Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Wiley Interdiscip Rev RNA. 2013 Jan-Feb;4(1):61-76. doi: 10.1002/wrna.1141. Epub 2012 Oct 16.
The removal of non-coding sequences, introns, from the mRNA precursors is an essential step in eukaryotic gene expression. U12-type introns are a minor subgroup of introns, distinct from the major or U2-type introns. U12-type introns are present in most eukaryotes but only account for less than 0.5% of all introns in any given genome. They are processed by a specific U12-dependent spliceosome, which is similar to, but distinct from, the major spliceosome. U12-type introns are spliced somewhat less efficiently than the major introns, and it is believed that this limits the expression of the genes containing such introns. Recent findings on the role of U12-dependent splicing in development and human disease have shown that it can also affect multiple cellular processes not directly related to the functions of the host genes of U12-type introns. At the same time, advances in understanding the regulation and phylogenetic distribution of the minor spliceosome are starting to shed light on how the U12-type introns and the minor spliceosome may have evolved.
从 mRNA 前体中去除非编码序列(内含子)是真核基因表达的一个重要步骤。U12 型内含子是内含子的一个小亚群,与主要的或 U2 型内含子不同。U12 型内含子存在于大多数真核生物中,但在任何给定的基因组中只占所有内含子的不到 0.5%。它们由一个特定的 U12 依赖性剪接体加工,该剪接体与主要剪接体相似,但又有所不同。U12 型内含子的剪接效率比主要内含子略低,人们认为这限制了含有这些内含子的基因的表达。最近关于 U12 依赖性剪接在发育和人类疾病中的作用的发现表明,它还可以影响多个与 U12 型内含子的宿主基因功能不直接相关的细胞过程。与此同时,对小剪接体的调节和系统发育分布的理解的进展开始揭示 U12 型内含子和小剪接体可能是如何进化的。