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

Authors :
Sonia Couture
Sherif Abou Elela
Julian P. Venables
Benoit Chabot
Anne Bramard
Elvy Lapointe
Eric Paquet
Panagiotis Prinos
Valérie Watier
Lyna Inkel
ChuShin Koh
Jean-François Lucier
Mathieu Durand
Ulrike Froehlich
Julien Gervais-Bird
Karine Tremblay
Roscoe Klinck
Source :
Molecular and Cellular Biology. 28:6033-6043
Publication Year :
2008
Publisher :
Informa UK Limited, 2008.

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.

Details

ISSN :
10985549
Volume :
28
Database :
OpenAIRE
Journal :
Molecular and Cellular Biology
Accession number :
edsair.doi.dedup.....ff3f1fb50043c598409b25a3b1ff60dc