Suppr超能文献

RAD1是酿酒酵母的一种切除修复基因,它也参与重组过程。

RAD1, an excision repair gene of Saccharomyces cerevisiae, is also involved in recombination.

作者信息

Schiestl R H, Prakash S

机构信息

Department of Biology, University of Rochester, New York 14627.

出版信息

Mol Cell Biol. 1988 Sep;8(9):3619-26. doi: 10.1128/mcb.8.9.3619-3626.1988.

Abstract

The RAD1 gene of Saccharomyces cerevisiae is required for the incision step of excision repair of damaged DNA. In this paper, we report our observations on the effect of the RAD1 gene on genetic recombination. Mitotic intrachromosomal and interchromosomal recombination in RAD+, rad1, rad52, and other rad mutant strains was examined. The rad1 deletion mutation and some rad1 point mutations reduced the frequency of intrachromosomal recombination of a his3 duplication, in which one his3 allele is deleted at the 3' end while the other his3 allele is deleted at the 5' end. Mutations in the other excision repair genes, RAD2, RAD3, and RAD4, did not lower recombination frequencies in the his3 duplication. As expected, recombination between the his3 deletion alleles in the duplication was reduced in the rad52 mutant. The frequency of HIS3+ recombinants fell synergistically in the rad1 rad52 double mutant, indicating that the RAD1 and RAD52 genes affect this recombination via different pathways. In contrast to the effect of mutations in the RAD52 gene, mutations in the RAD1 gene did not lower intrachromosomal and interchromosomal recombination between heteroalleles that carry point mutations rather than partial deletions; however, the rad1 delta mutation did lower the frequency of integration of linear plasmids and DNA fragments into homologous genomic sequences. We suggest that RAD1 plays a role in recombination after the formation of the recombinogenic substrate.

摘要

酿酒酵母的RAD1基因是受损DNA切除修复切口步骤所必需的。在本文中,我们报告了关于RAD1基因对基因重组影响的观察结果。检测了RAD+、rad1、rad52和其他rad突变菌株中的有丝分裂染色体内和染色体间重组。rad1缺失突变和一些rad1点突变降低了his3重复序列的染色体内重组频率,其中一个his3等位基因在3'端缺失,而另一个his3等位基因在5'端缺失。其他切除修复基因RAD2、RAD3和RAD4的突变并未降低his3重复序列中的重组频率。正如预期的那样,rad52突变体中重复序列中his3缺失等位基因之间的重组减少。在rad1 rad52双突变体中,HIS3+重组体的频率协同下降,表明RAD1和RAD52基因通过不同途径影响这种重组。与RAD52基因突变的影响相反,RAD1基因突变并未降低携带点突变而非部分缺失的异等位基因之间的染色体内和染色体间重组;然而,rad1缺失突变确实降低了线性质粒和DNA片段整合到同源基因组序列中的频率。我们认为RAD1在重组底物形成后在重组中发挥作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验