Khmel'nitskiĭ M I, Zlotnikov K M
Genetika. 1979;15(5):823-30.
Mutations prv1, prv2 and mutR34, increasing frequencies of intragenic recombinations, are found not to complement and therefore to be alleles of one gene. Checking for the influence of mutator genes mutS3, mutT1 and uvrE502 on the intragenic recombination in conjugational crossings has shown that mutators mutS3 and uvrE502 increase the frequency of intragenic recombinations while mutT1 does not change it. None of the examined mutator genes influence the conjugational frequencies of recombination. A supplementary analysis for the mutability of the mutant prv1 has been carried out. The prv1 mutation can induce mutations of the frameshift type. Mutations uvrA6, recB21, recC22 and lexA produce no influence on the display of a mutator effect of the prv1 mutation.
发现增加基因内重组频率的prv1、prv2和mutR34突变不能互补,因此是一个基因的等位基因。检查诱变基因mutS3、mutT1和uvrE502对接合杂交中基因内重组的影响表明,诱变剂mutS3和uvrE502增加了基因内重组的频率,而mutT1没有改变它。所检测的诱变基因均不影响重组的接合频率。已对突变体prv1的可突变性进行了补充分析。prv1突变可诱导移码型突变。uvrA6、recB21、recC22和lexA突变对prv1突变的诱变效应表现没有影响。