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[Rec41——一个参与酿酒酵母重组调控的新基因]

[Rec41--a new gene, participating in the control of recombination in Saccharomyces cerevisiae yeast].

作者信息

Chepurnaia O V, Kozhina T N, Peshekhonov V T, Korolev V G

出版信息

Genetika. 1993 Feb;29(2):246-56.

PMID:8486254
Abstract

We isolated a collection of rec- mutants. The mutant rec41 from this collection was studied in detail. The mutant demonstrated a reduced level of interplasmid recombination, did not grow at the elevated temperature (36 degrees C) and was sensitive to gamma-rays but not to ultraviolet irradiation. The rec41-1 mutation behaved as a semidominant nuclear mutation. Our study on inter- and intraplasmid recombination suggested that the rec41-1 mutation decreased the level of crossing over events significantly and the frequency of gene conversion events at a lower degree. We postulate that rec41 mutation reduces the efficiency of double-stranded break repair and this results in high sensitivity of mutant cells to methylenmethan-sulfonate and ionizing radiation. Using gamma-sensitivity of the mutant cells we isolated a rec41-1 complementing plasmid from a yeast genomic DNA library. The mapping of plasmid integration site allowed us to localize the REC41 gene on the left arm of the VII chromosome nearby LYS4 and CDC43 genes.

摘要

我们分离出了一系列rec-突变体。对该系列中的突变体rec41进行了详细研究。该突变体表现出质粒间重组水平降低,在高温(36摄氏度)下无法生长,对γ射线敏感,但对紫外线照射不敏感。rec41-1突变表现为半显性核突变。我们对质粒间和质粒内重组的研究表明,rec41-1突变显著降低了交换事件的水平,对基因转换事件频率的降低程度较小。我们推测rec41突变降低了双链断裂修复的效率,这导致突变细胞对甲磺酸甲酯和电离辐射高度敏感。利用突变细胞的γ敏感性,我们从酵母基因组DNA文库中分离出了一个rec41-1互补质粒。质粒整合位点的定位使我们能够将REC41基因定位在VII号染色体左臂上靠近LYS4和CDC43基因的位置。

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