Non-coding RNAs as direct and indirect modulators of epigenetic regulation

被引:390
|
作者
Peschansky, Veronica J.
Wahlestedt, Claes [1 ]
机构
[1] Univ Miami, Miller Sch Med, Ctr Therapeut Innovat, Miami, FL 33136 USA
关键词
H3; LYSINE-27; METHYLATION; INACTIVE X-CHROMOSOME; TUMOR-SUPPRESSOR; ENDOGENOUS SIRNA; DNA METHYLATION; CHROMATIN DOMAINS; DOWN-REGULATION; XIST GENE; ANTISENSE; EXPRESSION;
D O I
10.4161/epi.27473
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
Epigenetic regulation of gene expression is an increasingly well-understood concept that explains much of the contribution of an organism's environment and experience to its biology. However, discussion persists as to which mechanisms can be classified as epigenetic. Ongoing research continues to uncover novel pathways, including the important role of non-protein coding RNA transcripts in epigenetic gene regulation. We know that the majority of human and other mammalian transcripts are not translated but that many of these are nonetheless functional. These non-coding RNAs (ncRNAs) can be short (< 200 nt) or long (< 200 nt) and are further classified by genomic origin and mechanism of action. We discuss examples of ncRNAs that interact with histone modifying complexes or DNA methyltransferases to regulate gene expression, others that are targets of these epigenetic mechanisms, and propose a model in which such transcripts feed back into an epigenetic regulatory network. © 2014 Landes Bioscience.
引用
收藏
页码:3 / 12
页数:10
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