Source:http://linkedlifedata.com/resource/pubmed/id/18495665
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
29
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pubmed:dateCreated |
2008-7-14
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pubmed:abstractText |
Human DNA topoisomerase I plays a dual role in transcription, by controlling DNA supercoiling and by acting as a specific kinase for the SR-protein family of splicing factors. The two activities are mutually exclusive, but the identity of the molecular switch is unknown. Here we identify poly(ADP-ribose) as a physiological regulator of the two topoisomerase I functions. We found that, in the presence of both DNA and the alternative splicing factor/splicing factor 2 (ASF/SF2, a prototypical SR-protein), poly(ADP-ribose) affected topoisomerase I substrate selection and gradually shifted enzyme activity from protein phosphorylation to DNA cleavage. A likely mechanistic explanation was offered by the discovery that poly(ADP-ribose) forms a high affinity complex with ASF/SF2 thereby leaving topoisomerase I available for directing its action onto DNA. We identified two functionally important domains, RRM1 and RS, as specific poly(ADP-ribose) binding targets. Two independent lines of evidence emphasize the potential biological relevance of our findings: (i) in HeLa nuclear extracts, ASF/SF2, but not histone, phosphorylation was inhibited by poly(ADP-ribose); (ii) an in silico study based on gene expression profiling data revealed an increased incidence of alternative splicing within a subset of inflammatory response genes that are dysregulated in cells lacking a functional poly(ADP-ribose) polymerase-1. We propose that poly(ADP-ribose) targeting of topoisomerase I and ASF/SF2 functions may participate in the regulation of gene expression.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA Topoisomerases, Type I,
http://linkedlifedata.com/resource/pubmed/chemical/Histones,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Poly Adenosine Diphosphate Ribose,
http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Topoisomerase I Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/serine-arginine-rich splicing...
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
18
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pubmed:volume |
283
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
19991-8
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:18495665-Alternative Splicing,
pubmed-meshheading:18495665-Cell Nucleus,
pubmed-meshheading:18495665-DNA Topoisomerases, Type I,
pubmed-meshheading:18495665-Enzyme Activation,
pubmed-meshheading:18495665-Gene Expression Regulation,
pubmed-meshheading:18495665-HeLa Cells,
pubmed-meshheading:18495665-Histones,
pubmed-meshheading:18495665-Humans,
pubmed-meshheading:18495665-Nuclear Proteins,
pubmed-meshheading:18495665-Phosphorylation,
pubmed-meshheading:18495665-Poly Adenosine Diphosphate Ribose,
pubmed-meshheading:18495665-Protein Binding,
pubmed-meshheading:18495665-RNA-Binding Proteins,
pubmed-meshheading:18495665-Topoisomerase I Inhibitors
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pubmed:year |
2008
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pubmed:articleTitle |
Poly(ADP-ribose) binds to the splicing factor ASF/SF2 and regulates its phosphorylation by DNA topoisomerase I.
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pubmed:affiliation |
Department of Structural and Functional Biology, University Federico II, Via Cinthia, Monte S Angelo, Naples, Italy. malanga@unina.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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