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Allele-specific RNA-seq expression profiling of imprinted genes in mouse isogenic pluripotent states
Epigenetics & Chromatin volume 12, Article number: 14 (2019)
Genomic imprinting, resulting in parent-of-origin specific gene expression, plays a critical role in mammalian development. Here, we apply allele-specific RNA-seq on isogenic B6D2F1 mice to assay imprinted genes in tissues from early embryonic tissues between E3.5 and E7.25 and in pluripotent cell lines to evaluate maintenance of imprinted gene expression. For the cell lines, we include embryonic stem cells (ESCs) and epiblast stem cells (EpiSCs) derived from fertilized embryos and from embryos obtained after nuclear transfer (NT) or parthenogenetic activation (PGA).
As homozygous genomic regions of PGA-derived cells are not compatible with allele-specific RNA-seq, we developed an RNA-seq-based genotyping strategy allowing identification of informative heterozygous regions. Global analysis shows that proper imprinted gene expression as observed in embryonic tissues is largely lost in the ESC lines included in this study, which mainly consisted of female ESCs. Differentiation of ESC lines to embryoid bodies or NPCs does not restore monoallelic expression of imprinted genes, neither did reprogramming of the serum-cultured ESCs to the pluripotent ground state by the use of 2 kinase inhibitors. Fertilized EpiSC and EpiSC-NT lines largely maintain imprinted gene expression, as did EpiSC-PGA lines that show known paternally expressed genes being silent and known maternally expressed genes consistently showing doubled expression. Notably, two EpiSC-NT lines show aberrant silencing of Rian and Meg3, two critically imprinted genes in mouse iPSCs. With respect to female EpiSC, most of the lines displayed completely skewed X inactivation suggesting a (near) clonal origin.
Altogether, our analysis provides a comprehensive overview of imprinted gene expression in pluripotency and provides a benchmark to allow identification of cell lines that faithfully maintain imprinted gene expression and therefore retain full developmental potential.
Embryonic stem cells (ESCs) and epiblast stem cells (EpiSCs) are pluripotent cells derived from mouse embryos at embryonic day (E) E3.5–E4.5 and E6–E7, respectively [1,2,3,4]. Both ESCs and EpiSCs can be directed to differentiate into a wide variety of mature cell types. Therefore, these cells are important models for pre- and post-implantation embryonic development. As mouse ESCs are highly amenable to genetic manipulation and are capable of colonizing the germline of chimaeric mice , they are widely used for the generation of transgenic mice.
ESCs and EpiSCs are also promising tools in regenerative medicine due to their self-renewal and differentiation capacity. To avoid an allogeneic immune response during transplantation of these cells, a matching genotype between donor and recipient cells is of key importance. Induced pluripotency has emerged as one of the main methodologies to derive patient-specific pluripotent cells (iPSCs) by reprogramming of adult stem cells using defined reprogramming factors . Two more traditional approaches to obtain genetically matched pluripotent cells include somatic cell nuclear transfer (NT) and parthenogenetic activation (PGA) [7, 8]. During NT, the nucleus of a donor cell is introduced into an enucleated oocyte, after which ESC-NTs or EpiSCs-NTs are derived from the developing embryo. NT is a relatively inefficient process, but it has a significant advantage over transcription factor-mediated reprogramming in that ESC-NTs largely lack residual parental DNA methylation patterns as observed for iPSCs . PGA involves the stimulation of oocytes to produce diploid ESC-PGAs in the absence of fertilization . Although the genotype of the ESC-PGA cells is different from the female oocyte donor due to meiotic recombination occurring in the oocyte, subsequent matching of the ESC-PGAs based on the major histocompatibility complex antigens allows for engraftment of these cells in mouse recipients .
Genomic imprinting is an epigenetic process resulting in the expression of genes in a parent-of-origin specific manner. Current estimates suggest the presence of around 200 imprinted genes in mice, most of them having a role in development and social cognition [11, 12]. The importance of imprinting during embryonic development is further underpinned by the fact that androgenetic mice (derived from two paternal pronuclei) and gynogenetic mice (derived from two maternal pronuclei) are embryonic lethal [13, 14]. This is associated with the imprinted H19 and Dlk1-Dio3 loci, as manipulation of these loci enables the generation of viable and fertile bi-maternal mice . In line with this, proper imprinting of the Dlk1-Dio3 locus in iPSCs is essential for significant contribution to chimaeras and for the derivation of viable all-iPSC mice . Together, these studies show that maintenance of imprinted genes in embryonic cells is essential to retain full developmental potential. Additionally, loss of imprinting is highly correlated with transformation and cancer [17, 18], further highlighting the importance of assaying imprinted loci of cells.
Considering the critical role of imprinting in development , imprinted genes in ESC and EpiSC lines have been assayed in previous studies. This showed that mouse ESCs tend to lose imprinting upon prolonged culturing resulting in only few genes showing imprinted expression [20,21,22,23], while EpiSCs retain their imprints . In contrast to EpiSCs from normal fertilized mouse embryos, EpiSCs derived from NT were reported to show aberrant expression of imprinted genes . With regard to parthenogenesis, ESC-PGA cells were reported to show a surprisingly high efficiency in their contribution to chimaeric mice. This has been attributed to a loss of aberrant imprinting in the ESC-PGA cells , but this analysis was based on a very small number of loci. Interestingly, in human loss of imprinting in conventional ESCs is relatively rare, but occurs much more frequently in human ESC-NTs and iPSCs . Most of the studies assaying imprinted genes were performed on a restricted panel of imprinted genes, or in a non-allele-specific manner (i.e., without the knowledge if a gene is expressed from the maternally or paternally derived allele). There is only few studies that include profiling of imprinting in embryonic tissues, which is important for comparative analysis of ESC lines or EpiSC lines with their founder cells. Therefore, a global overview of allele-specific expression of imprinted genes, and how this contributes to the functionality of the ESCs and EpiSCs, is currently lacking.
To study the degree to which imprinted gene expression is preserved in pluripotent cell lines as compared to their founder mouse embryonic cells in vivo, we performed high-resolution allele-specific RNA-seq on embryonic tissues as well as on ESCs and EpiSCs derived after normal fertilization, NT and PGA. For the embryonic tissues, we focused on the very early embryonic stages (between E3.5 and E7.25 ) from which ESCs and EpiSCs are derived. Although two recent studies performed in-depth analysis of allelic gene expression during embryonic development, these studies focused on much later stages (from E9.5 onward) [11, 20]. Furthermore, previous studies were carried out on a variety of mouse genetic backgrounds, which is known to influence the efficiency of ESC derivation and to affect NT and PGA [29,30,31,32]. In our study, we make use of isogenic F1 hybrids of C57BL/6J (maternal) and DBA/2J (paternal) mouse inbred strains, previously also referred to as B6D2F1, B6D2 or BDF1. This cross has been shown to be relatively efficient in NT and PGA, and the use of isogenic tissues and cell lines eliminates complications arising from strain-specific differences in gene expression [30, 31, 33]. Importantly, when derived from hybrid F1 mice, ESC-PGAs contain a mosaic homo- and heterozygous genotype due to chromosomal crossover occurring in the parental B6D2F1 oocyte during meiosis . Since only the heterozygous part of the genome is compatible with allele-specific expression in RNA-seq, we developed a robust algorithm to reconstruct genotypes of cells derived by PGA based on the RNA-seq profiles we generated. This allowed us to gain insight in allele-specific gene expression of PGA cells at a global scale for the first time.
Experimental setup to study imprinted gene expression using allele-specific RNA-seq
To assay imprinted genes during embryogenesis and in the ESCs and EpiSCs, we made use of the B6D2F1 mouse model (Fig. 1a). Being an intercross of the genetically distant inbred strains C57BL/6J (referred to in this manuscript as B6) and DBA/2J (referred to as DBA2), the B6D2F1 mice contain around 5.2 million single nucleotide polymorphic sites (SNPs) genome-wide, corresponding to ~ 1 SNP per 520 bp [34,35,36,37]. These sites can be used to discriminate between expression from either the B6 maternally or the DBA2 paternally derived alleles in B6D2F1 cells by RNA-seq profiling.
To gain insight into the expression of imprinted genes in the developing B6D2F1 embryo in vivo, we used RNA-seq that we generated previously  on three replicate tissues of (1) Expanded Blastocyst: Inner cell mass (E3.5; “EBI”); (2) Epithelial cells of the pre-gastrulation Radially Symmetrical Epiblast (E6.25; “ERSE”); and (3) mid-gastrulation Anterior–Posterior Epiblast (E7.25; “APE”). Given the importance of imprinting in the placenta , Expanded Blastocyst: mural TrophEctoderm tissue (E3.5; “EB-TE”; two replicates), we performed RNA-seq profiling to provide insight into imprinted gene expression in the very early extraembryonic trophoblast lineage (Fig. 1a, b; Additional file 1: Table S1). With regard to the pluripotent cell lines, we performed RNA-seq on conventional B6D2F1 ESCs derived from fertilized embryos (two lines, referred to as ESC or fertilized ESC). We also included three ESC lines derived from nuclear transfer embryos generated using B6D2F1 mouse embryonic fibroblast donor nuclei (ESC-NT1) or B6D2F1 donor nuclei of cumulus cells (ESC-NT2 and ESC-NT3), as well as three ESC lines derived from PGA embryos generated using B6D2F1 oocytes (ESC-PGA) (Fig. 1a; Additional file 1: Table S1). Similarly, three replicas of fertilized B6D2F1 EpiSC lines and EpiSC lines derived from nuclear transfer embryos generated using a B6D2F1 donor nuclei of cumulus cells (EpiSC-NT) were included for RNA-seq (Fig. 1a; Additional file 1: Table S1). Lastly, we included two EpiSC-PGA lines which were previously described as EpiSC-NT lines , but which we here confirm to be of PGA origin (as further outlined below). As prolonged culture of ESCs has recently been associated with erosion of genomic imprints [39, 40], we used early passage ESCs (between passage 8 and 14; Additional file 1: Table S1). Using regular (non-allele specific) expression analysis of the RNA-seq, we validated the developmental stages of the samples and the RNA-seq profiling (Additional file 2: Fig. S1 and Fig. S2).
Genotyping of PGA samples using RNA-seq profiling
Cells containing a B6D2F1 genotype, such as the embryonic tissues and most of the cell lines included in this study, are compatible with global allele-specific analysis by RNA-seq. However, only part of the genome of B6D2F1-derived ESC-PGA lines can be utilized to call allele-specific expression using RNA-seq. During the most widely used method for PGA (resulting in p(MII)ESCs referred here as ESC-PGAs), metaphase II-halted oocytes are stimulated to proceed through meiosis in the absence of fertilization. Blocking the extrusion of the second polar body results in a diploid parthenote. Subsequent chemical activation toward further development allows for derivation of ESC-PGAs . Metaphase II oocytes have already undergone meiotic recombination, and therefore, the genotype of the subsequent ESC-PGA cells is different from the female oocyte donor: B6D2F1 ESC-PGA lines are homozygous proximal to the centromere, while they are heterozygous at distal regions for most chromosomes . The homozygous parts of the genome of the PGA lines lack SNPs required for allele-specific RNA-seq analysis. Thus, only the heterozygous parts of the genome of PGA lines can be utilized to call allele-specific expression. To identify these heterozygous parts, we used the allele-specific RNA-seq mapping counts over the B6/DBA2 polymorphic sites to calculate the relative contribution of either B6 (maternal) or DBA2 (paternal) in genomic bins, on which we applied a moving average over the individual chromosomes. Since we expect only 1 or few breakpoints per chromosome, we first analyzed at a low resolution to gain a comprehensive overview. Using a low-resolution binning size of 5 Mb (Fig. 1c), this RNA-seq SNP genotyping very clearly shows a pattern of recombination in all the ESC-PGAs. In contrast, the fertilized ESCs and ESC-NTs show a full heterozygous F1 genotype as expected (Fig. 1c, Additional file 2: Fig. S3). To better estimate the chromosomal breakpoints, we increased our resolution to 1 MB (Additional file 3: Table S2). Plotting of the allelic ratios of genes present within the parts of the genome in ESC-PGAs annotated as either B6, heterozygous or DBA2 shows the expected pattern (Fig. 1d). Genes present in the heterozygous part of the genome are largely expressed from both alleles, while alleles of genes present in the homozygous part of the genome cannot be discriminated. Therefore, these genes show a (near) complete bias according to their genotype. Together, this allowed us to only include genes present in the informative heterozygous parts in the genome (Additional file 3: Table S2) for further allele-specific RNA-seq analysis of the PGA lines.
To verify the genotype of the remaining embryonic tissues and EpiSC samples, we applied the same RNA-seq-based genotyping strategy. The in vivo embryonic tissues showed the expected heterozygous F1 genotype, except for the maternal B6 bias on the X chromosome which reflects the presence of male embryos in the pooled male and female embryos samples (Additional file 2: Fig. S4). All fertilized EpiSC and three of the EpiSC-NT lines also showed the expected F1 genotype as expected (Additional file 2: Fig. S5). Additionally, we identified two parthenogenetic EpiSC lines (Fig. 1e). These EpiSC-PGA lines have originally been reported as being derived after transfer of B6D2F1 donor nuclei of cumulus cells . Nevertheless, they show a clear mosaic genotype, not matching the expected F1 genotype as observed for the other three EpiSC-NT lines (Additional file 2: Fig. S5). Instead, these two EpiSC lines show a recombination pattern unique to PGA (Fig. 1e; cf Fig. 1c). To verify these two unexpected genotypes, we performed regular genotyping using genomic DNA, yielding results nearly identical to the RNA-seq genotyping, both at 5 MB resolution (Additional file 2: Fig. S6; cf Additional file 2: Fig. S5) and at 1 MB resolution (Additional file 4: Table S3). This further confirms the mosaic PGA-specific genotypes for both EpiSC lines, and these lines were included in this study accordingly. The accidental isolation of PGA-derived cells during nuclear transfer experiments is a serious concern  and is likely due to improper enucleation preceding the nuclear transfer resulting in PGA of the original nucleus after stimulation of the oocyte.
Finally, to validate our RNA-seq-based genotyping approach, we made further use of the direct comparison with regular DNA-based genotyping. At 1 MB resolution, the RNA-seq genotyping algorithm identified the exact same position of genomic breakpoints in 56% (23 of 41) of the cases as compared to DNA-based genotyping, while it shows an average accuracy of 2.9 MB in the EpiSC-PGAs (Additional file 4: Table S3). Notably, our RNA-seq-based genotyping algorithm also allows for identification of genomic alterations (Additional file 2: Fig. S8). Together, this shows the accuracy and sensitivity of our RNA-seq-based genotyping approach and further confirms our detection of the heterozygous parts of the PGA cell lines to be used in further analysis for imprinting.
Allele-specific expression of imprinted genes in embryonic tissues
For allele-specific expression, we applied a computational pipeline for unbiased allele-specific quantification of transcripts that we developed previously, obtaining quantitative allelic information for up ~ 5000 genes per sample (Additional file 2: Fig. S9) . On average, individual genes show equal expression from the B6- and DBA2-derived alleles in all samples, including in the heterozygous chromosomal regions of the PGA-derived lines, with only a small number of genes showing allelic bias in expression toward B6 or DBA2 as would be expected for imprinted genes (Additional file 2: Fig. S9). To determine allele-specific expression of imprinted genes, we compiled a list of 98 imprinted genes based on available data present in the two most widely used imprinting databases (www.geneimprint.com  and www.har.mrc.ac.uk/research/genomic_imprinting/ ) and in a recent comprehensive survey on imprinted genes over a large number of developmental stages and tissues  (Additional file 5: Table S4). Of these 98 genes, 20 genes had sufficient RNA-seq coverage over polymorphic sites (> 9 counts ) to quantify allele-specific expression in at least one of the samples included in our analysis (Fig. 2a; Additional file 6: Table S5). Notably, in order to obtain reliable allelic ratios, we only included a gene of an individual sample in our analysis if it showed consistent B6 versus DBA2 allelic ratios over all polymorphic sites that are present within the gene body (standard error of the mean < 0.15; see Methods section for more details). An overview of the RNA-seq data of all B6D2F1 samples over a selection of the imprinted genes is provided in Additional file 2: Fig. S10.
For the in vivo embryonic tissues, we obtained allelic information for 16 autosomal genes and 1 X-linked gene (Xist), while expression of Peg12, Peg10 and Plagl1 was too low in any of the samples to reliably call allelic ratios (Fig. 2a). From the 16 autosomal imprinted genes covered, 13 (81%) follow a pattern of (nearly) full imprinting in all samples for which we obtained allelic ratios (Fig. 2a). Another two genes (13%) show a strong parental bias (> 80%) toward either the maternal (H13) or the paternal allele (Phf17), in line with later embryonic stages or tissues for which these genes consistently show an allelic bias but not complete monoallelic expression [11, 45]. Interestingly, the imprinting pattern of the EB-TE trophectoderm samples was nearly identical to that observed for the other embryonic tissues, including the EBI embryoblast tissues obtained from the same embryonic stage E3.5. Previous studies focusing on mouse embryonic tissues at later stages (E9.5 and later) showed that imprinting of Phf17 was restricted to the mouse placenta and yolk salk . Here, we find that Phf17 also consistently shows allelic expression bias in early mouse embryonic inner cell mass tissue. This suggests that imprinting of Phf17 outside extra-embryonic tissue is lost shortly after the blastocyst stage. Ube3a, the only gene that consistently shows biallelic expression at all embryonic stages profiled, was originally identified as being imprinted in brain . Apparently, this gene is not imprinted during embryonic development. Finally, it should be noted that the individual in vivo embryonic tissues originate from a pool of male and female embryos, which complicates interpretation of allelic ratios of the X-linked gene Xist for these samples. Together, these results show that we robustly detect imprinting in B6D2F1 early (extra-)embryonic tissue for nearly all known imprinted genes covered in our transcriptomes, extending previous observations of highly conserved imprinting pattern across tissues  to early embryonic and extra-embryonic tissues.
Allele-specific expression of imprinted genes in ESCs
Most of the ESC lines, either fertilized ESCs, ESC-NTs or ESC-PGAs, show a very different pattern of imprinted gene expression as compared to the in vivo embryonic tissues, including the E3.5 inner cell mass tissue that they originate from (Fig. 2a). In the fertilized ESCs, 11 out of the 13 imprinted genes that contain sufficient coverage show biallelic expression in both ESC lines (Fig. 2a; Additional file 6: Table S5). Considering the pattern observed in the embryonic tissues, this strongly suggests that imprinted gene expression in fertilized ESCs is lost during outgrowth or maintenance of ESCs. In line, two out of three ESC-NT lines (ESC-NT2 and ESC-NT3) and all three ESC-PGA lines show biallelic expression for the majority of imprinted genes that contain sufficient coverage (11 out of 16 autosomal genes). In contrast to a previous study , we find monoallelic (imprinted) expression of Igf2r in the ESCs. This difference in allelic bias of Igf2r might be caused by a difference in mouse strains used, as we also find monoallelic expression of Igf2r in the B6D2F1 embryonic tissues (Fig. 2a). To gain further insight into the loss of imprinted gene expression, we performed allele-specific ChIP-Seq profiling of the posttranslational histone modifications H3K4me3 and H3K27me3, epigenetic marks associated with gene activity or gene silencing, respectively . In line with the biallelic expression of imprinted genes in ESCs, the imprinted monoallelic presence of H3K4me3 and H3K27me3 is largely lost in B6D2F1 fertilized ESCs, ESC-NTs or ESC-PGAs (Additional file 2: Fig. S11 and Fig. S12). Interestingly, one NT-derived ESC line (ESC-NT1) showed an allelic bias of > 80% for most of the genes which were covered by the allele-specific RNA-seq (Snrpn/Snurf, D7Ertd715e, Rian, Meg3 and Igf2r), similar to the monoallelic expression observed in the embryonic tissues (Fig. 2a). This suggests that the loss of monoallelic expression of imprinted genes observed for ESC-NT2 and ESC-NT3 is likely associated with the derivation and maintenance of the ESCs rather than with the nuclear transfer per se. Furthermore, this shows that occasionally ESC lines (largely) retain imprinted gene expression, in line with previous observations on the variation of imprinted gene expression in ESCs .
To investigate whether the observed loss of imprinted gene expression was B6D2F1-strain specific, we analyzed allele-specific RNA-seq profiles from fertilized ESCs originating from a cross between mouse strains Mus musculus (M.m.) domesticus 129/SV-Jae (129) and M.m. castaneus (Cast) (129xCast) that we generated previously (Additional file 2: Fig. S13; ESC 129CastF1 ). Similar to the B6D2F1 ESCs, almost all imprinted genes were biallelically expressed [< 80% allelic bias for 12 out of 13 genes (92%)], showing that the observed loss of imprinting in ESCs is independent of the genotype. We next asked whether the loss of imprinted gene expression is dependent on culture conditions. The B6D2F1 and 129CastF1 ESC lines are maintained in the presence of serum [either supplemented with LIF (129CastF1 ESCs) or on feeder cells (B6D2F1 ESCs)]. It has been shown that culturing ESCs in serum-free minimal media containing 2 kinase inhibitors (“2i”) maintains or reverts ESCs toward the ground state of pluripotency, resulting in an ESC transcriptome resembling the early in vivo tissue of the inner cell mass [49,50,51,52]. We therefore adapted the 129CastF1 ESCs to 2i media (> 12 days) and assayed imprinted genes by allele-specific RNA-seq. Adaptation to 2i did not result in major changes in the ratio of allelic expression of imprinted genes, and the majority of imprinted genes (17/19; 89%) still showed biallelic expression (Additional file 2: Fig. S13; ESC 129CastF1_2i). These results show the strong tendency of ESCs to lose imprinted gene expression.
The observed biallelic expression of imprinted genes in ESCs is likely to be the consequence of (1) a loss of epigenetic imprints at the imprinted control regions (ICRs); and/or (2) a relaxation in the ESCs to “read” these epigenetic imprints. Also, for some imprinted genes monoallelic expression only arises during development . To further investigate these issues, we differentiated ESCs to embryoid bodies (EBs) or neural progenitor cells (NPCs). EB differentiation of either 2i ESCs or serum ESCs did not change the biallelic expression of imprinted genes as observed in the undifferentiated ESCs (Fig. 2b; Additional file 2: Fig. S14). Most of the imprinted genes also remained biallelically expressed in the NPCs generated from the ESCs (Fig. 2b). Together, this shows that ESCs tend to lose imprinting and that imprints are not reinstalled upon differentiation of the ESCs toward developmentally more advanced cell types.
Allele-specific expression of imprinted genes in EpiSCs
In contrast to ESCs, fertilized EpiSCs and EpiSC-NTs largely retain allele-specific expression of imprinted genes as compared with the in vivo embryonic tissues, including their in vivo counterparts ERSE and APE (Fig. 2a). A total of 10 of the 15 genes that were imprinted or biased in the embryonic tissues show full imprinting in EpiSC and EpiSC-NT lines, while another two genes (Atp10a and H13) show a strong allelic bias. Additionally, Peg12, Peg10 and Plagl1, for which we obtained insufficient coverage of the RNA-seq in the embryonic tissues, show imprinted gene expression in the fertilized EpiSC and EpiSC-NT lines. Mcts2, Asb4 and Phf17 lost imprinted gene expression in the fertilized EpiSCs and EpiSC-NTs as compared to the embryonic tissues (Fig. 2a). Notably, Rian and Meg3 (also known as Gtl2) have very high coverage in the fertilized EpiSCs and in EpiSC-NT2, but lack sufficient coverage of the RNA-seq to determine allelic bias in the EpiSC-NT1 and EpiSC-NT3 (Fig. 2a; Additional file 6: Table S5). In line, expression of Rian and Meg3 is nearly absent in EpiSC-NT1 and EpiSC-NT3, in contrast to the high expression observed in the other EpiSC lines (Fig. 3a, b). This is reminiscent of the aberrant Rian and Meg3 silencing in iPSC lines, for which proper imprinting of both genes is essential to retain full developmental potential .
To study the effect of nuclear transfer at the total expression level of imprinted genes, we performed regular (non-allele specific) gene expression analysis of fertilized EpiSCs and EpiSC-NTs. Although only few imprinted genes were present among all differentially expressed genes (adjusted p value < 0.05; Additional file 7: Table S6), the imprinted genes Igf2 and Cdkn1c (p57) were among the most significant (Additional file 2: Fig. S16; Additional file 7: Table S6). Imprinting of Igf2 is relatively unstable  and loss of imprinting might therefore partly underlie the increased expression of Igf2 in the EpiSC-NT lines. However, Igf2 as well as Cdkn1c do not contain SNPs in the B6D2F1 genotype to confirm loss of imprinting in the current study. Functionally, Igf2 and Cdkn1c are important in control of cell proliferation and development . As such, misregulation of these genes as observed in EpiSC-NT cells might provide a selective growth advantage, as previously suggested for Igf2 in human ESCs .
Calling of allele-specific bias on the B6D2F1 heterozygous part of the EpiSC-PGA genomes clearly shows a (near) complete loss of monoallelic expression of imprinted genes, in line with the absence of paternal imprinting (Fig. 2a). For known paternally expressed genes included in Fig. 2a, this resulted in an average drop in expression of > fourfold in the EpiSC-PGAs (Fig. 3b, c). Seven of the twelve paternal imprinted genes as shown in Fig. 2a show a significant change in expression (adjusted p value < 0.05; Additional file 7: Table S6). The same trend was observed for other well-known paternally imprinted genes for which the B6D2F1 genotype does not have allelic coverage, such as Peg3 (Fig. 3c). In line, of all 77 genes that are significantly downregulated in EpiSC-PGAs as compared to fertilized EpiSCs (adjusted p value < 0.05), the top most downregulated genes are known imprinted genes (Additional file 7: Table S6). In contrast to paternally expressed genes, maternally expressed genes generally showed a minor (but occasional significant) upregulation in the EpiSC-PGAs. While no maternally expressed genes were significantly downregulated, three were significantly upregulated (out of a total of 47 upregulated genes (adjusted p value < 0.05) between EpiSC-PGAs and fertilized EpiSCs (Additional file 7: Table S6; Fig. 3c). The observed ~ twofold increase is in agreement with the lack of a silent, imprinted paternal allele in the EpiSC-PGAs. To gain further insight in the regulation of imprinted genes in EpiSC-PGAs, we performed global DNA methylation profiling using MethylCap-Seq. Analysis of the ICRs belonging to the imprinted genes in the EpiSC-PGAs showed (1) a loss of DNA methylation on the ICR for paternally imprinted (maternally expressed) genes; and (2) a twofold gain of DNA methylation on the ICR for maternally imprinted (paternally expressed) genes (Additional file 2: Fig. S17). Altogether, these results indicate that both alleles in the EpiSC-PGAs contain a maternal imprinting pattern, and therefore, imprinting in the EpiSC-PGAs is correctly maintained as both alleles are maternally derived. Interestingly, these observations in EpiSC-PGAs are different from ESC-PGAs, which tend to show a loss of genomic DNA methylation imprints (Fig. 2a) .
X inactivation in EpiSC: EpiSC clonality
For most of the EpiSC lines, we noticed a full allelic bias in Xist expression associated with X inactivation (Fig. 2a). Random X inactivation (rXCI) occurs in the mouse between E5.5 and E7.5 during which individual female cells in the epiblast randomly inactivate one of the two X chromosomes, which is stably propagated to daughter cells . Consequently, female founder cells of EpiSCs have usually undergone rXCI and EpiSC lines contain an active (Xa) as well as an inactive X chromosome (Xi) . The noncoding RNA Xist is required for X inactivation and is specifically expressed from the Xi [58, 59]. Considering that B6- and DBA2-derived X chromosomes have an equal chance to be inactivated during rXCI [as both contain the same X-controlling element “b” locus (Xceb)] , the ratio of female B6D2F1 cells within the epiblast that contain either an inactivated B6- or DBA2-derived X chromosome is around 0.5. Similarly, in case (some) founder cells initiate rXCI during derivation or early culturing of the EpiSC lines, the ratio is also around 0.5. Therefore, we expected that half of the cells within female EpiSC lines would contain an inactive B6-derived X chromosome, while the other half of the cells would contain an inactive DBA2-derived one. At population level of stable EpiSC lines, this would be represented by an equal allelic expression of Xist from the B6- and DBA2-derived X chromosome. However, most of the EpiSC lines that we included in our analysis show a full allelic bias of Xist (Fig. 2a).
To further investigate the allelic bias of Xist, we examined expression of Xist and other X-linked genes. As expected, Xist is highly expressed in all six female EpiSC lines, but not in the seven female ESC lines as the female ESC founder cells have not yet undergone rXCI. Also, Xist expression is absent in the single male ESC and the two male EpiSC lines that were included in this study (Fig. 4a, b). Independent of their origin (fertilized EpiSC, EpiSC-NT or EpiSC-PGA), five of the six female EpiSC lines showed full bias in allelic expression of Xist, with expression from the B6-derived X chromosome being observed in most of the EpiSC lines (Fig. 4b). In line with the allelic bias of Xist in these five EpiSC lines, we observed a (near) monoallelic expression of the far majority of X-linked genes reciprocal to the allelic ratio of Xist (Fig. 4c, d). EpiSC-NT3 is the only line which showed equal expression of X-linked genes from both B6 and DBA2 alleles (Fig. 4c, d), including Xist (Fig. 4b). We observed biallelic expression and an increased global expression of X-linked genes in the female ESC lines (except for ESC-NT2), in keeping with the presence of two active X chromosomes in ESCs (Fig. 4c, e; Additional file 2: Fig. S18a). ESC-NT1 is male and, therefore, only shows B6-derived RNA-seq signals from the X chromosome (Fig. 4c; Additional file 2: Fig. S18a). As female ESCs are prone to the loss of one X chromosome, we analyzed the karyotype of the ESC lines as a control (Additional file 1: Table S1; ). This showed that the ESC-NT2 line is largely X0, explaining the allelic bias and the reduction in X-linked gene expression for ESC-NT2 (Fig. 4c, e; Additional file 2: Fig. S18a). Together, our results indicate that 5 of the 6 female EpiSC lines show a complete skewing of XCI, with the DBA2-derived X chromosome being active (Xa) in 4 EpiSC lines and the B6-derived X chromosome being active (Xa) in the EpiSC-PGA2 line. The most likely explanation for the observed skewing is that the EpiSC lines are (largely) of clonal origin, as further outlined in the discussion. Only occasionally, EpiSC lines are derived from a mixed population of cells, as is the case for the EpiSC-NT3 line which consists of a mixed population of cells containing either an inactive B6- or an inactive DBA2-derived X chromosome. Since derivation of the EpiSCs was performed using standard protocols [1, 25, 62], clonality is likely to be a common phenomenon among EpiSC lines.
Genomic imprinting is critical for proper development, as alterations in imprinting gene dosage in early embryos are often associated with development defects (reviewed by Peters ). In line, we demonstrate that parent-specific monoallelic expression of imprinted genes is intact in pre- and post-implantation embryos. Within in vitro cultures, maintenance of imprinted gene expression in embryonic cells is essential to retain full developmental potential [13,14,15,16]. Considering this critical role, previous studies have assayed allelic bias of imprinted gene expression in fertilized ESCs and EpiSCs [24, 54, 64, 65]. However, most of these studies were performed on a restricted panel of imprinted genes by targeted sequencing of expressed SNPs in cDNA. In case of NT and PGA, allelic bias of imprinted genes in mouse ESCs or EpiSCs has mainly been assayed by non-allele-specific DNA methylation profiling, either at a genome-wide scale or using more targeted approaches [25, 26, 66,67,68]. Information on allele-specific expression of imprinted genes in NT and PGA lines is largely absent. Importantly, most of the studies investigating imprinting in ESCs and EpiSCs did not include analysis of the embryonic tissues and therefore cannot discriminate between lack of imprinting in embryonic tissue versus loss (or gain) of imprinting during derivation of ESCs and/or EpiSCs. The analysis performed here therefore extends previous studies by providing a comprehensive overview of imprinted gene expression in pluripotency. The use of isogenic tissues and cell lines in the current study allows for direct comparisons between pluripotent cells and as such provides a benchmark to allow identification of cell lines that faithfully maintain imprinted gene expression. A notable example showing the power of the dataset we generated represents the known imprinted gene Ube3a, for which the biallelic expression observed in the ESC and EpiSC lines is not due to a loss of imprinting, but due to absence of imprinting in the embryonic tissue of origin. It should be noted that the B6D2F1 hybrid mouse strain which we used for our analysis contains relatively few polymorphic sites (~ 5.2 million) as compared to other hybrid mouse crosses that are often used to study allelic gene expression (e.g., a 129xCast hybrid mouse strain contains ~ 20.8 million polymorphic sites ). Therefore, the coverage over imprinted genes to be included in our analysis is relatively low. However, the B6D2F1 genotype has been shown to be superior over other mouse strains in nuclear transfer and PGA (both in efficiency and in the development and quality of the embryos or pluripotent cell lines [31, 33, 69, 70]), which we used as main criteria for selecting the B6D2F1 strain for the current study.
To facilitate global allele-specific expression analysis of PGA-derived cell lines, we performed RNA-seq-based genotyping to determine the positions of genomic crossover. A direct comparison with regular DNA genotyping shows that the algorithm is robust and accurate in detecting chromosomal breakpoints. Despite the fact our RNA-seq genotyping method lacks resolution in “gene deserts” because of the absence of coverage of the RNA-seq, the position of the genomic breakpoints called from the RNA-seq exactly matches the DNA-based genotyping in over half of the cases. Previous studies reporting chromosomal breakpoints in human or mouse PGA p(MII)ESC lines used either (1) DNA genotyping of p(MII)ESCs derived from an F1 mouse cross similar to the DNA genotyping performed here used as a control (Additional file 2: Fig. S6) ; (2) the signature of heterozygous and homozygous signals over SNPs as obtained by DNA-based genotyping  or by RNA-seq . The latter method takes advantage of the fact that p(MII)ES cells retain pericentromeric homozygosity but show distal regions of heterozygosity due to crossing-over in the oocyte [10, 41] and is particularly powerful if parental genotypes are unknown. However, in the absence of parental genotypes, this method cannot discriminate between homozygotic parts of the genome being derived from either the paternal or the maternal parent of the oocyte donor. By taking advantage of mouse inbred strains and the known genomes of the B6 and DBA2 mouse strains, our method enables accurate characterization of the genotype of the PGA-derived ESC and EpiSC lines. This allowed us to comprehensively show for the first time that twofold upregulation of known maternally expressed genes in PGA-derived cells is caused by the activation of the paternal allele (which lacks the imprint in the PGA lines), as these genes show an equal biallelic expression in our allele-specific analysis. Next to its use for PGA lines, our RNA-seq-based genotyping method is applicable to F2 hybrids and subsequent generations of crossbreeds, as well as backcrosses, of (mouse) inbred strains. As such, genotypic information can conveniently be obtained for studies where gene expression analysis by RNA-seq has been performed.
Our genome-wide study shows that mouse ESCs tend to lose imprinting, while EpiSCs retain their imprints, similar to previous observations on a restricted panel of imprinted genes . In contrast to fertilized EpiSCs, EpiSCs derived after NT were reported to show aberrant expression of a large number of imprinted genes . However, this conclusion was largely based on analyses of EpiSC lines that accidentally originated from parthenogenesis (instead of NT), which indeed show loss of imprinted gene expression (Fig. 2a). Our current analyses, including proper genotyping as control for the nuclear transfer, show that allelic expression of imprinted genes is largely retained in EpiSC-NTs (Figs. 2, 3). Despite the similarity of EpiSC-NT lines to embryonic tissues or fertilized EpiSCs, the Dlk1-Dio3 imprinted gene cluster is notably different in expression. In this cluster, Rian and Meg3 are robustly expressed in the fertilized EpiSC lines and one EpiSC-NT line, while expression is absent in two EpiSC-NT lines. Aberrant silencing of Rian and Meg3 has previously been observed in iPSC lines. In contrast to iPSC lines with normal expression of Rian and Meg3, iPSC lines in which these genes are silenced contribute poorly to chimaeric mice and fail to support the development of entirely iPSC-derived mice . The misexpression in the Dlk1-Dio3 imprinted gene cluster has been associated with transcription factor-mediated reprogramming, as it has not been observed in other methods of reprogramming thus far. Although we only profiled a small sample set, our data suggest that silencing of Rian and Meg3 is a more general phenomenon in reprogramming and can also occur during nuclear transfer. In iPSCs, the presence of ascorbic acid during reprogramming prevents misexpression of the Dlk1-Dio3 cluster . It will be interesting to test whether the presence of ascorbic acid after nuclear transfer can similarly preserve a normal imprinting status at the Dlk1-Dio3 gene cluster in EpiSC-NTs. If so, this might underlie the beneficial effect of ascorbic acid on mouse nuclear transfer as reported recently .
EpiSCs are derived during in vitro outgrowth of post-implantation epiblasts on which colonies emerge. In order to obtain pure EpiSCs and get rid of the remainder of the mouse epiblast outgrowth, these EpiSC colonies are picked after a week of epiblast culture to be further expanded toward EpiSC lines [1, 25, 62]. It has been observed that the EpiSCs colonies emerging from the epiblast are generally localized close together  (Alice Jouneau, personal communication). The close concentration of EpiSC colonies might suggest a clonal origin of EpiSC lines. rXCI randomly occurs in early post-implantation female embryos (generally before collection of the epiblast for EpiSC derivation) and is stably maintained afterward. Therefore, full skewing of XCI is widely used to assess clonality . The use of mouse F1 hybrid in combination with allele-specific RNA-seq allows for convenient detection of skewing, which otherwise often remains unnoticed. Our analysis shows that five of the six female EpiSC lines as profiled here show a complete skewing of XCI (Fig. 4). Therefore, this strongly suggests that these EpiSC lines are clonal, although we cannot exclude that the EpiSC lines originate from two or more founder cells that inactivated the same copy of the X chromosome. In line, the EpiSC colonies emerging from the epiblast during derivation of the EpiSC-NT3 line (which showed biallelic expression of Xist) were spread over a much larger area of the epiblast, explaining the EpiSC-NT3 line not being clonal. Altogether, the skewed XCI observed for the majority of EpiSC lines included in the current study suggests that these lines originate from a single cell of the early epiblast that divided further during development and gave rise to multiple colonies during in vitro outgrowth, which were picked for further expansion. The discrete areas showing outgrowth of EpiSC colonies might reflect regions of the epiblast that are more permissive toward EpiSC derivation than other areas. This could be due to the heterogeneous nature of the epiblast, which contains a range of cells with different commitment toward the various embryonic lineages , and of which only a few cells might be susceptible for outgrowth toward EpiSC lines.
Collectively our observations yield insight into global imprinted gene expression patterns during early embryonic development, and the cell lines derived from these early embryonic stages. Thereby, it provides a benchmark to allow identification of cell lines that faithfully maintain imprinted gene expression and therefore retain full developmental potential. Our study provides further evidence that, in contrast to EpiSCs, ESCs are prone to lose allelic expression of imprinted genes. It should be noted that the majority of ES cell lines included in this study were female, which are more susceptible to losing imprinting as compared to male ESCs due to their hypomethylated state . Also, it has been shown that prolonged in vitro culture of ESCs in serum containing media perturbs the maintenance of methylation imprints that control the allelic expression of imprinted genes [20,21,22,23], which for the ESC lines included in this study largely occurred within 20–30 days (8–14 passages; Additional file 1: Table S1). EpiSC lines as included in this study were cultured in serum-free medium (CDM ), which might facilitate the maintenance of imprinting in EpiSCs, for both male and female EpiSCs (Additional file 1: Table S1). In recent years, the use of kinase inhibitors (“2i”) within a serum-free defined medium has enabled derivation of mouse ground state pluripotent ESCs that more faithfully reflect early in vivo cells of the inner cell mass as compared to conventional ESCs cultures in serum and LIF [49,50,51,52, 78]. Despite the fact that adaptation of conventional ESCs to 2i allows for reprogramming of the epigenome to the ground state [50, 79, 80], it does not rescue the imprinting pattern of founder embryonic cells (Additional file 2: Fig. S13). This is in line with very recent studies showing that the use of 2i-conditions results in erosion of DNA methylation at most ICRs in ESCs [39, 40]. Importantly, we show that the allelic expression of imprinted genes is not restored upon differentiation of the ESCs, while also conversion of ESCs to EpiSCs does not restore imprinting patterns . Together, this strongly suggests that the loss of imprinted gene expression as observed in ESCs is caused by an irreversible loss of epigenetic imprints (i.e., a loss of DNA methylation (or other epigenetic marks ) at ICRs), rather than a relaxation in ESCs to translate these imprints to monoallelic expression.
Based on a wide variety of features (including transcriptome, epigenome and signaling responses), conventional human ESCs are considered to be the human equivalent of mouse EpiSCs [1, 4, 82]. In line, imprinting in human ESCs has been considered to be relatively stable. Recently, various groups have reported the derivation of human ESCs in a naive state akin to mouse ESCs [83,84,85,86,87]. The DNA hypomethylation reported at ICRs in these naive human ESCs suggests that monoallelic expression of imprinted genes is lost, similar to mouse ESCs [88, 89]. However, only few ICRs are well documented, and it has been shown that imprinting can rely on other epigenetic features besides DNA methylation [27, 81, 90]. Therefore, global analysis of imprinted genes by allele-specific RNA-seq in naive human ESCs will be highly informative to further evaluate loss of imprinted gene expression. Also, such profiling will be helpful in the future to further evaluate optimized culture conditions for naive mouse and human ESCs.
In the current study, we performed allele-specific RNA-seq of early (extra-)embryonic tissues and various types of pluripotent cell lines in vitro using an isogenic mouse F1 genotype, allowing genome-wide comparative analysis of imprinting. This shows that mouse ESCs tend to lose imprinting during outgrowth, while EpiSCs largely retain imprints, even if they are derived from nuclear transfer embryos. Profiling of EpiSC-PGAs shows that known maternally imprinted (paternally expressed) genes are silent, while known paternally imprinted (maternally expressed) genes consistently have a twofold higher expression level in EpiSC-PGAs as compared to their fertilized counterparts. The upregulation of known maternally expressed genes in the EpiSC-PGAs is caused by the absence of the imprinted, silent paternal allele in the EpiSC-PGAs, as these genes show an equal biallelic expression in our allele-specific analysis. Differentiation of ESCs, as well as reversion of ESCs to the pluripotent ground state, does not restore monoallelic expression of imprinted genes, strongly suggesting that the loss of imprinting in ESCs is irreversible. This has important implications for the use of these cells in further applications, as correct imprinting is critical to retain full developmental potential. Together, our analysis provides a comprehensive overview of imprinted gene expression in pluripotency and provides a benchmark to allow identification of pluripotent cell lines that faithfully maintain imprinted gene expression.
Derivation and maintenance of B6D2F1 ESC and EpiSC lines is described in Kobolak et al.  and Maruotti et al. , respectively. B6D2F1 ESCs were cultured on mouse embryonic fibroblast (MEF) feeder cells in media containing fetal calf serum (FCS). B6D2F1 EpiSCs were maintained feeder-free in chemically defined medium (CDM; ) complemented with 20 ng/ml activin A and 12 ng/ml fibroblast growth factor 2 (FGF2), in the absence of fetal bovine serum. In order to get rid of the MEFs for RNA-seq or ChIP-Seq, ESCs were replated on 6 cm feeder-free culture dishes and incubated at 37 °C. After 30 min, floating ESCs were harvested, washed with PBS and collected. An extensive overview of the cell lines used in this study, including sex, passage number, karyotyping, genotype information and names as use previous studies (if the cell lines were derived before) is present in Additional file 1: Table S1. None of the ESC or EpiSC cell lines have tested for their capacity to form teratomas, for their contribution toward chimaeric mice or for their capacity to form completely ES cell-derived fetuses (/germline transmission).
Embryo sample preparation and RNA-seq
The embryo sample preparation and RNA-seq has been described previously . In short, for preimplantation B6D2F1 mouse embryonic tissues, samples were collected by flushing embryos out of the uterus. For isolation of the E3.5 inner cell mass (ICM) of the expanded blastocyst (Expanded Blastocyst: Inner cell mass; “EBI”), ICMs were isolated from E3.5 B6D2F1 blastocysts by immunosurgery . After removal of the zona pellucida by incubation in acid Tyrode’s solution (Sigma-Aldrich), blastocysts were collected in KSOM (potassium-supplemented simplex optimized medium) containing 20% anti-mouse serum (Sigma-Aldrich) for 30 min at 37 °C. After 3 times washing in KSOM, blastocysts were incubated for 5–10 min in guinea pig complement (Calbiochem-Merck) diluted 1:10 with KSOM. After serial washings, the embryos were cultured for 30–60 min in KSOM. Finally, the ICMs were pipetted through a thin micropipette in order to mechanically remove the lysed trophectoderm cells. For isolation of E3.5 mural trophectoderm (Expanded Blastocyst: mural TrophEctoderm; “EB-TE”), laser-assisted (XY Clone, Hamilton Thorne, UK) ICM isolation was performed on intact, expanded E3.5 blastocysts as previously described . The embryos were secured by two holding pipettes with the ICM being positioned at 9 o’clock. Once adequate tension was established, several (about 10–15) infrared laser pulses (300mW, 1 ms) were fired to section the blastocyst into two uneven portions, of which one consisted of the mural trophectoderm cells.
Tissues from post-implantation stages were obtained as in Brons et al. . Briefly, pregnant female animals were euthanized by cervical dislocation. After surgical removal of the uterine horns, decidua was removed using sharp fine edge forceps. After removing the embryo from the decidua, the Reichert’s membrane was torn out from the embryo and the ectoplacental cone trophoblast tissue was sliced out. The visceral endoderm was removed from the embryo after incubation in cell dissociation buffer (Invitrogen). At E6.25, radially symmetrical epiblast was dissected from the extra-embryonic ectoderm and collected as clean epiblast (Epithelial Radially Symmetrical Epiblast; “ERSE”). At E7.25, the anterior–posterior epiblast was collected with its attached mesodermal wings (Anterior–Posterior Epiblast; “APE”) but without any extraembryonic mesoderm tissues. Samples were harvested into TriZol and snap-frozen. RNA was isolated using the PureLink™ RNA Micro Kit (Invitrogen). 100 pg RNA of the embryo samples was used to prepare cDNA according to the SMARTer (Clontech) method and sequenced paired-end on Illumina Hi-Seq 2000. All RNA-seq of the embryonic tissue samples (FASTQ and BedGraph or wig files) are present in the NCBI GEO SuperSeries GSE53387. An overview of this data is present in Additional file 1: Table S1.
RNA isolation and cDNA synthesis of ESCs and EpiSCs
RNA was harvested (1) for the ESCs using the RNeasy Plus Mini Kit (QIAGEN) including gDNA eliminator treatment according to instructions of the manufacturer; and (2) for the EpiSCs using TriZol (Invitrogen) according to the manufacturer’s recommendations. Total RNA (100 μg) was subjected to two rounds of poly(A) selection (Oligotex mRNA Mini Kit; QIAGEN), followed by DNaseI treatment (QIAGEN). mRNA (100–200 ng) was fragmented by hydrolysis (5 × fragmentation buffer: 200 mM Tris acetate, pH8.2, 500 mM potassium acetate and 150 mM magnesium acetate) at 94 °C for 90 s and purified (RNAeasy Minelute Kit; QIAGEN). cDNA was synthesized using 5 μg random hexamers by Superscript III Reverse Transcriptase (Invitrogen). Double-stranded cDNA synthesis was performed in second strand buffer (Invitrogen) according to the manufacturer’s recommendations and purified (Minelute Reaction Cleanup Kit; QIAGEN).
RNA-seq, ChIP-seq and MethylCap-seq of ESCs and EpiSCs
ChIP-Seq was performed according to Marks et al. , MethylCap-Seq was performed according to Veillard et al. . For RNA-seq, cDNA was prepared for sequencing either by (1) end repair of 20 ng double-stranded cDNA as measured by Qubit (Invitrogen), ligation of adaptors to DNA fragments followed by size selection (~ 300 bp) and PCR amplification; or by (2) using the Kapa Hyper Prep kit (KAPA Biosystems) according to manufacturer’s protocol, followed by PCR amplification and size selection. Quality control of the adaptor-containing DNA libraries was performed by quantitative PCR and by running the products on an Automated Electrophoresis System [Experion (BioRad) or Bioanalyzer (Agilent)]. Cluster generation and sequencing was performed using the Illumina Genome Analyzer IIx, Hi-Seq 2000 or NextSeq 500 platforms according to standard Illumina protocols. Generation of FASTQ files and demultiplexing was performed using Illumina CASAVA. All sequencing analyses were conducted based on the M. musculus NCBI m37 genome assembly (MM9; assembly July 2007). Additional file 1: Table S1 summarizes the sequencing output. All RNA-seq data and ChIP-Seq data (FASTQ and WIG files) are present in the NCBI Gene Expression Omnibus (GEO) SuperSeries GSE101292. An overview of these profiles is present in Additional file 1: Table S1.
Allele-specific mapping using polymorphic sites between the B6 and DBA2 genomes
Known polymorphic sites between the Mus musculus domesticus mouse strains B6 and DBA2  (nucleotide substitutions, not indels) were collected using polymorphic sites determined by (1) the Sanger mouse sequencing project using the March 2011 release using the strains C57BL and DBA [35, 36]; and (2) the NIEHS/Perlegen mouse resequencing project  (we used the b04_Chr*_genotype.dat files for the species C57BL/6J (reference genome) and DBA/2J). This resulted in a total of 5,233,965 polymorphic sites between the genomes of B6 and DBA2. FASTQ files were mapped using GSNAP version 2012-07-20 . To avoid bias in the mapping of either the B6- or the DBA2-derived reads, the alternative alleles of polymorphic sites between the B6 and DBA2 genome were included in the reference during mapping (GSNAP SNP-tolerant mapping; flag—v). Only sequence tags aligning to a single position in the genome were included for further analysis. Within the individual samples, we used the mapped tags to determine the coverage per allele for each of the polymorphic sites using GSNAP tally. Per single polymorphic nucleotide, the pile-ups were subsequently assigned to either the B6 or the DBA2 allele using custom Perl-based scripts. Polymorphic sites and analysis for the 129xCast ESCs (Fig. 2b, Additional file 2: Figs. S13 and S14) are described in Marks et al. . Profiles used for the 129xCast ESC analysis were obtained from NCBI GEO SuperSeries GSE60738 .
RNA-seq genotyping was performed by determining the percentage of B6 for the sum of B6 or DBA2 allelic counts over all polymorphic sites (B6/(B6 + DBA2) × 100%) in 5 MB or 1 MB chromosomal bins. At 5 MB resolution, we subsequently applied a moving average over four bins for the allelic ratios of bins that contained > 40 counts over polymorphic sites summed for both alleles. Bins containing ≤ 40 SNP counts over polymorphic sites summed for both alleles were labeled “insufficient coverage.” 5 MB bins showing a B6 contribution between 0 and 31% were labeled “DBA2” (paternal; yellow), between 31 and 78.5% “B6/DBA2” (heterozygous; blue) and between 78.5 and 100% “B6” (maternal; red), unless specified otherwise. For the analysis at 1 MB resolution, bins containing > 10 (RNA sequencing) or > 15 (DNA sequencing) counts over polymorphic sites summed for both alleles were included in the analysis. To enable reliable calling of crossover breakpoints, we increased resolution and stringency: 1 MB bins showing a B6 contribution between 0 and 15% were considered DBA2, between 15 and 85% B6/DBA2 heterozygous and between 85 and 100% B6. The genotype at the start of the chromosome proximal to the centromere was assigned B6 or DBA2 if (1) ≥ 80% of 5 bins or (2) ≥ 60% of 10 bins were labeled as either DBA2 or B6; or heterozygous if > 5 consecutive bins were labeled heterozygous. Having characterized the genotype at the proximal part of the centromere, we applied a sliding window approach toward the distal part of the chromosome to estimate crossing-over breakpoints. These breakpoints were identified at positions after which > 5 consecutive bins lacked the label of the assigned genotype (or ≥ 4 consecutive bins of the same genotype at the very proximal end of the chromosome). The genotype present after the breakpoints was determined by applying the same 3 criteria as at the start of the chromosome, or by the ≥ 4 consecutive bins of the same genotype at the proximal end of the chromosome. Breakpoints within 15 MB were discarded if the genotype of the genomic regions neighboring the ≤ 15 MB region was same. The methods as described in this section were also applied for genotyping of the EpiSCs using genomic DNA (obtained from MethylCap-seq experiments present in NCBI GEO SuperSeries GSE47793) .
Gene expression analysis
In light of the difference in sequencing length between the samples (Additional file 1: Table S1), we only included the first 35 bp of the forward read for RPKM quantification, data visualization and PCA/clustering analysis. (In case of paired-end reads, we only included the forward read if the distance between read pairs was < 10 kb to exclude aspecifically mapped reads but to include reads covering introns.) To obtain RNA-seq gene expression values (RPKM), we converted the GSNAP output to Browser Extensible Data (BED) files which were used as input for Genomatix (ElDorado 08–2011) selecting RefSeq genes (NCBI m37 genome assembly; MM9; Additional file 8: Table S7). For viewing, profiles were normalized based on the total number of reads and converted to Wiggle (WIG) files. Differential gene expression was called using DE-Seq 2 applying a Wald test and parametric fitting to estimate dispersion, followed by multiple testing correction using the Benjamini–Hochberg procedure (“adjusted p value”), requiring a change > 1.5 fold.
Calling of allele-specific gene bias
Counts over polymorphic sites within exons of individual RefSeq genes for either B6 or DBA2 were summed to obtain allele-specific gene expression counts for both species (Additional file 8: Table S7). The ratio between the B6 counts or the DBA2 counts versus the total counts (B6 + DBA2) represent the relative contribution of the B6 or DBA2 allele, respectively, to expression of a particular gene. Alternatively, we used the ratio of all allelic counts within genes (log2 B6/DBA2). For analysis of imprinted genes in the various RNA-seq samples, we included genes that (1) contained a coverage of > 9 counts over the polymorphic sites present in the gene; and (2) showed a standard error of the mean (STDEM) of ≤ 0.15 over individual polymorphic sites within a gene (these sites were required to contain a coverage ≥ 3 from either the B6 or DBA2 allele to be included; only applicable if multiple of such polymorphic sites were present). For inclusion in the global allele-specific analysis, we required that individual genes contained coverage over polymorphic sites in each individual ESC, EpiSC or embryonic sample, with a total coverage over polymorphic sites of > 40 for all ESCs or EpiSCs samples and > 200 for all embryonic samples. Allelic bias was defined as > 80% contribution in expression from one allele. Genes showing < 80% allelic bias were considered to be biallelically expressed. For analysis of XCI, we included genes showing a < fourfold allelic bias between B6 and DBA2 in the EpiSC-NT3 line.
Analysis of epigenetic profiling
ChIP-Seq enriched regions (“peaks”) were determined on tag-normalized BED files using MACS version 1.4.2 at p value 10−6 for H3K4me3  or, for H3K27me3, using a minimum threshold of 24 overlapping tags, merging enriched regions within 1500 bp. Peak sets of either H3K4me3 or H3K27me3 were merged for all samples and quantified using the tag-normalized BED files by determining the number of reads present within the enriched regions for each of the profiles. Peaks were associated with the closest genes using Pinkthing . For allele-specific quantification of ChIP-Seq peaks, we summed the B6 or BDA2 counts over polymorphic sites within the peaks to calculate the contribution from each allele, similar to the method applied to calculate allelic ratios of gene expression from RNA-seq (see previous sections). Analysis of MethylCap-Seq was performed according to Veillard et al. .
Brons IG, Smithers LE, Trotter MW, Rugg-Gunn P, Sun B, Chuva de Sousa Lopes SM, et al. Derivation of pluripotent epiblast stem cells from mammalian embryos. Nature. 2007;448(7150):191–5.
Evans MJ, Kaufman MH. Establishment in culture of pluripotential cells from mouse embryos. Nature. 1981;292(5819):154–6.
Martin GR. Isolation of a pluripotent cell line from early mouse embryos cultured in medium conditioned by teratocarcinoma stem cells. Proc Natl Acad Sci USA. 1981;78(12):7634–8.
Tesar PJ, Chenoweth JG, Brook FA, Davies TJ, Evans EP, Mack DL, et al. New cell lines from mouse epiblast share defining features with human embryonic stem cells. Nature. 2007;448(7150):196–9.
Thomas KR, Capecchi MR. Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells. Cell. 1987;51(3):503–12.
Takahashi K, Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell. 2006;126(4):663–76.
Munsie MJ, Michalska AE, O’Brien CM, Trounson AO, Pera MF, Mountford PS. Isolation of pluripotent embryonic stem cells from reprogrammed adult mouse somatic cell nuclei. Curr Biol. 2000;10(16):989–92.
Robertson EJ, Evans MJ, Kaufman MH. X-chromosome instability in pluripotential stem cell lines derived from parthenogenetic embryos. J Embryol Exp Morphol. 1983;74:297–309.
Ma H, Morey R, O’Neil RC, He Y, Daughtry B, Schultz MD, et al. Abnormalities in human pluripotent cells due to reprogramming mechanisms. Nature. 2014;511(7508):177–83.
Kim K, Lerou P, Yabuuchi A, Lengerke C, Ng K, West J, et al. Histocompatible embryonic stem cells by parthenogenesis. Science. 2007;315(5811):482–6.
Babak T, DeVeale B, Tsang EK, Zhou Y, Li X, Smith KS, et al. Genetic conflict reflected in tissue-specific maps of genomic imprinting in human and mouse. Nat Genet. 2015;47(5):544–9.
DeVeale B, van der Kooy D, Babak T. Critical evaluation of imprinted gene expression by RNA-seq: a new perspective. PLoS Genet. 2012;8(3):e1002600.
Barton SC, Surani MA, Norris ML. Role of paternal and maternal genomes in mouse development. Nature. 1984;311(5984):374–6.
McGrath J, Solter D. Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell. 1984;37(1):179–83.
Kawahara M, Wu Q, Takahashi N, Morita S, Yamada K, Ito M, et al. High-frequency generation of viable mice from engineered bi-maternal embryos. Nat Biotechnol. 2007;25(9):1045–50.
Stadtfeld M, Apostolou E, Akutsu H, Fukuda A, Follett P, Natesan S, et al. Aberrant silencing of imprinted genes on chromosome 12qF1 in mouse induced pluripotent stem cells. Nature. 2010;465(7295):175–81.
Feinberg AP. Imprinting of a genomic domain of 11p15 and loss of imprinting in cancer: an introduction. Cancer Res. 1999;59(7 Suppl):1743s–6s.
Holm TM, Jackson-Grusby L, Brambrink T, Yamada Y, Rideout WM 3rd, Jaenisch R. Global loss of imprinting leads to widespread tumorigenesis in adult mice. Cancer Cell. 2005;8(4):275–85.
Bartolomei MS, Ferguson-Smith AC. Mammalian genomic imprinting. Cold Spring Harb Perspect Biol. 2011;3(7):a002592.
Andergassen D, Dotter CP, Wenzel D, Sigl V, Bammer PC, Muckenhuber M, et al. Mapping the mouse Allelome reveals tissue-specific regulation of allelic expression. eLife. 2017;6:e25125.
Dean W, Bowden L, Aitchison A, Klose J, Moore T, Meneses JJ, et al. Altered imprinted gene methylation and expression in completely ES cell-derived mouse fetuses: association with aberrant phenotypes. Development (Cambridge). 1998;125(12):2273–82.
Humpherys D, Eggan K, Akutsu H, Hochedlinger K, Rideout WM 3rd, Biniszkiewicz D, et al. Epigenetic instability in ES cells and cloned mice. Science. 2001;293(5527):95–7.
Szabo P, Mann JR. Expression and methylation of imprinted genes during in vitro differentiation of mouse parthenogenetic and androgenetic embryonic stem cell lines. Development (Cambridge). 1994;120(6):1651–60.
Sun B, Ito M, Mendjan S, Ito Y, Brons IG, Murrell A, et al. Status of genomic imprinting in epigenetically distinct pluripotent stem cells. Stem Cells. 2012;30(2):161–8.
Maruotti J, Dai XP, Brochard V, Jouneau L, Liu J, Bonnet-Garnier A, et al. Nuclear transfer-derived epiblast stem cells are transcriptionally and epigenetically distinguishable from their fertilized-derived counterparts. Stem Cells. 2010;28(4):743–52.
Horii T, Kimura M, Morita S, Nagao Y, Hatada I. Loss of genomic imprinting in mouse parthenogenetic embryonic stem cells. Stem Cells. 2008;26(1):79–88.
Bar S, Schachter M, Eldar-Geva T, Benvenisty N. Large-scale analysis of loss of imprinting in human pluripotent stem cells. Cell Rep. 2017;19(5):957–68.
Bernardo AS, Jouneau A, Marks H, Kensche P, Kobolak J, Freude K, et al. Mammalian embryo comparison identifies novel pluripotency genes associated with the naive or primed state. Biol Open. 2018;7(8):bio033282.
Czechanski A, Byers C, Greenstein I, Schrode N, Donahue LR, Hadjantonakis AK, et al. Derivation and characterization of mouse embryonic stem cells from permissive and nonpermissive strains. Nat Protoc. 2014;9(3):559–74.
Eggan K, Akutsu H, Loring J, Jackson-Grusby L, Klemm M, Rideout WM 3rd, et al. Hybrid vigor, fetal overgrowth, and viability of mice derived by nuclear cloning and tetraploid embryo complementation. Proc Natl Acad Sci USA. 2001;98(11):6209–14.
Ibanez E, Albertini DF, Overstrom EW. Effect of genetic background and activating stimulus on the timing of meiotic cell cycle progression in parthenogenetically activated mouse oocytes. Reproduction. 2005;129(1):27–38.
Rideout WM 3rd, Wakayama T, Wutz A, Eggan K, Jackson-Grusby L, Dausman J, et al. Generation of mice from wild-type and targeted ES cells by nuclear cloning. Nat Genet. 2000;24(2):109–10.
Gao S, McGarry M, Priddle H, Ferrier T, Gasparrini B, Fletcher J, et al. Effects of donor oocytes and culture conditions on development of cloned mice embryos. Mol Reprod Dev. 2003;66(2):126–33.
Frazer KA, Eskin E, Kang HM, Bogue MA, Hinds DA, Beilharz EJ, et al. A sequence-based variation map of 8.27 million SNPs in inbred mouse strains. Nature. 2007;448(7157):1050–3.
Keane TM, Goodstadt L, Danecek P, White MA, Wong K, Yalcin B, et al. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature. 2011;477(7364):289–94.
Yalcin B, Wong K, Agam A, Goodson M, Keane TM, Gan X, et al. Sequence-based characterization of structural variation in the mouse genome. Nature. 2011;477(7364):326–9.
Yang H, Wang JR, Didion JP, Buus RJ, Bell TA, Welsh CE, et al. Subspecific origin and haplotype diversity in the laboratory mouse. Nat Genet. 2011;43(7):648–55.
Cleaton MA, Edwards CA, Ferguson-Smith AC. Phenotypic outcomes of imprinted gene models in mice: elucidation of pre- and postnatal functions of imprinted genes. Annu Rev Genom Hum Genet. 2014;15:93–126.
Choi J, Huebner AJ, Clement K, Walsh RM, Savol A, Lin K, et al. Prolonged Mek1/2 suppression impairs the developmental potential of embryonic stem cells. Nature. 2017;548(7666):219–23.
Yagi M, Kishigami S, Tanaka A, Semi K, Mizutani E, Wakayama S, et al. Derivation of ground-state female ES cells maintaining gamete-derived DNA methylation. Nature. 2017;548(7666):224–7.
Kim K, Ng K, Rugg-Gunn PJ, Shieh JH, Kirak O, Jaenisch R, et al. Recombination signatures distinguish embryonic stem cells derived by parthenogenesis and somatic cell nuclear transfer. Cell Stem Cell. 2007;1(3):346–52.
Marks H, Kerstens HH, Barakat TS, Splinter E, Dirks RA, van Mierlo G, et al. Dynamics of gene silencing during X inactivation using allele-specific RNA-seq. Genome Biol. 2015;16:149.
Jirtle RL. Genomic imprinting and cancer. Exp Cell Res. 1999;248(1):18–24.
Williamson CM, Blake A, Thomas S, Beechey CV, Hancock J, Cattanach BM et al. MRC Harwell, Oxfordshire. World Wide Web Site—mouse imprinting data and references—http://www.har.mrc.ac.uk/research/genomic_imprinting/. 2013.
Wood AJ, Schulz R, Woodfine K, Koltowska K, Beechey CV, Peters J, et al. Regulation of alternative polyadenylation by genomic imprinting. Genes Dev. 2008;22(9):1141–6.
Vu TH, Hoffman AR. Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain. Nat Genet. 1997;17(1):12–3.
Latos PA, Stricker SH, Steenpass L, Pauler FM, Huang R, Senergin BH, et al. An in vitro ES cell imprinting model shows that imprinted expression of the Igf2r gene arises from an allele-specific expression bias. Development (Cambridge). 2009;136(3):437–48.
Bernstein BE, Mikkelsen TS, Xie X, Kamal M, Huebert DJ, Cuff J, et al. A bivalent chromatin structure marks key developmental genes in embryonic stem cells. Cell. 2006;125(2):315–26.
Boroviak T, Loos R, Bertone P, Smith A, Nichols J. The ability of inner-cell-mass cells to self-renew as embryonic stem cells is acquired following epiblast specification. Nat Cell Biol. 2014;16(6):516–28.
Marks H, Kalkan T, Menafra R, Denissov S, Jones K, Hofemeister H, et al. The transcriptional and epigenomic foundations of ground state pluripotency. Cell. 2012;149(3):590–604.
Marks H, Stunnenberg HG. Transcription regulation and chromatin structure in the pluripotent ground state. Biochim Biophys Acta. 2014;1839(3):129–37.
van Mierlo G, Dirks RAM, De Clerck L, Brinkman AB, Huth M, Kloet SL, et al. Integrative proteomic profiling reveals PRC2-dependent epigenetic crosstalk maintains ground-state pluripotency. Cell Stem Cell. 2019;24(1):123.e8–137.e8.
Plasschaert RN, Bartolomei MS. Genomic imprinting in development, growth, behavior and stem cells. Development (Cambridge). 2014;141(9):1805–13.
Rugg-Gunn PJ, Ferguson-Smith AC, Pedersen RA. Status of genomic imprinting in human embryonic stem cells as revealed by a large cohort of independently derived and maintained lines. Hum Mol Genet. 2007;16(Spec No. 2):R243–51.
Caspary T, Cleary MA, Perlman EJ, Zhang P, Elledge SJ, Tilghman SM. Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome. Genes Dev. 1999;13(23):3115–24.
Augui S, Nora EP, Heard E. Regulation of X-chromosome inactivation by the X-inactivation centre. Nat Rev Genet. 2011;12(6):429–42.
Guo G, Yang J, Nichols J, Hall JS, Eyres I, Mansfield W, et al. Klf4 reverts developmentally programmed restriction of ground state pluripotency. Development (Cambridge). 2009;136(7):1063–9.
Borsani G, Tonlorenzi R, Simmler MC, Dandolo L, Arnaud D, Capra V, et al. Characterization of a murine gene expressed from the inactive X chromosome. Nature. 1991;351(6324):325–9.
Brockdorff N, Ashworth A, Kay GF, Cooper P, Smith S, McCabe VM, et al. Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome. Nature. 1991;351(6324):329–31.
Plenge RM, Percec I, Nadeau JH, Willard HF. Expression-based assay of an X-linked gene to examine effects of the X-controlling element (Xce) locus. Mamm Genome. 2000;11(5):405–8.
Kobolak J, Mamo S, Rungsiwiwut R, Ujhelly O, Csonka E, Hadlaczky G, et al. Comparative analysis of nuclear transfer embryo-derived mouse embryonic stem cells. Part I: cellular characterization. Cell Reprogr. 2012;14(1):56–67.
Rugg-Gunn P. Derivation and culture of epiblast stem cell (EpiSC) lines. Cold Spring Harb Protoc. 2017;2017(1):pdb.prot093971.
Peters J. The role of genomic imprinting in biology and disease: an expanding view. Nat Rev Genet. 2014;15(8):517–30.
Adewumi O, Aflatoonian B, Ahrlund-Richter L, Amit M, Andrews PW, Beighton G, et al. Characterization of human embryonic stem cell lines by the international stem cell initiative. Nat Biotechnol. 2007;25(7):803–16.
Frost J, Monk D, Moschidou D, Guillot PV, Stanier P, Minger SL, et al. The effects of culture on genomic imprinting profiles in human embryonic and fetal mesenchymal stem cells. Epigenetics. 2011;6(1):52–62.
Kim K, Doi A, Wen B, Ng K, Zhao R, Cahan P, et al. Epigenetic memory in induced pluripotent stem cells. Nature. 2010;467(7313):285–90.
Wakayama S, Jakt ML, Suzuki M, Araki R, Hikichi T, Kishigami S, et al. Equivalency of nuclear transfer-derived embryonic stem cells to those derived from fertilized mouse blastocysts. Stem Cells. 2006;24(9):2023–33.
Li C, Chen Z, Liu Z, Huang J, Zhang W, Zhou L, et al. Correlation of expression and methylation of imprinted genes with pluripotency of parthenogenetic embryonic stem cells. Hum Mol Genet. 2009;18(12):2177–87.
Gao S, Czirr E, Chung YG, Han Z, Latham KE. Genetic variation in oocyte phenotype revealed through parthenogenesis and cloning: correlation with differences in pronuclear epigenetic modification. Biol Reprod. 2004;70(4):1162–70.
Wakayama T, Yanagimachi R. Mouse cloning with nucleus donor cells of different age and type. Mol Reprod Dev. 2001;58(4):376–83.
Weissbein U, Schachter M, Egli D, Benvenisty N. Analysis of chromosomal aberrations and recombination by allelic bias in RNA-seq. Nat Commun. 2016;7:12144.
Stadtfeld M, Apostolou E, Ferrari F, Choi J, Walsh RM, Chen T, et al. Ascorbic acid prevents loss of Dlk1-Dio3 imprinting and facilitates generation of all-iPS cell mice from terminally differentiated B cells. Nat Genet. 2012;44(4):398–405, s1–2.
Mallol A, Santalo J, Ibanez E. Improved development of somatic cell cloned mouse embryos by vitamin C and latrunculin A. PLoS ONE. 2015;10(3):e0120033.
Beutler E, Yeh M, Fairbanks VF. The normal human female as a mosaic of X-chromosome activity: studies using the gene for C-6-PD-deficiency as a marker. Proc Natl Acad Sci USA. 1962;48:9–16.
Scialdone A, Tanaka Y, Jawaid W, Moignard V, Wilson NK, Macaulay IC, et al. Resolving early mesoderm diversification through single-cell expression profiling. Nature. 2016;535(7611):289–93.
Zvetkova I, Apedaile A, Ramsahoye B, Mermoud JE, Crompton LA, John R, et al. Global hypomethylation of the genome in XX embryonic stem cells. Nat Genet. 2005;37(11):1274–9.
Johansson BM, Wiles MV. Evidence for involvement of activin A and bone morphogenetic protein 4 in mammalian mesoderm and hematopoietic development. Mol Cell Biol. 1995;15(1):141–51.
Ying QL, Wray J, Nichols J, Batlle-Morera L, Doble B, Woodgett J, et al. The ground state of embryonic stem cell self-renewal. Nature. 2008;453(7194):519–23.
Ficz G, Hore TA, Santos F, Lee HJ, Dean W, Arand J, et al. FGF signaling inhibition in ESCs drives rapid genome-wide demethylation to the epigenetic ground state of pluripotency. Cell Stem Cell. 2013;13(3):351–9.
Habibi E, Brinkman AB, Arand J, Kroeze LI, Kerstens HH, Matarese F, et al. Whole-genome bisulfite sequencing of two distinct interconvertible DNA methylomes of mouse embryonic stem cells. Cell Stem Cell. 2013;13(3):360–9.
Inoue A, Jiang L, Lu F, Suzuki T, Zhang Y. Maternal H3K27me3 controls DNA methylation-independent imprinting. Nature. 2017;547(7664):419–24.
Rossant J. Stem cells and early lineage development. Cell. 2008;132(4):527–31.
Chan YS, Goke J, Ng JH, Lu X, Gonzales KA, Tan CP, et al. Induction of a human pluripotent state with distinct regulatory circuitry that resembles preimplantation epiblast. Cell Stem Cell. 2013;13(6):663–75.
Gafni O, Weinberger L, Mansour AA, Manor YS, Chomsky E, Ben-Yosef D, et al. Derivation of novel human ground state naive pluripotent stem cells. Nature. 2013;504(7479):282–6.
Takashima Y, Guo G, Loos R, Nichols J, Ficz G, Krueger F, et al. Resetting transcription factor control circuitry toward ground-state pluripotency in human. Cell. 2014;158(6):1254–69.
Theunissen TW, Powell BE, Wang H, Mitalipova M, Faddah DA, Reddy J, et al. Systematic identification of culture conditions for induction and maintenance of naive human pluripotency. Cell Stem Cell. 2014;15(4):471–87.
Ware CB, Nelson AM, Mecham B, Hesson J, Zhou W, Jonlin EC, et al. Derivation of naive human embryonic stem cells. Proc Natl Acad Sci USA. 2014;111(12):4484–9.
Pastor WA, Chen D, Liu W, Kim R, Sahakyan A, Lukianchikov A, et al. Naive human pluripotent cells feature a methylation landscape devoid of blastocyst or germline memory. Cell Stem Cell. 2016;18(3):323–9.
Theunissen TW, Friedli M, He Y, Planet E, O’Neil RC, Markoulaki S, et al. Molecular criteria for defining the naive human pluripotent state. Cell Stem Cell. 2016;19(4):502–15.
Leick MB, Shoff CJ, Wang EC, Congress JL, Gallicano GI. Loss of imprinting of IGF2 and the epigenetic progenitor model of cancer. Am J Stem Cells. 2012;1(1):59–74.
Kobolak J, Bodo S, Rungsiwiwut R, Meng Q, Adorjan M, Virutamasen P, et al. Generation of mouse embryonic stem cell lines from zona-free nuclear transfer embryos. Cell Reprogr. 2010;12(1):105–13.
Solter D, Knowles BB. Immunosurgery of mouse blastocyst. Proc Natl Acad Sci USA. 1975;72(12):5099–102.
Tanaka N, Takeuchi T, Neri QV, Sills ES, Palermo GD. Laser-assisted blastocyst dissection and subsequent cultivation of embryonic stem cells in a serum/cell free culture system: applications and preliminary results in a murine model. J Transl Med. 2006;4:20.
Veillard AC, Marks H, Bernardo AS, Jouneau L, Laloe D, Boulanger L, et al. Stable methylation at promoters distinguishes epiblast stem cells from embryonic stem cells and the in vivo epiblasts. Stem Cells Dev. 2014;23(17):2014–29.
Wu TD, Nacu S. Fast and SNP-tolerant detection of complex variants and splicing in short reads. Bioinformatics. 2010;26(7):873–81.
Zhang Y, Liu T, Meyer CA, Eeckhoute J, Johnson DS, Bernstein BE, et al. Model-based analysis of ChIP-seq (MACS). Genome Biol. 2008;9(9):R137.
Nielsen FG, Kooyman M, Kensche P, Marks H, Stunnenberg H, Huynen M. The PinkThing for analysing ChIP profiling data in their genomic context. BMC Res Notes. 2013;6:133.
Mikkelsen TS, Ku M, Jaffe DB, Issac B, Lieberman E, Giannoukos G, et al. Genome-wide maps of chromatin state in pluripotent and lineage-committed cells. Nature. 2007;448(7153):553–560.
Ferguson-Smith AC. Genomic imprinting: the emergence of an epigenetic paradigm. Nat Rev Genet. 2011;12(8):565–575.
RAM performed RNA-seq profiling, assisted in data analysis and generating the figures, and helped drafting the manuscript. GvM assisted in designing the study and helped drafting the manuscript. HHDK designed data analysis pipelines. JM derived EpiSCs. ASB isolated ERSE and APE tissues. RA provided ERSE and APE tissues. JK and IB provided RNA of ESCs for RNA-seq and isolated EBI and EB-TE tissues. AD provided ESCs for epigenetic profiling as well as EBI and EB-TE tissues. MAH assisted in data analysis. AJ provided EpiSCs, designed the study and assisted in data analysis. HM initiated, designed, conceived and coordinated the study, performed RNA-seq profiling and data analysis, generated the figures and drafted the manuscript. All authors read and approved the final manuscript.
We thank Olga Ujhelly for culture and harvest of ESCs used for ChIP-Seq, Eva Janssen-Megens and Yan Tan for technical sequencing support, Kees-Jan François and Rita Bylsma for bioinformatic support and Henk Stunnenberg for discussion and advice.
The authors declare that they have no competing interests.
Availability of data and materials
All RNA-seq data and ChIP-Seq data of ESCs and EpiSCs are present in the NCBI Gene Expression Omnibus (GEO) SuperSeries GSE101292. All RNA-seq of the embryonic tissue samples are present in the NCBI GEO SuperSeries GSE53387.
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Ethics approval and consent to participate
This work was supported by the European Union grant PluriSys (FP7/2009: 223485); the Netherlands Organization for Scientific Research (NWO-VIDI 864.12.007 to H.M.); and a Van Gogh programme grant (VGP.17/13 to A.J. and H.M). Part of the computational analysis was carried out on the Dutch national e-infrastructure with the support of SURF Cooperative.
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Dirks, R.A.M., Mierlo, G., Kerstens, H.H.D. et al. Allele-specific RNA-seq expression profiling of imprinted genes in mouse isogenic pluripotent states. Epigenetics & Chromatin 12, 14 (2019) doi:10.1186/s13072-019-0259-8
- Genomic imprinting
- Allele-specific RNA-seq
- Mouse embryo
- Embryonic stem cells
- Parthenogenetic activation (PGA)
- Nuclear transfer (NT)