选择性剪接:真核生物基因组功能创新的潜在来源。

Lu Chen, Jaime M Tovar-Corona, Araxi O Urrutia
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引用次数: 76

摘要

选择性剪接(AS)是真核生物中常见的转录后过程,通过该过程,单个基因可以产生多个不同功能的转录本。公布的人类基因组草图显示的基因数量比预期的要少得多。由于其在扩大蛋白质多样性方面的潜在作用,在过去的十年中,人们对选择性剪接的兴趣越来越大。虽然最近的研究表明,94%的人类多外显子基因经历了AS,但AS的进化及其在真核生物基因组功能创新中的潜在作用在很大程度上仍未被探索。在这里,我们回顾现有的证据,关于演变的流行和功能作用。此外,我们强调需要纠正AS检测中转录覆盖的强大影响,并制定策略,最终阐明AS在基因组尺度上功能创新中的作用程度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Alternative splicing: a potential source of functional innovation in the eukaryotic genome.

Alternative splicing: a potential source of functional innovation in the eukaryotic genome.

Alternative splicing: a potential source of functional innovation in the eukaryotic genome.

Alternative splicing: a potential source of functional innovation in the eukaryotic genome.

Alternative splicing (AS) is a common posttranscriptional process in eukaryotic organisms, by which multiple distinct functional transcripts are produced from a single gene. The release of the human genome draft revealed a much smaller number of genes than anticipated. Because of its potential role in expanding protein diversity, interest in alternative splicing has been increasing over the last decade. Although recent studies have shown that 94% human multiexon genes undergo AS, evolution of AS and thus its potential role in functional innovation in eukaryotic genomes remain largely unexplored. Here we review available evidence regarding the evolution of AS prevalence and functional role. In addition we stress the need to correct for the strong effect of transcript coverage in AS detection and set out a strategy to ultimately elucidate the extent of the role of AS in functional innovation on a genomic scale.

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