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rdf:type |
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lifeskim:mentions |
umls-concept:C0205245,
umls-concept:C0381107,
umls-concept:C0381108,
umls-concept:C0381109,
umls-concept:C1514562,
umls-concept:C1514873,
umls-concept:C1546857,
umls-concept:C1556066,
umls-concept:C1619636,
umls-concept:C1704675,
umls-concept:C1879547,
umls-concept:C1880022,
umls-concept:C1880389,
umls-concept:C1883204,
umls-concept:C1883221
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pubmed:issue |
41
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pubmed:dateCreated |
1996-11-19
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pubmed:abstractText |
The Elongin (SIII) complex stimulates the rate of elongation by RNA polymerase II by suppressing transient pausing by polymerase at many sites along DNA templates. The Elongin (SIII) complex is composed of a transcriptionally active A subunit, a chaperone-like B subunit, which promotes assembly and enhances stability of the Elongin (SIII) complex, and a regulatory C subunit, which (i) functions as a potent activator of Elongin A transcriptional activity, (ii) interacts specifically with Elongin B to form an isolable Elongin BC complex, and (iii) is bound and negatively regulated in vitro by the product of the von Hippel-Lindau tumor suppressor gene. As part of our effort to understand how Elongin C regulates the activity of the Elongin (SIII) complex, we are characterizing Elongin C functional domains. In this report, we identify Elongin C mutants that fall into multiple functional classes based on their abilities to bind Elongin B and to bind and activate Elongin A under our assay conditions. Characterization of these mutants suggests that Elongin C is composed of multiple overlapping regions that mediate functional interactions with Elongin A and B.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Ligases,
http://linkedlifedata.com/resource/pubmed/chemical/Macromolecular Substances,
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/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Ubiquitin-Protein Ligases,
http://linkedlifedata.com/resource/pubmed/chemical/VHL protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Von Hippel-Lindau Tumor Suppressor...,
http://linkedlifedata.com/resource/pubmed/chemical/elongin
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0021-9258
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
11
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pubmed:volume |
271
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
25562-8
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:8810329-Amino Acid Sequence,
pubmed-meshheading:8810329-Animals,
pubmed-meshheading:8810329-Binding Sites,
pubmed-meshheading:8810329-Genes, Tumor Suppressor,
pubmed-meshheading:8810329-Humans,
pubmed-meshheading:8810329-Kinetics,
pubmed-meshheading:8810329-Ligases,
pubmed-meshheading:8810329-Macromolecular Substances,
pubmed-meshheading:8810329-Molecular Sequence Data,
pubmed-meshheading:8810329-Mutagenesis, Site-Directed,
pubmed-meshheading:8810329-Proteins,
pubmed-meshheading:8810329-RNA Polymerase II,
pubmed-meshheading:8810329-Rats,
pubmed-meshheading:8810329-Recombinant Proteins,
pubmed-meshheading:8810329-Sequence Deletion,
pubmed-meshheading:8810329-Sequence Homology, Amino Acid,
pubmed-meshheading:8810329-Transcription, Genetic,
pubmed-meshheading:8810329-Transcription Factors,
pubmed-meshheading:8810329-Tumor Suppressor Proteins,
pubmed-meshheading:8810329-Ubiquitin-Protein Ligases,
pubmed-meshheading:8810329-Von Hippel-Lindau Tumor Suppressor Protein,
pubmed-meshheading:8810329-von Hippel-Lindau Disease
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pubmed:year |
1996
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pubmed:articleTitle |
Characterization of elongin C functional domains required for interaction with elongin B and activation of elongin A.
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pubmed:affiliation |
Program in Molecular and Cell Biology, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma 73104, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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