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异质性核糖核蛋白L在哺乳动物mRNA加工中的多种作用:微阵列和RNA干扰联合分析

Diverse roles of hnRNP L in mammalian mRNA processing: a combined microarray and RNAi analysis.

作者信息

Hung Lee-Hsueh, Heiner Monika, Hui Jingyi, Schreiner Silke, Benes Vladimir, Bindereif Albrecht

机构信息

Institute of Biochemistry, Justus-Liebig-University of Giessen, D-35392 Giessen, Germany.

出版信息

RNA. 2008 Feb;14(2):284-96. doi: 10.1261/rna.725208. Epub 2007 Dec 11.

Abstract

Alternative mRNA splicing patterns are determined by the combinatorial control of regulator proteins and their target RNA sequences. We have recently characterized human hnRNP L as a global regulator of alternative splicing, binding to diverse C/A-rich elements. To systematically identify hnRNP L target genes on a genome-wide level, we have combined splice-sensitive microarray analysis and an RNAi-knockdown approach. As a result, we describe 11 target genes of hnRNP L that were validated by RT-PCR and that represent several new modes of hnRNP L-dependent splicing regulation, involving both activator and repressor functions: first, intron retention; second, inclusion or skipping of cassette-type exons; third, suppression of multiple exons; and fourth, alternative poly(A) site selection. In sum, this approach revealed a surprising diversity of splicing-regulatory processes as well as poly(A) site selection in which hnRNP L is involved.

摘要

可变mRNA剪接模式由调节蛋白及其靶RNA序列的组合控制决定。我们最近将人类hnRNP L鉴定为可变剪接的全局调节因子,它与多种富含C/A的元件结合。为了在全基因组水平上系统地鉴定hnRNP L的靶基因,我们结合了剪接敏感微阵列分析和RNA干扰敲低方法。结果,我们描述了hnRNP L的11个靶基因,这些基因通过RT-PCR得到验证,代表了hnRNP L依赖性剪接调控的几种新模式,涉及激活和抑制功能:第一,内含子保留;第二,盒式外显子的包含或跳过;第三,多个外显子的抑制;第四,可变聚腺苷酸化位点选择。总之,这种方法揭示了hnRNP L所涉及的剪接调控过程以及聚腺苷酸化位点选择的惊人多样性。

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