- Research article
- Open Access
Identification of regulatory elements flanking human XIST reveals species differences
© Chang and Brown; licensee BioMed Central Ltd. 2010
Received: 28 October 2009
Accepted: 8 March 2010
Published: 8 March 2010
The transcriptional silencing of one X chromosome in eutherians requires transcription of the long non-coding RNA gene, XIST. Many regulatory elements have been identified downstream of the mouse Xist gene, including the antisense Tsix gene. However, these elements do not show sequence conservation with humans, and the human TSIX gene shows critical differences from the mouse. Thus we have undertaken an unbiased identification of regulatory elements both downstream and upstream of the human XIST gene using DNase I hypersensitivity mapping.
Downstream of XIST a single DNase I hypersensitive site was identified in a mouse undifferentiated ES cell line containing an integration of the human XIC region. This site was not observed in somatic cells. Upstream of XIST, the distance to the flanking JPX gene is expanded in humans relative to mice, and we observe a hypersensitive site 65 kb upstream of XIST, in addition to hypersensitive sites near the XIST promoter. This -65 region has bi-directional promoter activity and shows sequence conservation in non-rodent eutheria.
The lack of regulatory elements corresponding to human TSIX lends further support to the argument that TSIX is not a regulator of XIST in humans. The upstream hypersensitive sites we identify show sequence conservation with other eutheria, but not with mice. Therefore the regulation of XIST seems to be different between mice and man, and regulatory sequences upstream of XIST may be important regulators of XIST in non-rodent eutheria instead of Tsix which is critical for Xist regulation in rodents.
The Tsix gene encodes an untranslated RNA antisense to Xist that is transcribed across the Xist locus, extending beyond the promoter of the sense strand [9, 11]. A critical role for Tsix in regulating Xist expression was demonstrated by augmented Tsix expression resulting in inhibition of Xist accumulation  while deletion of the Tsix promoter resulted in primary non-random inactivation of the mutant X in females . DXPas34, a 1.2 kb CG-rich region located 750 bp downstream of the Tsix major promoter, is critical for Xist and Tsix regulation, and shows bi-directional promoter activity [14, 15]. Xite, named as the X-inactivation intergenic transcription element, was identified by DNase I hypersensitive mapping, and is also a site of bi-directional transcription, although the transcripts themselves are not necessary for Xite to promote Tsix persistence on the active X . Homologous pairing of a region downstream of Xist, encompassing Tsix, DXPas34 and Xite, is necessary for the initiation of X inactivation [16, 17]. This pairing can be recapitulated by sub-fragments which contain a high density of CTCF sites, and CTCF as well as transcription is essential for the establishment of pairing .
While the mouse system provides an excellent framework from which we can understand the process of X inactivation, how human fits into this framework is not clear. XIST and Xist share sequence homology [3, 4] and are each sufficient to initiate silencing [18, 19]; however, there are substantial differences between the two species in other aspects of X-chromosome inactivation. Significantly, X inactivation is imprinted in mouse extraembryonic tissues  but not in humans (reviewed in ) and Tsix is very different from TSIX in patterns of expression and extent of transcription across the sense strand [22–24]. Human TSIX has been observed in embryoid bodies and a human embryonal carcinoma cell line, but also in chorionic villus cells [22, 24]. TSIX is also expressed in mouse ES-10 cells carrying a multi-copy integration of a 480 kb XIST-containing human YAC transgene  and in L1.10.1, a clone of a somatic male cell line transfected with a human XIST-containing PAC, which contains at least 50 kb of flanking genomic DNA . While these cells did not show identical initiation sites for the TSIX transcript, in all cases the TSIX transcript truncated well before the 5' end of XIST. As human ES cells have been variable in their X inactivation status (e.g.), mouse ES cells with a human transgene remain one of the best models for human X inactivation. Multi-copy integrations of the 480-kb transgene containing human XIST display partial X inactivation center function upon in vitro differentiation of male mouse embryonic stem cells, including activation in some cells of the endogenous mouse Xist locus [28, 29].
Given the importance of XIST for X inactivation, it is perhaps surprising that the X inactivation center region shows little sequence conservation surrounding XIST between mouse and human [30, 31]. In addition to XIST, the region contains several conserved genes and a number of non-coding RNAs and pseudogenes. Downstream of Xist the closest gene is the testes-specific Tsx gene in mouse, however TSX is a pseudogene in human . The closest gene upstream of XIST is the JPX (also known as ENOX) non-coding RNA gene. Interestingly, the region between JPX and XIST is ~90 kb in human, which is approximately 9 times larger than that of mouse. Thus rearrangements downstream of XIST where the mouse regulatory elements are found may have been compensated for by regulatory regions upstream of the gene. To identify such regulatory elements in the absence of substantial sequence conservation we have used DNase I hypersensitive site mapping as an unbiased approach to identify cis-acting regulatory elements in humans. Genomic regions hypersensitive to DNase I digestion (DHS sites) have been shown to harbour cis-regulatory elements critical for gene regulation , and both of the mouse Xist regulatory regions DXPas34 and Xite show DNase I hypersensitivity . Here, we report the identification of three previously unknown hypersensitive sites surrounding the human XIST locus.
Identification of DHS sites 3' to human XIST
The critical timing for XIST regulation is early in development and thus for mapping of DHS sites 3' to human XIST we used the mouse undifferentiated embryonic stem cell line ES-10 which contains a human XIST transgene. We also examined the L1.10.1 cell line which is a somatic male HT1080 cell line transfected with a PAC containing the XIST region, and which expresses XIST as well as TSIX. Additionally, we examined mouse/human somatic cell hybrids containing either the human active (Xa) or inactive (Xi) chromosome, which provide a unique opportunity to compare the chromatin structure between the Xi and Xa independent of each other without requiring allele-specific detection. We generated three probes downstream of XIST that were able to detect six overlapping restriction fragments allowing the analysis of a 43 kb region (see Figure 1B). Only one DHS site, located approximately 12 - 13 kb downstream of XIST, was identified in the ES-10 cells. This DHS site does not correspond to the cluster of four TSIX transcription start sites described in these cells, which are located approximately 14 kb further from the 3' end of XIST. The DHS site is close to the antisense transcription start in L1.10.1 cells. Interestingly, however, the DHS site was not found in L1.10.1 (Figure 1B), nor were any others, despite previous detection of antisense transcript both with RT-PCR and FISH in this cell line . We confirmed the ongoing presence of antisense transcript in the L1.10.1 cells used for DHS mapping by RT-PCR (data not shown). DHS mapping in both Xi and Xa hybrids did not show the presence of any DHS site downstream of XIST, including at the region identified to contain a DHS in ES-10 cells (Figure 1B). It thus appears that, unlike the situation in mouse where there are both developmental-specific and constitutive DHS sites downstream of Xist, in humans there is only a single developmental-specific DHS site downstream of XIST.
Identification of DHS sites 5' to human XIST
The lack of putative regulatory elements 3' to XIST, where many of the mouse transcriptional regulatory sites are located, led us to examine the region 5' to XIST which is larger in humans than it is in mouse . We generated three probes to examine the region upstream of human XIST for DHS sites. Almost 80% of the just over 90 kb region upstream of XIST is comprised of repetitive elements, predominantly LINE1 (39.5%) and ALU (27.3%) as identified by repeatmasker (http://www.repeatmasker.org/). This high repeat content precluded examination of the entire region and the restriction fragments assessed by the three probes interrogate a total of 39 kb in the 90 kb region.
X-chromosome inactivation in both humans and mice requires the presence in cis of the X-inactivation center, and the XIST/Xist gene contained therein. Interestingly, the XIST gene appears to have evolved in eutherians from a protein-coding gene, Lnx3, and while critical regions such as the 5' A repeats required for silencing are conserved [19, 35], other regions of XIST are more variable amongst the eutheria . Extensive studies in mouse models have defined a wide variety of regulatory elements for Xist including Tsix, DXPas34 and Xite. These elements are all located 3' to Xist, between Xist and the adjacent testes-specific Tsx gene. In humans TSX is a non-expressed pseudogene, and the blocks of sequence conservation previously reported between humans and mice 3' to XIST are ancestral TSX exons [31, 32]. The human TSIX region lacks an equivalent to the mouse CpG island that was shown to be essential for function of Tsix[13, 32, 37]. Other significant differences between mouse and human Tsix/TSIX include a lower level of human TSIX transcription and termination of human TSIX prior to the XIST promoter [24, 32], while antisense transcription across the mouse Xist promoter region is necessary for antisense function . In addition, Migeon et al. (2002), using RNA FISH for cellular localization of transcripts, showed that human TSIX transcripts are co-expressed with XIST from the inactive X throughout human embryonic development, suggesting that this antisense is unable to repress XIST leading to the argument that Tsix regulation of Xist may be specific to mouse .
Upstream of XIST/Xist the adjacent gene is JPX/ENOX, which is conserved in humans and mice , although the distance to the JPX CpG island and first exon is larger in humans (~90 kb) than in mice (less than 10 kb) . JPX is a non-coding RNA gene including different repetitive elements in different species, and the promoter of the mouse Jpx gene has been shown to interact with the Xist promoter in undifferentiated ES cells . No sequence conservation between humans and mice is found in the region between Jpx and Xist; however, there is conservation between humans and cows (and also dogs, data not shown), including an exon of the Rasl11c pseudogene .
The lack of sequence conservation between human and mouse in the region flanking XIST/Xist, as well as the differences in the TSIX/Tsix transcript, led us to undertake this study to identify potential regulatory elements for XIST by using DHS mapping both downstream and upstream of XIST. Downstream of XIST in the region where most regulatory elements are observed for mouse Xist we find only a single DHS, and this is only observed in undifferentiated mouse ES cells containing a human XIC transgene. While this site mapped close to one of the previously described human TSIX transcription start sites, the presence of the DHS did not correlate with TSIX transcription, and thus we consider it more likely that this DHS is reflective of a developmental event not regulating antisense transcription. As previously reported there is no substantial sequence conservation between cow, human and mouse downstream of XIST[24, 30], and dog also fails to show homologous regions (data not shown). In this region downstream of XIST the human sequence is enriched for LTR class repetitive elements, while mouse and dog are enriched in LINE elements. It has been demonstrated that in addition to a cis-regulatory role in XIST regulation, the mouse Tsix and Xite regulatory elements are also involved in a trans-regulation involving a transitory pairing of homologous X chromosomes proposed to establish the mutually exclusive choice of the future active and inactive X chromosomes in females . As the human XIC transgene in the ES-10 cells studied is capable of inducing expression of the single Xist gene in these male ES cells , it is plausible that the DHS identified in the transgene 3' to XIST is involved in such trans-interactions. There is now genome-wide mapping of DNase I hypersensitive sites  as well as histone modifications and CTCF binding sites, which often mark promoters and enhancers [43, 44] in a number of cultured cell lines or human CD4+ cells. The genome-wide mapping of CTCF sites in somatic cells did not identify any enrichment in the region of this 3' DHS. However, we also did not observe this DHS in somatic cells. Enhancer sequences have been reported to show cell-type specific patterns , so this region may contain an enhancer specific to undifferentiated cells.
We found evidence for DHS sites near the transcriptional start site of XIST in both somatic and ES-10 cells. XIST is expressed in the ES-10 cells prior to differentiation, however it is not expressed in the Xa-containing hybrid cells, thus these sites are observed independent of XIST expression. We did not refine the localization of these sites, as they likely correspond to the minimal XIST promoter and regulatory elements. The minimal mouse promoter has been shown to have a cluster of DHS sites [46, 47]. In agreement with the previously defined human minimal promoter  we detected strong promoter activity in our transient luciferase assay using 1 kb of DNA surrounding the XIST transcription start site (data not shown). Although a CTCF binding site has previously been defined at -43 bp of the XIST promoter , genome-wide mapping in CD4+ T cells only identified CTCF binding further upstream . This would correspond to our fragment 3 which showed limited promoter or enhancer activity in the 'reverse' orientation, but was unable to be cloned in the 'forward' orientation where it would be aligned with the test promoter in the same orientation it is aligned to XIST in the human genome. Genome-wide mapping of DHS sites identified a DHS site approximately three kb upstream of the promoter, in the vicinity of the CTCF site, as well as sites further within XIST that our analysis would not have detected . Thus it appears that there is a regulatory element for human XIST ~three kb upstream of the XIST promoter which includes CTCF binding sequences.
Further 5' to XIST we find a DHS site in a region sharing sequence conservation with cow and dog (data not shown). A DHS site in this region can also be observed in the genome-wide mapping in CD4+ T cells, and furthermore genome-wide H3K4me1 enrichment, which is characteristic of enhancers, flanks the site . We refined the location of the DHS to between 73,053,323 and 73,053,866, while the DHS site identified by the global mapping is slightly proximal at 73,053,237- 73,053,138. This might reflect subtle discrepancies in mapping, or between cell types. The region cloned for subsequent enhancer and promoter activity analysis was 73,054,787 -73,053,643 and would contain the H3K4me1 marked regions  and the majority of the region to which our DHS site was mapped, but be just upstream of the DHS site mapped in CD4+ cells .
Overall we find fewer regulatory elements in human than have been identified in mice. This could be due to higher repetitive element content in human which made analyzing the whole region challenging. Furthermore, the repetitive elements themselves might harbour regulatory elements. Indeed, the TSIX transcription starts mapped by Migeon et al. were to MER58B, AluY and L2 class repetitive elements , and conservation of repetitive elements between the mouse Tsix transcription start and humans was noted by Cohen et al. . While acquisition of repetitive elements may have led to an expansion of the XIC region in humans compared to mice, the conservation upstream of XIST between humans and other eutheria, including homology to an exon of the Rasl gene of chicken  suggests that this region was likely lost in rodents.
While many XIST regulatory elements do not appear to be conserved between humans and mice, many of the basic events required for X-chromosome inactivation must be conserved (reviewed in ). The 3' DHS site might demarcate a developmental-specific regulatory region that participates in the trans pairing interactions involved in initiation [17, 41]. It has been proposed that a critical function of TSIX is to partition chromatin domains in the XIC. Perhaps the 5' regulatory regions we have identified are capable of recapitulating such a function in humans. However we did not observe a consistent difference between the active and inactive X chromosomes for these DHS sites, and genome-wide chromatin mapping in somatic cells does not show evidence for a chromatin domain ending at the -65 DHS. Ultimately testing whether human X inactivation involves regulatory processes related to those detailed in mouse will require the challenging investigation of human XIST expression during early development. It has been shown that X chromosome inactivation is initiated in human preimplantation embryos ; however, human ES cells have shown considerable variability (e.g. ), making mouse ES cells with human XIST transgenes one of the best current models to study regulation of human XIST.
DNase I hypersensitivity mapping around the human XIST gene has identified fewer candidate regulatory regions than are observed flanking mouse Xist. In particular, 3' to XIST only a single, developmental-specific DHS site was observed in undifferentiated mouse ES cells with an integration of the human XIST domain. 5' to XIST a DHS site was identified in a region of sequence conservation amongst non-rodent eutheria. This region showed bi-directional promoter and enhancer activity. The lack of conservation of regulatory elements for XIST lends support to previous conjectures that human TSIX is no longer a functional regulator of XIST.
Tissue Culture & Cell Lines
ES-10 cells, a derivative of J1 male mouse embryonic stem cells with a 480-kb human XIC transgene, were generously provided by Dr. B. Migeon and maintained as described . The L1.10.1 transgenic derivative of human male fibrosarcoma cell line HT-1080 was grown as described . Mouse-human somatic cell hybrids t11-4Aaz5 (containing a human Xi as well as six human autosomes in addition to mouse chromosomes) and t60-12 (containing a human Xa) were maintained as described .
DNase I Hypersensitivity Mapping
Primers for probe generation
Sequence (5' to 3')
Sequence Comparisons, Plasmid Construction and Luciferase Assay
Primers for cloning
Sequence (5' to 3')
XIST promoter, positive control
1 kb upstream of XIST promoter
-1 kb F
-1 kb R
2 kb upstream of XIST promoter
-2 kb F
-2 kb R
3 kb upstream of XIST promoter
-3 kb F
-3 kb R
65 kb upstream of XIST, covers HS 101
-65 kb F
-65 kb R
Funding for this study was provided by Canadian Institute of Health Research Operating Grant MOP-13690. The ES-10 cells were generously provided by Dr. B. Migeon. The authors would like to thank Drs. Hugh Brock and Dixie Mager for helpful suggestions and Jakub Minks and other members of the Brown laboratory for advice and critical review of the manuscript.
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