Source:http://linkedlifedata.com/resource/pubmed/id/10930409
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
42
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pubmed:dateCreated |
2000-11-20
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pubmed:abstractText |
The human protein MED1 (also known as MBD4) was previously isolated in a two-hybrid screening using the mismatch repair protein MLH1 as a bait, and shown to have homology to bacterial base excision repair DNA N-glycosylases/lyases. To define the mechanisms of action of MED1, we implemented a sensitive glycosylase assay amenable to kinetic analysis. We show that MED1 functions as a mismatch-specific DNA N-glycosylase active on thymine, uracil, and 5-fluorouracil when these bases are opposite to guanine. MED1 lacks uracil glycosylase activity on single-strand DNA and abasic site lyase activity. The glycosylase activity of MED1 prefers substrates containing a G:T mismatch within methylated or unmethylated CpG sites; since G:T mismatches can originate via deamination of 5-methylcytosine to thymine, MED1 may act as a caretaker of genomic fidelity at CpG sites. A kinetic analysis revealed that MED1 displays a fast first cleavage reaction followed by slower subsequent reactions, resulting in biphasic time course; this is due to the tight binding of MED1 to the abasic site reaction product rather than a consequence of enzyme inactivation. Comparison of kinetic profiles revealed that the MED1 5-methylcytosine binding domain and methylation of the mismatched CpG site are not required for efficient catalysis.
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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 |
Oct
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
20
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pubmed:volume |
275
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
32422-9
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:10930409-Base Pair Mismatch,
pubmed-meshheading:10930409-Base Sequence,
pubmed-meshheading:10930409-DNA Repair,
pubmed-meshheading:10930409-Endodeoxyribonucleases,
pubmed-meshheading:10930409-Humans,
pubmed-meshheading:10930409-Kinetics,
pubmed-meshheading:10930409-Molecular Sequence Data,
pubmed-meshheading:10930409-Mutagenesis,
pubmed-meshheading:10930409-Oligodeoxyribonucleotides,
pubmed-meshheading:10930409-Recombinant Proteins,
pubmed-meshheading:10930409-Sensitivity and Specificity,
pubmed-meshheading:10930409-Sequence Deletion,
pubmed-meshheading:10930409-Substrate Specificity
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pubmed:year |
2000
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pubmed:articleTitle |
Biphasic kinetics of the human DNA repair protein MED1 (MBD4), a mismatch-specific DNA N-glycosylase.
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pubmed:affiliation |
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, 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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