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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
17
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pubmed:dateCreated |
1993-10-5
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pubmed:abstractText |
The kinetically component open complexes formed at prokaryotic and eukaryotic transcription start sites are efficiently nicked by the chemical nuclease activity of the 2:1 1,10-phenanthroline-copper(I) complex [(OP)2Cu+] and hydrogen peroxide. This reaction specificity has been attributed to the creation of a binding site(s) for redox-active tetrahedral (OP)2Cu+ when RNA polymerase form productive complexes with promoters. This proposal has been confirmed for the Escherichia coli lac UV-5 promoter by the demonstration that the 2:1 2,9-dimethyl-1,10-phenanthroline-copper(I) complex [(Me2OP)2Cu+], a redox-inactive isostere of (OP)2-Cu+, protects the transcription start site from scission by the chemical nuclease activity. (Me2OP)2Cu+ is also an effective inhibitor of transcription. The inhibition of transcription and the protection from scission of the open complex by (OP)2Cu+ exhibit the same dependence on the concentration of (Me2OP)2Cu+. This redox- and exchange-stable species is a previously undescribed transcription inhibitor that binds to a site generated by the interaction of RNA polymerase with the promoter. Unlike the intercalating agent proflavine, which is also an effective transcription inhibitor, it does not displace the enzyme from the promoter. The ability of (Me2OP)2Cu+ to inhibit transcription may be partially responsible for its potent cytotoxicity.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-1280856,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-1310361,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-1377020,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-14875144,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-1536005,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-1579168,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-1695832,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-1868543,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-1881889,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-2176843,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-2185756,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-2328244,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-2668879,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-2722774,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-2904147,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-3016894,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-3131344,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-3415689,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-3889902,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-3896304,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-3900414,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-3986288,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-4092055,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-6123596,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-6206781,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-6302514,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-6320169,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-6573669,
http://linkedlifedata.com/resource/pubmed/commentcorrection/8367475-6651879
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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 |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0027-8424
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
90
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
8140-4
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:8367475-Cross-Linking Reagents,
pubmed-meshheading:8367475-DNA, Bacterial,
pubmed-meshheading:8367475-DNA-Directed RNA Polymerases,
pubmed-meshheading:8367475-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:8367475-Escherichia coli,
pubmed-meshheading:8367475-Kinetics,
pubmed-meshheading:8367475-Phenanthrolines,
pubmed-meshheading:8367475-Promoter Regions, Genetic,
pubmed-meshheading:8367475-Transcription, Genetic
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pubmed:year |
1993
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pubmed:articleTitle |
A transcription inhibitor specific for unwound DNA in RNA polymerase-promoter open complexes.
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pubmed:affiliation |
Department of Biological Chemistry, School of Medicine, University of California, Los Angeles 90024-1570.
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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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