Novel players in X inactivation: insights into Xist-mediated gene silencing and chromosome conformation

被引:99
作者
da Rocha, Simao T. [1 ]
Heard, Edith [2 ]
机构
[1] Univ Lisbon, Inst Med Mol, Fac Med, Lisbon, Portugal
[2] PSL Univ, CNRS UMR3215, INSERM U934, Mammalian Dev Epigenet Grp,Inst Curie, Paris, France
基金
欧洲研究理事会;
关键词
TUMOR 1-ASSOCIATING PROTEIN; MESSENGER-RNA; TRANSCRIPTIONAL REPRESSION; NUCLEAR COMPARTMENT; LIVING CELLS; HUMAN GENOME; HNRNP U; SAF-A; REVEALS; BINDING;
D O I
10.1038/nsmb.3370
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
The nuclear long noncoding RNA (lncRNA) Xist ensures X-chromosome inactivation (XCI) in female placental mammals. Although Xist is one of the most intensively studied lncRNAs, the mechanisms associated with its capacity to trigger chromosome-wide gene silencing, the formation of facultative heterochromatin and an unusual 3D conformation of the inactive X chromosome (Xi) have remained elusive. Now researchers have identified novel functional partners of Xist in a series of breakthrough studies, using unbiased techniques to isolate Xist-bound proteins, as well as forward genetic screens. In addition, important insights into the 3D organization of Xi and its relation to gene expression have been obtained. In this Review, we discuss how this new information is providing a recipe for deciphering XCI mechanisms by which a multitasking RNA can structurally and functionally transform an active chromosome into uniquely organized facultative heterochromatin.
引用
收藏
页码:197 / 204
页数:8
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