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在酿酒酵母中无法诱导DNA修复基因RAD54并不影响DNA修复或重组表型。

Failure to induce a DNA repair gene, RAD54, in Saccharomyces cerevisiae does not affect DNA repair or recombination phenotypes.

作者信息

Cole G M, Mortimer R K

机构信息

Genetics Department, University of California, Berkeley 94720.

出版信息

Mol Cell Biol. 1989 Aug;9(8):3314-22. doi: 10.1128/mcb.9.8.3314-3322.1989.

Abstract

The Saccharomyces cerevisiae RAD54 gene is transcriptionally regulated by a broad spectrum of DNA-damaging agents. Induction of RAD54 by DNA-damaging agents is under positive control. Sequences responsible for DNA damage induction (the DRS element) lie within a 29-base-pair region from -99 to -70 from the most proximal transcription start site. This inducible promoter element is functionally separable from a poly(dA-dT) region immediately downstream which is required for constitutive expression. Deletions which eliminate induction of RAD54 transcription by DNA damage but do not affect constitutive expression have no effect on growth or survival of noninducible strains relative to wild-type strains in the presence of DNA-damaging agents. The DRS element is also not required for homothallic mating type switching, transcriptional induction of RAD54 during meiosis, meiotic recombination, or spontaneous or X-ray-induced mitotic recombination. We find no phenotype for a lack of induction of RAD54 message via the damage-inducible DRS, which raises significant questions about the physiology of DNA damage induction in S. cerevisiae.

摘要

酿酒酵母RAD54基因受多种DNA损伤剂的转录调控。DNA损伤剂对RAD54的诱导处于正调控之下。负责DNA损伤诱导的序列(DRS元件)位于距最近端转录起始位点-99至-70的29个碱基对区域内。这种可诱导的启动子元件在功能上可与紧邻下游的聚(dA-dT)区域分离,后者是组成型表达所必需的。消除DNA损伤对RAD54转录的诱导但不影响组成型表达的缺失,在存在DNA损伤剂的情况下,相对于野生型菌株,对不可诱导菌株的生长或存活没有影响。DRS元件对于同宗配合型转换、减数分裂期间RAD54的转录诱导、减数分裂重组或自发或X射线诱导的有丝分裂重组也不是必需的。我们发现通过损伤诱导的DRS缺乏对RAD54信息的诱导没有表型,这对酿酒酵母中DNA损伤诱导的生理学提出了重大问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f7f/362376/b468e9ba4177/molcellb00056-0174-a.jpg

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