首页> 美国卫生研究院文献>Nucleic Acids Research >Recovery of RNA polymerase II synthesis following DNA damage in mutants of Saccharomyces cerevisiae defective in nucleotide excision repair.
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Recovery of RNA polymerase II synthesis following DNA damage in mutants of Saccharomyces cerevisiae defective in nucleotide excision repair.

机译:在核苷酸切除修复缺陷的酿酒酵母突变体中DNA损伤后RNA聚合酶II合成的恢复。

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摘要

We have measured the kinetics of the recovery of mRNA synthesis in the inducible GAL10 and RNR3 genes after exposure of yeast cells to ultraviolet (UV) radiation. Such recovery is abolished in mutant strains defective in nucleotide excision repair (NER) of DNA, including a rad23 mutant. Mutants defective in the RAD7 or RAD16 genes, which are required for the repair of the non-transcribed strand but not the transcribed strand of transcriptionally active genes, show slightly faster recovery of RNA synthesis than wild-type strains. A strain deleted of the RAD26 gene, which is known to be required for strand-specific NER in yeast, manifested delayed recovery of mRNA synthesis, whereas a rad28 mutant, which does not show defective strand-specific repair, showed normal kinetics of recovery. Measurement of the recovery of expression of selected individual yeast genes by Northern analysis following exposure of cells to UV radiation apparently correlates directly with the capacity of cells for strand-specific NER.
机译:我们已经测量了酵母细胞暴露于紫外线(UV)辐射后诱导型GAL10和RNR3基因中mRNA合成恢复的动力学。在DNA的核苷酸切除修复(NER)有缺陷的突变株中,包括rad23突变株,废除了这种恢复。 RAD7或RAD16基因有缺陷的突变体是修复转录活性基因的非转录链而非转录链所必需的,与野生型菌株相比,其RNA合成的恢复略快。已知RAD26基因缺失的菌株是酵母中链特异性NER所必需的,表现出mRNA合成的延迟恢复,而没有显示缺陷的链特异性修复的rad28突变体显示出正常的恢复动力学。将细胞暴露于紫外线辐射后,通过Northern分析测量所选单个酵母基因表达的恢复,显然与细胞产生链特异性NER的能力直接相关。

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