Long non-coding RNAs: spatial amplifiers that control nuclear structure and gene expression

被引:461
作者
Engreitz, Jesse M. [1 ,2 ]
Ollikainen, Noah [3 ]
Guttman, Mitchell [3 ]
机构
[1] Broad Inst Harvard & Massachusetts Inst Technol M, Cambridge, MA 02142 USA
[2] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02142 USA
[3] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
基金
美国国家卫生研究院;
关键词
INACTIVE X-CHROMOSOME; XIST RNA; FACULTATIVE HETEROCHROMATIN; CHROMATIN ARCHITECTURE; HISTONE MODIFICATION; RESOLUTION REVEALS; POLYCOMB PROTEINS; ACTIVE CHROMATIN; MATRIX PROTEIN; MAPS REVEAL;
D O I
10.1038/nrm.2016.126
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Over the past decade, it has become clear that mammalian genomes encode thousands of long non-coding RNAs (lncRNAs), many of which are now implicated in diverse biological processes. Recent work studying the molecular mechanisms of several key examples-including Xist, which orchestrates Xchromosome inactivation-has provided new insights into how lncRNAs can control cellular functions by acting in the nucleus. Here we discuss emerging mechanistic insights into how lncRNAs can regulate gene expression by coordinating regulatory proteins, localizing to target loci and shaping three-dimensional (3D) nuclear organization. We explore these principles to highlight biological challenges in gene regulation, in which lncRNAs are well-suited to perform roles that cannot be carried out by DNA elements or protein regulators alone, such as acting as spatial amplifiers of regulatory signals in the nucleus.
引用
收藏
页码:756 / 770
页数:15
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