Khan Dilshad H, Jahan Sanzida, Davie James R
Manitoba Institute of Child Health, University of Manitoba, Winnipeg, Manitoba, R3E 3P4 Canada.
Adv Biol Regul. 2012 Sep;52(3):377-88. doi: 10.1016/j.jbior.2012.04.003. Epub 2012 Apr 28.
Epigenetics refer to a variety of processes that have long-term effects on gene expression programs without changes in DNA sequence. Key players in epigenetic control are histone modifications and DNA methylation which, in concert with chromatin remodeling complexes, nuclear architecture and microRNAs, define the chromatin structure of a gene and its transcriptional activity. There is a growing awareness that histone modifications and chromatin organization influence pre-mRNA splicing. Further there is emerging evidence that pre-mRNA splicing itself influences chromatin organization. In the mammalian genome around 95% of multi-exon genes generate alternatively spliced transcripts, the products of which create proteins with different functions. It is now established that several human diseases are a direct consequence of aberrant splicing events. In this review we present the interplay between epigenetic mechanisms and splicing regulation, as well as discuss recent studies on the role of histone deacetylases in splicing activities.
表观遗传学是指一系列对基因表达程序具有长期影响且不改变DNA序列的过程。表观遗传控制的关键因素是组蛋白修饰和DNA甲基化,它们与染色质重塑复合物、核结构和微小RNA协同作用,决定基因的染色质结构及其转录活性。人们越来越意识到组蛋白修饰和染色质组织会影响前体mRNA剪接。此外,越来越多的证据表明,前体mRNA剪接本身也会影响染色质组织。在哺乳动物基因组中,约95%的多外显子基因会产生可变剪接转录本,其产物会产生具有不同功能的蛋白质。现已确定,几种人类疾病是异常剪接事件的直接后果。在本综述中,我们阐述了表观遗传机制与剪接调控之间的相互作用,并讨论了关于组蛋白去乙酰化酶在剪接活动中作用的最新研究。