Roles of long, non-coding RNA in chromosome-wide transcription regulation: Lessons from two dosage compensation systems

被引:20
作者
Maenner, Sylvain [1 ]
Mueller, Marisa
Becker, Peter B.
机构
[1] Univ Munich, Adolf Butenandt Inst, D-80336 Munich, Germany
关键词
Dosage compensation; Chromatin; Long non-coding RNAs; Epigenetic regulation; Histone modifications; INACTIVE X-CHROMOSOME; MALE-SPECIFIC LETHAL-2; ES CELL-DIFFERENTIATION; DNA-BINDING PROTEIN; MOUSE XIST GENE; MSL COMPLEX; DROSOPHILA-MELANOGASTER; CHROMATIN-STRUCTURE; HISTONE H3; SEX-LETHAL;
D O I
10.1016/j.biochi.2011.12.026
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
A large part of higher eukaryotic genomes is transcribed into RNAs lacking any significant open reading frame. This "non-coding part" has been shown to actively contribute to regulating gene expression, but the mechanisms are largely unknown. Particularly instructive examples are provided by the dosage compensation systems, which assure that the single X chromosome in male cells and the two X chromosomes in female cells give rise to similar amounts of gene product. Although this is achieved by very different strategies in mammals and fruit flies, long, non-coding RNAs (lncRNAs) are involved in both cases. Here we summarize recent progress towards unraveling the mechanisms, by which the Xist and roX RNAs mediate the selective association of regulators with individual target chromosomes, to initiate dosage compensation in mammals and fruit flies, respectively. (c) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1490 / 1498
页数:9
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