Source:http://linkedlifedata.com/resource/pubmed/id/18260644
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2008-3-5
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pubmed:abstractText |
The Y-family DNA polymerase Dpo4, from the archaeon bacterium Sulfolobus solfataricus, is a member of the DinB family, which also contains human Pol kappa. It has a spacious active site that can accommodate two templating bases simultaneously, with one of them skipped by the incoming dNTP. Assays of single dNTP insertion opposite a benzo[ a]pyrene-derived N (2)-dG adduct, 10 S(+)- trans- anti-[BP]- N (2)-dG ([BP]G*), reveal that an incoming dATP is significantly preferred over the other three dNTPs in the TG 1*G 2 sequence context. Molecular modeling and dynamics simulations were carried out to interpret this experimental observation on a molecular level. Modeling studies suggest that the significant preference for dATP insertion observed experimentally can result from two possible dATP incorporation modes. The dATP can be inserted opposite the T on the 5' side of the adduct G 1*, using an unusual 5'-slippage pattern, in which the unadducted G 2, rather than G 1*, is skipped, to produce a -1 deletion. In addition, the dATP can be misincorporated opposite the adduct. The 5'-slippage pattern may be generally facilitated in cases where the base 3' to the lesion is the same as the adducted base.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2'-deoxyadenosine triphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Archaeal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Benzopyrenes,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Directed DNA Polymerase,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxyadenine Nucleotides,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxyguanosine,
http://linkedlifedata.com/resource/pubmed/chemical/Nucleotides,
http://linkedlifedata.com/resource/pubmed/chemical/benzo(a)pyrene N2-dG adduct
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0006-2960
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
4
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pubmed:volume |
47
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2701-9
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pubmed:meshHeading |
pubmed-meshheading:18260644-Archaeal Proteins,
pubmed-meshheading:18260644-Base Pairing,
pubmed-meshheading:18260644-Base Sequence,
pubmed-meshheading:18260644-Benzopyrenes,
pubmed-meshheading:18260644-Binding Sites,
pubmed-meshheading:18260644-Computer Simulation,
pubmed-meshheading:18260644-DNA-Directed DNA Polymerase,
pubmed-meshheading:18260644-Deoxyadenine Nucleotides,
pubmed-meshheading:18260644-Deoxyguanosine,
pubmed-meshheading:18260644-Models, Molecular,
pubmed-meshheading:18260644-Molecular Structure,
pubmed-meshheading:18260644-Nucleotides,
pubmed-meshheading:18260644-Substrate Specificity,
pubmed-meshheading:18260644-Sulfolobus solfataricus
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pubmed:year |
2008
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pubmed:articleTitle |
Nucleotide selectivity opposite a benzo[a]pyrene-derived N2-dG adduct in a Y-family DNA polymerase: a 5'-slippage mechanism.
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pubmed:affiliation |
Department of Biology, New York University, 1009 Silver Center, 100 Washington Square East, New York City, New York 10003, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, N.I.H., Extramural
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