Schild D
Life Sciences Division, Lawrence Berkeley Laboratory, California 94720, USA.
Genetics. 1995 May;140(1):115-27. doi: 10.1093/genetics/140.1.115.
The RAD52 gene of Saccharomyces cerevisiae is involved both in the recombinational repair of DNA damage and in mitotic and meiotic recombination. A new allele of rad52 has been isolated that has unusual properties. Unlike other alleles of rad52, this allele (rad52-20) is partially suppressed by an srs2 deletion; srs2 mutations normally act to suppress only rad6 and rad18 mutations. In addition, although haploid rad52-20 strains are very X-ray sensitive, diploids homozygous for this allele are only slightly X-ray sensitive and undergo normal meiosis and meiotic recombination. Because rad52-20 diploids homozygous for mating type are very X-ray sensitive, mating-type heterozygosity is acting to suppress rad52-20. Mating-type heterozygosity suppresses this allele even in haploids, because sir mutations, which result in expression of the normally silent mating-type cassettes, were identified among the extragenic revertants of rad52-20. A new allele of srs2 and alleles of the transcriptional regulatory genes ccr4 and caf1 were among the other extragenic revertants of rad52-20. Because other researchers have shown that the RAD51 and RAD52 proteins interact, RAD51 on a high copy number plasmid was tested and found to suppress the rad52-20 allele, but RAD54, 55 and 57 did not suppress. The RAD51 plasmid did not suppress rad52-1. The rad52-20 allele may encode a protein that has low affinity binding to the RAD51 protein. To test whether the selected revertants suppressed rad52-20 by elevating the expression of RAD51, an integrated RAD51-lacZ fusion was genetically crossed into each revertant. Because none of the revertants increased the level of RAD51-lacZ, the revertants must exert their effect by one or more mechanisms that are not mediated by RAD51.
酿酒酵母的RAD52基因参与DNA损伤的重组修复以及有丝分裂和减数分裂重组。已分离出一个具有异常特性的rad52新等位基因。与rad52的其他等位基因不同,该等位基因(rad52 - 20)被srs2缺失部分抑制;srs2突变通常仅作用于抑制rad6和rad18突变。此外,尽管单倍体rad52 - 20菌株对X射线非常敏感,但该等位基因的纯合二倍体仅对X射线有轻微敏感性,并且能进行正常的减数分裂和减数分裂重组。由于交配型纯合的rad52 - 20二倍体对X射线非常敏感,交配型杂合性起到了抑制rad52 - 20的作用。交配型杂合性甚至在单倍体中也能抑制该等位基因,因为在rad52 - 20的基因外回复突变体中鉴定出了sir突变,这些突变导致通常沉默的交配型盒式结构表达。srs2的一个新等位基因以及转录调控基因ccr4和caf1的等位基因也在rad52 - 20的其他基因外回复突变体中。因为其他研究人员已表明RAD51和RAD52蛋白相互作用,所以对高拷贝数质粒上的RAD51进行了测试,发现它能抑制rad52 - 20等位基因,但RAD54、55和57不能抑制。RAD51质粒不能抑制rad52 - 1。rad52 - 20等位基因可能编码一种与RAD51蛋白结合亲和力较低的蛋白质。为了测试所选的回复突变体是否通过提高RAD51的表达来抑制rad52 - 20,将一个整合的RAD51 - lacZ融合基因通过遗传杂交导入每个回复突变体中。由于没有一个回复突变体提高RAD51 - lacZ的水平,回复突变体必定是通过一种或多种不由RAD51介导的机制发挥其作用