The Ftx Noncoding Locus Controls X Chromosome Inactivation Independently of Its RNA Products

被引:78
作者
Furlan, Giulia [1 ]
Hernandez, Nancy Gutierrez [1 ]
Huret, Christophe [1 ]
Galupa, Rafael [2 ]
van Bemmel, Joke Gerarda [2 ,3 ]
Romito, Antonio [1 ]
Heard, Edith [2 ]
Morey, Celine [1 ]
Rougeulle, Claire [1 ]
机构
[1] Univ Paris Diderot, Sorbonne Paris Cite, CNRS, UMR 7216,Epigenet & Cell Fate, Paris, France
[2] PSL Res Univ, CNRS, INSERM,Mammalian Dev Epigenet Grp, Inst Curie,UMR3215,U934 Genet & Dev Biol Unit, F-75005 Paris, France
[3] Erasmus MC, Dept Dev Biol, Wytemaweg 80, NL-3015 CN Rotterdam, Netherlands
基金
欧洲研究理事会;
关键词
CHROMATIN-STRUCTURE; XIST TRANSCRIPTION; CENTER REGION; TSIX; GENE; EXPRESSION; MOUSE; CONFORMATION; CTCF; ACTIVATION;
D O I
10.1016/j.molcel.2018.03.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Accumulation of the Xist long noncoding RNA (lncRNA) on one X chromosome is the trigger for X chromosome inactivation (XCI) in female mammals. Xist expression, which needs to be tightly controlled, involves a cis-acting region, the X-inactivation center (Xic), containing many lncRNA genes that evolved concomitantly to Xist from protein-coding ancestors through pseudogeneization and loss of coding potential. Here, we uncover an essential role for the Xic-linked noncoding gene Ftx in the regulation of Xist expression. We show that Ftx is required in cis to promote Xist transcriptional activation and establishment of XCI. Importantly, we demonstrate that this function depends on Ftx transcription and not on the RNA products. Our findings illustrate the multiplicity of layers operating in the establishment of XCI and highlight the diversity in the modus operandi of the noncoding players.
引用
收藏
页码:462 / +
页数:19
相关论文
共 40 条
[1]   A Multiplexed Single-Cell CRISPR Screening Platform Enables Systematic Dissection of the Unfolded Protein Response [J].
Adamson, Britt ;
Norman, Thomas M. ;
Jost, Marco ;
Cho, Min Y. ;
Nunez, James K. ;
Chen, Yuwen ;
Villalta, Jacqueline E. ;
Gilbert, Luke A. ;
Horlbeck, Max A. ;
Hein, Marco Y. ;
Pak, Ryan A. ;
Gray, Andrew N. ;
Gross, Carol A. ;
Dixit, Atray ;
Parnas, Oren ;
Regev, Aviv ;
Weissman, Jonathan S. .
CELL, 2016, 167 (07) :1867-+
[2]   CHARACTERIZATION OF A MURINE GENE EXPRESSED FROM THE INACTIVE X-CHROMOSOME [J].
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 .
NATURE, 1991, 351 (6324) :325-329
[3]   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
[4]   Comparative sequence analysis of the X-inactivation center region in mouse, human, and bovine [J].
Chureau, C ;
Prissette, M ;
Bourdet, A ;
Barbe, V ;
Cattolico, L ;
Jones, L ;
Eggen, A ;
Avner, P ;
Duret, L .
GENOME RESEARCH, 2002, 12 (06) :894-908
[5]   Ftx is a non-coding RNA which affects Xist expression and chromatin structure within the X-inactivation center region [J].
Chureau, Corinne ;
Chantalat, Sophie ;
Romito, Antonio ;
Galvani, Angelique ;
Duret, Laurent ;
Avner, Philip ;
Rougeulle, Claire .
HUMAN MOLECULAR GENETICS, 2011, 20 (04) :705-718
[6]   Novel players in X inactivation: insights into Xist-mediated gene silencing and chromosome conformation [J].
da Rocha, Simao T. ;
Heard, Edith .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2017, 24 (03) :197-204
[7]  
Davies JOJ, 2016, NAT METHODS, V13, P74, DOI [10.1038/NMETH.3664, 10.1038/nmeth.3664]
[8]  
Debrand E, 1999, MOL CELL BIOL, V19, P8513
[9]   Local regulation of gene expression by lncRNA promoters, transcription and splicing [J].
Engreitz, Jesse M. ;
Haines, Jenna E. ;
Perez, Elizabeth M. ;
Munson, Glen ;
Chen, Jenny ;
Kane, Michael ;
McDonel, Patrick E. ;
Guttman, Mitchell ;
Lander, Eric S. .
NATURE, 2016, 539 (7629) :452-455
[10]   Function and evolution of the long noncoding RNA circuitry orchestrating X-chromosome inactivation in mammals [J].
Furlan, Giulia ;
Rougeulle, Claire .
WILEY INTERDISCIPLINARY REVIEWS-RNA, 2016, 7 (05) :702-722