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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptHHS Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
 
Cell Stem Cell. Author manuscript; available in PMC 2014 April 4.
Published in final edited form as:
PMCID: PMC3684274
NIHMSID: NIHMS446857

Stage-Specific Roles for Tet1 and Tet2 in DNA Demethylation in Primordial Germ Cells

SUMMARY

Primordial germ cells (PGCs) undergo dramatic rearrangements to their methylome during embryo-genesis, including initial genome-wide DNA demethylation that establishes the germline epigenetic ground state. The role of the 5-methylcytosine (5mC) dioxygenases Tet1 and Tet2 in the initial genome-wide DNA demethylation process has not been examined directly. Using PGCs differentiated from either control or Tet2−/−; Tet1 knockdown embryonic stem cells (ESCs), we show that in vitro PGC (iPGC) formation and genome-wide DNA demethylation are unaffected by the absence of Tet1 and Tet2, and thus 5-hydroxymethylcytosine (5hmC). However, numerous promoters and gene bodies were hypermethylated in mutant iPGCs, which is consistent with a role for 5hmC as an intermediate in locus-specific demethylation. Altogether, our results support a revised model of PGC DNA demethylation in which the first phase of comprehensive 5mC loss does not involve 5hmC. Instead, Tet1 and Tet2 have a locus-specific role in shaping the PGC epige-nome during subsequent development.

INTRODUCTION

DNA methylation is an epigenetic mark involving the addition of a methyl group to the fifth carbon of a cytosine base (5mC). In mammalian cells, DNA methylation is established and maintained mostly in CG sequence contexts, and the amount of cytosine methylation in a given genome is relatively stable (Feng et al., 2010). Despite this stability, there are periods in embryonic development where DNA methylation is significantly reduced, including after oocyte fertilization, during preimplantation embryo development, and during primordial germ cell (PGC) formation (Gkountela et al., 2012; Guibert et al., 2012; Hackett et al., 2013; Hajkova et al., 2008; Hajkova et al., 2002; Hajkova et al., 2010; Monk et al., 1987; Okano et al., 1999; Popp et al., 2010; Seisenberger et al., 2012; Seki et al., 2005; Smith et al., 2012). Recent work has revealed a critical role for the oxidation of 5mC to 5-hydroxymethylcytosine (5hmC) by Tet methylcytosine dioxygenase 1 (Tet1) and Tet2 in locus-specific DNA demethylation in PGCs (Yamaguchi et al., 2012; Hackett et al., 2013). However, a role for 5hmC in the initial widespread (global) depletion of DNA demethylation in PGCs has not been addressed (Figure 1A).

Figure 1
Generation of PGCs from ESCs Results in a Significant Decrease in CG Methylation

PGCs are the founder cells of the metazoan germline, and abnormal PGC development causes infertility or cancer. Mammalian PGCs are specified de novo in each generation from the epiblast (Lawson and Hage, 1994; Ohinata et al., 2006; Tam and Zhou, 1996; Ying et al., 2001) and begin as highly methylated cells (Seki et al., 2005). Although methylation is critical for lineage specialization (Lei et al., 1996), it poses an inherent problem for PGCs, which become globally depleted of DNA methylation by e13.5 (Guibert et al., 2012; Kafri et al., 1992; Monk et al., 1987; Popp et al., 2010). This differential has lead to a longstanding hypothesis that a loss of methylation in PGCs prior to e13.5 is necessary to restore the germline epigenetic ground state, but the mechanisms for this restoration are not well understood (Reik and Walter, 2001).

PGCs undergo DNA demethylation in two phases (Seisenberger et al., 2012) (Figure 1A). The first phase involves global depletion of cytosine methylation with the retention of locus-specific methylation at imprinting control centers (ICCs), single copy genes, and repetitive elements (Guibert et al., 2012; Hackett et al., 2013; Hajkova et al., 2002; Lane et al., 2003; Lees-Murdock et al., 2003; Seki et al., 2005). The second phase occurs from e9.5 to e13.5, where methylation is depleted from the PGC genome in a locus-specific manner (Guibert et al., 2012; Hackett et al., 2013; Hajkova et al., 2008; Hajkova et al., 2002; Hajkova et al., 2010; Popp et al., 2010; Seisenberger et al., 2012; Yamaguchi et al., 2012). Recent work has revealed a role for Tet1 in the locus-specific demethylation of meiotic genes (Yamaguchi et al., 2012). However, given that 5hmC levels were reduced by only 45% in this model, it is conceivable that a second Tet protein may have compensated for loss of Tet1. More recently, a double knockdown of Tet1 and Tet2 in embryonic stem cell (ESC)-derived PGCs revealed a role for Tet1 and Tet2 in the demethylation of germline genes Deleted in azoospermia-like (Dazl), Maelstrom (Mael), and Synaptonemal complex protein 3 (Sycp3) (Hackett et al., 2013). However, it was not determined whether Tet1 and Tet2 act to regulate global DNA demethylation in phase 1.

In the current study, our goal was to evaluate the role of Tet1 and Tet2 in genome-wide DNA demethylation by differentiating in vitro PGCs (iPGCs) from ESCs. It has previously been reported that this method robustly captures immature PGCs transcriptionally younger than e10.5 of development at high purity (Vincent et al., 2011). However, it is not known whether global DNA demethylation occurs in this model. Therefore, this study had two goals. The first goal was to examine whether the differentiation of iPGCs from ESCs involves a genome-wide depletion of DNA methylation from the iPGC genome and, if so, the second goal was to use this model to determine whether Tet1 and Tet2 regulate phase 1 genome-wide demethylation in PGCs.

RESULTS

PGCs undergo DNA demethylation in two phases (Seisenberger et al., 2012). In phase 1, 5mC is depleted globally from the genome with rare, locus-specific retention of methylation, including the ICC of Snrpn (Figure S1A–S1D available online). To determine whether ESC-derived iPGCs undergo genome-wide demethylation, we used two independently derived ESC lines (V6.5 and Rosa26-GFP) and differentiated iPGCs with embryoid body (EB) differentiation. The iPGCs were sorted on day 6 with surface markers stage-specific embryonic antigen 1 (SSEA1) and c-kit and then gated on the SSEA1+ and c-kitbright double positive population (Figure S1F). The transcriptional identity of iPGCs was confirmed with single-cell gene expression analysis of 40 SSEA1+c-kitbright cells from the XY V6.5 background (Figure 1B). In this study, a higher cross threshold (Ct) indicated lower gene expression, and black indicated no detectable Ct and therefore no expression. We found that 38 of 40 iPGCs coexpressed the PGC genes Blimp1 and Dppa3 and that single iPGC sheterogeneously expressedDead end homolog 1 (Dnd1), as previously reported (Vincent et al., 2011). We also determined that the XY iPGCs do not express the spermatogonial marker Plzf and are negative for somatic lineage markers Hoxa1 and Hoxb1. Using bisulfite (BS) treatment of iPGC DNA followed by PCR amplification of the Snprn ICC, we demonstrate that iPGCs on day 6 are methylated, indicating that iPGCs have not completed phase 2 demethylation (Figure S1E).

Next, we performed whole-genome BS sequencing (BS-seq) to compare cytosine methylation in ESCs and iPGCs (Table S1). Notably, BS treatment does not distinguish between 5mC and 5hmC (Huang et al., 2010). Therefore, the use of BS was for detecting the sum of 5mC and 5hmC. Cytosine methylation was mapped with the use of BS Seeker (Chen et al., 2010) with mouse genome build mm9 (UCSC Genome Browser) allowing up to three mismatches. Using this approach, we quantified a statistically significant (p < 0.05) reduction in the levels of CG methylation in iPGCs relative to ESCs (Figure 1C). Specifically, we determined that, on average, 75% of cytosines in a CG sequence context in ESCs were methylated, whereas, in iPGCs, this was reduced to 47%. Cytosine methylation was also observed in non-CG contexts. However, the amounts of non-CG methylation were low, at around 2% or less (Table S1). Though non-CG methylation in iPGCs trended toward depletion, this trend did not reach statistical significance.

To map genomic regions where a loss of CG methylation occurred, we sequenced undifferentiated ESCs to 6.8× and iPGCs to 6.9× coverage per strand, resulting in 478,482,437 cytosines covered ≥ 4× in both samples. Sites with delta methylation levels ≥ 30% were subject to two-way binomial tests, which yielded 11,994,107 CG sites for further analysis. We determined that 8,623,115 methylated cytosines in a CG sequence context were significantly decreased in iPGCs, whereas only 81,884 methylated cytosines in a CG sequence context were significantly increased in iPGCs relative to ESCs (FDR ≤ 5%). Chromosomal views of iPGCs in 1 million bp windows revealed a chromosome-wide depletion of CG methylation across all chromosomes (Figure S1G). Metaplots of reference genes showed typical depletion of CG methylation at the transcription start site (TSS) in both iPGCs and ESCs but general hypomethylation in iPGCs across all upstream and downstream regions (Figure 1D). Examination of repeat regions including nuclear elements (SINEs and LINEs) revealed a similar depletion in CG methylation (Figure S1H and S1I). Next, we used a Shannon entropy calculation to capture the heterogeneity of methylated cytosines between samples (Figure S1J). We found that the entropy was considerably higher in iPGCs in comparison to ESCs. This was true for genes, pseudogenes, exons, and introns. The one exception was gene promoters (defined as −800 bp to +200 bp of the TSS), where the entropy was almost equivalent between ESCs and iPGCs. Altogether, we conclude that the loss of cytosine methylation from iPGCs occurred genome-wide and that the increased entropy indicates that the iPGC population is heterogeneously (not synchronously) undergoing demethylation.

To determine whether global changes in cytosine methylation correlate with global changes in gene expression, we plotted differentially methylated CG sites (DMS) against the average change in gene expression between ESCs and iPGCs for each reference gene (Figure 1E). ESC and iPGC gene expression data were obtained from Vincent et al., 2011. A Pearson correlation coefficient for all comparisons revealed that the DMS at promoters, gene bodies, exons, and introns exhibited no correlation to either an increase or a decrease in gene expression in iPGCs relative to ESCs (Figure 1E and Figure S1K). Unlike the majority of the PGC genome, analysis of CG islands (CGIs) revealed no change in the percentage of CG methylation (Figure 1F). However, a small number of promoter CGIs significantly gained methylation in iPGCs, and these were enriched in gene ontology groups associated with meiosis (Figure 1G and Table S2). This was confirmed by bisulfite PCR of the meiotic gene Tex12 CGI (Figure 1H). Altogether, these data demonstrate that methylation at CGIs undergoes dynamic and unique reorganization with iPGC differentiation.

Next, we evaluated changes in the distribution of methylated CGs in ESCs and iPGCs by mapping methylation levels from 0% to 100% as a fraction of total cytosine methylation (Figure 1I). Cytosine methylation in ESCs exhibited a typical bimodal distribution where 59.6% of cytosines had ≥80% methylation (red, high), whereas 12.2% of cytosines had ≤20% methylation (blue, low). In contrast, in iPGCs, we observed a substantial loss of cytosine methylation from the high category and a near doubling of cytosines in the low category (from 12.2% to 21.6%). The largest change between ESCs and iPGCs was in their progression to the intermediate category (yellow, > 0.2 and < 0.8), where methylation more than doubled (from 28.2% to 65.3%).

Finally, we evaluated the symmetry of cytosine methylation (Figure 1J). In this analysis, mC+mG refers to symmetrically methylated CG sites where the cytosine from both strands of DNA (with the opposite strand read as G) are methylated. Similarly, a symmetrically unmethylated site is represented by uC+uG. Our analysis shows that, when iPGCs are differentiated from ESCs, there is a loss in symmetrical methylation and a 3-fold increase in asymmetrical methylation (Figure 1J). Altogether, the differentiation of iPGCs from ESCs results in a genome-wide reduction in cytosine methylation similar to what was previously reported for immature PGCs in phase 1 (Seisenberger et al., 2012).

Tet Proteins and 5hmC Are Found in PGCs In Vivo and In Vitro

Given the role for Tet-mediated conversion of 5mC to 5hmC as an intermediate in locus-specific DNA demethylation (Hackett et al., 2013), we were interested in examining expression of Tet genes at a single-cell level in Oct4-GFP+ PGCs at e9.25, e10.25, and e11.5 (Figure 2A–2D) as well as iPGCs sorted at day 6 of EB differentiation (Figure 2E). Quantitative RT-PCR and RNA sequencing have been used to evaluate Tet gene expression in Oct4-GFP+ PGCs (Hajkova et al., 2010; Yamaguchi et al., 2012; Hackett et al., 2013); however, the heterogeneity between PGCs in sequential developmental ages has not been well defined. Single-cell analysis revealed that Tet1 is expressed as early as e9.25, and it was detected in every Dppa3+ PGC examined to e11.5. In contrast, Tet2 was heterogeneously expressed at e9.25 and e10.25 (51% and 57% of cells, respectively). At e11.5, the number of Tet2+ PGCs increased substantially to be expressed in almost every Dppa3+ PGC along with Tet1. Unlike Tet1 and Tet2, Tet3 was expressed in rare Dppa3+ PGCs at e11.5. The cytidine deaminase Aid was negative, suggesting that Aid does not act during this period. Comparably, by analyzing iPGCs, we discovered that 40 of 40 iPGCs expressed Tet1 and that almost every single iPGC (39 of 40) also expressed Tet2 (Figure 2E). Similar to PGCs from the embryo, we did not find Aid expression in iPGCs, and Tet3 was rarely expressed (Figure 2E).

Figure 2
Tet1, Tet2, and 5-Hydroxymethylcytosine Are Present in PGCs and iPGCs

Given the expression of at least one or two Tet genes in PGCs, we analyzed 5hmC by immunostaining (Figure 2F and 2G). We used the commercially available 5hmC antibody that was previously confirmed as specifically recognizing 5hmC and not cytosine or 5mC (Iqbal et al., 2011). To confirm specificity, we transiently transfected 293T cells with a plasmid encoding the Tet1 catalytic domain, and a 5hmC-specific signal was only found in transfected cells (Figure S2A). Next, using this antibody, we show that 5hmC is present in e10.5 SSEA1+ PGCs (arrow heads) at levels similar to somatic cells (Figure 2F). The expression of 5hmC was mostly uniform through the PGC nucleus. However, by e13.5, 5hmC exhibits a characteristic punctate pattern that overlaps with DAPI+ pericentromeric heterochromatin (Figure S2B). Immunohistochemistry of sorted iPGCs and control SSEA1+ undifferentiated V6.5 ESCs revealed 5hmC enrichment in both cell types (Figure 2G) (Ficz et al., 2011).

To quantify global levels of 5hmC and 5mC, we used combined liquid chromatography electro-spray ionization tandem mass spectrometry with multiple-reaction monitoring (LC-ESI-MS/MS-MRM) (Figure 2H and 2I). With the use of this technique, 5.1% of total cytosines in V6.5 ESCs were methylated (Figure 2H) in a manner consistent with our previous report (Le et al., 2011). Next, we found that the levels of 5mC in iPGCs were significantly reduced to an average of 2.5%, whereas 5mC levels in somatic cells from the same EB were 4.9%. Furthermore, V6.5 ESCs and iPGCs had a similar 5hmC to 5mC ratio wherein 5hmC is approximately 50-fold lower in abundance than 5mC (Figure 2I). In contrast, analysis of somatic cells from the EB at day 6 revealed a significant reduction in 5hmC relative to ESCs, as previously reported (Koh et al., 2011; Tahiliani et al., 2009). Altogether, the differentiation of iPGCs from ESCs is not associated with a significant reduction in 5hmC in comparison to somatic cells, and this suggests that iPGCs uniquely regulate 5hmC modification during differentiation.

Tet1 and Tet2 Do Not Regulate Genome-Wide Demethylation in iPGCs

Given that 5hmC is found on less than 1% of cytosines in undifferentiated ESCs and iPGCs and that Tet1 and Tet2 are coexpressed, we considered two alternate hypotheses for the role of Tet1 and Tet2 in phase 1 genome-wide DNA demethylation. First, we could hypothesize that 5mC oxidation by Tet1 and Tet2 is required for genome-wide DNA demethylation in iPGCs and that this is initiated extensively in immature PGCs during EB formation. Therefore, the small measureable amounts of 5hmC in iPGCs at day 6 would underestimate the total 5mC to 5hmC conversion that occurred. A second hypothesis could be that 5hmC plays no role in phase 1 DNA demethylation in iPGCs.

To address these possibilities, we designed an experiment to generate iPGCsfrom Tet2−/− ESCs transduced with a lentivirally (LV)-delivered small hairpin RNA (shRNA) against Tet1 (shTet1 LV). We used this approach because iPGCs (and many endogenous PGCs) coexpress Tet1 and Tet2 (Figure 2E), and the depletion of Tet1 and Tet2 alone in ESCs results in only mild to moderate changes in 5hmC (Koh et al., 2011). We found no statistically significant difference in the percentage of iPGCs differentiated from Tet2−/− ESCs transduced with a control LV (Tet2−/− control LV) relative to Tet2−/− ESCs transduced with the Tet1 shRNA LV (Tet2−/−; shTet1 LV) (Figure 3A). To determine knockdown in sorted iPGCs, we used fluorescence-activated cell sorting (FACS) to isolate iPGCs and examined Tet gene expression by real-time PCR (Figure 3B). As a positive control for Tet2, we sorted iPGCs differentiated from V6.5 ESCs transduced with control LV (WT; control LV). Tet1 RNA was successfully depleted up to 80% with shTet1 LV in iPGCs (Figure 3B). Tet2 was undetectable in Tet2−/− ESCs, and Tet3 levels were very low relative to Tet1 and were unchanged in the context of Tet2 deletion with or without Tet1 knockdown (Figure 3B and 3C). Therefore, modulating Tet gene expression in iPGCs does not resultin the compensatory expression of other Tet genes, similar to what was reported in undifferentiated ESCs (Dawlaty et al., 2011; Koh et al., 2011). We also analyzed the PGC-expressed genes Blimp1 (a determinant of PGC fate), Dppa3, Prdm14 (a determinant of PGC fate), and Dnd1 and found that the manipulation of Tet1 and Tet2 had no significant effect on the expression of these genes relative to control genes (Figure 3D).

Figure 3
Tet1 and Tet2 Do Not Regulate Phase 1 Global DNA Demethylation in iPGCs

Finally, we asked whether Tet1 and Tet2 regulate genome-wide DNA demethylation with iPGC differentiation. If we accept the hypothesis that Tet1 and/or Tet2 are required for regulating genome-wide DNA demethylation, we would anticipate that cytosine methylation should significantly increase in Tet2−/−; shTet1 LV iPGCs in comparison to Tet2−/−; control LV. To reject the hypothesis and find that Tet1 and Tet2 have no major role in genome-wide iPGC demethylation, we would expect that Tet2−/−; shTet1 LV iPGCs would have DNA methylation levels equivalent to wild-type iPGCs (Figure 1C). Using LC-ESI-MS/ MS-MRM, we found that 5hmC was no longer detectable in Tet2−/−; shTet1 iPGCs relative to Tet2−/−; control LV (Figure 3E). We also found that, at the start of differentiation (day 6 posttransduction), the Tet2−/−; shTet1 LV ESC samples had undetectable levels of 5hmC and no change in 5mC levels in comparison to Tet2−/−; control LV (Figure S2C and S2D). Finally, analysis of 5mC by mass spectrometry revealed no increase in methylation in iPGCs with depleted 5hmC (Figure 3F). Thus, we conclude that Tet1 and Tet2 do not regulate global DNA demethylation.

Using an alternate approach, whole genome BS-seq in biological triplicate, we identified 6,866,888 CG dinucleotides that were represented in all six libraries, and, in agreement with the LC-ESI-MS/MS-MRM assay, we show no significant change in the percentage of CG methylation between Tet2−/−; shTet1 LV iPGCs in comparison to Tet2−/−; control LV iPGCs (Figure 3G). Combined, our data reject the first hypothesis that Tet1 and Tet2 regulate genome-wide DNA demethylation during iPGC differentiation. However, the BS-seq results reveal a small (~4%) increase in methylation in the Tet1 and Tet2 mutant iPGCs, which suggests locus-specific effects. Indeed, we found that knockdown of Tet1 in a Tet2−/− background had a local effect on promoter and gene body methylation in iPGCs when compared to Tet2−/− iPGCs transduced with a control LV (Table S2). Importantly, the most significant directional change observed was CG hypermethylation in Tet2−/−; shTet1 LV iPGCs in comparison to Tet2−/−; control LV reference iPGCs (Figure 3H and 3I). Some notable hypermethylated promoters included the genome defense genes Tudor domain containing protein 5 (Tdrd5) and Piwi-like 4 (Piwil4), which are required to repress transposons later in germ cell development, and Tdrd7, Spag8, and Pramel1, which are expressed in adult testis (Figure 3J). Curiously, gene body hypermethylation was discovered on the germ cell-expressed genes Nanos3, Blimp1, and Dppa2 and the imprinted genes Peg3 and Snrpn (Figure 3K). However, the increase in gene body methylation at Blimp1 did not alter expression (Figure 3D). We noted that olfactory receptor (Olfr) RNA and microRNAs (miRNAs) were highly represented in both promoter and gene body classifications, and shown here are an Olfr (Olfr1226) and a miRNA (mir133b) that exhibited hypomethylation in the Tet1- and Tet2-depleted iPGCs (Figure 3J and 3K). Altogether, this leads to a model where phase 1 PGC demethylation involving the bulk removal of DNA methylation is Tet1 and Tet2 independent.

DISCUSSION

Our genome-wide analysis of cytosine methylation with the use of BS-seq of iPGCs revealed a statistically significant and reproducible genome-wide depletion of cytosine methylation similar to what was recently reported by Seisenberger et al., 2012. Specifically, the iPGC model reported here captures the reorganization of cytosine methylation at meiotic CGIs relative to undifferentiated ESCs and represents a heterogeneous population of PGCs undergoing global phase 1 DNA demethylation and the initiation of some locus-specific, Tet-dependent DNA demethylation in phase 2. Although Tet1 and Tet2 were recently reported to regulate locus-specific demethylation in PGCs (Yamaguchi et al., 2012; Hackett et al., 2013), it was unknown whether the initial global depletion of DNA methylation required a 5hmC intermediate. Here, we show that Tet1, Tet2, and 5hmC are dispensable for the initial global depletion of 5mC from the PGC genome. Instead, Tet depletion induces promoter and gene body hypermethylation that is consistent with 5hmC having a locus-specific role in DNA demethylation in PGCs (Hackett et al., 2013).

Our genome-wide analysis reveals approximately 1,000 promoters and gene bodies that are differentially methylated in Tet1and Tet 2 mutant iPGCs, and the vast majority exhibit significant hypermethylation. Our data set revealed that Dazl, Sycp3, and Mael promoter methylation levels were all increased in the Tet1 and Tet2 mutants, as previously reported (Yamaguchi et al., 2012; Hackett et al., 2013). However, these changes did not reach statistical significance in our study, perhaps because the iPGCs here are younger than e10.5. One interesting observation was the discovery of important Tet-regulated germ cell-expressed genes, including Tdrd5, Piwil4 (also called Miwi2), and Tdrd7 that function in the male germline after e13.5 (Carmell et al., 2007; Tanaka et al., 2011; Yabuta et al., 2011). This suggests that 5hmC may prepare the germline epigenome for future functional events unique to this lineage.

If 5mC oxidation and deamination (Popp et al., 2010) are not responsible for driving genome-wide depletion in DNA demethylation in PGCs, what could be the mechanism? One possibility is that global demethylation is linked to abnormalities in replication-coupled methylation inheritance prior to e9.5. This could be caused by mislocalization, inactivation, or repression of DNA methyltransferase 1 (Dnmt1) (Lei et al., 1996) or its cofactor Uhrf1 during DNA synthesis (Bostick etal., 2007). Hairpin BS-seq (Laird et al., 2004), which detects methylation on complementary strands of DNA, is one way to address this in the ESC to iPGC model.

In conclusion, we propose that the differentiation of iPGCs represents a heterogeneous population of immature PGCs in the process of undergoing global genome-wide depletion of methylation during phase 1 and the beginning of Tet-dependent demethylation in phase 2. Our study demonstrates that Tet1 and Tet2 do not regulate initial genome-wide depletion of 5mC (Figure 1A) and instead clarifies the model to demonstrate that Tet1 and Tet2 function to regulate locus-specific methylation during PGC development.

EXPERIMENTAL PROCEDURES

Embryonic Stem Cell Culture and iPGC Differentiation

Mouse ESC maintenance, differentiation, and isolation of iPGCs were performed as previously described (Vincent et al., 2011). For the Tet studies, lenti-viruses were modified from Ambartsumyan et al., 2010, to carry shRNA directed against Tet1 mRNA harboring hygromycin resistance. Cells were transduced with the indicated VSV-G pseudotyped virus at a multiplicity of infection of 1 and selected in 200 µg/ml hygromycin on inactivated DR4 mouse embryonic fibroblasts. EB differentiation was performed with hygromycin in the media for 6 days prior to FACS.

Mouse Studies

Oct4-GFP+ embryos were used to isolate PGCs by FACS, as previously described (Vincent et al., 2011). All research protocols were approved by the Animal Care and Use Committee at UCLA.

Single-Cell PCR

Single-cell analysis was performed with the use of the Fluidigm BioMark microfluidics PCR system, as previously described, and involved an 18 cycle Specific Target Amplification reaction (Vincent et al., 2011). Heatmaps of Ct values were generated with Fluidigm PCR data analysis software.

Whole-Genome Bisulfite Sequencing

BS-seq libraries were prepared as previously described (Feng et al., 2011). Libraries were all single-end reads containing premethylated illumina adaptors. Libraries were sequenced on either a Genome Analyzer II or HiSeq 2000 and the percent methylation did not change between machines. Mapping was performed with the use of BS Seeker, and methylation levels for each cytosine were determined by measuring the ratio of Cs to Cs plus Ts that align to each genomic cytosine (Chen et al., 2010). Read lengths ranged from 50 to 80 after trimming 20 bases from the 3′ end. Multiple reads mapped to the same location were considered only once. For deep sequencing of libraries mB557 and mB556 (Table S1), only cytosines with coverage ≥ 4 were included for the downstream analysis (478,482,437 cytosines). This set was used to acquire chromosome views, metaplots, Shannon entropy, distribution plots, and analysis of symmetry. To generate a metaplot of genes, the transcription start and end sites of selected genes were fixed and the upstream, body, and downstream regions were binned into windows. For each window, the average methylation level was calculated. Therefore, a metagene plot summarized the average methylation level per window and was plotted from the upstream to downstream direction. Shannon entropy was calculated equation M1 where mi is the methylation levels estimated at the i-th CG site. In the comparison, we took the average of Shannon entropy (i.e., divided by n). To map DMS CG, sites were selected with the use of the criteria of delta methylation levels ≥ 30% and subjected to two-way binomial tests. This yielded 11,994,107 CG sites for analysis with a false discovery rate (FDR) of ≤ 5%. In the scatter plots, the points show the [increment] methylation level between the two samples versus the changes of expression (log2 microarray 1–log2 microarray2). Distribution plots of methylation levels were calculated at each cytosine as the ratio of Cs to Cs plus Ts that align to each genomic cytosine. The methylation levels of all cytosines with coverage ≥ 4× were plotted as a histogram. To calculate symmetry, the methylation status of these cytosines is based on an FDR of 1% and a sequencing error of 1% (Lister et al., 2009). As a result, the methylation status (methylated or not methylated) of all eligible cytosines were determined by counting the numbers of both methylated (mC+mG), one methylated and one unmethylated (mC+uG), and both unmethylated (uC+uG) among CpG pairs in mBS48 and mBS49. For analysis of Tet2−/−; LVandTet2−/−;Tet1shLV samples, n = 3 libraries were prepared in biological triplicate in samples that exhibited knockdown of Tet1 that was ≥ 69% oftheTet2−/−; control sample. This analysis yielded 6,866,888 CG dinucleotides that were represented in all six libraries and used to calculate the percent of CG methylation. We used t tests to calculate the significance between two groups.

LC-ESI-MS/MS-MRM

DNA was extracted from freshly sorted cell populations by FACS with a Zymo Quick-gDNA MiniPrep kit, and LC-ESI-MS/MS-MRM was used to determine the proportional content of 5mC or 5hmC relative to total cytosine levels, according to Le et al., 2011.

Immunofluorescence

Paraffin-embedded tissue staining was performed with conventional protocols with some exceptions. For 5mC and 5hmC staining, tissue was first stained for other markers, postfixed, and denatured for 10 min in 4 N HCl prior to overnight incubation with the appropriate antibodies. The following antibodies were used: Oct4 (Santa Cruz Biotechnology), E-cadherin (BD Biosciences), SSEA1 (Developmental Studies Hybridoma Bank), 5mC (Aviva Biosciences), and 5hmC (Active Motif). Fluorescent visualization was performed with the use of isotype-specific secondary antibodies conjugated to either fluorescein isothiocyanate or Alexa Fluor 594 (Jackson ImmunoResearch). All images were acquired on a Zeiss LSM 780 confocal microscope.

Supplementary Material

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ACKNOWLEDGMENTS

This work is supported by grant R01HD058047 from the National Institutes of Health (NIH) and a Research Award from the Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research to A.T.C. and NIH grants R01 HD065812 and CA151535 to A.R. The sequencing and FACS experiments were performed at the Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research Sequencing Center and FACS facility. J.J.V. is supported by a Dissertation Year Fellowship from UCLA. Y.H. and S.F. are supported by postdoctoral fellowships from the Leukemia & Lymphoma Society and J.H.C. is supported by fellowship TG2-01169 from the California Institute for Regenerative Medicine. Requests for Tet2−/− ESCs should be directed to A.R. at the La Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.

Footnotes

ACCESSION NUMBERS

All BS-seq data reported have been uploaded to the Gene Expression Omnibus (GEO) at accession number GSE44092.

SUPPLEMENTAL INFORMATION

Supplemental Information contains two figures and two tables and can be found with this article online at http://dx.doi.org/10.1016/j.stem.2013.01.016.

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