Literature DB >> 8231822

Mutagenic specificity of the base analog 6-N-hydroxylaminopurine in the URA3 gene of the yeast Saccharomyces cerevisiae.

P V Shcherbakova1, Y I Pavlov.   

Abstract

The mutational specificity of the base analog 6-N-hydroxylaminopurine (HAP) was studied in the URA3 gene of the yeast Saccharomyces cerevisiae. Twenty-nine independent HAP-induced ura3 mutations were sequenced. GC-->AT transitions were found most frequently (21 out of 29) while AT-->GC transitions were less abundant (five out of 29). Three GC-->TA transversions were also detected. Two interesting features of DNA context were revealed for transition mutations. One third of the transitions occurred at one site within short direct imperfect repeats converting them to perfect repeats. A model involving complementary interaction of imperfect repeats is proposed to explain the origin of these mutations. Nearly all of the rest of the GC-->AT as well as the AT-->GC transitions were found in the runs of several identical base pairs, predominantly in the middle or at the 3' template nucleotide of (G)n and (A)n runs.

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Year:  1993        PMID: 8231822     DOI: 10.1093/mutage/8.5.417

Source DB:  PubMed          Journal:  Mutagenesis        ISSN: 0267-8357            Impact factor:   3.000


  10 in total

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Journal:  Environ Mol Mutagen       Date:  2012-10-10       Impact factor: 3.216

2.  The yeast HSM3 gene acts in one of the mismatch repair pathways.

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Journal:  Genetics       Date:  1998-03       Impact factor: 4.562

3.  A new reversion assay for measuring all possible base pair substitutions in Saccharomyces cerevisiae.

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4.  3'-->5' exonucleases of DNA polymerases epsilon and delta correct base analog induced DNA replication errors on opposite DNA strands in Saccharomyces cerevisiae.

Authors:  P V Shcherbakova; Y I Pavlov
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6.  DNA polymerase ζ-dependent lesion bypass in Saccharomyces cerevisiae is accompanied by error-prone copying of long stretches of adjacent DNA.

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7.  Nucleotide selectivity defect and mutator phenotype conferred by a colon cancer-associated DNA polymerase δ mutation in human cells.

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  10 in total

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