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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
13
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pubmed:dateCreated |
1985-8-7
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pubmed:abstractText |
Complexes between Bacillus subtilus RNA polymerase and 32P-labeled DNA were irradiated with UV light and digested with nuclease; electrophoresis and autoradiography were used to identify the polymerase subunits cross-linked to DNA. These experiments showed: 1) that cross-linkage of promoter complexes yielded predominantly the beta and sigma subunits; 2) that beta, beta', and sigma were detected in non-promoter complexes; 3) that addition of the delta subunit or high concentrations of NaCl decreased cross-linkage of all subunits, especially the cross-linkage of the sigma subunit in non-promoter complexes and the binding of polymerase at DNA ends; 4) that different patterns of cross-linkage were obtained at 0 degrees C (conditions favoring the formation of closed complexes) and 37 degrees C (conditions favoring the formation of open complexes); and 5) predominantly beta and possibly alpha were cross-linked by irradiation of core-DNA complexes whereas similar experiments with core-delta complexed to DNA showed the efficient cross-linkage of beta' and beta.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
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 |
5
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pubmed:volume |
260
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
8121-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3924912-Bacillus subtilis,
pubmed-meshheading:3924912-Bacteriophages,
pubmed-meshheading:3924912-DNA, Viral,
pubmed-meshheading:3924912-DNA-Directed RNA Polymerases,
pubmed-meshheading:3924912-Operon,
pubmed-meshheading:3924912-Plasmids,
pubmed-meshheading:3924912-Sodium Chloride,
pubmed-meshheading:3924912-Temperature,
pubmed-meshheading:3924912-Ultraviolet Rays
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pubmed:year |
1985
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pubmed:articleTitle |
UV cross-linking of the Bacillus subtilis RNA polymerase to DNA in promoter and non-promoter complexes.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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