|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
6
|
|
pubmed:dateCreated |
1997-4-24
|
|
pubmed:abstractText |
Mammalian cells contain activities that amplify the effects of activators on class II gene transcription in vitro. The molecular identity of several of these cofactor activities is still unknown. Here we identify poly(ADP-ribose) polymerase (PARP) as one functional component of the positive cofactor 1 activity. PARP enhances transcription by acting during preinitiation complex formation, but at a step after binding of transcription factor IID. This transcriptional activation requires the amino-terminal DNA-binding domain, but not the carboxyl-terminal catalytic region. In purified systems, coactivator function requires a large molar excess of PARP over the number of templates, as reported for other DNA-binding cofactors such as topoisomerase I. PARP effects on supercoiled templates are DNA concentration-dependent and do not depend on damaged DNA. The PARP coactivator function is suppressed by NAD+, probably as a result of auto-ADP-ribosylation. These observations provide another example of the potentiation of trancription by certain DNA-binding cofactors and may point to interactions of PARP with RNA polymerase II-associated factors in special situations.
|
|
pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-1549180,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-1796908,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-1889091,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-1907890,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-2109322,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-2123876,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-3118181,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-3120719,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-3155867,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-6304101,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-7578423,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-7628453,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-7698643,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-7774019,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-7797075,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-7898477,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-7969171,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-7984410,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8001135,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8062255,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8062391,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8062392,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8187178,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8193132,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8196633,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8265582,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8396729,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8396762,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8451755,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8533153,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8598913,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8609996,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8794742,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8811195,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8870494,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8870495,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8870497,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8870498,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9122182-8946909
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/GAL4 protein, S cerevisiae,
http://linkedlifedata.com/resource/pubmed/chemical/NAD,
http://linkedlifedata.com/resource/pubmed/chemical/Poly(ADP-ribose) Polymerases,
http://linkedlifedata.com/resource/pubmed/chemical/Poly Adenosine Diphosphate Ribose,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA Polymerase II,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/poly(ADP)-ribosylated proteins
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
0027-8424
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
18
|
|
pubmed:volume |
94
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
2261-5
|
|
pubmed:dateRevised |
2009-11-19
|
|
pubmed:meshHeading |
pubmed-meshheading:9122182-Animals,
pubmed-meshheading:9122182-Cell Nucleus,
pubmed-meshheading:9122182-Cloning, Molecular,
pubmed-meshheading:9122182-DNA-Binding Proteins,
pubmed-meshheading:9122182-Fungal Proteins,
pubmed-meshheading:9122182-HeLa Cells,
pubmed-meshheading:9122182-Humans,
pubmed-meshheading:9122182-Kinetics,
pubmed-meshheading:9122182-Mammals,
pubmed-meshheading:9122182-NAD,
pubmed-meshheading:9122182-Poly(ADP-ribose) Polymerases,
pubmed-meshheading:9122182-Poly Adenosine Diphosphate Ribose,
pubmed-meshheading:9122182-Proteins,
pubmed-meshheading:9122182-RNA Polymerase II,
pubmed-meshheading:9122182-Recombinant Proteins,
pubmed-meshheading:9122182-Saccharomyces cerevisiae Proteins,
pubmed-meshheading:9122182-Transcription, Genetic,
pubmed-meshheading:9122182-Transcription Factors,
pubmed-meshheading:9122182-Transcriptional Activation
|
|
pubmed:year |
1997
|
|
pubmed:articleTitle |
Poly(ADP-ribose) polymerase enhances activator-dependent transcription in vitro.
|
|
pubmed:affiliation |
Laboratorium für Molekulare Biologie-Genzentrum, der Ludwig-Maximilians-Universitat Munchen, Munich, Germany. meister@lmb.uni-muenchen.de
|
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|
