Frequencies of mutagen-induced coincident mitotic recombination at unlinked loci in Saccharomyces cerevisiae
Frequencies of coincident genetic events were measured in strain D7 of Saccharomyces cerevisiae. This diploid strain permits the detection of mitotic gene conversion involving the trp5-12 and trp5-27 alleles, mitotic crossing-over and gene conversion leading to the expression of the ade2-40 and ade2...
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Veröffentlicht in: | Mutation Research-Fundamental and Molecular Mechanisms of Mutagenesis 2007-03, Vol.616 (1), p.119-132 |
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Zusammenfassung: | Frequencies of coincident genetic events were measured in strain D7 of
Saccharomyces cerevisiae. This diploid strain permits the detection of mitotic gene conversion involving the
trp5-12 and
trp5-27 alleles, mitotic crossing-over and gene conversion leading to the expression of the
ade2-40 and
ade2-119 alleles as red and pink colonies, and reversion of the
ilv1-92 allele. The three genes are on different chromosomes, and one might expect that coincident (simultaneous) genetic alterations at two loci would occur at frequencies predicted by those of the single alterations acting as independent events. Contrary to this expectation, we observed that
ade2 recombinants induced by bleomycin, β-propiolactone, and ultraviolet radiation occur more frequently among
trp5 convertants than among total colonies. This excess among
trp5 recombinants indicates that double recombinants are more common than expected for independent events. No similar enrichment was found among Ilv
+ revertants. The possibility of an artifact in which haploid yeasts that mimic mitotic recombinants are generated by a low frequency of cryptic meiosis has been excluded. Several hypotheses that can explain the elevated incidence of coincident mitotic recombination have been evaluated, but the cause remains uncertain. Most evidence suggests that the excess is ascribable to a subset of the population being in a recombination-prone state. |
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ISSN: | 0027-5107 1386-1964 1873-135X 0027-5107 |
DOI: | 10.1016/j.mrfmmm.2006.11.014 |