- Open Access
HIRA dependent H3.3 deposition is required for transcriptional reprogramming following nuclear transfer to Xenopus oocytes
© Jullien et al.; licensee BioMed Central Ltd. 2012
- Received: 27 July 2012
- Accepted: 4 September 2012
- Published: 29 October 2012
Nuclear reprogramming is potentially important as a route to cell replacement and drug discovery, but little is known about its mechanism. Nuclear transfer to eggs and oocytes attempts to identify the mechanism of this direct route towards reprogramming by natural components. Here we analyze how the reprogramming of nuclei transplanted to Xenopus oocytes exploits the incorporation of the histone variant H3.3.
After nuclear transplantation, oocyte-derived H3.3 but not H3.2, is deposited on several regions of the genome including rDNA, major satellite repeats, and the regulatory regions of Oct4. This major H3.3 deposition occurs in absence of DNA replication, and is HIRA-and transcription-dependent. It is necessary for the shift from a somatic- to an oocyte-type of transcription after nuclear transfer.
This study demonstrates that the incorporation of histone H3.3 is an early and necessary step in the direct reprogramming of somatic cell nuclei by oocyte. It suggests that the incorporation of histone H3.3 is necessary during global changes in transcription that accompany changes in cell fate.
- Xenopus Oocyte
- Nuclear Transfer
- Nuclear Transplantation
- Germinal Vesicle
- Histone Variant
Nuclear reprogramming is characterized by a global shift in gene expression. The mechanisms underlying this phenomenon are not well understood but are likely to involve changes to chromatin. For example, an increase in histone H3K4 methylation has been observed in nuclei following nuclear transfer (NT) and during iPS production [1, 2]. Alternatively, the incorporation of histone variants into chromatin can provide another way to drastically alter the structure of chromatin. Nucleosomes containing core histone variants H3.3 or macroH2A have been associated with the active and inactive states of a gene, respectively. MacroH2A restricts the reactivation of pluripotency genes from mouse nuclei transplanted to Xenopus oocytes . In nuclear transfer to Xenopus eggs, histone H3.3 participates in the transmission of an active state of a gene, even in embryonic lineages where genes should be silenced . Furthermore, histone variants are also positively involved in the mechanism of transcriptional reprogramming. We have previously shown that the incorporation of histone B4, an oocyte specific linker histone variant, is a necessary step for nuclear reprogramming following nuclear transfer . A number of histone changes are already known to be associated with nuclear reprogramming by eggs and oocytes. While those observed in eggs may well be related to DNA synthesis and cell replication coupled events during the cell cycle, those that take place in somatic nuclei transplanted to oocytes which do not replicate DNA and are arrested in prophase I of meiosis are associated essentially with new transcription and are independent of cell cycle progression.
Here we investigate the dynamics of histone H3 variants in the reprogramming of mammalian nuclei transplanted to Xenopus oocytes. In this type of reprogramming there is no cell division and new cell types are not derived. However, the transplanted nuclei undergo dramatic changes in their pattern of gene expression so that transcription is switched directly from a somatic to an oocyte type. The evolutionarily conserved histone variant H3.3 has been found to be especially enriched in the coding region of transcriptionally active genes as well as in gene regulatory elements . This histone is often associated with histone modifications related to gene activation [7, 8]. Histone H3.3 can be incorporated into chromatin throughout the cell cycle in a replication independent manner by the histone chaperone HIRA [9, 10], which is also found to be required for global H3.3 deposition in the male pronucleus after fertilization in Drosophila . This association between histone H3.3 and the HIRA deposition pathway has been further demonstrated to play a critical role during a major change in gene expression at gastrulation in Xenopus. Finally, early work showed that plasmid DNA injected to oocytes is differently transcribed depending on whether its chromatin has been assembled in a DNA synthesis dependent or independent manner . Together these findings prompted us to investigate the importance of the histone variant H3.3 and its deposition in transcriptional reprogramming of nuclei transplanted to Xenopus oocytes. We demonstrate that the deposition of H3.3 by HIRA is necessary for transcriptional reprogramming. We also observe that HIRA mediated H3.3 deposition and transcription are interdependent in somatic nuclei transplanted to Xenopus oocytes.
Gain and loss of histone H3 variants
We have then asked whether the loading of oocyte H3.3 onto transplanted chromatin is associated with the loss of H3.2 or H3.3 from donor nuclei. For that purpose we have used donor nuclei containing cherry labeled H3.2 or H3.3. Quantitation of the level of cherry labeled histones that remain associated with donor nuclei after transplantation to oocytes was done by confocal microscopy. We observed that during the first 12 h after nuclear transfer 15% and 19% of H3.2-cherry or H3.3-cherry, respectively, are lost from transplanted nuclei (Figure 1D). This suggests that following nuclear transfer to Xenopus oocytes, a significant fraction of H3.2 and H3.3 in donor nuclei is replaced by oocyte H3.3. The mobility of core histones on the chromatin of nuclei transplanted to Xenopus oocytes is not known. Changes in histone mobility have been proposed to account for plasticity in transcription  and could therefore account for the change in gene expression observed after nuclear transfer. We therefore investigated whether histone H3.3 incorporated after transplantation corresponds to a fraction of the transplanted nuclear core histone that has become highly mobile. When tested by FRAP analysis over a period of 20 min, we observed that oocyte derived H3.3 loaded onto transplanted chromatin does not recover above the level of H3.3 found in the surrounding germinal vesicle (Figure 1E). By contrast oocyte derived HP1-alpha fully recovers within the 20 min following photo bleaching, indicating that within the imaging conditions used some chromatin associated protein exhibits rapid turnover. We therefore conclude that, once incorporated into transplanted nuclei, the newly loaded H3.3 is not turning over rapidly. Thus transplanted nuclei incorporate H3.3 readily from the oocyte, thereby changing their chromatin landscape and possibly reprogramming transcription.
Timing of H3.3 incorporation and transcription
By qRT-PCR we have confirmed that 4-day retinoic acid (RA) treatment of the reporter ES cell line ESC#5 (RA-ESC#5) induces silencing of the endogenous pluripotency genes Sox2 and Oct4 as well as of the Oct4 transgene (Additional file 1: Figure S3). To confirm that the oocyte successfully reactivates the Oct4 transgene, a transcription analysis was carried out with RA-ESC #5 nuclei carrying the silent Oct4 array analyzed at various times after NT. We observe transcription of the rDNA 28S, major satellite repeat, as well as the previously silent Oct4 reporter within 12 to 20 h after nuclear transfer (Figure 2B). The level of all three kinds of transcript is greatly increased from 20 h to 48 h after transplantation. In particular, we note that transcripts from the rDNA and major satellite regions are accumulated to levels that largely exceed those observed in the donor nuclei immediately after nuclear transfer (at least 20-fold, Figure 2B, compare 0 h and 48 h after transplantation). The observed increase in rRNA and major satellite transcripts after nuclear transfer suggests transcriptional reprogramming of these parts of the genome too. However since both rDNA and pericentric heterochromatin can be transcribed in cultured cells, the observed accumulation of transcripts from these regions following nuclear transfer (Figure 2B) could result from a somatic type of transcription associated with increased transcript stability in the oocyte.
To confirm transcriptional reprogramming of these genomic regions we have directly measured whether their rate of transcription from transplanted nuclei changes after nuclear transfer. In order to measure changes in rate of transcription we have labeled new transcripts produced from transplanted nuclei by injecting BrUTP into the oocyte (Figure 2C). BrUTP was injected at different times after nuclear transfer and oocytes collected 12 h after injection. In that way the transcripts are labeled with BrUTP for 12-h periods covering the 48 h after nuclear transplantation. The labeled transcripts are then immunoprecipitated with an anti-BrdUTP antibody and analyzed by qRT-PCR, providing a measurement of transcript production per 12-h period. We observe that the rate of transcription from rDNA and major satellites increases approximately five times between the 12 to 24 h and 24 to 36 h periods that follow nuclear transplantation (Figure 2C). Therefore the reprogramming of transplanted nuclei to an oocyte type of transcription includes reactivation of silent genes such as Oct4, and an increased transcription of rDNA and pericentric chromatin. We point out that transcription of the latter has been observed in several instances, especially at the time of early embryonic development when heterochromatin is established [15, 20].
We then compared the extent of the oocyte-expressed H3.3 and H3.2 incorporation into the transplanted chromatin analyzing different regions of the transplanted nuclei. For this purpose we expressed in the oocyte HA tagged H3.3 or H3.2 prior to nuclear transfer. The level of HA-H3 and HA-H3.3 obtained by mRNA injection is similar to that of their endogenous counterpart stored in the oocyte (Additional file 1: Figure S1 and Figure 1A). At 24 h after nuclear transfer of RA-ESC #5, the oocytes were cross-linked and analyzed by ChIP with an antibody recognizing the HA-tag in order to determine the extent of incorporation of histones from the oocyte. We found that HA-H3.3 was incorporated with an approximately 8-10-fold higher efficiency compared to the background level of HA-H3.2, not only over the Oct4 promoter but also over the major satellite region and ribosomal DNA (Figure 2D). Therefore the incorporation of oocyte H3.3 as opposed to H3.2 into transplanted nuclear chromatin as seen by immunofluorescence analysis (Figure 1C) is also observed by ChIP analysis. We conclude that H3.3 but not H3.2 is preferentially deposited on transplanted nuclear chromatin including regulatory regions such as in the Oct4 promoter.
Our results so far indicate that H3.3 deposition is an early event following NT but do not show whether it precedes or follows the switch from somatic type to oocyte type transcription. To address this we focused on Oct4 reactivation and investigated the time at which various parts of the Oct4 regulatory region exhibit histone H3.3 incorporation. The oocytes were injected with mRNA encoding HA-H3.3 as before and the next day RA ESC #5 nuclei were used for NT. The oocytes were then incubated and cross-linked at indicated time points prior to ChIP analysis for the well conserved proximal promoter (PP), proximal enhancer (PE), and the distal enhancer (DE) of Oct4. We found that histone H3.3 incorporation increased greatly during the first 20 h and then reached a plateau around 24 h after NT (Figure 2E). No difference in the extent of H3.3 incorporation between the promoter and enhancers was seen for up to 72 h, indicating a uniform exchange over the entire regulatory region of Oct4 after NT. At 20 h after nuclear transfer, both gene reactivation (qRT-PCR, Figure 2B) and H3.3 incorporation can be detected (ChIP, Figure 2E). However, whereas H3.3 incorporation on Oct4 regulatory regions reaches a maximum level around 24 h after nuclear transfer (Figure 2E), the quantity of accumulated Oct4 transcript increases massively after that time (Figure 2B). This observation is consistent with the hypothesis whereby H3.3 is incorporated onto a gene (and reach a maximum plateau level) while enabling activation and subsequent continuous accumulation of the transcribed mRNAs.
H3.3 incorporation requires HIRA
Interestingly when HIRA mediated H3.3 deposition is inhibited an increased deposition of H3.2 is observed (Figure 3A, compare lane 5 with lane 7). In the presence of alpha-amanitin, neither H3.3 nor H3.2 is deposited onto transplanted chromatin (Figure 3A). We conclude that following nuclear transfer, H3.3 deposition on the tested genomic region is a HIRA- and transcription-dependent process. We have conducted a complementary analysis of H3.3 loading, this time on a global level, by monitoring H3.3-GFP accumulation onto transplanted chromatin by confocal microscopy. Similar to the ChIP analysis, we observed that H3.3 deposition is inhibited by both anti-HIRA antibody and alpha-amanitin injection (Figure 3B).
Together these data demonstrate that H3.3 deposition on a global nuclear level is HIRA- and largely transcription-dependent.
The alternative deposition of H3.2 in response to anti-HIRA injection is also observed on a global nuclear level when monitored by confocal microscopy, albeit on a subset of transplanted nuclei only (Additional file 1: Figure S5). This heterogeneous behavior of transplanted nuclei might reflect the various phases of the cell cycle that are represented in the donor nuclei population. Further investigations will be needed to describe the mechanism by which HIRA inhibition following nuclear transfer to Xenopus oocytes leads to H3.2 incorporation.
H3.3 incorporation and transcription are interdependent
We next ask whether HIRA mediated H3.3 deposition is required for transcriptional reprogramming. Inhibition of HIRA by antibody injection greatly impairs transcriptional reprogramming as shown by the reduced expression of Oct4 reporter, rDNA, and major satellite from transplanted nuclei (qRT-PCR analysis, Figure 3C). Overexpression of HIRA by mRNA injection into oocytes prior to anti-HIRA antibody injection and nuclear transfer partially rescues the effect of antibody injection (Figure 3D and E). This observation confirms that the antibody effect is through inhibition of HIRA. We conclude that HIRA is required for the reprogramming from a somatic to an oocyte type of transcription. The alternative H3.2 deposition observed when HIRA is inhibited (Figure 3A) is not sufficient to promote transcriptional reprogramming (Figure 3C). This indicates that a specific deposition of H3.3 is required for efficient reprogramming.
From a mechanistic point of view the requirement for H3.3 is mediated by HIRA. H3.3 incorporation and transcription seem to act in a cooperative and interdependent way. In cultured cells, inhibition of HIRA does not interfere with transcription . However in the context of the developing embryo, HIRA activity is necessary at gastrulation where cell lineages are determined . Together with these findings, our results reveal an involvement of this histone chaperone in the genome wide remodeling of transcription associated with major transition between cell states. Importantly, physical interactions between HIRA and the transcription machinery has recently been observed . A requirement for H3.3 deposition in the reprogramming of somatic nuclei to an oocyte type of transcription may depend on an interaction between RNA polymerase II and HIRA.
Nuclear transfer procedure
TAU gel analysis
We prepared germinal vesicles (GV) soluble extracts , and soluble fractions from eggs and stage 28 embryos using the High Speed Egg (HSE) extract protocol . We analyzed those extracts by electrophoresis in a Triton Acetic acid Urea (TAU) gel that separates histone subtypes .
We used the following primary antibodies: anti-H3 (Abcam ab1791; 1:1,000 dilution), anti- H3.3 (Abnova H00003021-M01; 1:40), anti-HA (Roche Diagnostics Clone 3 F10; 1:1,000), anti-xHIRA (; 1:2,000), anti-GFP (Santa Cruz #SC8334; 1:500), anti-actin (SIGMA; AC15, 1:5,000).
We would like to thank all the member of the Gurdon lab for critical reading of the manuscript. This work was supported by grants from the Wellcome Trust and the Medical Research Council, UK.
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