Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
46
|
pubmed:dateCreated |
1994-12-19
|
pubmed:abstractText |
The spectrum of mutations induced upon in vivo replication of an M13 genome containing a site-specifically located propanodeoxyguanosine (PdG) adduct was determined. PdG was used as a model for the major deoxyguanosine adduct produced on reaction of DNA with the endogenous genotoxin malondialdehyde. PdG was introduced at position 6256 of M13MB102 by ligating the oligodeoxynucleotide 5'-GGT(PdG)TCCG-3' into an 8-base gap in the (-)-strand of duplex M13MB102. Replication of the adducted strand was maximized by incorporation of uracil into the unadducted (+)-strand. Following replication of dG-containing and PdG-containing M13MB102 genomes in Escherichia coli JM105, frameshift mutations were detected as phenotypic changes in the lacZ alpha marker gene. Base pair substitutions were detected by differential hybridization using 32P-labeled 13-mers bearing different bases opposite position 6256. Neither frameshift nor base pair substitution mutations were detected following replication of PdG-adducted genomes in non-SOS-induced JM105. However, PdG-->T transversions and PdG-->A transitions were detected following transformation of PdG-adducted M13MB102 into SOS-induced JM105. Both types of mutations were detected at comparable frequencies, and the total mutation frequency was approximately 2%. The results indicate that PdG is an efficient premutagenic lesion in E. coli strains in which the SOS response is induced.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1,N(2)-propanodeoxyguanosine,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Adducts,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxyguanosine,
http://linkedlifedata.com/resource/pubmed/chemical/Mutagens
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0021-9258
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
18
|
pubmed:volume |
269
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
28844-50
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:7961843-Bacteriophage M13,
pubmed-meshheading:7961843-Base Sequence,
pubmed-meshheading:7961843-Cell Line,
pubmed-meshheading:7961843-DNA Adducts,
pubmed-meshheading:7961843-DNA Damage,
pubmed-meshheading:7961843-DNA Primers,
pubmed-meshheading:7961843-Deoxyguanosine,
pubmed-meshheading:7961843-Genome, Viral,
pubmed-meshheading:7961843-Molecular Sequence Data,
pubmed-meshheading:7961843-Mutagenesis, Site-Directed,
pubmed-meshheading:7961843-Mutagens,
pubmed-meshheading:7961843-Nucleic Acid Hybridization
|
pubmed:year |
1994
|
pubmed:articleTitle |
Site-specific mutagenesis by a propanodeoxyguanosine adduct carried on an M13 genome.
|
pubmed:affiliation |
A. B. Hancock, Jr. Memorial Laboratory for Cancer Research, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|