Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, 1649-028 Lisboa, Portugal.
Trends Biochem Sci. 2012 Jun;37(6):248-53. doi: 10.1016/j.tibs.2012.02.002. Epub 2012 Mar 5.
In human cell nuclei, the vast majority of mRNA precursors (pre-mRNA) are spliced in more than one way. The process of alternative splicing creates enormous biological complexity from a limited number of genes, and its misregulation often leads to disease. Splicing regulation relies primarily on RNA-binding proteins that recognize specific target features in the pre-mRNA. Evidence accumulated over the past decade has further shown that most splicing occurs co-transcriptionally and that transcription modulates splicing. More recently, chromatin emerged as a novel node in the network of splicing regulatory interactions. Chromatin structure influences splicing choices but splicing can also actively modulate the pattern of histone modification in chromatin. This review discusses how splicing, transcription and chromatin are interwoven bi-directionally.
在人类细胞核中,绝大多数 mRNA 前体(pre-mRNA)都以不止一种方式进行剪接。可变剪接过程从有限数量的基因中产生了巨大的生物复杂性,其调控失常常常导致疾病。剪接调控主要依赖于 RNA 结合蛋白,这些蛋白识别 pre-mRNA 中的特定靶特征。过去十年积累的证据进一步表明,大多数剪接发生在转录过程中,并且转录调节剪接。最近,染色质成为剪接调控相互作用网络中的一个新节点。染色质结构影响剪接选择,但剪接也可以主动调节染色质中组蛋白修饰的模式。这篇综述讨论了剪接、转录和染色质如何双向交织在一起。