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将可变剪接和mRNA编辑纳入复杂性状的遗传分析。

Incorporating alternative splicing and mRNA editing into the genetic analysis of complex traits.

作者信息

Hassan Musa A, Saeij Jeroen P J

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.

出版信息

Bioessays. 2014 Nov;36(11):1032-40. doi: 10.1002/bies.201400079. Epub 2014 Aug 29.

Abstract

The nomination of candidate genes underlying complex traits is often focused on genetic variations that alter mRNA abundance or result in non-conservative changes in amino acids. Although inconspicuous in complex trait analysis, genetic variants that affect splicing or RNA editing can also generate proteomic diversity and impact genetic traits. Indeed, it is known that splicing and RNA editing modulate several traits in humans and model organisms. Using high-throughput RNA sequencing (RNA-seq) analysis, it is now possible to integrate the genetics of transcript abundance, alternative splicing (AS) and editing with the analysis of complex traits. We recently demonstrated that both AS and mRNA editing are modulated by genetic and environmental factors, and potentially engender phenotypic diversity in a genetically segregating mouse population. Therefore, the analysis of splicing and RNA editing can expand not only the regulatory landscape of transcriptome and proteome complexity, but also the repertoire of candidate genes for complex traits.

摘要

复杂性状潜在候选基因的提名通常集中在那些改变mRNA丰度或导致氨基酸非保守变化的遗传变异上。尽管在复杂性状分析中不那么显眼,但影响剪接或RNA编辑的遗传变异也能产生蛋白质组多样性并影响遗传性状。事实上,已知剪接和RNA编辑会调节人类和模式生物中的多种性状。利用高通量RNA测序(RNA-seq)分析,现在有可能将转录本丰度、可变剪接(AS)和编辑的遗传学与复杂性状分析整合起来。我们最近证明,AS和mRNA编辑都受到遗传和环境因素的调节,并可能在基因分离的小鼠群体中产生表型多样性。因此,剪接和RNA编辑的分析不仅可以扩展转录组和蛋白质组复杂性的调控格局,还可以扩展复杂性状候选基因的范围。

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