X chromosome inactivation (XCI) is a dosage compensation mechanism essential for embryonic development and cell physiology. Human embryonic stem cells (hESCs) derived from inner cell mass (ICM) of blastocyst stage embryos have been used as a model system to understand XCI initiation and maintenance. Previous studies of undifferentiated female hESCs at intermediate passages have shown three possible states of XCI; 1) cells in a pre-XCI state, 2) cells that already exhibit XCI, or 3) cells that never undergo XCI even upon differentiation. In this study, XCI status was assayed in ten female hESC lines between passage 5 and 15 to determine whether XCI variations occur in early passages of hESCs. Our results show that three different states of XCI already exist in the early passages of hESC. In addition, we observe one cell line with skewed XCI and preferential expression of X-linked genes from the paternal allele, while another cell line exhibits random XCI. Skewed XCI in undifferentiated hESCs may be due to clonal selection in culture instead of non-random XCI in ICM cells. We also found that XIST promoter methylation is correlated with silencing of XIST transcripts in early passages of hESCs, even in the pre-XCI state. In conclusion, XCI variations already take place in early passages of hESCs, which may be a consequence of in vitro culture selection during the derivation process. Nevertheless, we cannot rule out the possibility that XCI variations in hESCs may reflect heterogeneous XCI states in ICM cells that stochastically give rise to hESCs.
Citation: Dvash T, Lavon N, Fan G (2010) Variations of X Chromosome Inactivation Occur in Early Passages of Female Human Embryonic Stem Cells. PLoS ONE 5(6): e11330. doi:10.1371/journal.pone.0011330
Editor: Gert Jan C. Veenstra, Radboud University Nijmegen, Netherlands
Received: February 1, 2010; Accepted: May 27, 2010; Published: June 25, 2010
Copyright: © 2010 Dvash et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The research was supported by the California Institute of Regenerative Medicine training grant TG2-01169 to T.D. and comprehensive grant RC1-0111 to G.F. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Human embryonic stem cells (hESCs) are an invaluable tool for regenerative medicine and a model for early human embryogenesis . Numerous studies in the past ten years have described the capacity of hESCs to differentiate into specialized cells from the three germ layers . In certain instances, in vitro differentiated hESCs can be integrated and become functional in transplantation experiments , . Due to the wide applications of hESCs, there have been increasing demands for more newly derived hESC lines. This interest allows comparison of different properties among various hESC lines and can potentially create a gold standard for the characterization of hESC lines. Therefore, efforts have been made to generate gene expression and epigenetic profiles for hESCs , , , , . Although it seems that the gene expression profile is quite consistent for all hESC lines, the epigenetic status varies significantly , . For example, XIST gene expression varies among different hESC lines and even within the same cell line , , , .
In mice, Xist is known to play a major role in X chromosome inactivation (XCI) during female mammalian embryogenesis. In this process, genetic and epigenetic events, beginning with expression of Xist, allow equal expression from the X chromosome in male and female cells. In the mouse model system, XCI occurs in two waves during embryogenesis. At the two-cell stage, the imprinted paternal X chromosome is exclusively inactivated. During blastocyst formation, cells in the inner cell mass (ICM) reactivate the paternal X chromosome whereas the trophectoderm and primitive endoderm retain their imprinted XCI. Upon differentiation, the second wave of XCI occurs in a random fashion; thus each somatic cell will possess either maternal or paternal active X chromosome (reviewed in ref. ). Furthermore, it was shown that mouse ESCs (mESCs) and induced pluripotent stem cells (iPSCs) recapitulate random XCI upon differentiation , . Due to prominent developmental differences between mouse and human, XCI patterns between the two species are not well conserved. Indeed, both random and skewed XCI patterns are observed in human extra-embryonic tissue (placenta), but not mouse extra-embryonic tissue, which show exclusive paternal X chromosome inactivation . Therefore, an assessment of the XCI during early human embryogenesis is still needed.
A recent study in pre-implantation human embryos reported that XIST transcript accumulation on the X chromosome is initiated in the eight-cell stage embryo with full establishment of XIST clouds in the blastocyst stage . However, the identity of the cells showing XIST accumulation is not obvious due to three distinct cell populations found in the blastocyst stage embryos, namely trophectoderm, primitive endoderm and ICM. Furthermore, the XCI pattern (skewed or random) is still unclear. Questions regarding the XCI status of the ICM and the pattern of XCI in human pre-implantation embryos still remain to be resolved.
Since differentiation of hESCs can be used to model human embryogenesis in vitro, they are examined for the initiation and maintenance of XCI. Several research groups including ours reported that XCI in hESCs, unlike their rodent counterparts, is unstable and prone to changes during culture , , , , . Recent in depth XCI studies with several hESC lines described three different states of XCI in these cells , ,  (reviewed by Dvash and Fan, 2009 ). The first or “naïve” state refers to undifferentiated hESCs that possess two active X chromosomes. However, upon differentiation, they acquire one inactivated X chromosome. The second or intermediate state refers to hESCs that show XCI markers in both undifferentiated and differentiated states. The third state describes hESCs that do not show any XCI markers in both undifferentiated and differentiated states. Interestingly, it has been suggested that hESCs progress gradually during culture from the first “naïve” state, to the second stage exhibiting XCI, then to the third state where all XCI marks are irreversibly lost  . Furthermore, there is a correlation between the inability to express XCI marks and biallelic methylation pattern on the XIST promoter . Importantly, all the above mentioned studies used mid to late passage hESCs (∼p20–p100), that have been exposed to long term culture effects.
It is therefore better to evaluate the status of XCI in early passages of undifferentiated hESCs that have been minimally exposed to culture effects. Hereby we report the status of XCI in ten lines of female hESC at the earliest passages available. Our results indicate that the three distinct states of XCI can be observed even in minimally passaged hESCs. In addition, we investigated the pattern of XCI in two cell lines- one showed random XCI reminiscent of mESCs, while the other showed non-random XCI. Consistently, we found that the methylation pattern of the XIST promoter is tightly associated with silencing of XIST expression in early passages of female hESCs.
XIST expression analysis in CSES cell lines at early passages
Recent studies have identified three distinct states of XCI in a variety of female hESCs , , . These studies have also implied that these three XCI states are the consequence of long term culture conditions. We hypothesized that by using early passage hESCs, which have minimal exposure to culture effects, we may be able to better evaluate XCI status in the derivation of hESCs. For this purpose, we used newly derived CSES cell lines  at the earliest available stage such as passage five (p5) for some of the cell lines to study XCI.
Relative expression levels of XIST were assessed in all ten female cell lines (CSES1, 2, 3, 5, 6, 7, 8, 10, 11 and 14) by using real-time PCR analysis. In the undifferentiated state, four of the examined cell lines (CSES 1, 8, 10 and 11) expressed XIST while all the other lines did not show any XIST expression (Fig 1A). We then asked whether XIST expression can be induced in hESCs that do not express XIST upon teratoma differentiation. Consistent with previous findings  all cell lines that expressed XIST in the undifferentiated state were able to maintain and even up-regulate XIST expression upon differentiation. Interestingly, two of the cell lines (CSES2 and CSES7) that did not express XIST in the undifferentiated state were able to induce XIST expression upon differentiation, though at a lower level (Fig 1B). However, four cell lines (CSES3, CSES5, CSES6 and CSES14) did not express XIST both at the undifferentiated and differentiated state. These results clearly demonstrate that three different states of XCI exist in hESCs even after a short culture period. We conclude that CSES2 and CSES7 cells are in the “naïve” state, showing XIST expression only upon differentiation; CSES1, 8, 10 and 11 cells are in the intermediate state, showing XIST expression at the undifferentiated state and further induction upon differentiation; and CSES 3, 5, 6, 14 cells are in the third “culture affected” state, showing no XIST expression regardless of undifferentiated or differentiated conditions.
(A) XIST relative expression levels in CSES undifferentiated cells. (B) XIST relative expression levels in teratomas derived from CSES cells. (C) Pluripotency gene expression by Delta Ct in CSES cell lines in different passages as well as in H1 (male) cell line. (D) XIST expression by Delta Ct in all CSES cell lines analyzed compared to H1 (male) cell line. Significant values (p<0.01) are marked by asterisks.
It has been shown that XCI initiation correlates with low levels of pluripotency related factors in mouse ES cells . To exclude the possibility that XIST expression in undifferentiated hESCs occurs due to differentiation in culture, we analyzed pluripotency gene expression along with XIST expression by using the ABI human stem cell pluripotency low density array. Delta Ct values were calculated for each gene compared to the control gene, beta actin (Fig. 1C, D). Brown-Forsthye test shows that all pluripotency genes are expressed with small variance between different cell lines analyzed (p = 0.27) (Fig. 1C), whereas XIST expression varied significantly (p = 2.2×10−17) (Fig. 1D). These results were supported by our observation of simultaneous appearance of XCI markers and undifferentiated stem cell markers such as OCT4 by immunostaining (Fig. 2G).
(A) CSES1 shows positive punctate staining for H3K27me3 (indicated by the arrow heads). CSES3 cells do not show punctate staining pattern for H3K27me3 in (B) late or (C) early passages. (D) Shown is XIST RNA coating of Xi by FISH in CSES1 cell line (indicated by the arrow heads). (E) CSES3 lack XIST RNA coating of Xi as indicated by FISH analysis. (F) CSES3 is positively stained for OCT4 (green) at p6. (G) CSES8 at p8 shows H3K27me3 punctate staining along with OCT4 staining; however, the relative expression of XIST is reduced in this cell line at p14. This observation is supported by a decrease in the cell population with H3K27me3 punctae in p17 (48% of the cells).
To visualize XCI states at a single cell resolution, we assayed for XIST RNA coating of the inactive X (Xi) by using FISH analysis or enrichment of histone 3 lysine 27 tri-methylation (H3K27me3) by immunocytochemistry , . Consistent with XIST expression, cell lines such as CSES1 showed punctate staining for H3K27me3 on the Xi (Fig. 2A). XIST RNA coating was also identified on one of the X chromosomes in virtually all of the cells (Fig. 2D). In contrast, cell lines such as CSES3 lack both H3K27me3 punctate staining and XIST RNA coating of the Xi (Fig. 2B, E). Interestingly, CSES3 lacks XCI markers at early passages (p6) (Fig. 2C, F) and upon long term culture (p31) (Fig. 2B, E). In addition, these cells lack the capability to induce XCI upon teratoma formation (Fig 1 B).
Low level of XIST expression as seen in CSES10 (Fig. 1A, D) can be explained either by uniformly low XIST expression in the entire cell population or by high expression from a small subset of cells. In order to distinguish between the two possibilities, we calculated the percentage of cells exhibiting punctate H3K27me3 staining. Indeed, all cell lines that do not express XIST also do not show any H3K27me3 punctate staining. However, in intermediate state (state II) cells, we observed a significant number of cells with punctate staining for H3K27me3 (Fig. S1). Therefore, low level of XIST expression in CSES10 p15 cells correlates with a lower number of H3K27me3 positive cells, indicating a low number of XIST expressing cells. Furthermore, all H3K27me3 positive cells were positively stained for OCT4 (data not shown), which again suggests that XCI can occur in undifferentiated hESCs.
Finally, we also observed the transition from the XIST + to the XIST − XCI state in subcultures of early passage hESCs. In CSES8, H3K27me3 punctate staining can be detected at a high percentage in p8 (n = 257, 87%); however the number of positively-stained cells was significantly reduced by p17 (n = 403, 48%). In parallel, XIST mRNA expression was dramatically reduced in p17 CSES8 hESCs (Fig 2G).
Skewed versus random XCI pattern in CSES cell lines
During mouse embryogenesis, imprinted XCI of the paternal X chromosome occurs prior to the blastocyst formation whereas random XCI is initiated upon differentiation. However, previously we observed non-random XCI in later passages of female hESC lines . Given that the XCI states seems to be affected by culture and that culture pressure could result in clonal selection, we were curious to see whether XCI is random or skewed in early passages of hESCs.
We chose to analyze the pattern of XCI in two cell lines, CSES1 and CSES8, because both showed XCI markers. In order to verify the parental origin of the active X chromosome, we used maternal DNA that was extracted from granulosa cells, which are somatic cells that surround the oocyte during maturation. These cells are normally removed at the time of egg retrieval during IVF procedure in order to expose the oocyte surface for fertilization. Frozen granulosa cells for CSES1 and CSES8 were used for DNA extraction. Following DNA amplification these samples were hybridized to Affymetrix SNP array (250k Sty) side by side with the corresponding hESC DNA. The results from this analysis enabled us to choose SNPs within X-linked genes that were identified as heterozygous in the hESC lines and homozygous in the maternal DNA.
In order to verify the maternity of the granulosa DNA sample with the corresponding hESC sample, we performed identical by state (IBS) analysis to show that our samples are genetically related. For instance, comparison of CSES1 and its corresponding maternal sample showed that in 71.7% of the SNPs both alleles are shared (IBS = 2) and in 28% of the SNPs one of the alleles is shared (IBS = 1). This indicates that 99.7% of SNPs show at least one allele shared between the samples. Overall 85.7% of SNPs are shared between CSES1 and its maternal sample. This indicates close genetic relationship between the two samples (Fig. S2). In order to perform SNP expression analysis, we selected genes that show moderate to high expression in undifferentiated hESCs. Consequently, we analyzed the expression of seven SNPs for CSES1 and nine SNPs for CSES8 along the X chromosome (Table 1, 2, Fig. S3, S4).
Our results indicate discrepancies between the two hESC lines with regard to the pattern of XCI. In the CSES8 cell line at both p5 and p14, we consistently observed bi-allelic expression of X-linked genes, indicating that random XCI has occurred. On the other hand, CSES1 at p5 showed preferential expression of the paternal allele suggesting skewed XCI with six out seven X-linked genes exhibiting mono-allelic expression from the paternal X. Theoretically, the probability of having maternal or paternal allele expressed per SNP is 50%. According to binomial distribution B(x = 6; n = 7, p = 0.5), the cumulative probability of getting as many as six out of seven SNPs with paternal expression is 0.0625. Since this probability is very small, it argues against the hypothesis of random XCI in this case. Therefore, the preferential expression from the paternal allele is due to skewed maternal X inactivation. Moreover, upon prolonged culture of CSES1 cell line, we observe partial reactivation of the second allele that coincides with the loss of XIST expression at later passages. For example, rs41537046 expressed only the paternal allele (A) at p5, whereas both paternal and maternal alleles are expressed (A/G) by p14 (Table 1 and Fig. S3). This is consistent with our previous observation that loss of XIST expression would lead to partial reactivation of a portion of previously silenced genes in Xi .
XIST promoter methylation status correlates with the three different states of XCI in hESCs
The variability of XCI status in early passages may indicate epigenetic modifications of the XIST promoter that occur either prior or subsequent to the hESCs derivation process. Indeed, it was previously suggested that XIST promoter methylation pattern is correlated with the XCI status of the cells , . Consistently, our analysis demonstrates that CSES1 at p11 expresses XCI markers and have ∼50% methylation at the XIST promoter (Fig. 3). This result is consistent with the observation that one of the XIST alleles in these cells expresses XIST in the undifferentiated state as well as upon teratomas differentiation. In addition, the XIST promoter shows ∼90% methylation in later passages of CSES8 (p28) consistent with silencing of both XIST alleles and the loss of XCI markers upon long-term culture (data not shown). We also observed 70–96% methylation in the XIST promoter of CSES3 and CSES5 (Fig. 3), even in early passages (p11 and p12 respectively). This is correlated with the inability of these cell lines to induce XCI in either undifferentiated state or upon teratomas differentiation (Fig. 1B). Interestingly, both CSES2 and CSES7, which exhibit XCI only upon differentiation, also showed 80–87% methylation of the XIST promoter in early passages (p12 and p10 respectively) (Fig. 1B and Fig. S5). This observation suggests that DNA methylation is also involved in repression of XIST gene expression in the pre-XCI state.
Schematic of XIST promoter CpG sites and bisulfite sequencing results of the corresponding CpG sites in the XIST promoter in each cell line. Open circle represents unmethylated CpG site and closed circle represents methylated CpG site.
In this study, we attempted to minimize the in vitro culture effects by using hESCs at the earliest available time. It has been shown that long term culture can contribute to the variation in XCI status of hESCs , , . We found that early passage cell lines already exhibit various XCI states similar to cell lines after prolonged culture. While it is formally possible that culture variations in the first few weeks of hESC derivation and expansion may yield XCI variation, we cannot rule out the alternative possibility that XCI variations may reflect innate heterogeneity of the original cells found in the ICM of the human embryo. This hypothesis is supported by a study on cultured mouse ICM cells reporting that these cells can undertake different paths- such as differentiation to epiblast, reversion into pre-blastocyst embryonic cell stage or selective expansion of a distinct subpopulation- and therefore differ in their XCI status . Of note, mouse EpiSCs exhibit XCI as they are derived from a later stage of mouse embryogenesis and resemble the morphology and the expression patterns of the hESCs , , . Thus, it is formally possible that at the time of the hESCs derivation, some of ICM cells have already progressed to a more committed state and already initiate XCI , whereas other ICM cells are still at a pre-XCI stage that eventually give rise of hESCs in the “naïve” pre-XCI state.
Here we show that variations of XCI are already present from early passage (p5) to later passage (p14) of the same cell line (CSES8), supporting the notion that XCI is highly affected by culture conditions , even at the earliest stages of culturing. Very recently, it was demonstrated that derivation of hESCs in physiological oxygen concentration (5%) allows establishment of hESC in a naïve pre-XCI state, with two active X chromosome . Irreversible XCI occurs when the naïve female hESCs are cultured in atmospheric oxygen concentration (20%) conditions. This is consistent with the previous notions that female hESCs can switch from a pre-XCI state to established XCI status upon culture selection.
Concerning the pattern of XCI in hESCs at the early passages, our SNP analysis revealed random XCI for one line of hESCs (CSES8) while skewed XCI for the other cell line (CSES1) with preferential expression from the paternal X chromosome. Skewed XCI is known to happen during mouse embryogenesis at the two cell stage until the blastocyst stage when the inactive paternal X becomes reactivated. In this case, the inactivation is imprinted and the paternal X chromosome is inactivated. In hESCs, methylation specific analysis of a polymorphic tri-nucleotide repeat at the HUMARA gene show three out of four hESC lines possess skewed XCI while one has a random pattern of inactivation . Interestingly, this research group also analyzed a triploid (3PN) hESC line and showed a progression from a random XCI to a skewed pattern of XCI. Similarly, transition of naïve hESCs, possessing two active X chromosomes under physiological oxygen concentrations to atmospheric oxygen concentrations also result in skewed XCI . We show that in CSES1 cells the maternal X chromosome is inactivated. Our observations for CSES1 cell line combined with the observation from Liu et al.  and Lengner et al.  suggest that culture selection during hESC culture may results in skewed XCI as reported , , .
The mechanism underlying the initiation and loss of XCI markers in hESCs is largely unknown. It is known that Xist promoter is 50% methylated in undifferentiated female mESCs . However, the methylation status of human XIST promoter in the pre-XCI state is previously unknown. In order to gain some insight into this mechanism, we analyzed the methylation patterns of XIST promoter in early passages of hESCs. Cells that show XCI markers both prior and post differentiation have approximately 50% methylation of the XIST promoter as expected. We also observe gain of methylation in the XIST promoter region upon further passages, which is also associated with loss of XIST expression and other XCI markers in the case of CESE8 hESCs. Here we show that hypermethylation of the XIST promoter is also observed in short term culture (CSES3 and CSES5). This correlates with the inability of these cells to initiate XCI upon differentiation. Surprisingly, cell lines such as CSES2 and CSES7 were able to initiate XCI upon differentiation but showed relative high methylation on the XIST promoter in the undifferentiated state, consistent with reports by Lengner et al.  for their hESCs in the pre-XCI state. The ability of these two CSES cell lines to initiate XIST expression upon differentiation suggests two possibilities: (i) there might be an additional XCI state in hESC where hypermethylation of the XIST promoter is reversed and consequently XIST transcript is expressed, or (ii) only a minority of the cells within the teratomas express XIST whereas the majority of cells do not express XIST.
In this study, we propose that XCI occurs in undifferentiated hESC in a random manner and the observations of skewed XCI are probably a result of a clonal selection occurring in hESC culture. It was recently shown that mouse induced pluripotent cells (miPSC) recapitulate XCI patterns of mESCs . Therefore, analysis of human iPSCs may elucidate whether these cells can reactivate both X chromosomes and maintain their active state in the undifferentiated state, or whether XCI occur in these cells in the undifferentiated state as in hESCs. Moreover, previous reports have demonstrated the involvement of pluripotency factors in the initiation of XCI in mESCs . Since hESCs and mEpiSCs seems to represent a more committed derivative of the ICM it is possible that a different set or levels of transcription factors present in these cells are responsible for the different patterns of XCI between mouse and human ESCs.
Overall the variability in the status of XCI among the cell lines indicates either rapid epigenetic culture effect or the potential heterogeneity of the original ICM cells. It seems that the cells, even in early passages, tend to undergo XCI and later on lose the XCI markers. Thus, XCI process is highly affected by culture conditions and inactivation of one of the X chromosomes may provide an advantage in the current culture condition. We propose that a careful re-examination of XCI status in human ICM will shed light on the status and pattern of XCI in these cells. It is known that normal XCI is critical in the embryonic development  and inappropriate XCI is involved in different pathologies such as cancer . Therefore, routine evaluation of XCI status should be a standard procedure for any pluripotent cells, including iPSCs, when they are applied to regenerative medicine.
Materials and Methods
This research was approved by UCLA Embryonic stem cells research oversight (ESCRO) committee.
Human ESC culture and differentiation
Cedars Sinai Embryonic Stem cell lines (CSES) were derived as described  and were cultured on mouse embryonic fibroblasts (MEF) in hESC medium  supplemented with 30ng/ml bFGF until cell line establishment. Upon establishment bFGF concentration was reduced to 5ng/ml. Manual passaging method was applied until a stable cell line was established (normally between p4 to p8), and thereafter enzymatic transfers were done either by using Trypsin/EDTA or collagenase type IV . Cells were allowed to undergo in vivo differentiation by injection of 5×106 cells under the kidney capsule of Nude mice. A month after injection, the mice were euthanized and teratomas were removed for RNA extraction. The care of the animals was in accordance with the institutional guidelines, as approved by Cedars Sinai Medical Center Institutional Animal Care and Use Committee, according to protocol 2182. In vitro differentiation was carried out on matrigel coated plates and the cells were cultured in hESC medium without bFGF supplemented with 2 µM retinoic acid (Sigma) for seven days.
RNA extraction and real time polymerase chain reaction analysis
Total RNA was extracted using RNeasy mini kit (Qiagen, Valencia, CA http://www1.qiagen.com) and was treated with DNase I as described in the RNeasy mini kit protocol. 1 µg of DNase treated RNA was subjected to reverse transcription by iScript cDNA synthesis kit (Bio-Rad, Hercules, CA http://www.bio-rad.com). cDNA was either subjected to PCR amplification for SNP analysis as described below or for real-time PCR that was carried out with Bio-Rad iCycler using IQ™ SYBR® green supermix (Bio-rad) with XIST and GAPDH human specific primers (see table S1 for primer sequences). Relative XIST gene expression levels were calculated after they were normalized with expression levels of GAPDH.
Gene expression analysis by low density arrays
RNA from undifferentiated hESCs were analyzed by a Taqman© based assay, using the human stem cell pluripotency array (ABI, foster city,CA). Delta Ct values were obtained by identifying the number of amplification cycles needed to reach the common threshold (Ct) value for each gene. Then, these values were normalized by subtraction of the Ct values obtained for a control gene (beta-Actin) for the same sample. In order to show that XIST expression variation among the different cell lines is not due to differentiation in culture, we performed a Brown-Forsthye test.
Genomic DNA from the hESC lines was extracted using DNeasy kit (Qiagene). Due to low amount of starting cells, DNA for Granulosa cells was extracted with the same kit and was subjected to whole genome amplification using REPLI-g mini kit (Qiagene). DNA from CSES1 (p14), CSES8 (p12) and their corresponding maternal granulosa cells were hybridized to Affymetrix 250k Sty SNP array (Affymetrix, Santa Clara, CA http://Affymmetirx.com). The microarray data have been deposited in GEO and given the series accession number GSE2167. SNPs were selected for analysis along the X chromosome according to the following criteria: the gene is X-linked and expressed in hESCs in moderate to high levels, and the SNP is heterozygous in the hESC line and homozygous in the corresponding maternal DNA. Genotype was validated for the selected SNPs by direct sequencing (see table S1 for primer sequences). In order to assess the expression from a specific SNP in CSES1 and CSES8 hESC lines, we used cDNA that was treated with DNase I as described above to avoid DNA contamination and amplified the specific regions. Amplicons were separated using an ethidium bromide stained 2% agarose gel, followed by gel-purification (Wizard ® SV Gel and PCR clean up system, Promega http://www.promega.com) and direct sequencing reaction to identify the expressed allele.
Bisulfite genomic sequencing analysis
Genomic DNA samples for CSES1, 2, 3, 5 and 7 were digested with BglII overnight and treated the following day with sodium bisulfite for 15 hours as previously described . Converted DNA samples were cleaned using Wizard® DNA Clean Up Kit (Promega) and were amplified by a single PCR reaction. PCR products were cloned into the Topo TA Vector 4.0 (Invitrogen). Individual colonies were picked for sequencing to identify the allelic methylation patterns. XIST promoter Bisulfite PCR primers were designed using the MethPrimer online software http://www.urogene.org/methprimer/index1.html.
Immunocytochemistry and XIST RNA-FISH analysis
Cells for immunostaining were first fixed with 4% PFA/PBS for 20 minutes at room temperature and washed with PBS. Cells were then permeabilized by 0.4% Triton-X in TBST for 20 min and blocked in 10% milk and 1% normal goat serum for 1 hour. Cover slips were incubated 1 hour at room temperature with primary antibodies diluted in 3% BSA in TBST [monoclonal mouse anti-OCT4 (1∶20, Santa Cruz) and polyclonal rabbit anti-H3K27me3 (1∶1000, a gift from Yi Zhang, University of North Carolina, Chapel Hill, NC)]. After being washed three times with PBS, cover slips were incubated in fluorochrome-conjugated secondary antibodies for 1 hour at room temperature with protection from light. Hoechst dye #33342 was used to label cell nuclei. XIST RNA-FISH was performed as described  by using three 50-mer DNA probes designed from consensus sequences of map positions 6183-6232, 62234-6283 and 6368-6417 (accession No. L04961), which are in repeat D of XIST.
(0.05 MB DOC)
Percentage of undifferentiated cells positively stained for H3K27me3. Intermediate state (state II) cells show significant number of cells with punctate staining for H3K27me3 CSES1 p15 (n = 511, 94%), CSES8 p8 (n = 257, 87%) CSES10 p15 (n = 257, 32%) and CSES11 p12 (n = 655, 84%).
(4.55 MB TIF)
Identical by state (IBS) analysis for CSES1 and its granulosa cells. Proportion of IBS = 0, 0.3% (no shared alleles), IBS = 1, 28% (one shared allele) and IBS = 2, 71.7% (two shared alleles). Overall, 85.7% of the alleles are shared, clearly indicating for close genetic relationship between the samples.
(8.34 MB TIF)
SNP sequences for CSES1 samples. SNP rs6620161 shows biallelic expression in p5 with one of the alleles more prominently expressed. However, in p14 both alleles are expressed at the same level. rs41537046 shows monoallelic expression at p5, but at p14 both of the alleles are already expressed. SNP rs5914796 shows expression of the paternal allele both at p5 and p14.
(9.12 MB TIF)
SNP sequences for CSES8 samples. Representing SNP sequences for CSES8 cell line. SNPs rs1204399, rs42890 and rs6625472 all show biallelic expression both at p5 and p14.
(9.24 MB TIF)
Induction of XCI in CSES upon Retinoic Acid differentiation. XCI detected by immunostaining for H3K27me3 and pluripotency detected by staining for OCT4 were tested in the three different classes of CSES cells. In CSES2 and CSES7 (A–D), representing class I cells, we were able to detect induction of XCI upon differentiation in CSES2 (A, B) but not for CSES7 (C, D). CSES3 representing class II cells were not able to induce XCI upon differentiation (E, F). In CSES8, we were able to detect XCI markers both in the undifferentiated and differentiated cells (G, H).
(9.89 MB TIF)
We greatly thank Professor Nissim Benvenisty for reagents and many helpful discussions during the course of this study and Professor Rita Cantor for statistical analysis of the data presented. We would also like to thank Kavita Narwani and Dr. Juan-Carlos Biancotti for their help in the derivation and characterization of the CSES cell lines, Shaily Shah for her help in the SNP analysis and Kevin Huang and Thuc Le for proofreading this manuscript.
Conceived and designed the experiments: TD GF. Performed the experiments: TD. Analyzed the data: TD GF. Contributed reagents/materials/analysis tools: TD NL. Wrote the paper: TD GF.
- 1. Dvash T, Benvenisty N (2004) Human embryonic stem cells as a model for early human development. Best Pract Res Clin Obstet Gynaecol 18: 929–940.
- 2. Itskovitz-Eldor J, Schuldiner M, Karsenti D, Eden A, Yanuka O, et al. (2000) Differentiation of human embryonic stem cells into embryoid bodies compromising the three embryonic germ layers. Mol Med 6: 88–95.
- 3. Lu B, Malcuit C, Wang S, Girman S, Francis P, et al. (2009) Long-term Safety and Function of RPE from Human Embryonic Stem Cells in Preclinical Models of Macular Degeneration. Stem Cells.
- 4. van Laake LW, Passier R, Monshouwer-Kloots J, Verkleij AJ, Lips DJ, et al. (2007) Human embryonic stem cell-derived cardiomyocytes survive and mature in the mouse heart and transiently improve function after myocardial infarction. Stem Cell Res 1: 9–24.
- 5. Adewumi O, Aflatoonian B, Ahrlund-Richter L, Amit M, Andrews PW, et al. (2007) Characterization of human embryonic stem cell lines by the International Stem Cell Initiative. Nat Biotechnol 25: 803–816.
- 6. Kim KP, Thurston A, Mummery C, Ward-van Oostwaard D, Priddle H, et al. (2007) Gene-specific vulnerability to imprinting variability in human embryonic stem cell lines. Genome Res 17: 1731–1742.
- 7. Lister R, Pelizzola M, Dowen RH, Hawkins RD, Hon G, et al. (2009) Human DNA methylomes at base resolution show widespread epigenomic differences. Nature 462: 315–322.
- 8. Doi A, Park IH, Wen B, Murakami P, Aryee MJ, et al. (2009) Differential methylation of tissue- and cancer-specific CpG island shores distinguishes human induced pluripotent stem cells, embryonic stem cells and fibroblasts. Nat Genet 41: 1350–1353.
- 9. Laurent L, Wong E, Li G, Huynh T, Tsirigos A, et al. (2010) Dynamic changes in the human methylome during differentiation. Genome Res 20: 320–331.
- 10. Tanasijevic B, Dai B, Ezashi T, Livingston K, Roberts RM, et al. (2009) Progressive accumulation of epigenetic heterogeneity during human ES cell culture. Epigenetics 4:
- 11. Dhara SK, Benvenisty N (2004) Gene trap as a tool for genome annotation and analysis of X chromosome inactivation in human embryonic stem cells. Nucleic Acids Res 32: 3995–4002.
- 12. Hoffman LM, Hall L, Batten JL, Young H, Pardasani D, et al. (2005) X-inactivation status varies in human embryonic stem cell lines. Stem Cells 23: 1468–1478.
- 13. Shen Y, Matsuno Y, Fouse SD, Rao N, Root S, et al. (2008) X-inactivation in female human embryonic stem cells is in a nonrandom pattern and prone to epigenetic alterations. Proc Natl Acad Sci U S A 105: 4709–4714.
- 14. Navarro P, Avner P (2009) When X-inactivation meets pluripotency: an intimate rendezvous. FEBS Lett 583: 1721–1727.
- 15. Panning B, Dausman J, Jaenisch R (1997) X chromosome inactivation is mediated by Xist RNA stabilization. Cell 90: 907–916.
- 16. Maherali N, Sridharan R, Xie W, Utikal J, Eminli S, et al. (2007) Directly reprogrammed fibroblasts show global epigenetic remodeling and widespread tissue contribution. Cell Stem Cell 1: 55–70.
- 17. Zeng SM, Yankowitz J (2003) X-inactivation patterns in human embryonic and extra-embryonic tissues. Placenta 24: 270–275.
- 18. van den Berg IM, Laven JS, Stevens M, Jonkers I, Galjaard RJ, et al. (2009) X chromosome inactivation is initiated in human preimplantation embryos. Am J Hum Genet 84: 771–779.
- 19. Silva SS, Rowntree RK, Mekhoubad S, Lee JT (2008) X-chromosome inactivation and epigenetic fluidity in human embryonic stem cells. Proc Natl Acad Sci U S A 105: 4820–4825.
- 20. Hall LL, Byron M, Butler J, Becker KA, Nelson A, et al. (2008) X-inactivation reveals epigenetic anomalies in most hESC but identifies sublines that initiate as expected. J Cell Physiol 216: 445–452.
- 21. Dvash T, Fan G (2009) Epigenetic regulation of X-inactivation in human embryonic stem cells. Epigenetics 4: 19–22.
- 22. Lavon N, Narwani K, Golan-Lev T, Buehler N, Hill D, et al. (2008) Derivation of euploid human embryonic stem cells from aneuploid embryos. Stem Cells 26: 1874–1882.
- 23. Navarro P, Chambers I, Karwacki-Neisius V, Chureau C, Morey C, et al. (2008) Molecular coupling of Xist regulation and pluripotency. Science 321: 1693–1695.
- 24. Enver T, Soneji S, Joshi C, Brown J, Iborra F, et al. (2005) Cellular differentiation hierarchies in normal and culture-adapted human embryonic stem cells. Hum Mol Genet 14: 3129–3140.
- 25. Plath K, Fang J, Mlynarczyk-Evans SK, Cao R, Worringer KA, et al. (2003) Role of histone H3 lysine 27 methylation in X inactivation. Science 300: 131–135.
- 26. Thomson JA, Itskovitz-Eldor J, Shapiro SS, Waknitz MA, Swiergiel JJ, et al. (1998) Embryonic stem cell lines derived from human blastocysts. Science 282: 1145–1147.
- 27. Reubinoff BE, Pera MF, Fong CY, Trounson A, Bongso A (2000) Embryonic stem cell lines from human blastocysts: somatic differentiation in vitro. Nat Biotechnol 18: 399–404.
- 28. Tesar PJ, Chenoweth JG, Brook FA, Davies TJ, Evans EP, et al. (2007) New cell lines from mouse epiblast share defining features with human embryonic stem cells. Nature 448: 196–199.
- 29. Brons IG, Smithers LE, Trotter MW, Rugg-Gunn P, Sun B, et al. (2007) Derivation of pluripotent epiblast stem cells from mammalian embryos. Nature 448: 191–195.
- 30. Reijo Pera RA, DeJonge C, Bossert N, Yao M, Hwa Yang JY, et al. (2009) Gene expression profiles of human inner cell mass cells and embryonic stem cells. Differentiation 78: 18–23.
- 31. Lengner CJ, Gimelbrant AA, Erwin JA, Cheng AW, Guenther MG, et al. (2010) Derivation of Pre-X Inactivation Human Embryonic Stem Cells under Physiological Oxygen Concentrations. Cell 141: 872–883.
- 32. Guo G, Yang J, Nichols J, Hall JS, Eyres I, et al. (2009) Klf4 reverts developmentally programmed restriction of ground state pluripotency. Development 136: 1063–1069.
- 33. Liu W, Sun X (2009) Skewed X chromosome inactivation in diploid and triploid female human embryonic stem cells. Hum Reprod.
- 34. Zvetkova I, Apedaile A, Ramsahoye B, Mermoud JE, Crompton LA, et al. (2005) Global hypomethylation of the genome in XX embryonic stem cells. Nat Genet 37: 1274–1279.
- 35. Tomkins DJ, McDonald HL, Farrell SA, Brown CJ (2002) Lack of expression of XIST from a small ring X chromosome containing the XIST locus in a girl with short stature, facial dysmorphism and developmental delay. Eur J Hum Genet 10: 44–51.
- 36. Ganesan S, Richardson AL, Wang ZC, Iglehart JD, Miron A, et al. (2005) Abnormalities of the inactive X chromosome are a common feature of BRCA1 mutant and sporadic basal-like breast cancer. Cold Spring Harb Symp Quant Biol 70: 93–97.
- 37. Clark SJ, Harrison J, Paul CL, Frommer M (1994) High sensitivity mapping of methylated cytosines. Nucleic Acids Res 22: 2990–2997.
- 38. Michienzi A, Rossi JJ (2001) Intracellular applications of ribozymes. Methods Enzymol 341: 581–596.