Department of Microbiology and Molecular Genetics, University of California, Irvine, CA 92697, United States of America.
Department of Microbiology and Molecular Genetics, University of California, Irvine, CA 92697, United States of America.
Biochim Biophys Acta Gene Regul Mech. 2019 Nov-Dec;1862(11-12):194392. doi: 10.1016/j.bbagrm.2019.06.003. Epub 2019 Jul 2.
The generation of protein coding mRNAs from pre-mRNA is a fundamental biological process that is required for gene expression. Alternative pre-mRNA splicing is responsible for much of the transcriptomic and proteomic diversity observed in higher order eukaryotes. Aberrations that disrupt regular alternative splicing patterns are known to cause human diseases, including various cancers. Alternative splicing is a combinatorial process, meaning many factors affect which two splice sites are ligated together. The features that dictate exon inclusion are comprised of splice site strength, intron-exon architecture, RNA secondary structure, splicing regulatory elements, promoter use and transcription speed by RNA polymerase and the presence of post-transcriptional nucleotide modifications. A comprehensive view of all of the factors that influence alternative splicing decisions is necessary to predict splicing outcomes and to understand the molecular basis of disease. This article is part of a Special Issue entitled: RNA structure and splicing regulation edited by Francisco Baralle, Ravindra Singh and Stefan Stamm.
从前体 mRNA 生成蛋白质编码 mRNA 是一个基本的生物学过程,是基因表达所必需的。选择性前体 mRNA 剪接是高等真核生物中观察到的转录组和蛋白质组多样性的主要原因。已知扰乱正常选择性剪接模式的异常会导致人类疾病,包括各种癌症。选择性剪接是一个组合过程,这意味着许多因素会影响两个剪接位点连接在一起。决定外显子包含的特征包括剪接位点强度、内含子-外显子结构、RNA 二级结构、剪接调控元件、启动子的使用以及 RNA 聚合酶的转录速度,以及转录后核苷酸修饰的存在。为了预测剪接结果并理解疾病的分子基础,需要全面了解影响选择性剪接决策的所有因素。本文是由 Francisco Baralle、Ravindra Singh 和 Stefan Stamm 编辑的题为“RNA 结构和剪接调控”的特刊的一部分。