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理解可变剪接:迈向一种细胞编码。

Understanding alternative splicing: towards a cellular code.

作者信息

Matlin Arianne J, Clark Francis, Smith Christopher W J

机构信息

Department of Biochemistry, 80 Tennis Court Road, University of Cambridge, CB2 1GA, UK.

出版信息

Nat Rev Mol Cell Biol. 2005 May;6(5):386-98. doi: 10.1038/nrm1645.

Abstract

In violation of the 'one gene, one polypeptide' rule, alternative splicing allows individual genes to produce multiple protein isoforms - thereby playing a central part in generating complex proteomes. Alternative splicing also has a largely hidden function in quantitative gene control, by targeting RNAs for nonsense-mediated decay. Traditional gene-by-gene investigations of alternative splicing mechanisms are now being complemented by global approaches. These promise to reveal details of the nature and operation of cellular codes that are constituted by combinations of regulatory elements in pre-mRNA substrates and by cellular complements of splicing regulators, which together determine regulated splicing pathways.

摘要

可变剪接违反了“一个基因,一种多肽”的规则,使单个基因能够产生多种蛋白质异构体,从而在生成复杂蛋白质组中发挥核心作用。可变剪接在定量基因控制中也有一个很大程度上隐藏的功能,即通过将RNA靶向无义介导的衰变。传统的逐个基因研究可变剪接机制现在正得到全局方法的补充。这些方法有望揭示细胞编码的性质和运作细节,这些编码由前体mRNA底物中的调控元件组合以及剪接调节因子的细胞互补物构成,它们共同决定了受调控的剪接途径。

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