Co-regulation of alternative splicing by diverse splicing factors in Caenorhabditis elegans

被引:19
|
作者
Barberan-Soler, Sergio
Medina, Pedro
Estella, Jeffrey
Williams, James
Zahler, Alan M. [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Mol Cell & Dev Biol, Santa Cruz, CA 95064 USA
基金
美国国家卫生研究院;
关键词
PRE-MESSENGER-RNA; GENOME-WIDE ANALYSIS; SR PROTEINS; MEC-8; GENE; HNRNP PROTEINS; FAMILY; MUSCLE; UNC-52; FOX-1; EXPRESSION;
D O I
10.1093/nar/gkq767
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of alternative splicing is controlled by pre-mRNA sequences (cis-elements) and trans-acting protein factors that bind them. The combinatorial interactions of multiple protein factors with the cis-elements surrounding a given alternative splicing event lead to an integrated splicing decision. The mechanism of multifactorial splicing regulation is poorly understood. Using a splicing-sensitive DNA microarray, we assayed 352 Caenorhabditis elegans alternative cassette exons for changes in embryonic splicing patterns between wild-type and 12 different strains carrying mutations in a splicing factor. We identified many alternative splicing events that are regulated by multiple splicing factors. Many splicing factors have the ability to behave as splicing repressors for some alternative cassette exons and as splicing activators for others. Unexpectedly, we found that the ability of a given alternative splicing factor to behave as an enhancer or repressor of a specific splicing event can change during development. Our observations that splicing factors can change their effects on a substrate during development support a model in which combinatorial effects of multiple factors, both constitutive and developmentally regulated ones, contribute to the overall splicing decision.
引用
收藏
页码:666 / 674
页数:9
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