Fair Benjamin Jung, Pleiss Jeffrey A
Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, 14853, USA.
Curr Genet. 2017 Jun;63(3):375-380. doi: 10.1007/s00294-016-0647-6. Epub 2016 Sep 14.
Pre-mRNA splicing is an essential component of eukaryotic gene expression. Many metazoans, including humans, regulate alternative splicing patterns to generate expansions of their proteome from a limited number of genes. Importantly, a considerable fraction of human disease causing mutations manifest themselves through altering the sequences that shape the splicing patterns of genes. Thus, understanding the mechanistic bases of this complex pathway will be an essential component of combating these diseases. Dating almost to the initial discovery of splicing, researchers have taken advantage of the genetic tractability of budding yeast to identify the components and decipher the mechanisms of splicing. However, budding yeast lacks the complex splicing machinery and alternative splicing patterns most relevant to humans. More recently, many researchers have turned their efforts to study the fission yeast, Schizosaccharomyces pombe, which has retained many features of complex splicing, including degenerate splice site sequences, the usage of exonic splicing enhancers, and SR proteins. Here, we review recent work using fission yeast genetics to examine pre-mRNA splicing, highlighting its promise for modeling the complex splicing seen in higher eukaryotes.
前体mRNA剪接是真核基因表达的一个重要组成部分。包括人类在内的许多后生动物通过调控可变剪接模式,从有限数量的基因中产生蛋白质组的扩展。重要的是,相当一部分导致人类疾病的突变是通过改变影响基因剪接模式的序列来表现自身的。因此,了解这一复杂途径的机制基础将是对抗这些疾病的一个重要组成部分。几乎从剪接最初被发现起,研究人员就利用芽殖酵母的遗传易处理性来鉴定剪接成分并解读剪接机制。然而,芽殖酵母缺乏与人类最相关的复杂剪接机制和可变剪接模式。最近,许多研究人员将精力转向研究裂殖酵母(粟酒裂殖酵母),它保留了复杂剪接的许多特征,包括简并剪接位点序列、外显子剪接增强子的使用以及SR蛋白。在这里,我们综述了利用裂殖酵母遗传学研究前体mRNA剪接的近期工作,突出了其在模拟高等真核生物中所见复杂剪接方面的前景。