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酿酒酵母中同源重组的诱导

Induction of homologous recombination in Saccharomyces cerevisiae.

作者信息

Simon J R, Moore P D

机构信息

Department of Microbiology and Immunology, University of Illinois College of Medicine, Chicago 60612.

出版信息

Mol Gen Genet. 1988 Sep;214(1):37-41. doi: 10.1007/BF00340176.

Abstract

We have investigated the effects of UV irradiation of Saccharomyces cerevisiae in order to distinguish whether UV-induced recombination results from the induction of enzymes required for homologous recombination, or the production of substrate sites for recombination containing regions of DNA damage. We utilized split-dose experiments to investigate the induction of proteins required for survival, gene conversion, and mutation in a diploid strain of S. cerevisiae. We demonstrate that inducing doses of UV irradiation followed by a 6 h period of incubation render the cells resistant to challenge doses of UV irradiation. The effects of inducing and challenge doses of UV irradiation upon interchromosomal gene conversion and mutation are strictly additive. Using the yeast URA3 gene cloned in non-replicating single- and double-stranded plasmid vectors that integrate into chromosomal genes upon transformation, we show that UV irradiation of haploid yeast cells and homologous plasmid DNA sequences each stimulate homologous recombination approximately two-fold, and that these effects are additive. Non-specific DNA damage has little effect on the stimulation of homologous recombination, as shown by studies in which UV-irradiated heterologous DNA was included in transformation/recombination experiments. We further demonstrate that the effect of competing single- and double-stranded heterologous DNA sequences differs in UV-irradiated and unirradiated cells, suggesting an induction of recombinational machinery in UV-irradiated S. cerevisiae cells.

摘要

我们研究了紫外线照射酿酒酵母的影响,以区分紫外线诱导的重组是源于同源重组所需酶的诱导,还是含有DNA损伤区域的重组底物位点的产生。我们利用分剂量实验来研究二倍体酿酒酵母菌株中生存、基因转换和突变所需蛋白质的诱导情况。我们证明,诱导剂量的紫外线照射后经过6小时的孵育,使细胞对紫外线照射的挑战剂量具有抗性。诱导剂量和挑战剂量的紫外线照射对染色体间基因转换和突变的影响严格相加。使用克隆在非复制型单链和双链质粒载体中的酵母URA3基因,这些载体在转化时整合到染色体基因中,我们表明单倍体酵母细胞和同源质粒DNA序列的紫外线照射各自刺激同源重组约两倍,并且这些效应是相加的。如在转化/重组实验中包含紫外线照射的异源DNA的研究所表明的,非特异性DNA损伤对同源重组的刺激影响很小。我们进一步证明,在紫外线照射和未照射的细胞中,竞争性单链和双链异源DNA序列的影响不同,这表明紫外线照射的酿酒酵母细胞中诱导了重组机制。

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