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MUTATIONAL SPECIFICITY OF ULTRAVIOLET LIGHT IN ESCHERICHIA COLI WITH AND WITHOUT THE R PLASMID pKM101
Author(s) -
Robert G. Fowler,
L McGinty,
Kristien Mortelmans
Publication year - 1981
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1093/genetics/99.1.25
Subject(s) - frameshift mutation , biology , escherichia coli , genetics , nucleotide , microbiology and biotechnology , ultraviolet light , mutation , plasmid , mutagenesis , reversion , pyrimidine dimer , missense mutation , dna , dna repair , gene , chemistry , phenotype , photochemistry
Plasmid pKM101 provides UV protection and increases the frequency of spontaneous and UV-induced mutations in Escherichia coli. By analyzing reversion patterns of defined trpA alleles, we showed that pKM101 altered the mutational specificity of UV-induced mutations. Certain UV-induced base-pair substitutions were strongly enhanced, while others were decreased in frequency in the presence of pKM101. This result suggests an interaction between cellular misrepair and an error-prone repair function(s) provided by pKM101. We have also examined UV mutational specificity in the absence of pKM101 and found the following: (1) UV preferentially enhances missense, as well as nonsense, intergenic suppressor mutations; (2) UV causes all possible base-pair substitutions as well as frameshift mutations; (3) G·C base pairs are more susceptible to UV mutagenesis than A·T base pairs at the same nucleotide positions; and (4) UV-induced mutations can occur at nucleotide positions that are not part of pyrimidine-pyrimidine sequences.

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