RNF12 Activates Xist and Is Essential for X Chromosome Inactivation

被引:115
作者
Barakat, Tahsin Stefan [1 ]
Gunhanlar, Nilhan [1 ]
Pardo, Cristina Gontan [1 ]
Achame, Eskeatnaf Mulugeta [1 ]
Ghazvini, Mehrnaz [1 ,2 ]
Boers, Ruben [1 ]
Kenter, Annegien [1 ]
Rentmeester, Eveline [1 ]
Grootegoed, J. Anton [1 ]
Gribnau, Joost [1 ]
机构
[1] Univ Med Ctr, Erasmus MC, Dept Reprod & Dev, Rotterdam, Netherlands
[2] Univ Med Ctr, Erasmus MC, Erasmus Stem Cell Inst, Rotterdam, Netherlands
关键词
MOUSE; GENE; PLURIPOTENCY; RECRUITMENT; METHYLATION; TSIX; MICE; RLIM; CTCF;
D O I
10.1371/journal.pgen.1002001
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In somatic cells of female placental mammals, one of the two X chromosomes is transcriptionally silenced to accomplish an equal dose of X-encoded gene products in males and females. Initiation of random X chromosome inactivation (XCI) is thought to be regulated by X-encoded activators and autosomally encoded suppressors controlling Xist. Spreading of Xist RNA leads to silencing of the X chromosome in cis. Here, we demonstrate that the dose dependent X-encoded XCI activator RNF12/RLIM acts in trans and activates Xist. We did not find evidence for RNF12-mediated regulation of XCI through Tsix or the Xist intron 1 region, which are both known to be involved in inhibition of Xist. In addition, we found that Xist intron 1, which contains a pluripotency factor binding site, is not required for suppression of Xist in undifferentiated ES cells. Analysis of female Rnf12(-/-) knockout ES cells showed that RNF12 is essential for initiation of XCI and is mainly involved in the regulation of Xist. We conclude that RNF12 is an indispensable factor in up-regulation of Xist transcription, thereby leading to initiation of random XCI.
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页数:12
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共 29 条
[1]  
Ahn Janice Y, 2010, BMC Dev Biol, V10, P90, DOI 10.1186/1471-213X-10-90
[2]   RLIM inhibits functional activity of LIM homeodomain transcription factors via recruitment of the histone deacetylase complex [J].
Bach, I ;
Rodriguez-Esteban, C ;
Carrière, C ;
Bhushan, A ;
Krones, A ;
Rose, DW ;
Glass, CK ;
Andersen, B ;
Belmonte, JCI ;
Rosenfeld, MG .
NATURE GENETICS, 1999, 22 (04) :394-399
[3]   X-changing information on X inactivation [J].
Barakat, Tahsin Stefan ;
Jonkers, Iris ;
Monkhorst, Kim ;
Gribnau, Joost .
EXPERIMENTAL CELL RESEARCH, 2010, 316 (05) :679-687
[4]   CONSERVATION OF POSITION AND EXCLUSIVE EXPRESSION OF MOUSE XIST FROM THE INACTIVE X-CHROMOSOME [J].
BROCKDORFF, N ;
ASHWORTH, A ;
KAY, GF ;
COOPER, P ;
SMITH, S ;
MCCABE, VM ;
NORRIS, DP ;
PENNY, GD ;
PATEL, D ;
RASTAN, S .
NATURE, 1991, 351 (6324) :329-331
[5]   THE PRODUCT OF THE MOUSE XIST GENE IS A 15 KB INACTIVE X-SPECIFIC TRANSCRIPT CONTAINING NO CONSERVED ORF AND LOCATED IN THE NUCLEUS [J].
BROCKDORFF, N ;
ASHWORTH, A ;
KAY, GF ;
MCCABE, VM ;
NORRIS, DP ;
COOPER, PJ ;
SWIFT, S ;
RASTAN, S .
CELL, 1992, 71 (03) :515-526
[6]   A GENE FROM THE REGION OF THE HUMAN X-INACTIVATION CENTER IS EXPRESSED EXCLUSIVELY FROM THE INACTIVE X-CHROMOSOME [J].
BROWN, CJ ;
BALLABIO, A ;
RUPERT, JL ;
LAFRENIERE, RG ;
GROMPE, M ;
TONLORENZI, R ;
WILLARD, HF .
NATURE, 1991, 349 (6304) :38-44
[7]   EVIDENCE OF NONRANDOM X-CHROMOSOME ACTIVITY IN MOUSE [J].
CATTANACH, BM ;
WILLIAMS, CE .
GENETICS RESEARCH, 1972, 19 (03) :229-+
[8]   Vive la Difference: Males vs females in flies vs worms [J].
Cline, TW ;
Meyer, BJ .
ANNUAL REVIEW OF GENETICS, 1996, 30 :637-702
[9]   Identification of a Ctcf cofactor, Yy1, for the X chromosome binary switch [J].
Donohoe, Mary E. ;
Zhang, Li-Feng ;
Xu, Na ;
Shi, Yang ;
Lee, Jeannie T. .
MOLECULAR CELL, 2007, 25 (01) :43-56
[10]   The pluripotency factor Oct4 interacts with Ctcf and also controls X-chromosome pairing and counting [J].
Donohoe, Mary E. ;
Silva, Susana S. ;
Pinter, Stefan F. ;
Xu, Na ;
Lee, Jeannie T. .
NATURE, 2009, 460 (7251) :128-U147