Multiple and Specific mRNA Processing Targets for the Major Human hnRNP Proteins

Author:

Venables Julian P.1,Koh Chu-Shin1,Froehlich Ulrike1,Lapointe Elvy1,Couture Sonia1,Inkel Lyna1,Bramard Anne1,Paquet Éric R.1,Watier Valérie1,Durand Mathieu1,Lucier Jean-François1,Gervais-Bird Julien1,Tremblay Karine1,Prinos Panagiotis1,Klinck Roscoe12,Elela Sherif Abou12,Chabot Benoit12

Affiliation:

1. Laboratoire de Génomique Fonctionnelle de l'Université de Sherbrooke

2. Département de Microbiologie et d'Infectiologie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, Québec J1H 5N4, Canada

Abstract

ABSTRACT Alternative splicing is a key mechanism regulating gene expression, and it is often used to produce antagonistic activities particularly in apoptotic genes. Heterogeneous nuclear ribonucleoparticle (hnRNP) proteins form a family of RNA-binding proteins that coat nascent pre-mRNAs. Many but not all major hnRNP proteins have been shown to participate in splicing control. The range and specificity of hnRNP protein action remain poorly documented, even for those affecting splice site selection. We used RNA interference and a reverse transcription-PCR screening platform to examine the implications of 14 of the major hnRNP proteins in the splicing of 56 alternative splicing events in apoptotic genes. Out of this total of 784 alternative splicing reactions tested in three human cell lines, 31 responded similarly to a knockdown in at least two different cell lines. On the other hand, the impact of other hnRNP knockdowns was cell line specific. The broadest effects were obtained with hnRNP K and C, two proteins whose role in alternative splicing had not previously been firmly established. Different hnRNP proteins affected distinct sets of targets with little overlap even between closely related hnRNP proteins. Overall, our study highlights the potential contribution of all of these major hnRNP proteins in alternative splicing control and shows that the targets for individual hnRNP proteins can vary in different cellular contexts.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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