Shukla Sanjeev, Oberdoerffer Shalini
Mouse Cancer Genetics Program, NCI- Frederick, NIH, Frederick, MD 21702, USA.
Biochim Biophys Acta. 2012 Jul;1819(7):673-83. doi: 10.1016/j.bbagrm.2012.01.014. Epub 2012 Feb 2.
While studies of alternative pre-mRNA splicing regulation have typically focused on RNA-binding proteins and their target sequences within nascent message, it is becoming increasingly evident that mRNA splicing, RNA polymerase II (pol II) elongation and chromatin structure are intricately intertwined. The majority of introns in higher eukaryotes are excised prior to transcript release in a manner that is dependent on transcription through pol II. As a result of co-transcriptional splicing, variations in pol II elongation influence alternative splicing patterns, wherein a slower elongation rate is associated with increased inclusion of alternative exons within mature mRNA. Physiological barriers to pol II elongation, such as repressive chromatin structure, can thereby similarly impact splicing decisions. Surprisingly, pre-mRNA splicing can reciprocally influence pol II elongation and chromatin structure. Here, we highlight recent advances in co-transcriptional splicing that reveal an extensive network of coupling between splicing, transcription and chromatin remodeling complexes. This article is part of a Special Issue entitled: Chromatin in time and space.
虽然对可变前体mRNA剪接调控的研究通常集中于RNA结合蛋白及其在新生信使中的靶序列,但越来越明显的是,mRNA剪接、RNA聚合酶II(pol II)延伸和染色质结构是错综复杂地交织在一起的。高等真核生物中的大多数内含子在转录本释放之前以依赖于通过pol II转录的方式被切除。由于共转录剪接,pol II延伸的变化会影响可变剪接模式,其中较慢的延伸速率与成熟mRNA中可变外显子的包含增加有关。因此,pol II延伸的生理障碍,如抑制性染色质结构,同样会影响剪接决定。令人惊讶的是,前体mRNA剪接可以相互影响pol II延伸和染色质结构。在这里,我们重点介绍了共转录剪接的最新进展,这些进展揭示了剪接、转录和染色质重塑复合体之间广泛的耦合网络。本文是名为:《时空染色质》的特刊的一部分。