Functional characterization of SR and SR-related genes in Caenorhabditis elegans
The SR proteins constitute a family of nuclear phosphoproteins, which are required for constitutive splicing and also influence alternative splicing regulation. Initially, it was suggested that SR proteins were functionally redundant in constitutive splicing. However, differences have been observed...
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Published in | The EMBO journal Vol. 19; no. 7; pp. 1625 - 1637 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Chichester, UK
John Wiley & Sons, Ltd
03.04.2000
Nature Publishing Group UK Blackwell Publishing Ltd Oxford University Press |
Subjects | |
Online Access | Get full text |
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Summary: | The SR proteins constitute a family of nuclear phosphoproteins, which are required for constitutive splicing and also influence alternative splicing regulation. Initially, it was suggested that SR proteins were functionally redundant in constitutive splicing. However, differences have been observed in alternative splicing regulation, suggesting unique functions for individual SR proteins. Homology searches of the
Caenorhabditis elegans
genome identified seven genes encoding putative orthologues of the human factors SF2/ASF, SRp20, SC35, SRp40, SRp75 and p54, and also several SR‐related genes. To address the issue of functional redundancy, we used dsRNA interference (RNAi) to inhibit specific SR protein function during
C.elegans
development. RNAi with CeSF2/ASF caused late embryonic lethality, suggesting that this gene has an essential function during
C.elegans
development. RNAi with other SR genes resulted in no obvious phenotype, which is indicative of gene redundancy. Simultaneous interference of two or more SR proteins in certain combinations caused lethality or other developmental defects. RNAi with CeSRPK, an SR protein kinase, resulted in early embryonic lethality, suggesting an essential role for SR protein phosphorylation during development. |
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Bibliography: | ark:/67375/WNG-8PKXDVRJ-Q ArticleID:EMBJ7592274 istex:2525DCCE2B545C5102CBDBFCAF9ED1B3AF32E2AB ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 Corresponding author e-mail: Javier.Caceres@hgu.mrc.ac.uk |
ISSN: | 0261-4189 1460-2075 1460-2075 |
DOI: | 10.1093/emboj/19.7.1625 |