Knowledge

XIST

Source πŸ“

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open and closed circles are medium and strongly reactive, respectively (reactivity suggests that a nucleotide is unpaired or loosely structured). Consistent and compensatory mutations (single and double point mutations that preserve pairing) are annotated in blue and purple, respectively. Base pairs that are 100% conserved in rodents are bold and black, while those conserved in rodents and mammals are in green. The data and model are taken from
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chromatin-binding region was functionally mapped and evaluated by using an approach for studying noncoding RNA function in living cells called peptide nucleic acid (PNA) interference mapping. In the reported experiments, a single 19-bp antisense cell-permeating PNA targeted against a particular region of Xist RNA caused the disruption of the Xi. The association of the Xi with macro-histone H2A is also disturbed by PNA interference mapping.
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The A region appears to encode two long stem-loop RNA structures that each include four repeats. An ortholog of the Xist RNA gene in humans has been identified in mice. This ortholog encodes a 15 kb Xist transcript that is also localized in the nucleus. However, the ortholog does not feature conserved repeats. The Xist RNA gene is located within the Xist Inactivation Center (XIC), which plays a major role in X-inactivation.
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of the X chromosomes from one of the sexes are Tsix antisense gene, DNA methylation and DNA acetylation; however, the definite mechanism of X-inactivation is still poorly understood. If one of the X chromosomes is not inactivated or is partially expressed, it could lead to over expression of the X chromosome and it could be lethal in some cases.
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the in vivo data, this revised model is highly conserved in rodents and mammals (including humans) suggesting functional importance for repA structure. Although the exact function of the repA region is uncertain, it was shown that the entire region is needed for efficient binding to the Suz12 protein.
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mechanisms that allow for equal expression of the X and autosomal chromosomes. Different species have different dosage compensation methods, with all of the methods involving the regulation of an X chromosome from one of the either sexes. Some methods involved in dosage compensation to inactivate one
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The functional role of the Xist transcript was definitively demonstrated in mouse female ES cells using a novel antisense technology, called peptide nucleic acid (PNA) interference mapping. In the reported experiments, a single 19-bp antisense cell-permeating PNA targeted against a particular region
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The Xist RNA gene lies within the X-inactivation centre (XIC), which plays a major role in Xist expression and X-inactivation. The XIC is located on the q arm of the X chromosome (Xq13). XIC regulates Xist in cis X-inactivation, where Tsix, an antisense of Xist, downregulates the expression of Xist.
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1 at the binding site of these factors on the Xist gene, which inhibits Xist expression A study was conducted where Nanog or Oct4 transcription factors were depleted in pluripotent cells, which resulted in the upregulation of Xist. From this study, it is proposed that Nanog and Oct4 are involved in
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is an RNAi enzyme and it is believed to cleave the duplex of Xist and Tsix at the beginning of X-inactivation, to small ~30 nucleotide RNAs, which have been termed xiRNAs, These xiRNAs are believed to be involved in repressing Xist on the probable active X chromosome based upon studies. A study was
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Structure model of the repeat A (repA) region of Xist based on in vivo biochemical structure probing and comparative sequence analysis. Repeats 1 to 8(1/2) are numbered and boxed - they are shown in red on the cartoon of repA in the upper left hand panel. Reactive nucleotides are colored red, where
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The human Xist RNA gene is located on the long (q) arm of the X chromosome. The Xist RNA gene contains conserved repeats within its structure. Its gene product is largely localized in the nucleus. The Xist RNA gene features a conserved A region, which contains 8 repeats separated by U-rich spacers.
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structures. A recent study using in vivo biochemical probing and comparative sequence analysis proposed a revision of the repA structure model that includes both intra-repeat and inter-repeat folding found in previous models as well as novel features (see Figure). In addition to its agreement with
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and sperm do not express Xist and the X chromosome remains active. After fertilization, when the cells are in the 2 to 4 cell stage, Xist transcripts are expressed from paternal X chromosome(Xp) in every cell, causing that X chromosome to become imprinted and inactivated. Some cells develop into
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is one example of where dosage compensation does not equally express the X chromosome, and in females one of the X chromosomes is missing or has abnormalities, which leads to physical abnormalities and also gonadal dysfunction in females due to the one missing or abnormal X chromosome. Turner's
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The Xist RNA directly binds to the inactive X-chromosome through a chromatin binding region of the RNA transcript. The Xist chromatin binding region was first elucidated in female mouse fibroblastic cells. The primary chromatin binding region was shown to localize to the C-repeat region. The
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In addition to being expressed in nearly all females, XIST is expressed in narrow developmental contexts in males including human preimplantation embryos, primordial germ cells, testicular germ cell tumors, and a subset of male cancers of diverse lineages. It may be involved in the dosage
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conducted where normal endogenous Dicer levels were decreased to 5%, which led to an increase in Xist expression in undifferentiated cells, thus supporting the role of xiRNAs in Xist repression. The role and mechanism of xiRNAs is still under examination and debate.
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of Xist RNA prevented the formation of Xi and inhibited cis-silencing of X-linked genes. The association of the Xi with macro-histone H2A is also disturbed by PNA interference mapping. The X-inactivation process occurs in mice even in the absence of this gene via
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to repress the transcription of Xist, which negatively regulates its expression. The mechanism behind how Tsix modulates Xist activity in cis is poorly understood; however, there are a few theories on its mechanism. One theory is that Tsix is involved in
891:. The inactive X chromosome is coated with this transcript, which is essential for the inactivation. X chromosomes lacking Xist will not be inactivated, while duplication of the Xist gene on another chromosome causes inactivation of that chromosome. 2039:
Borsani G, Tonlorenzi R, Simmler MC, Dandolo L, Arnaud D, Capra V, Grompe M, Pizzuti A, Muzny D, Lawrence C, Willard HF, Avner P, Ballabio A (May 1991). "Characterization of a murine gene expressed from the inactive X chromosome".
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The Xist RNA contains a region of conservation called the repeat A (repA) region that contains up to nine repeated elements. It was initially suggested that repA repeats could fold back on themselves to form local intra-repeat
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domain. The zinc finger domain is believed to bind to the RNA molecule. The PRC2 has been observed to repress Xist expression independent of the Tsix antisense transcript, although the definite mechanism is still not known.
1247:, but the Xist is maintained in epiblast, an X is inactivated and the Xist allele is turned off in the active X chromosome. In maturing XX primordial germ cells, Xist is downregulated and X reactivation occurs once again. 2999:
Brown CJ, Ballabio A, Rupert JL, Lafreniere RG, Grompe M, Tonlorenzi R, Willard HF (January 1991). "A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome".
2146:, Ashworth A, Kay GF, McCabe VM, Norris DP, Cooper PJ, Swift S, Rastan S (1992). "The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus". 3717:
Brockdorff N, Ashworth A, Kay GF, Cooper P, Smith S, McCabe VM, Norris DP, Penny GD, Patel D, Rastan S (May 1991). "Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome".
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Brockdorff N, Ashworth A, Kay GF, Cooper P, Smith S, McCabe VM, Norris DP, Penny GD, Patel D, Rastan S (May 1991). "Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome".
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Ganesan S, Silver DP, Greenberg RA, Avni D, Drapkin R, Miron A, Mok SC, Randrianarison V, Brodie S, Salstrom J, Rasmussen TP, Klimke A, Marrese C, Marahrens Y, Deng CX, Feunteun J, Livingston DM (November 2002).
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Plenge RM, Hendrich BD, Schwartz C, Arena JF, Naumova A, Sapienza C, Winter RM, Willard HF (November 1997). "A promoter mutation in the XIST gene in two unrelated families with skewed X-chromosome inactivation".
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Brown CJ, Lafreniere RG, Powers VE, Sebastio G, Ballabio A, Pettigrew AL, Ledbetter DH, Levy E, Craig IW, Willard HF (January 1991). "Localization of the X inactivation centre on the human X chromosome in Xq13".
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Ganesan S, Silver DP, Greenberg RA, Avni D, Drapkin R, Miron A, Mok SC, Randrianarison V, Brodie S, Salstrom J, Rasmussen TP, Klimke A, Marrese C, Marahrens Y, Deng CX, Feunteun J, Livingston DM (November 2002).
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Brown CJ, Ballabio A, Rupert JA, Lafreniere RG, Grompe M, Tonlorenzi R, Willard HF (Jan 1991). "A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome".
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that seem to play a role in repressing Xist. In the absence of Tsix in pluripotent cells, Xist is repressed, where a mechanism has been proposed that these transcription factors cause splicing to occur at
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Nesterova TB, Mermoud JE, Hilton K, Pehrson J, Surani MA, McLaren A, Brockdorff N (January 2002). "Xist expression and macroH2A1.2 localisation in mouse primordial and pluripotent embryonic germ cells".
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Kawakami T, Okamoto K, Sugihara H, Hattori T, Reeve AE, Ogawa O, Okada Y (April 2003). "The roles of supernumerical X chromosomes and XIST expression in testicular germ cell tumors".
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27 (K27), which results in chromatin repression, and thus leads to transcriptional silencing. Xist RNA recruits polycomb complexes to the inactive X chromosome at the onset of XCI.
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Maenner S, Blaud M, Fouillen L, Savoye A, Marchand V, Dubois A, Sanglier-CianfΓ©rani S, Van Dorsselaer A, Clerc P, Avner P, Visvikis A, Branlant C (January 2010). Hall K (ed.).
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Mak W, Nesterova TB, de Napoles M, Appanah R, Yamanaka S, Otte AP, Brockdorff N (January 2004). "Reactivation of the paternal X chromosome in early mouse embryos".
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where it coats the inactive X chromosome. Alternatively spliced transcript variants have been identified, but their full length sequences have not been determined.
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Navarro P, Chambers I, Karwacki-Neisius V, Chureau C, Morey C, Rougeulle C, Avner P (September 2008). "Molecular coupling of Xist regulation and pluripotency".
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The Xist RNA, a large (17 kb in humans) transcript, is expressed on the inactive chromosome and not on the active one. It is processed in a similar way to
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Duret L, Chureau C, Samain S, Weissenbach J, Avner P (June 2006). "The Xist RNA gene evolved in eutherians by pseudogenization of a protein-coding gene".
566: 2422:"Tsix transcription across the Xist gene alters chromatin conformation without affecting Xist transcription: implications for X-chromosome inactivation" 3380:"Familial cases of point mutations in the XIST promoter reveal a correlation between CTCF binding and pre-emptive choices of X chromosome inactivation" 547: 55:, DXS1089, DXS399E, LINC00001, NCRNA00001, SXI1, swd66, X inactive specific transcript (non-protein coding), X inactive specific transcript, Xist 2367:
Nesterova TB, Popova BC, Cobb BS, Norton S, Senner CE, Tang YA, Spruce T, Rodriguez TA, Sado T, Merkenschlager M, Brockdorff N (October 2008).
1373: 1501:"The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus" 1243:
cells are then formed and they begin to be differentiated, and the Xist is upregulated from either of the two X chromosomes and at random in
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Hong YK, Ontiveros SD, Strauss WM (March 2000). "A revision of the human XIST gene organization and structural comparison with mouse Xist".
1355: 929:). The process is regulated by several factors, including a region of chromosome X called the X-inactivation center (XIC). The XIST gene is 3448:
Cohen HR, Panning B (August 2007). "XIST RNA exhibits nuclear retention and exhibits reduced association with the export factor TAP/NXF1".
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Chenga MK, Nguyena KD, Disteche CM (2006). "Dosage compensation of the X chromosome and Turner syndrome=International-Congress-series".
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Pugacheva EM, Tiwari VK, Abdullaev Z, Vostrov AA, Flanagan PT, Quitschke WW, Loukinov DI, Ohlsson R, Lobanenkov VV (April 2005).
1396: 1235:(the inner cell mass) when the blastocyte forms. There, the imprint is removed, leading to the downregulation of Xist and thus 3676:"A novel role for Xist RNA in the formation of a repressive nuclear compartment into which genes are recruited when silenced" 3093:"XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure" 1338: 1060:
The Xist promoter of XIC is the master regulator of X-inactivation. X-inactivation plays a key role in dosage compensation.
3880: 3136:"Identification and characterization of the human XIST gene promoter: implications for models of X chromosome inactivation" 1317: 3890: 2235:
Herzing LB, Romer JT, Horn JM, Ashworth A (March 1997). "Xist has properties of the X-chromosome inactivation centre".
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Plath K, Mlynarczyk-Evans S, Nusinow DA, Panning B (2002). "Xist RNA and the mechanism of X chromosome inactivation".
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Vincent-Salomon A, Ganem-Elbaz C, ManiΓ© E, Raynal V, Sastre-Garau X, Stoppa-Lyonnet D, Stern MH, Heard E (June 2007).
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Lee JT (2011). "Gracefully ageing at 50, X-chromosome inactivation becomes a paradigm for RNA and chromatin control".
2640:"Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation" 1239:
of the inactive X chromosome. Recent data suggests that Xist activity is regulated by an anti-sense transcript. The
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de Napoles M, Mermoud JE, Wakao R, Tang YA, Endoh M, Appanah R, Nesterova TB, Silva J, Otte AP, Vidal M, Koseki H,
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Lee JT, Davidow LS, Warshawsky D (April 1999). "Tsix, a gene antisense to Xist at the X-inactivation centre".
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Lee JT, Davidow LS, Warshawsky D (April 1999). "Tsix, a gene antisense to Xist at the X-inactivation centre".
2369:"Dicer regulates Xist promoter methylation in ES cells indirectly through transcriptional control of Dnmt3a" 887:. It has been suggested that this RNA gene evolved at least partly from a protein-coding gene that became a 592: 3861: 139: 114: 64: 3254:"An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells" 1445:
Chureau C, Prissette M, Bourdet A, Barbe V, Cattolico L, Jones L, Eggen A, Avner P, Duret L (June 2002).
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antisense gene is a transcript of the Xist gene at the XIC center. The Tsix antisense transcript acts in
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Xist expression and X-inactivation change throughout embryonic development. In early embryogenesis, the
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Nguyen DK, Disteche CM (January 2006). "Dosage compensation of the active X chromosome in mammals".
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Brockdorff N (July 2002). "X-chromosome inactivation: closing in on proteins that bind Xist RNA".
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structures. Later work using in vitro biochemical structure probing proposed several inter-repeat
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Brown CJ, Hendrich BD, Rupert JL, Lafrenière RG, Xing Y, Lawrence J, Willard HF (October 1992).
1447:"Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine" 1152: 1073: 2332:
Senner CE, Brockdorff N (April 2009). "Xist gene regulation at the onset of X inactivation".
1256: 1148: 918: 884: 3818: 3727: 3586: 3498: 3265: 3055: 3009: 2810: 2590: 2535: 2482: 2244: 2101: 2049: 1888: 1829: 1728: 1669: 1557: 1214: 1082: 934: 128: 1877:"Evidence of Xist RNA-independent initiation of mouse imprinted X-chromosome inactivation" 1423: 84: 8: 3487:"Inducible XIST-dependent X-chromosome inactivation in human somatic cells is reversible" 1934:"Somatic XIST activation and features of X chromosome inactivation in male human cancers" 1289: 1207: 926: 3822: 3769:
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
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Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
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Ganesan S, Silver DP, Drapkin R, Greenberg R, Feunteun J, Livingston DM (January 2004).
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Chow JC, Yen Z, Ziesche SM, Brown CJ (2005). "Silencing of the mammalian X chromosome".
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pathway have been also proposed to play a role in regulation of the Xist Promoter.
1009: 999: 899: 333: 264: 208: 163: 3556: 3539: 3341: 2981: 76: 3865: 2656: 2639: 2635: 2143: 2006: 1657: 1107: 1004: 930: 895: 880: 308: 92: 3853: 3765:"Advances in understanding chromosome silencing by the long non-coding RNA Xist" 1378:
National Center for Biotechnology Information, U.S. National Library of Medicine
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National Center for Biotechnology Information, U.S. National Library of Medicine
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process in mammalian females that transcriptionally silences one of the pair of
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Proceedings of the National Academy of Sciences of the United States of America
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Proceedings of the National Academy of Sciences of the United States of America
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Proceedings of the National Academy of Sciences of the United States of America
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Chow JC, Hall LL, Baldry SE, Thorogood NP, Lawrence JB, Brown CJ (June 2007).
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through a cDNA library screening and then characterized in collaboration with
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Sadagopan A, Nasim IT, Li J, Achom M, Zhang CZ, Viswanathan SR (2022-11-16).
1620: 1111: 3511: 3431: 3414: 2822: 2602: 2579:"Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome" 2547: 2494: 1569: 469: 347: 3838: 3798: 3780: 3709: 3623: 3594: 3565: 3530: 3469: 3440: 3405: 3370: 3333: 3297: 3278: 3236: 2973: 2931: 2913: 2874: 2830: 2760: 2703: 2665: 2620: 2555: 2512: 2455: 2406: 2353: 2307: 2213: 2182: 2025: 1967: 1918: 1861: 1842: 1791: 1639: 1577: 1480: 1431: 1023: 942: 922: 876: 827: 326: 105: 3747: 3658: 3252:
Hall LL, Byron M, Sakai K, Carrel L, Willard HF, Lawrence JB (June 2002).
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Kalantry S, Purushothaman S, Bowen RB, Starmer J, Magnuson T (July 2009).
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Vasques LR, Stabellini R, Xue F, Tian XC, Soukoyan M, Pereira LV (2007).
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exclusively from the XIC of the inactive X chromosome. The transcript is
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compensation of supernumerary X chromosomes in the latter two cases.
844:– X-chromosome inactivation centre – along with two other RNA genes ( 511: 292: 279: 191: 178: 80: 3308:"BRCA1 supports XIST RNA concentration on the inactive X chromosome" 2948:"BRCA1 supports XIST RNA concentration on the inactive X chromosome" 1783: 641: 637: 3572: 2695: 2322: 1816:
Beletskii A, Hong YK, Pehrson J, Egholm M, Strauss WM (July 2001).
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Fang R, Moss WN, Rutenberg-Schoenberg M, Simon MD (December 2015).
925:, thus providing dosage equivalence between males and females (see 831: 791: 2898:"Association of BRCA1 with the inactive X chromosome and XIST RNA" 2471:"Intersection of the RNA interference and X-inactivation pathways" 2420:
Navarro P, Pichard S, Ciaudo C, Avner P, Rougeulle C (June 2005).
988:"Probing Xist RNA Structure in Cells Using Targeted Structure-Seq" 979: 3633:"X chromosome inactivation is mediated by Xist RNA stabilization" 2299: 2205: 1874: 1644:
Figure 1 Xist RNA encompasses the X from which it is transcribed.
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Clemson CM, McNeil JA, Willard HF, Lawrence JB (February 1996).
68: 3377: 2038: 1227: 1186: 1165: 775: 533: 3348: 3044: 2998: 2895: 2851: 2800: 1717: 1660:(1996). "Requirement for Xist in X chromosome inactivation". 1547: 1498: 1272: 1190: 1131: 1123: 872: 3090: 1444: 3716: 3176: 2142: 2090: 1178: 1160: 1156: 1143: 1127: 1069: 857: 3673: 3304: 2944: 2633: 2577:
Zhao J, Sun BK, Erwin JA, Song JJ, Lee JT (October 2008).
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Chaumeil J, Le Baccon P, Wutz A, Heard E (August 2006).
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syndrome is also referred to as a monosomy X condition.
316: 3484: 2724: 1655: 3630: 3133: 2773: 1931: 481: 3415:"XIST repression in the absence of DNMT1 and DNMT3B" 3251: 3214: 2285: 2191: 1397:"Entrez Gene: XIST X (inactive)-specific transcript" 953:, but Xist is required to stabilize this silencing. 3631:Panning B, Dausman J, Jaenisch R (September 1997). 1598: 1409: 1081:modification at the Xist locus and another is that 1599:Ng K, Pullirsch D, Leeb M, Wutz A (January 2007). 1334: 1332: 1330: 1313: 1311: 1309: 1092: 2855:Differentiation; Research in Biological Diversity 1811: 1809: 263: 162: 3872: 3134:Hendrich BD, Plenge RM, Willard HF (July 1997). 2576: 2331: 2084: 1983: 1981: 1979: 1977: 1327: 1306: 1102:The Tsix antisense is believed to activate DNA 3762: 2725:Csankovszki G, Nagy A, Jaenisch R (May 2001). 2681: 1806: 1339:GRCm38: Ensembl release 89: ENSMUSG00000086503 1255:Mutations in the XIST promoter cause familial 1172: 1138: 1054: 2677: 2675: 2334:Current Opinion in Genetics & Development 1868: 1494: 1492: 1490: 1391: 1389: 1387: 3447: 2938: 2889: 2032: 1974: 1412:Annual Review of Genomics and Human Genetics 1063: 2468: 1318:GRCh38: Ensembl release 89: ENSG00000229807 3601: 2672: 1711: 1656:Penny GD, Kay GF, Sheardown SA, Rastan S, 1487: 1384: 1193:is a component of the PRC2 and contains a 969: 3788: 3699: 3648: 3555: 3520: 3510: 3430: 3395: 3323: 3287: 3277: 3159: 3116: 2963: 2921: 2750: 2655: 2610: 2502: 2445: 2396: 2386: 2015: 2005: 1949: 1908: 1851: 1841: 1629: 1619: 1516: 1470: 1013: 1003: 1763: 1144:Pluripotent cell transcriptional factors 978: 3805: 1221: 3873: 3587:10.1146/annurev.genet.36.042902.092433 1201: 894:The human Xist gene was discovered by 822:(X-inactive specific transcript) is a 3763:Sado T, Brockdorff N (January 2013). 2469:Ogawa Y, Sun BK, Lee JT (June 2008). 1772:Nature Reviews Molecular Cell Biology 1424:10.1146/annurev.genom.6.080604.162350 834:that acts as a major effector of the 268: 229: 224: 167: 126: 121: 1541: 1769: 1206:X-inactivation plays a key role in 1169:the repression of Xist expression. 13: 2991: 1250: 838:process. It is a component of the 14: 3902: 3847: 3363:10.1097/01.ju.0000044927.23323.5a 2867:10.1046/j.1432-0436.2002.690415.x 1601:"Xist and the order of silencing" 1117: 937:but apparently does not encode a 1703: 1089:play a role in Xist repression. 960: 941:. The transcript remains in the 252: 245: 239: 216: 151: 144: 138: 113: 29: 2845: 2794: 2767: 2718: 2627: 2570: 2519: 2462: 2413: 2360: 2279: 2228: 2136: 1925: 1649: 1592: 1262: 1177:Polycomb repressive complex 2 ( 1093:Regulation of the Xist promoter 386:epithelium of lactiferous gland 3831:10.1126/science.340.6135.910-a 1438: 1403: 1366: 1348: 1151:express transcription factors 1097: 470:More reference expression data 1: 3650:10.1016/S0092-8674(00)80355-4 3616:10.1016/S0168-9525(02)02717-8 3557:10.1158/0008-5472.CAN-07-0465 3325:10.1016/S0092-8674(02)01052-8 2965:10.1016/S0092-8674(02)01052-8 2776:International Congress Series 1300: 237: 136: 2657:10.1016/j.devcel.2004.10.005 2160:10.1016/0092-8674(92)90519-I 2007:10.1371/journal.pbio.1000276 1518:10.1016/0092-8674(92)90520-M 1005:10.1371/journal.pgen.1005668 7: 3881:Genes on human chromosome X 3097:The Journal of Cell Biology 2731:The Journal of Cell Biology 2374:Epigenetics & Chromatin 1278: 1173:Polycomb repressive complex 1139:Tsix independent mechanisms 1055:X-inactivation centre (XIC) 1045: 974: 909: 10: 3907: 1951:10.1016/j.cels.2022.10.002 452:sexually immature organism 3891:Sex-determination systems 3575:Annual Review of Genetics 3462:10.1007/s00412-007-0100-1 2788:10.1016/j.ics.2006.06.012 2346:10.1016/j.gde.2009.03.003 1374:"Mouse PubMed Reference:" 1356:"Human PubMed Reference:" 1064:Tsix antisense transcript 806: 801: 797: 790: 774: 755: 742: 738: 723: 719: 712: 699: 695: 680: 676: 669: 658: 654: 635: 631: 622: 609: 605: 590: 586: 577: 564: 560: 545: 541: 532: 517: 510: 506: 494: 489: 480: 467: 416: 407: 354: 345: 315: 307: 303: 286: 273: 236: 215: 206: 202: 185: 172: 135: 112: 103: 99: 62: 59: 49: 42: 37: 28: 23: 3384:Human Molecular Genetics 1621:10.1038/sj.embor.7400871 768:Chr X: 102.5 – 102.53 Mb 3680:Genes & Development 3512:10.1073/pnas.0610946104 2823:10.1126/science.1092674 2603:10.1126/science.1163045 2548:10.1126/science.1160952 2495:10.1126/science.1157676 2426:Genes & Development 1570:10.1126/science.1126316 1267:XIST has been shown to 970:Transcript organization 761:Chr X: 73.82 – 73.85 Mb 3781:10.1098/rstb.2011.0325 3351:The Journal of Urology 3279:10.1073/pnas.132468999 3152:10.1093/nar/25.13.2661 3140:Nucleic Acids Research 2914:10.1098/rstb.2003.1371 1843:10.1073/pnas.161173098 1149:Pluripotent stem cells 1029: 883:. However, it remains 432:neural layer of retina 3432:10.1093/dnares/dsi013 3229:10.1007/s003350010040 3109:10.1083/jcb.132.3.259 2743:10.1083/jcb.153.4.773 2388:10.1186/1756-8935-1-2 1257:skewed X-inactivation 1083:transcription factors 982: 951:epigenetic regulation 826:transcribed from the 1222:X-inactivation cycle 231:X chromosome (mouse) 129:X chromosome (human) 3859:lncRNAdb Xist entry 3823:2013Sci...340Q.910P 3732:1991Natur.351..329B 3503:2007PNAS..10410104C 3270:2002PNAS...99.8677H 3060:1991Natur.349...82B 3014:1991Natur.349...38B 2815:2004Sci...303..666M 2595:2008Sci...322..750Z 2540:2008Sci...321.1693N 2487:2008Sci...320.1336O 2249:1997Natur.386..272H 2106:1991Natur.351..329B 2054:1991Natur.351..325B 1901:10.1038/nature08161 1893:2009Natur.460..647K 1834:2001PNAS...98.9215B 1733:1991Natur.349...38B 1674:1996Natur.379..131P 1562:2006Sci...312.1653D 1556:(5780): 1653–1655. 1290:Dosage compensation 1208:dosage compensation 1202:Dosage compensation 1104:methyl transferases 927:dosage compensation 378:germinal epithelium 270:X D|X 46.15 cM 3864:2015-12-22 at the 3775:(1609): 20110325. 3692:10.1101/gad.380906 3604:Trends in Genetics 3397:10.1093/hmg/ddi089 3192:10.1038/ng1197-353 2644:Developmental Cell 2438:10.1101/gad.341105 1944:(11): 932–944.e5. 1030: 612:ENSMUSG00000086503 456:intercostal muscle 420:epithelium of lens 370:right uterine tube 2481:(5881): 1336–41. 1463:10.1101/gr.152902 1233:pluripotent cells 1215:Turner's Syndrome 1087:pluripotent cells 832:placental mammals 817: 816: 813: 812: 786: 785: 751: 750: 732: 731: 708: 707: 689: 688: 665: 664: 648: 647: 618: 617: 599: 598: 573: 572: 554: 553: 502: 501: 498: 497: 476: 475: 463: 462: 401: 400: 299: 298: 198: 197: 3898: 3842: 3802: 3792: 3759: 3740:10.1038/351329a0 3726:(6324): 329–31. 3713: 3703: 3670: 3652: 3627: 3598: 3569: 3559: 3534: 3524: 3514: 3481: 3444: 3434: 3409: 3399: 3374: 3345: 3327: 3301: 3291: 3281: 3248: 3217:Mammalian Genome 3211: 3173: 3163: 3130: 3120: 3087: 3068:10.1038/349082a0 3041: 3022:10.1038/349038a0 2986: 2985: 2967: 2942: 2936: 2935: 2925: 2893: 2887: 2886: 2849: 2843: 2842: 2798: 2792: 2791: 2771: 2765: 2764: 2754: 2722: 2716: 2715: 2679: 2670: 2669: 2659: 2631: 2625: 2624: 2614: 2574: 2568: 2567: 2534:(5896): 1693–5. 2523: 2517: 2516: 2506: 2466: 2460: 2459: 2449: 2417: 2411: 2410: 2400: 2390: 2364: 2358: 2357: 2329: 2320: 2319: 2283: 2277: 2276: 2257:10.1038/386272a0 2232: 2226: 2225: 2189: 2180: 2179: 2140: 2134: 2133: 2114:10.1038/351329a0 2100:(6324): 329–31. 2088: 2082: 2081: 2062:10.1038/351325a0 2036: 2030: 2029: 2019: 2009: 1985: 1972: 1971: 1953: 1929: 1923: 1922: 1912: 1887:(7255): 647–51. 1872: 1866: 1865: 1855: 1845: 1813: 1804: 1803: 1767: 1761: 1760: 1741:10.1038/349038a0 1715: 1709: 1708: 1707: 1701: 1682:10.1038/379131a0 1653: 1647: 1646: 1633: 1623: 1605: 1604:(Review Article) 1596: 1590: 1589: 1545: 1539: 1538: 1520: 1496: 1485: 1484: 1474: 1442: 1436: 1435: 1407: 1401: 1400: 1393: 1382: 1381: 1370: 1364: 1363: 1352: 1346: 1336: 1325: 1315: 1027: 1017: 1007: 998:(12): e1005668. 900:Carolyn J. Brown 799: 798: 770: 763: 746: 736: 735: 727: 717: 716: 713:RefSeq (protein) 703: 693: 692: 684: 674: 673: 652: 651: 629: 628: 603: 602: 584: 583: 558: 557: 539: 538: 508: 507: 487: 486: 472: 412: 410:Top expressed in 405: 404: 390:lactiferous duct 350: 348:Top expressed in 343: 342: 322: 321: 305: 304: 295: 282: 271: 256: 249: 243: 232: 220: 204: 203: 194: 181: 170: 155: 148: 142: 131: 117: 101: 100: 95: 93:XIST - orthologs 54: 47: 33: 21: 20: 3906: 3905: 3901: 3900: 3899: 3897: 3896: 3895: 3871: 3870: 3866:Wayback Machine 3854:NCBI Xist entry 3850: 3845: 3686:(16): 2223–37. 3550:(11): 5134–40. 3544:Cancer Research 3497:(24): 10104–9. 3264:(13): 8677–82. 3180:Nature Genetics 3146:(13): 2661–71. 3008:(6304): 38–44. 2994: 2992:Further reading 2989: 2943: 2939: 2908:(1441): 123–8. 2894: 2890: 2861:(4–5): 216–25. 2850: 2846: 2809:(5658): 666–9. 2799: 2795: 2772: 2768: 2723: 2719: 2684:Nature Genetics 2680: 2673: 2632: 2628: 2589:(5902): 750–6. 2575: 2571: 2524: 2520: 2467: 2463: 2432:(12): 1474–84. 2418: 2414: 2365: 2361: 2330: 2323: 2288:Nature Genetics 2284: 2280: 2243:(6622): 272–5. 2233: 2229: 2194:Nature Genetics 2190: 2183: 2141: 2137: 2089: 2085: 2048:(6324): 325–9. 2037: 2033: 2000:(1): e1000276. 1986: 1975: 1930: 1926: 1873: 1869: 1828:(16): 9215–20. 1814: 1807: 1784:10.1038/nrm3231 1768: 1764: 1727:(6304): 38–44. 1716: 1712: 1702: 1668:(6561): 131–7. 1654: 1650: 1603: 1597: 1593: 1546: 1542: 1497: 1488: 1451:Genome Research 1443: 1439: 1408: 1404: 1395: 1394: 1385: 1372: 1371: 1367: 1354: 1353: 1349: 1337: 1328: 1316: 1307: 1303: 1281: 1265: 1253: 1251:Disease linkage 1224: 1204: 1175: 1146: 1141: 1120: 1100: 1095: 1066: 1057: 1048: 977: 972: 963: 912: 896:Andrea Ballabio 881:polyadenylation 808:View/Edit Mouse 803:View/Edit Human 766: 759: 756:Location (UCSC) 744: 725: 701: 682: 640: 593:ENSG00000229807 468: 459: 454: 450: 446: 442: 438: 434: 430: 426: 424:renal corpuscle 422: 408: 397: 392: 388: 384: 380: 376: 372: 368: 366:mucosa of ileum 364: 360: 346: 290: 277: 269: 259: 258: 257: 250: 230: 207:Gene location ( 189: 176: 168: 158: 157: 156: 149: 127: 104:Gene location ( 63: 50: 43: 17: 12: 11: 5: 3904: 3894: 3893: 3888: 3886:Non-coding RNA 3883: 3869: 3868: 3856: 3849: 3848:External links 3846: 3844: 3843: 3803: 3760: 3714: 3671: 3628: 3599: 3570: 3535: 3482: 3445: 3410: 3375: 3357:(4): 1546–52. 3346: 3318:(3): 393–405. 3302: 3249: 3212: 3174: 3131: 3088: 3054:(6304): 82–4. 3042: 2995: 2993: 2990: 2988: 2987: 2958:(3): 393–405. 2937: 2888: 2844: 2793: 2766: 2717: 2696:10.1038/ng1705 2671: 2626: 2569: 2518: 2461: 2412: 2359: 2321: 2278: 2227: 2181: 2135: 2083: 2031: 1973: 1924: 1867: 1805: 1778:(12): 815–26. 1762: 1710: 1648: 1591: 1540: 1486: 1457:(6): 894–908. 1437: 1402: 1383: 1365: 1347: 1326: 1304: 1302: 1299: 1298: 1297: 1292: 1287: 1285:X-inactivation 1280: 1277: 1264: 1261: 1252: 1249: 1223: 1220: 1203: 1200: 1174: 1171: 1145: 1142: 1140: 1137: 1119: 1118:dsRNA and RNAi 1116: 1099: 1096: 1094: 1091: 1065: 1062: 1056: 1053: 1047: 1044: 976: 973: 971: 968: 962: 959: 915:X-inactivation 911: 908: 836:X-inactivation 824:non-coding RNA 815: 814: 811: 810: 805: 795: 794: 788: 787: 784: 783: 781: 779: 772: 771: 764: 757: 753: 752: 749: 748: 740: 739: 733: 730: 729: 721: 720: 714: 710: 709: 706: 705: 697: 696: 690: 687: 686: 678: 677: 671: 667: 666: 663: 662: 656: 655: 649: 646: 645: 633: 632: 626: 620: 619: 616: 615: 607: 606: 600: 597: 596: 588: 587: 581: 575: 574: 571: 570: 562: 561: 555: 552: 551: 543: 542: 536: 530: 529: 524: 519: 515: 514: 504: 503: 500: 499: 496: 495: 492: 491: 484: 478: 477: 474: 473: 465: 464: 461: 460: 458: 457: 453: 449: 445: 441: 437: 433: 429: 425: 421: 417: 414: 413: 402: 399: 398: 396: 395: 391: 387: 383: 379: 375: 371: 367: 363: 359: 355: 352: 351: 339: 338: 330: 319: 313: 312: 309:RNA expression 301: 300: 297: 296: 288: 284: 283: 275: 272: 267: 261: 260: 251: 244: 238: 234: 233: 228: 222: 221: 213: 212: 200: 199: 196: 195: 187: 183: 182: 174: 171: 166: 160: 159: 150: 143: 137: 133: 132: 125: 119: 118: 110: 109: 97: 96: 61: 57: 56: 48: 40: 39: 35: 34: 26: 25: 16:Non-coding RNA 15: 9: 6: 4: 3: 2: 3903: 3892: 3889: 3887: 3884: 3882: 3879: 3878: 3876: 3867: 3863: 3860: 3857: 3855: 3852: 3851: 3840: 3836: 3832: 3828: 3824: 3820: 3817:(6135): 910. 3816: 3812: 3808: 3804: 3800: 3796: 3791: 3786: 3782: 3778: 3774: 3770: 3766: 3761: 3757: 3753: 3749: 3745: 3741: 3737: 3733: 3729: 3725: 3721: 3715: 3711: 3707: 3702: 3697: 3693: 3689: 3685: 3681: 3677: 3672: 3668: 3664: 3660: 3656: 3651: 3646: 3643:(5): 907–16. 3642: 3638: 3634: 3629: 3625: 3621: 3617: 3613: 3609: 3605: 3600: 3596: 3592: 3588: 3584: 3580: 3576: 3571: 3567: 3563: 3558: 3553: 3549: 3545: 3541: 3536: 3532: 3528: 3523: 3518: 3513: 3508: 3504: 3500: 3496: 3492: 3488: 3483: 3479: 3475: 3471: 3467: 3463: 3459: 3456:(4): 373–83. 3455: 3451: 3446: 3442: 3438: 3433: 3428: 3424: 3420: 3416: 3411: 3407: 3403: 3398: 3393: 3390:(7): 953–65. 3389: 3385: 3381: 3376: 3372: 3368: 3364: 3360: 3356: 3352: 3347: 3343: 3339: 3335: 3331: 3326: 3321: 3317: 3313: 3309: 3303: 3299: 3295: 3290: 3285: 3280: 3275: 3271: 3267: 3263: 3259: 3255: 3250: 3246: 3242: 3238: 3234: 3230: 3226: 3222: 3218: 3213: 3209: 3205: 3201: 3197: 3193: 3189: 3185: 3181: 3175: 3171: 3167: 3162: 3157: 3153: 3149: 3145: 3141: 3137: 3132: 3128: 3124: 3119: 3114: 3110: 3106: 3103:(3): 259–75. 3102: 3098: 3094: 3089: 3085: 3081: 3077: 3073: 3069: 3065: 3061: 3057: 3053: 3049: 3043: 3039: 3035: 3031: 3027: 3023: 3019: 3015: 3011: 3007: 3003: 2997: 2996: 2983: 2979: 2975: 2971: 2966: 2961: 2957: 2953: 2949: 2941: 2933: 2929: 2924: 2919: 2915: 2911: 2907: 2903: 2899: 2892: 2884: 2880: 2876: 2872: 2868: 2864: 2860: 2856: 2848: 2840: 2836: 2832: 2828: 2824: 2820: 2816: 2812: 2808: 2804: 2797: 2789: 2785: 2781: 2777: 2770: 2762: 2758: 2753: 2748: 2744: 2740: 2737:(4): 773–84. 2736: 2732: 2728: 2721: 2713: 2709: 2705: 2701: 2697: 2693: 2689: 2685: 2678: 2676: 2667: 2663: 2658: 2653: 2650:(5): 663–76. 2649: 2645: 2641: 2637: 2630: 2622: 2618: 2613: 2608: 2604: 2600: 2596: 2592: 2588: 2584: 2580: 2573: 2565: 2561: 2557: 2553: 2549: 2545: 2541: 2537: 2533: 2529: 2522: 2514: 2510: 2505: 2500: 2496: 2492: 2488: 2484: 2480: 2476: 2472: 2465: 2457: 2453: 2448: 2443: 2439: 2435: 2431: 2427: 2423: 2416: 2408: 2404: 2399: 2394: 2389: 2384: 2380: 2376: 2375: 2370: 2363: 2355: 2351: 2347: 2343: 2339: 2335: 2328: 2326: 2317: 2313: 2309: 2305: 2301: 2297: 2293: 2289: 2282: 2274: 2270: 2266: 2262: 2258: 2254: 2250: 2246: 2242: 2238: 2231: 2223: 2219: 2215: 2211: 2207: 2203: 2199: 2195: 2188: 2186: 2177: 2173: 2169: 2165: 2161: 2157: 2154:(3): 515–26. 2153: 2149: 2145: 2139: 2131: 2127: 2123: 2119: 2115: 2111: 2107: 2103: 2099: 2095: 2087: 2079: 2075: 2071: 2067: 2063: 2059: 2055: 2051: 2047: 2043: 2035: 2027: 2023: 2018: 2013: 2008: 2003: 1999: 1995: 1991: 1984: 1982: 1980: 1978: 1969: 1965: 1961: 1957: 1952: 1947: 1943: 1939: 1935: 1928: 1920: 1916: 1911: 1906: 1902: 1898: 1894: 1890: 1886: 1882: 1878: 1871: 1863: 1859: 1854: 1849: 1844: 1839: 1835: 1831: 1827: 1823: 1819: 1812: 1810: 1801: 1797: 1793: 1789: 1785: 1781: 1777: 1773: 1766: 1758: 1754: 1750: 1746: 1742: 1738: 1734: 1730: 1726: 1722: 1714: 1706: 1699: 1695: 1691: 1687: 1683: 1679: 1675: 1671: 1667: 1663: 1659: 1652: 1645: 1641: 1637: 1632: 1627: 1622: 1617: 1613: 1609: 1602: 1595: 1587: 1583: 1579: 1575: 1571: 1567: 1563: 1559: 1555: 1551: 1544: 1536: 1532: 1528: 1524: 1519: 1514: 1511:(3): 527–42. 1510: 1506: 1502: 1495: 1493: 1491: 1482: 1478: 1473: 1468: 1464: 1460: 1456: 1452: 1448: 1441: 1433: 1429: 1425: 1421: 1417: 1413: 1406: 1398: 1392: 1390: 1388: 1379: 1375: 1369: 1361: 1357: 1351: 1344: 1340: 1335: 1333: 1331: 1323: 1319: 1314: 1312: 1310: 1305: 1296: 1293: 1291: 1288: 1286: 1283: 1282: 1276: 1274: 1270: 1260: 1258: 1248: 1246: 1242: 1238: 1234: 1229: 1219: 1216: 1212: 1209: 1199: 1196: 1192: 1188: 1184: 1180: 1170: 1167: 1162: 1158: 1154: 1150: 1136: 1133: 1129: 1125: 1115: 1113: 1109: 1105: 1090: 1088: 1084: 1080: 1075: 1071: 1061: 1052: 1043: 1040: 1036: 1025: 1021: 1016: 1011: 1006: 1001: 997: 993: 992:PLOS Genetics 989: 981: 967: 961:Gene location 958: 954: 952: 946: 944: 940: 936: 932: 928: 924: 923:X chromosomes 920: 919:developmental 916: 907: 905: 901: 897: 892: 890: 886: 882: 878: 874: 869: 867: 863: 859: 858:protein genes 855: 854: 849: 848: 843: 842: 837: 833: 829: 825: 821: 809: 804: 800: 796: 793: 789: 782: 780: 777: 773: 769: 765: 762: 758: 754: 747: 741: 737: 734: 728: 722: 718: 715: 711: 704: 698: 694: 691: 685: 679: 675: 672: 670:RefSeq (mRNA) 668: 661: 657: 653: 650: 644: 643: 639: 634: 630: 627: 625: 621: 614: 613: 608: 604: 601: 595: 594: 589: 585: 582: 580: 576: 569: 568: 563: 559: 556: 550: 549: 544: 540: 537: 535: 531: 528: 525: 523: 520: 516: 513: 509: 505: 493: 488: 485: 483: 479: 471: 466: 455: 451: 447: 443: 439: 435: 431: 427: 423: 419: 418: 415: 411: 406: 403: 393: 389: 385: 381: 377: 373: 369: 365: 361: 357: 356: 353: 349: 344: 341: 340: 337: 335: 331: 329: 328: 324: 323: 320: 318: 314: 310: 306: 302: 294: 289: 285: 281: 276: 266: 262: 255: 248: 242: 235: 227: 223: 219: 214: 210: 205: 201: 193: 188: 184: 180: 175: 165: 161: 154: 147: 141: 134: 130: 124: 120: 116: 111: 107: 102: 98: 94: 90: 86: 82: 78: 74: 70: 66: 58: 53: 46: 41: 36: 32: 27: 22: 19: 3814: 3810: 3772: 3768: 3723: 3719: 3683: 3679: 3640: 3636: 3610:(7): 352–8. 3607: 3603: 3578: 3574: 3547: 3543: 3494: 3490: 3453: 3449: 3425:(5): 373–8. 3422: 3419:DNA Research 3418: 3387: 3383: 3354: 3350: 3315: 3311: 3261: 3257: 3223:(3): 220–4. 3220: 3216: 3186:(3): 353–6. 3183: 3179: 3143: 3139: 3100: 3096: 3051: 3047: 3005: 3001: 2955: 2951: 2940: 2905: 2901: 2891: 2858: 2854: 2847: 2806: 2802: 2796: 2779: 2775: 2769: 2734: 2730: 2720: 2690:(1): 47–53. 2687: 2683: 2647: 2643: 2636:Brockdorff N 2629: 2586: 2582: 2572: 2531: 2527: 2521: 2478: 2474: 2464: 2429: 2425: 2415: 2378: 2372: 2362: 2340:(2): 122–6. 2337: 2333: 2300:10.1038/7734 2294:(4): 400–4. 2291: 2287: 2281: 2240: 2236: 2230: 2206:10.1038/7734 2200:(4): 400–4. 2197: 2193: 2151: 2147: 2144:Brockdorff N 2138: 2097: 2093: 2086: 2045: 2041: 2034: 1997: 1994:PLOS Biology 1993: 1941: 1938:Cell Systems 1937: 1927: 1884: 1880: 1870: 1825: 1821: 1775: 1771: 1765: 1724: 1720: 1713: 1665: 1661: 1658:Brockdorff N 1651: 1643: 1614:(1): 34–39. 1611: 1608:EMBO Reports 1607: 1594: 1553: 1549: 1543: 1508: 1504: 1454: 1450: 1440: 1415: 1411: 1405: 1377: 1368: 1359: 1350: 1266: 1263:Interactions 1254: 1244: 1237:reactivation 1225: 1213: 1205: 1176: 1147: 1121: 1101: 1067: 1058: 1049: 1031: 995: 991: 964: 955: 947: 917:is an early 913: 904:Hunt Willard 893: 885:untranslated 870: 865: 861: 851: 845: 840: 828:X chromosome 819: 818: 743: 724: 700: 681: 659: 636: 610: 591: 565: 546: 526: 521: 332: 325: 291:102,526,860 278:102,503,972 60:External IDs 18: 1195:zinc finger 1098:Methylation 382:pericardium 362:skin of hip 190:73,852,723 177:73,820,649 38:Identifiers 3875:Categories 3581:: 233–78. 3450:Chromosoma 1345:, May 2017 1324:, May 2017 1301:References 1183:histone H3 889:pseudogene 875:, through 856:) and two 394:left ovary 336:(ortholog) 3807:Pennisi E 1960:2405-4712 1418:: 69–92. 1110:the Xist 1108:methylate 1079:chromatin 1039:stem-loop 1035:stem-loop 931:expressed 512:Orthologs 81:GeneCards 3862:Archived 3839:23704542 3799:23166390 3710:16912274 3667:17987743 3624:12127775 3595:12429693 3566:17545591 3531:17537922 3470:17333237 3441:16769694 3406:15731119 3371:12629412 3334:12419249 3298:12072569 3245:21921352 3237:10723727 3208:23338176 2974:12419249 2932:15065664 2883:32840485 2875:11841480 2839:37749083 2831:14752160 2761:11352938 2704:16341221 2666:15525528 2638:(2004). 2621:18974356 2564:42703823 2556:18802003 2513:18535243 2456:15964997 2407:19014663 2381:(1): 2. 2354:19345091 2316:30636065 2308:10192391 2222:30636065 2214:10192391 2176:19889657 2026:20052282 1968:36356577 1919:19571810 1862:11481485 1800:21881827 1792:22108600 1640:17203100 1586:28145201 1578:16778056 1535:13141516 1481:12045143 1432:16124854 1341:– 1320:– 1279:See also 1269:interact 1241:epiblast 1112:promoter 1046:C region 1024:26646615 975:A region 910:Function 877:splicing 792:Wikidata 448:gastrula 3819:Bibcode 3811:Science 3790:3539355 3756:4342551 3748:2034279 3728:Bibcode 3701:1553206 3659:9298902 3522:1891207 3499:Bibcode 3478:7947134 3266:Bibcode 3200:9354806 3170:9185579 3127:8636206 3118:2120729 3084:4360783 3076:1985270 3056:Bibcode 3038:4332325 3030:1985261 3010:Bibcode 2923:1693294 2811:Bibcode 2803:Science 2782:: 3–8. 2752:2192370 2712:2898893 2612:2748911 2591:Bibcode 2583:Science 2536:Bibcode 2528:Science 2504:2584363 2483:Bibcode 2475:Science 2447:1151664 2273:4371247 2265:9069284 2245:Bibcode 2168:1423610 2130:4342551 2122:2034279 2102:Bibcode 2078:4239301 2070:2034278 2050:Bibcode 2017:2796953 1910:2754729 1889:Bibcode 1830:Bibcode 1757:4332325 1749:1985261 1729:Bibcode 1698:4329368 1690:8538762 1670:Bibcode 1631:1796754 1558:Bibcode 1550:Science 1527:1423611 1472:1383731 1343:Ensembl 1322:Ensembl 1015:4672913 943:nucleus 939:protein 935:spliced 830:of the 624:UniProt 579:Ensembl 518:Species 444:condyle 440:utricle 311:pattern 45:Aliases 3837:  3797:  3787:  3754:  3746:  3720:Nature 3708:  3698:  3665:  3657:  3622:  3593:  3564:  3529:  3519:  3476:  3468:  3439:  3404:  3369:  3342:372211 3340:  3332:  3296:  3289:124357 3286:  3243:  3235:  3206:  3198:  3168:  3161:146792 3158:  3125:  3115:  3082:  3074:  3048:Nature 3036:  3028:  3002:Nature 2982:372211 2980:  2972:  2930:  2920:  2881:  2873:  2837:  2829:  2759:  2749:  2710:  2702:  2664:  2619:  2609:  2562:  2554:  2511:  2501:  2454:  2444:  2405:  2398:257704 2395:  2352:  2314:  2306:  2271:  2263:  2237:Nature 2220:  2212:  2174:  2166:  2128:  2120:  2094:Nature 2076:  2068:  2042:Nature 2024:  2014:  1966:  1958:  1917:  1907:  1881:Nature 1860:  1850:  1798:  1790:  1755:  1747:  1721:Nature 1696:  1688:  1662:Nature 1638:  1628:  1584:  1576:  1533:  1525:  1479:  1469:  1430:  1228:oocyte 1187:lysine 1166:intron 1022:  1012:  778:search 776:PubMed 567:213742 534:Entrez 482:BioGPS 428:dermis 169:Xq13.2 69:314670 3752:S2CID 3663:S2CID 3474:S2CID 3338:S2CID 3241:S2CID 3204:S2CID 3080:S2CID 3034:S2CID 2978:S2CID 2879:S2CID 2835:S2CID 2708:S2CID 2560:S2CID 2312:S2CID 2269:S2CID 2218:S2CID 2172:S2CID 2126:S2CID 2074:S2CID 1853:55400 1796:S2CID 1753:S2CID 1694:S2CID 1582:S2CID 1531:S2CID 1273:BRCA1 1271:with 1191:SUZ12 1153:Nanog 1132:Dicer 1124:dsRNA 1106:that 873:mRNAs 866:Cnbp2 527:Mouse 522:Human 436:fossa 374:vulva 358:tibia 334:Mouse 327:Human 274:Start 209:Mouse 173:Start 106:Human 77:98974 3835:PMID 3795:PMID 3744:PMID 3706:PMID 3655:PMID 3637:Cell 3620:PMID 3591:PMID 3562:PMID 3527:PMID 3466:PMID 3437:PMID 3402:PMID 3367:PMID 3330:PMID 3312:Cell 3294:PMID 3233:PMID 3196:PMID 3166:PMID 3123:PMID 3072:PMID 3026:PMID 2970:PMID 2952:Cell 2928:PMID 2871:PMID 2827:PMID 2780:1298 2757:PMID 2700:PMID 2662:PMID 2617:PMID 2552:PMID 2509:PMID 2452:PMID 2403:PMID 2350:PMID 2304:PMID 2261:PMID 2210:PMID 2164:PMID 2148:Cell 2118:PMID 2066:PMID 2022:PMID 1964:PMID 1956:ISSN 1915:PMID 1858:PMID 1788:PMID 1745:PMID 1686:PMID 1636:PMID 1574:PMID 1523:PMID 1505:Cell 1477:PMID 1428:PMID 1295:Tsix 1179:PRC2 1161:Sox2 1159:and 1157:Oct4 1128:RNAi 1126:and 1070:Tsix 1068:The 1020:PMID 902:and 879:and 864:and 850:and 820:Xist 548:7503 317:Bgee 265:Band 226:Chr. 164:Band 123:Chr. 85:XIST 65:OMIM 52:XIST 24:XIST 3827:doi 3815:340 3785:PMC 3777:doi 3773:368 3736:doi 3724:351 3696:PMC 3688:doi 3645:doi 3612:doi 3583:doi 3552:doi 3517:PMC 3507:doi 3495:104 3458:doi 3454:116 3427:doi 3392:doi 3359:doi 3355:169 3320:doi 3316:111 3284:PMC 3274:doi 3225:doi 3188:doi 3156:PMC 3148:doi 3113:PMC 3105:doi 3101:132 3064:doi 3052:349 3018:doi 3006:349 2960:doi 2956:111 2918:PMC 2910:doi 2906:359 2863:doi 2819:doi 2807:303 2784:doi 2747:PMC 2739:doi 2735:153 2692:doi 2652:doi 2607:PMC 2599:doi 2587:322 2544:doi 2532:321 2499:PMC 2491:doi 2479:320 2442:PMC 2434:doi 2393:PMC 2383:doi 2342:doi 2296:doi 2253:doi 2241:386 2202:doi 2156:doi 2110:doi 2098:351 2058:doi 2046:351 2012:PMC 2002:doi 1946:doi 1905:PMC 1897:doi 1885:460 1848:PMC 1838:doi 1780:doi 1737:doi 1725:349 1678:doi 1666:379 1626:PMC 1616:doi 1566:doi 1554:312 1513:doi 1467:PMC 1459:doi 1420:doi 1245:ICM 1185:on 1085:of 1074:cis 1010:PMC 1000:doi 868:). 862:Tsx 853:Ftx 847:Jpx 841:Xic 745:n/a 726:n/a 702:n/a 683:n/a 660:n/a 490:n/a 287:End 186:End 89:OMA 73:MGI 3877:: 3833:. 3825:. 3813:. 3793:. 3783:. 3771:. 3767:. 3750:. 3742:. 3734:. 3722:. 3704:. 3694:. 3684:20 3682:. 3678:. 3661:. 3653:. 3641:90 3639:. 3635:. 3618:. 3608:18 3606:. 3589:. 3579:36 3577:. 3560:. 3548:67 3546:. 3542:. 3525:. 3515:. 3505:. 3493:. 3489:. 3472:. 3464:. 3452:. 3435:. 3423:12 3421:. 3417:. 3400:. 3388:14 3386:. 3382:. 3365:. 3353:. 3336:. 3328:. 3314:. 3310:. 3292:. 3282:. 3272:. 3262:99 3260:. 3256:. 3239:. 3231:. 3221:11 3219:. 3202:. 3194:. 3184:17 3182:. 3164:. 3154:. 3144:25 3142:. 3138:. 3121:. 3111:. 3099:. 3095:. 3078:. 3070:. 3062:. 3050:. 3032:. 3024:. 3016:. 3004:. 2976:. 2968:. 2954:. 2950:. 2926:. 2916:. 2904:. 2900:. 2877:. 2869:. 2859:69 2857:. 2833:. 2825:. 2817:. 2805:. 2778:. 2755:. 2745:. 2733:. 2729:. 2706:. 2698:. 2688:38 2686:. 2674:^ 2660:. 2646:. 2642:. 2615:. 2605:. 2597:. 2585:. 2581:. 2558:. 2550:. 2542:. 2530:. 2507:. 2497:. 2489:. 2477:. 2473:. 2450:. 2440:. 2430:19 2428:. 2424:. 2401:. 2391:. 2377:. 2371:. 2348:. 2338:19 2336:. 2324:^ 2310:. 2302:. 2292:21 2290:. 2267:. 2259:. 2251:. 2239:. 2216:. 2208:. 2198:21 2196:. 2184:^ 2170:. 2162:. 2152:71 2150:. 2124:. 2116:. 2108:. 2096:. 2072:. 2064:. 2056:. 2044:. 2020:. 2010:. 1996:. 1992:. 1976:^ 1962:. 1954:. 1942:13 1940:. 1936:. 1913:. 1903:. 1895:. 1883:. 1879:. 1856:. 1846:. 1836:. 1826:98 1824:. 1820:. 1808:^ 1794:. 1786:. 1776:12 1774:. 1751:. 1743:. 1735:. 1723:. 1692:. 1684:. 1676:. 1664:. 1642:. 1634:. 1624:. 1610:. 1606:. 1580:. 1572:. 1564:. 1552:. 1529:. 1521:. 1509:71 1507:. 1503:. 1489:^ 1475:. 1465:. 1455:12 1453:. 1449:. 1426:. 1414:. 1386:^ 1376:. 1358:. 1329:^ 1308:^ 1275:. 1259:. 1155:, 1122:A 1018:. 1008:. 996:11 994:. 990:. 906:. 293:bp 280:bp 192:bp 179:bp 87:; 83:: 79:; 75:: 71:; 67:: 3841:. 3829:: 3821:: 3801:. 3779:: 3758:. 3738:: 3730:: 3712:. 3690:: 3669:. 3647:: 3626:. 3614:: 3597:. 3585:: 3568:. 3554:: 3533:. 3509:: 3501:: 3480:. 3460:: 3443:. 3429:: 3408:. 3394:: 3373:. 3361:: 3344:. 3322:: 3300:. 3276:: 3268:: 3247:. 3227:: 3210:. 3190:: 3172:. 3150:: 3129:. 3107:: 3086:. 3066:: 3058:: 3040:. 3020:: 3012:: 2984:. 2962:: 2934:. 2912:: 2885:. 2865:: 2841:. 2821:: 2813:: 2790:. 2786:: 2763:. 2741:: 2714:. 2694:: 2668:. 2654:: 2648:7 2623:. 2601:: 2593:: 2566:. 2546:: 2538:: 2515:. 2493:: 2485:: 2458:. 2436:: 2409:. 2385:: 2379:1 2356:. 2344:: 2318:. 2298:: 2275:. 2255:: 2247:: 2224:. 2204:: 2178:. 2158:: 2132:. 2112:: 2104:: 2080:. 2060:: 2052:: 2028:. 2004:: 1998:8 1970:. 1948:: 1921:. 1899:: 1891:: 1864:. 1840:: 1832:: 1802:. 1782:: 1759:. 1739:: 1731:: 1700:. 1680:: 1672:: 1618:: 1612:8 1588:. 1568:: 1560:: 1537:. 1515:: 1483:. 1461:: 1434:. 1422:: 1416:6 1399:. 1380:. 1362:. 1028:. 1026:. 1002:: 860:( 642:a 638:n 211:) 108:) 91::

Index


Aliases
XIST
OMIM
314670
MGI
98974
GeneCards
XIST
OMA
XIST - orthologs
Human
X chromosome (human)
Chr.
X chromosome (human)
X chromosome (human)
Genomic location for XIST
Genomic location for XIST
Band
bp
bp
Mouse
X chromosome (mouse)
Chr.
X chromosome (mouse)
Genomic location for XIST
Genomic location for XIST
Band
bp
bp

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