N6-Adenosine methylation on mRNA is recognized by YTH2 domain protein of human malaria parasite Plasmodium falciparum

Background Plasmodium falciparum exhibits high translational plasticity during its development in RBCs, yet the regulation at the post-transcriptional level is not well understood. The N6-methyl adenosine (m6A) is an important epigenetic modification primarily present on mRNA that controls the levels of transcripts and efficiency of translation in eukaryotes. Recently, the dynamics of m6A on mRNAs at all three developmental stages of P. falciparum in RBCs have been profiled; however, the proteins that regulate the m6A containing mRNAs in the parasites are unknown. Results Using sequence analysis, we computationally identified that the P. falciparum genome encodes two putative YTH (YT521-B Homology) domain-containing proteins, which could potentially bind to m6A containing mRNA. We developed a modified methylated RNA immunoprecipitation (MeRIP) assay using PfYTH2 and find that it binds selectively to m6A containing transcripts. The PfYTH2 has a conserved aromatic amino acid cage that forms the methyl-binding pocket. Through site-directed mutagenesis experiments and molecular dynamics simulations, we show that F98 residue is important for m6A binding on mRNA. Fluorescence depolarization assay confirmed that PfYTH2 binds to methylated RNA oligos with high affinity. Further, MeRIP sequencing data revealed that PfYTH2 has more permissive sequence specificity on target m6A containing mRNA than other known eukaryotic YTH proteins. Taken together, here we identify and characterize PfYTH2 as the major protein that could regulate m6A containing transcripts in P. falciparum. Conclusion Plasmodium spp. lost the canonical m6A-specific demethylases in their genomes, however, the YTH domain-containing proteins seem to be retained. This study presents a possibility that the YTH proteins are involved in post-transcriptional control in P. falciparum, and might orchestrate the translation of mRNA in various developmental stages of P. falciparum. This is perhaps the first characterization of the methyl-reading function of YTH protein in any parasites.

in the human host. Comparative transcriptomic and proteomic studies of different P. falciparum stages have shown that there is a marked delay between mRNA synthesis and protein expression for nearly 30% of the 2584 analyzed genes [3]. Importantly, developmental switches in P. falciparum are marked by broad changes in transcriptional activity [4][5][6]. These findings suggest that Plasmodium spp. have distinct regulatory mechanisms, both at the post-transcriptional and translational levels that regulate various developmental stages of the Plasmodium lifecycle. Such unique mechanisms to fine-tune the global gene expression might help P. falciparum to establish successful pathogenesis inside the human host.
Epigenetic modifications such as DNA and histonemethylation play a pivotal role in regulating gene expression and safeguarding genome integrity. Nevertheless, the knowledge of the nucleic acid methylome in human malaria parasite is limited. Discovery of reversible adenine methylation on mRNA in many higher eukaryotes has opened new avenues to explore the post-transcriptional gene regulation in eukaryotic pathogens [7,8]. Interestingly, some apicomplexan parasites have lost DNA methylation machinery, but retain the cytosine-5 methyltransferase that methylate tRNA rather than DNA [9][10][11]. However, residual levels of DNA methylation have been detected in the genome of P. falciparum [12]. In addition to this, the number of transcription-associated proteins, such as specific transcription factors and the subunits of the mediator complex, are fewer in P. falciparum and P. vivax, as compared to other eukaryotes [13][14][15][16].
Presence of only a few transcription factors suggests that parasite might have a unique modes of gene regulation at the RNA level [17,18]. The mRNA of P. falciparum may undergo stringent regulation to facilitate delayed protein synthesis in a stage-dependent manner. The stability and fine-tuning of mRNA processing could happen at two levels: (i) addition of poly (A) tails at 3′ end of RNA and/or (ii) epigenetic modifications of mRNA, particularly N 6 -adenosine methylation of the matured mRNA. RNA modifications have emerged as critical biological regulators of tRNA, rRNA, and mRNA homeostasis in eukaryotes [19]. For instance, in eukaryotes the C38 modification of tRNA aspartic acid regulates the stability of tRNA [20], whereas in P. falciparum tRNA methylation may have a significant role in the regulation of poly-aspartic acid containing proteins [9]. Importantly, dynamics of tRNA modifications has been shown to control the stage-specific gene expression in P. falciparum [19].
In higher eukaryotes, N 6 -methyl adenosine (m6A) modifications of mRNA and lncRNAs regulate the RNA tertiary structure and recruit the m6A binding proteins [21]. m6A is a highly conserved eukaryotic modification on DNA and RNA. However, the functions of mRNA adenosine methylation are less understood in many organisms, particularly in apicomplexan parasites such as P. falciparum. Recently, m6A has been identified as predominant modification on mRNAs of P. falciparum and that this post-transcriptional modification is dynamically distributed [22].
In this study, we aimed to identify and characterize the potential m6A modification methyl-reader proteins in P. falciparum. We searched YTH-specific homologue in the genome of the parasite and identified two putative proteins in P. falciparum (PfYTH), in concordance with a previous report [22]. As PfYTH2 showed higher similarity with other known eukaryotic YTH proteins, here we functionally characterized this putative methyl-binding protein. For this, we developed a modified MeRIP assay with PfYTH2 and identified that it binds strongly to m6A containing mRNA and RNA oligos in vitro. Importantly, PfYTH2 forms the m6A binding pocket with a cluster of aromatic amino acids that preferentially binds to m6A containing mRNA with high affinity. Experimental sitedirected mutagenesis followed by molecular dynamics simulation analysis revealed reduced binding of PfYTH2 mutant protein to m6A-containing RNA. Next, we developed a modified methylated RNA immunoprecipitation (MeRIP) assay using recombinant PfYTH2 protein. We used this assay, along with NGS sequencing to identify the m6A specificity of PfYTH2. Interestingly, the PfYTH2 protein has more permissive sequence specificity on m6A containing mRNA than the YTH proteins of other organisms. Such permissive binding has a potential role in the regulation of selective/delayed translation of specific transcripts in P. falciparum during its development in RBCs. We anticipate that the findings presented here will propel further research in elucidating the role(s) of m6A on P. falciparum mRNAs and PfYTH proteins in regulating the development and pathogenicity of the parasite.

Identification and biochemical characterization of PfYTH2 protein
Plasmodium falciparum exhibits a high translational shift in the RBC stages during its development [3], but the regulators that facilitate these translational shifts, at the post-transcriptional level are unknown. As the P. falciparum mRNAs are enriched with m6A modifications, we searched for the m6A reader protein YTH homologs in the genome of P. falciparum. The YTH domain family proteins are known to bind m6A on mRNA in other eukaryotes [23,24]. We performed sequence analysis and found that the P. falciparum genome encoded two YTH domain-containing proteins (PfYTH1 and PfYTH2), as previously reported by Baumgarten et al. [22]. Importantly, we found that PfYTH2 protein contains conserved aromatic amino acids that are essential to bind methylated adenosine (Additional file 1: Figure S1). We then cloned the PfYTH2 domain protein, expressed and purified as GST tagged protein (Additional file 1: Figure  S2A-C and Fig. 1a). Next, we tested if PfYTH2 protein binds to P. falciparum m6A mRNAs. For this, we developed a modified MeRIP assay using PfYTH2 protein and performed methylated RNA immunoprecipitation to identify the m6A specific interaction. ImageJ analyses showed that the quality of the PfYTH2 is nearly 80%, and sufficient to perform in vitro pull-down assays (Additional file 1: Figure S3A, B). To identify the m6A enrichment in the PfYTH2 MeRIP assay, we performed dot blot assay using RNA enriched with MeRIP and probed with anti-m6A antibody. We found strong binding of PfYTH2 protein to m6A-containing RNAs compared to negligible binding in the GST control samples (Fig. 1b). This indicates that the PfYTH2 protein has the methyl-binding ability and can bind to m6A-containing transcripts.

PfYTH2 binds to methylated mRNA via methyl-binding pocket
To obtain mechanistic insights into the PfYTH2 interaction to m6A-containing RNA, we generated the homology model of PfYTH2 protein with human YTH as a template [23] using Swiss-Model with default parameters. We found that PfYTH2 forms a methyl-binding pocket with conserved aromatic amino acids (Fig. 1c). We superimposed the m6A-containing RNA ligand with the PfYTH2 model and found that methyl adenosine precisely fits the methyl-binding pocket surrounded with aromatic amino acids in the PfYTH2 (Fig. 1d). Calculation of the electrostatic potential for the PfYTH2 homology model using the PDB2PQR server [25] (http:// nbcr-222.ucsd.edu/pdb2p qr_2.0.0/) with default parameters revealed that PfYTH2 forms basic amino acid patches to bind with the negatively charged m6A-containing RNA ligand (Fig. 1c, d). To identify the potential aromatic amino acids that mediate interaction to m6A, we selected aromatic amino acids W46, F98, W114 from the methyl-binding pocket and mutated them to alanine by site-directed mutagenesis and confirmed the mutation by DNA sequencing (Additional file 1: Figures S2D and  S4A). We purified the mutant proteins of similar quality (Additional file 1: Figure S4B) and tested their m6A specific interaction with RNA using modified MeRIP assay. We observed a significant reduction in binding to m6A containing mRNA for PfYTH2 F98A mutant protein, and a slight reduction in W46A mutant, whereas the W114A mutant did not show any significant loss of binding (Fig. 1e, f ). Collectively, these results indicate that the P. falciparum PfYTH2 protein contains a functional methyl-binding pocket, which is essential to interact with m6A containing mRNA, with a possible role in regulating the mRNA functions in different stages of the parasite development in RBCs.

Molecular dynamics simulations highlight that F98 residue is important for PfYTH2 binding to m6A containing mRNA
To consolidate the m6A-specific interaction of PfYTH2 protein, we performed MeRIP pull-down assay with PfYTH2 F98A methyl-binding pocket mutant and found a significant loss of interaction with m6A containing mRNA (Fig. 1e, f ). To further rationalize our observations, PfYTH2 point mutations (W46A, F98A, and W114A) were computationally designed by considering initial protein coordinates from modeled PfYTH2 structure using rosetta software package suite (https ://www. roset tacom mons.org/). To study the effect of the point mutations on RNA binding, we performed atomic-level molecular dynamics simulations of the mutant protein-RNA complexes for 30 ns using Gromacs simulation package [26,27]. However, based on backbone root mean square deviation (RMSD) observations further analyses of protein-RNA complex simulations were restricted to 5-30 ns time scale to minimize the pre-equilibration artifacts (Fig. 2a).   We first assessed the overall potential energy changes of the protein-RNA complex to comprehend the effect of point mutations. Potential energies were calculated for wild type (WT) and mutant protein-RNA complexes over the simulation timescale. Interestingly, protein-RNA complexes with F98A point mutation showed a significant drift of − 122.349 (kJ/mol) over the timescale. This suggests a reduced binding interaction between the mutant PfYTH2 F98A and m6A-mRNA, corroborating well with our modified MeRIP assay, where a significant loss in binding is observed between mutant protein F98A and m6A-containing mRNA (Figs. 1e, 2b-d). In line with this observation, the average distance fluctuations monitored between F98A mutant protein and RNA also revealed significant variations compared to wild type, W46A and W114A mutations, over the simulated time scale (Fig. 2b). In addition, a higher resolution assessment between m6A residue and active site residues F98A and W46A from protein-RNA complexes revealed the minute drifting fluctuations of m6A from the residues F98A and W46A inside the active pocket compared to wild type and W114A point mutation (Fig. 2c, d). Collectively, these results highlight the importance of F98 and a possible role of W46 residues of PfYTH2 in binding with m6A mRNA.

PfYTH2 is the m6A-specific methyl-reader protein of P. falciparum
We next tested if PfYTH2 protein interacted with mRNAs in an m6A-dependent manner. To validate the m6A specificity of PfYTH2 protein, we adopted a twopronged approach. First, we performed PfYTH2 pulldown experiments with in vitro transcribed RNA as control and Pf RNA as a test (Additional file 1: Figure  S5A). We found a stronger interaction of PfYTH2 to Pf RNA than in vitro transcribed RNA (Fig. 3a, b). Second, we used synthetic RNA oligos containing m6A modification as a test and unmodified RNA oligos as control (Additional file 1: Figure S5B). We performed MeRIP pull-down assay for PfYTH2 protein, and dot blot assay was performed to confirm the m6A RNA oligos enrichment. We observed that PfYTH2 binds strongly to the m6A-containing RNA oligos than the unmodified RNA oligos (Fig. 3c, d).
To determine the binding affinity of PfYTH2 protein to the m6A-containing RNA, we performed fluorescence depolarization assay in solution. For this, we used cy5 fluorophore labeled m6A modified and unmodified RNA oligos. The free RNA oligos are highly depolarized with excitation of cy5 fluorophore, whereas binding of PfYTH2 protein decreases the mobility of RNA oligos and leads to increased polarization (anisotropy). To measure the binding affinity, various concentrations of PfYTH2 proteins were added to the cuvette containing m6A-containing RNA oligos. Fluorescence depolarization measurements revealed that PfYTH2 binds to m6A-containing RNA oligos with high affinity than to unmodified RNA oligos (Fig. 4a, b). The data points were fitted using a binding model and the binding constant calculation yielded K d 0.4 ± 0.07 μM for PfYTH2 with m6A-modified RNA oligos (Fig. 4b). Based on our above experimental and MD simulation findings, we hypothesized that F98 is essential for high-affinity binding of PfYTH2 to m6A RNA. To test this, we performed the depolarization assay with PfYTH2 F98A mutant protein and found a significant loss of its binding to m6A-containing RNA oligos (Fig. 4c). The calculated dissociation constant for wild-type protein to m6A RNA oligos is four times higher affinity than the mutant F98A protein (Fig. 4d). Taken together, these results establish that PfYTH2 protein is an m6A modification reader protein, facilitated by F98 residue and may have a significant role in controlling the fate of m6A containing mRNA in P. falciparum.

PfYTH2 binds to methylated mRNAs with permissive sequence selectivity
We performed a modified MeRIP assay with fragmented Pf RNA coupled with next-generation sequencing to identify m6A-containing mRNAs that are read by PfYTH2 protein (Fig. 5a, Additional file 1: Figure S6A, B). We next prepared the library from the enriched mRNA (Additional file 1: Figure S7) and sequenced using Illumina NextSeq Single-end sequencing with 75Χ1, and obtained an average of 24.16 million reads. More than 80% of the sequencing reads were successfully aligned to the P. falciparum genome, using Bowtie2 (Additional file 1: Figure S8). The PfYTH2 specific pull-down sample was normalized to the input control. Next, we investigated for the PfYTH2-specific enrichment of aligned reads to the genome and found that more than 60% of aligned reads corresponds to the transcription termination site (TTS), at the 3′ end of the gene (Fig. 5b). The PfYTH2-specific enrichment of sequence reads to the TTS region suggests that m6A methyl marks in P. falciparum are highly enriched at the 3′ end of the transcript. Notably, some of the PfYTH2-specific transcripts that are mapped to TTS regions are transcription factors and metabolism-associated genes ( Table 1). This explains that expression of transcription factors and metabolic pathway proteins could be tightly regulated through PfYTH2-m6A modification specific interaction on mRNA of P. falciparum.
Next, we aimed to identify sequence patterns that PfYTH2 could specifically recognize or bind to. For this, we searched for potential binding motifs that a b c d Fig. 3 PfYTH2 specifically binds to m6A-containing RNA. a A representative dot blot image for the transcripts from MeRIP assay with in vitro transcribed RNA (negative control) and Pf RNA (positive control). The eluted fractions were spotted on membrane and probed with anti-m6A antibody. b The bar plot shows the intensity of spots and the distribution of data points from three independent experiments and error bar represents SEM of three biological replicate samples. The dot plot graph on the right side represents the distribution of data points from same three independent experiments. c A representative dot blot image for the transcripts from MeRIP assay with synthetic RNA oligos (positive control) with m6A modification and unmodified RNA oligos (negative control). The MeRIP assay with PfYTH2 F98A methyl-binding pocket mutant shows reduced interaction. The eluted fractions were spotted on membrane and probed with anti-m6A antibody. d The bar plot shows intensity of spots from three independent experiments and error bar represents SEM of three biological replicates. The dot plot graph on the right side represents the distribution of data points from same three independent experiments. Statistical significance was assessed using paired t-test could be enriched in the PfYTH2 protein-specific TTS reads. We found a motif A(C)G(AU)G(A)AA(UC) U(C) with guanine or adenine at −1 position to target adenine, purines at −2 and adenine at −3 to be significantly enriched in more than 80% of the TTS reads (Fig. 5c). We validated the PfYTH2 pull-down assay experiments for the 6 candidates that are transcripts of genes associated with transcription and/or metabolism, followed by qRT-PCR analysis. We found a statistically significant enrichment of the PfYTH2-specific interaction of m6A containing transcripts compared to the GST control (Fig. 5d). The structural and biophysical data of YTH proteins from higher eukaryotes show that YTH protein strongly prefers the guanine base at −1 and −2 positions to target adenine and cytosine base at +1 position and disfavor the adenine at these positions [23,24]. The motif analyses for MeRIP sequence reads revealed that PfYTH2 has more permissible flank sequence specificity to methylated adenosine, unlike YTH proteins from higher eukaryotic organisms. This relaxation in sequence specificity could be due to the presence of only two YTH domain proteins in P. falciparum, as against multiple YTH domain-containing proteins in eukaryotes. Collectively, these results establish that PfYTH2 selectively binds to m6A mRNA, and has more permissive sequence specificity for binding with target methylated adenosine on mRNA of P. falciparum.

Discussion
Accumulating evidences suggest that m6A modification on mRNA is a major epigenetic player that regulates the mRNA fate, translation, and stability in diverse eukaryotes [28][29][30]. The role of m6A modification in post-transcriptional regulation in Plasmodium spp. has not been studied in detail. The m6A-based regulation of mRNA is achieved through N 6 -adenosine d c a b Fig. 5 Modified MeRIP analysis using PfYTH2. a The experimental flow of modified MeRIP using PfYTH2. b Pie chart represents the PfYTH2 specific MeRIP enriched reads mapped to the genome that are normalized to GST control. More than 60% of transcripts mapped to TTS region. c The motif analysis of TTS specific reads enriched in PfYTH2 samples. About 80% of reads mapped to the represented motif with a significant p-value. d Validation of the PfYTH2 specific enrichment of 6 candidate transcripts by qRT-PCR analysis. PfYTH2 and GST specific enrichment was calculated to percentage input of samples, the error bar represents SEM (n = 3). Statistical significance was calculated using paired t-test methyltransferases (writer), adenine demethylases (erasers), and methyl-reader proteins such as the YTH family of proteins. In this study, we have identified m6A-specific methyl-binding protein PfYTH2 in P. falciparum, and characterized its m6A-specific binding and showed that the protein has relaxed sequence specificity to recognize the m6A containing mRNAs. Multiple YTH domain-containing proteins are encoded by eukaryotic genome; for instance, five YTH domain-containing proteins have been identified in humans [31]. However, P. falciparum genome encodes only two YTH homology domain proteins [22]. Human YTH domain proteins have a stringent sequence specificity to bind with m6A containing mRNA. For instance, human YTHDC1 strictly prefers guanine at − 1 and − 2 positions to target methylated adenine [23]. Similarly, the YTH domain protein from rat prefers guanine at − 1 to target methylated adenine [32]. These findings clearly suggest that the flanking sequence of target methylated adenine is an important determinant of YTH2 binding and subsequent post-transcriptional regulation mediated by the methyl-binding proteins. Contrary to the observations made across different eukaryotic YTH2 proteins, here we identified that PfYTH2 protein has relaxed flanking sequence specificity. Importantly, Baumgarten et al., reported the presence of cytosine at +1 to the target methylated adenine in P. falciparum [22]. Our PfYTH2 pull-down data corroborate with this study as we observed cytosine as well as adenine and thymine nucleotides. However, the number of m6A-specific enriched transcripts identified in our PfYTH2 MeRIP is fewer than anti-m6A antibody MeRIP used by Baumgarten et al. These differences may have resulted from the differences in experimental setups as Baumgarten et al., used anti-m6A antibody for the MeRIP assay, whereas we used PfYTH2 recombinant protein to enrich the m6A-containing transcripts. Because of the high-affinity nature, the anti-m6A antibody could bind to a large number of transcripts than the recombinant protein that we used in our assay. Moreover, the binding of recombinant YTH protein to m6A-containing transcripts is influenced by flanking bases adjacent to target m6A on RNA. Nevertheless, the six candidate transcripts obtained in PfYTH2 pull-down NGS data analysis, that we validated by qRT-PCR were also identified in anti-m6A antibody MeRIP [22] (Fig. 5d). The relaxed sequence specificity of PfYTH2 might be essential to bind with diverse methylated transcripts to regulate the functions of m6A containing mRNAs in P. falciparum. Surprisingly, the apicomplexa group of parasites, including P. falciparum contains conserved writer complexes (mRNA N6-adenosine methyltransferase) [22], but does not encode a homolog for FTO and ALKBH5 proteins, well-known m6A specific demethylases in eukaryotes. The apicomplexa parasites encode the methyl-reader proteins, but the absence of adenine demethylases in their genome suggests that regulation of m6A-containing mRNA are largely controlled by YTH methyl-binding proteins in P. falciparum. Given these findings, it is tempting to speculate that YTH proteins may have significant functions to regulate differential stage-specific global gene expression patterns in P. falciparum.

Conclusion
Apicomplexa parasites including P. falciparum lead a complex life cycle for multiplication to establish infection in the host(s). This parasite undergoes multiple developmental stages in different hosts and employs stringent gene regulatory mechanisms to achieve the optimal gene expression during various developmental stages. The stage-specific transcriptome and proteome analysis of P. falciparum have shown a delay in mRNA synthesis and its corresponding proteins between various developmental stages [3]. This suggests that strong post-transcriptional mechanisms might be involved to regulate protein synthesis in the parasite. The accumulating evidences in many eukaryotes has shown that epi-transcriptome modification on mRNAs such as m6A modification has an important role(s) in the regulation of the mRNA stability and translation. In this study, we report the m6A-specific methyl-binding activity of PfYTH2 in P. falciparum, and showed that the protein has relaxed sequence specificity to recognize the m6A containing mRNAs. This study sheds light on the thus far unknown layer of regulatory processes that is essential for post-transcriptional regulation in various stages of parasite development to finetune the stage-specific translation in P. falciparum.

Plasmodium falciparum 3D7 culture maintenance
The blood stage of P. falciparum 3D7 was cultured in the 37 °C incubator with 5% haematocrit in RPMI 1640 (Gibco Cat # 11875093) supplemented with 10% of O+ve plasma and 0.5% albumax II (Gibco Cat # 11021037) and maintained by sub-culturing when sufficient parasitemia was achieved. Growth of P. falciparum was verified by preparing the thin smear followed by Giemsa staining and proceeded to RNA isolation.

Cloning, expression and purification of PfYTH2 protein
The putative YTH2-specific sequence was amplified from cDNA prepared from mRNA isolated from trophozoite culture of P. falciparum 3D7. The ORF sequence for each gene was cloned in pGEX6P2 (GE Healthcare) vector using restriction sites BamH1 in the forward primer and Xho1 site in the reverse primer (Additional file 1: Table S1). The PfYTH2 clone was verified by double digestion with BamHI and XhoI sites and further confirmed by DNA sequencing. The site-directed mutagenesis was performed with mutant primer by rolling circle amplification and the presence of specific mutations in the plasmids was confirmed by DNA sequencing. The expression of PfYTH2 wild type and PfYTH2 mutant proteins were carried out in BL21DE3 cells and the cells were lysed in lysis buffer (20 mM HEPES pH 7.5, 500 mM KCL, 1 mM EDTA, 1 mM DTT, 10% glycerol) using sonicator. The cell lysate was centrifuged to remove the cell debris and the supernatant passed through the GST-Sepharose beads (GE Healthcare) chromatography column and washed with lysis buffer. The GST tagged YTH proteins were eluted using elution lysis buffer containing 40 mM reduced glutathione (Sigma-Merck). The protein was subjected to dialysis process in two different dialysis buffers (dialysis buffer I-20 mM HEPES pH 7.5, 200 mM KCL, 1 mM EDTA, 1 mM DTT, 10% glycerol; dialysis buffer II-20 mM HEPES pH 7.5, 200 mM KCL, 1 mM EDTA, 1 mM DTT, 60% glycerol). The quality of the proteins was analyzed on 12% SDS-PAGE gel and stained with Coomassie brilliant blue.

RNA isolation from P. falciparum
RNA was isolated from the fresh parasite pellets by lysing the parasite cells with Trizol reagent followed by Qiagen RNA isolation kit (Cat # 74104). The quality of the RNA was analyzed on formaldehyde-denatured gel and the RNA stored at − 80 °C for further experiments.

Dot blot assay
The dot blot assay was carried out to detect the presence of methyl adenines in the immunoprecipitated RNA from MeRIP assay. The MeRIP enriched RNA was spotted on positively charged nylon membrane (GE Healthcare Cat # RPN303B) and RNA was cross-linked using UV crosslinker with 0.1 J for 6 min. Presence of RNA in the membrane was confirmed by Methylene blue staining and the stain was washed using 1X TBST, and the membrane was blocked in 5% skimmed milk overnight. The mouse anti-m6A antibody (Diagenode-Cat # C15200082) was used to probe m6A on RNA and anti-mouse HRP conjugated was used as secondary antibody. The blot was developed using chemiluminescence ECL substrate (Bio-Rad # 1705061).

Fluorescence depolarization assay
We performed fluorescence depolarization assay to calculate the binding affinity of PfYTH2 with m6A-containing RNA oligos using fluorescence spectrophotometer.
The assay was performed with 50 nM of m6A modified and unmodified RNA oligos (Additional file 1: Figure  S5B) labeled with cy5 fluorophore by titrating with varying concentrations of PfYTH2 wild type and F98A mutation proteins. The reactions were carried out in binding buffer containing 50 mM Tris pH 7.5, 100 mM NaCl, 1 mM EDTA and 0.05% NP40. The protein-RNA interaction was studied using fluorescence depolarization with the excitation wavelength at 633 nm (band-width 10 nm) and the emission wavelength at 665 nm (bandwidth 10 nm). The interaction reaction was initiated with 50 nM of Cy5-labeled RNA oligos in binding buffer and increasing concentration of proteins were added for each measurement. The measurements were collected for each concentration of proteins after incubation of protein and RNA complexes at room temperature for 3 min. Each protein concentration was measured in triplicate and the average values were taken for the analysis. The data were fitted to a binary binding equilibrium to determine the equilibrium binding constant using the Microsoft excel solver module.

MeRIP assay for synthetic RNA oligos containing m6A modification
We used methylated RNA immunoprecipitation (MeRIP) to study the m6A specificity for PfYTH2 in vitro using synthetic RNA oligos. We procured synthetic RNA oligos containing m6A with appropriate flanks and unmodified oligos for control experiments (Eurogentec, Belgium). The RNA oligos were reconstituted in RNAsefree water and the presence of m6A was verified by dot blot assay (Additional file 1: Figure S5B). We used 4 µg of RNA oligos to each modified and unmodified reaction and performed pull-down assay with PfYTH2 wild type and F98A mutant proteins. The bound RNA oligos were eluted as described above using competitor molecule. The specific enrichment of the interaction of the RNA oligos to the proteins was studied using dot blot assay. The pull-down experiment was repeated thrice and standard error of mean (SEM) was calculated. The p-values were estimated using paired t test to assess the significance of enrichment of m6A-containing RNA oligos with YTH2 in MeRIP assay.

Computational design of mutant PfYTH2
PfYTH2 point mutation models (W46A, F98A, and W114A) for molecular dynamics simulations were computationally designed for modeled PfYTH2 using rosetta backrub method for flexible backbone design described [33]. A total of 100 models were constructed for each point mutation design, the best models were selected based on the rosetta score obtained using rosetta ref2015 scoring function [34,35] by calculating the energy of all atomic interactions in the protein.

Molecular dynamics simulations
The all-atom molecular dynamics simulations were carried out using GROMACS 2019.3 molecular dynamics simulation package [26,27]. The additive Charm36 force field files were obtained for Gromacs from a previous study [36] to describe the protein-RNA complex with modified N 6 -methyl adenosine base. The protein-RNA complex was solvated by TIP3P water model in a cubic box with a distance cutoff 10 Å between the edge of the periodic box and surface of the protein-RNA complex.
The system was neutralized with Na + counter ions followed by energy minimization using steepest-descent algorithm down to a 1000 kJ/mol/nm till the energy gets converged. Before production run, all systems were equilibrated for pressure and temperature by position restraining the protein-RNA for 100 ps using canonical Number of particles (N), Pressure (P) Temperature (T) and Number of particles (N), Volume (V), Temperature (T) ensembles at respective temperatures. The longrange electrostatic interactions were calculated using Particle Mesh Ewald (PME) [37] method with a grid spacing of 0.16 nm and a cutoff of 1.0 nm was used for shortrange electrostatic and van der Waals interactions. Bond lengths were constrained using LINCS algorithm [38]. All simulations were performed using a 2-fs integration time step, with a coupling coefficient of tT − 0.1 ps using modified Berendsen thermostat [39], and Parrinello-Rahman pressure-coupling at 1 bar with a coupling coefficient of tP = 1 ps. All the results were analyzed using Gromacs 2019.3 package.

Library preparation and sequencing
DNA libraries were prepared with illumine compatible SMARTer Stranded Total RNA-Seq Kit v2 (Takara Bio USA, Inc. Cat # 634411). 400 pg of total RNA was taken for first strand synthesis followed by second strand synthesis by template switching mechanism. This was further processed with addition of Illumina adaptors and barcode as per SMARTer Stranded Total RNA-Seq Kitv2 in final PCR amplification of 16 cycles. The bar code ligated libraries were purified using HighPrep beads (Cat # AC-60050) followed by library quality control check. Illumina-compatible sequencing library was quantified by Qubit fluorometer (Thermo Scientific, MA, USA) and the fragment size distribution was analyzed on Agilent 2200 Tapestation. We got Illumina-compatible sequencing libraries with mean fragment size of ~ 338 bp.

MeRIP sequencing data analysis
The generated raw data was checked for the quality using FastQC software and reads were preprocessed to remove the adapter sequences and removal of the low quality bases (< q30) towards 3′-end using TrimGalore. We downloaded the reference genome P. falciparum 3D7 from PlasmoDB (https ://plasm odb.org/commo n/downl oads/relea se-24/Pfalc iparu m3D7/) and mapped the sequencing reads using Bowtie2 v0.9.6 tool with default parameters (Additional file 1: Figure S8). The transcript abundance was estimated using HTSeq-count v0.6.1. The MACS2 v2.1.4 software was used to identify peaks in GST and YTH sample with respect to input sample. MACS2 function was used to call peaks from alignment results. The input for this command includes the alignment files for IP and the control (input) samples along with the q value (minimum FDR) cutoff to call significant regions. The enriched peaks with q-value 0.01 obtained using MACS2 and fold enrichment for each peak summit was calculated against random Poisson distribution with local lambda. The MACS tool was used for peak identification, during the peak calling step. The location with the highest fragment pileup is referred as the absolute summit which provides the details about precise binding location. Further, the precise m6A position was used for HOMER annotation for the details of annotated regions. The summit file had only one base (m6A) information identified by MACS which was used as input for HOMER annotation. The HOMER annotation includes peaks in Transcription Start Site (TSS; the region that spans from core promoter and 5′ UTR), Transcription Termination Site (TTS; the region present at 3′ UTR, which could be a single nucleotide or could be short region averaged over a small population of RNA molecules), Exon (Coding), Intronic, or Intergenic. To identify the target motif and annotate transcripts from MeRIP analysis, we used HOMER software. The HOMER helps in motif identification, considering peaks with ≥ onefold change. We identified the enriched motifs in these peak regions. For this, the broad peak sequences for both samples are fetched out and analyzed for possible motifs. With total number of target sequences, the HOMER identified 120 (81.6%) number of target sequences are with the motif. It uses default the find MotifsGenome program and performs de novo motif discovery as well as checks for the enrichment of motifs. Further, the peaks are annotated using reference genome annotation file by annotate peaks program in HOMER tool with default parameter. This program first determines the distance to the nearest TTS and assigns the peak to that gene and subsequently determines the genomic annotation of the region occupied by the center of the peak/region.

qRT-PCR analysis of PfYTH2 MeRIP enriched transcripts
To validate the NGS data of PfYTH2 pull-down samples, we performed MeRIP using PfYTH2 and GST as control for P. falciparum RNA. The bound RNA from PfYTH2 protein was eluted using elution buffer containing competitor (Abcam Cat # ab145715) for m6A modification. The eluted RNA was used for cDNA synthesis. We performed a cDNA synthesis using Maxima H minus First strand synthesis kit (Thermo Scientific Cat # K1681). Briefly, the eluted RNA from YTH, GST and the input RNA were subjected to DNase digestion with 10× DNase buffer for 2 min at 37 °C in the preheated water bath separately. Then, oligo dT primers, random hexamer and 10 mM dNTPs were added to the DNase treated tubes and reaction volume was made up to 15 µl. The reaction mixtures were mixed gently and incubated at 65 °C for 5 min. Then 5× reverse transcriptase buffer, Maxima H Minus enzyme mix were added and volume of the mixtures were made up to 20 µl. Afterwards, cDNA synthesis for all the reactions were carried out in PCR machine using following conditions, 25 °C for 10 min followed by 50 °C for 15 min,