Livingstone-Zatchej M, Meier A, Suter B, Thoma F
Institut für Zellbiologie, ETH-Zürich, Hönggerberg, CH-8093 Zürich, Switzerland.
Nucleic Acids Res. 1997 Oct 1;25(19):3795-800. doi: 10.1093/nar/25.19.3795.
Yeast uses nucleotide excision repair (NER) and photolyase (photoreactivation) to repair cyclobutane pyrimidine dimers (CPDs) generated by ultraviolet light. In active genes, NER preferentially repairs the transcribed strand (TS). In contrast, we recently showed that photolyase preferentially repairs the non-transcribed strands (NTS) of the URA3 and HIS3 genes in minichromosomes. To test whether photoreactivation depends on transcription, repair of CPDs was investigated in the transcriptionally regulated GAL10 gene in a yeast strain deficient in NER [AMY3 (rad1Delta)]. In the active gene (cells grown in galactose), photoreactivation was fast in the NTS and slow in the TS demonstrating preferential repair of the NTS. In the inactive gene (cells grown in glucose), both strands were repaired at similar rates. This suggests that RNA polymerases II blocked at CPDs inhibit accessibility of CPDs to photolyase. In a strain in which both pathways are operational [W303-1a (RAD1)], no strand bias was observed either in the active or inactive gene, demonstrating that photoreactivation of the NTS compensates preferential repair of the TS by NER. Moreover, repair of the NTS was more quickly in the active gene than in the repressed gene indicating that transcription dependent disruption of chromatin facilitates repair of an active gene.
酵母利用核苷酸切除修复(NER)和光解酶(光复活作用)来修复由紫外线产生的环丁烷嘧啶二聚体(CPD)。在活跃基因中,NER优先修复转录链(TS)。相比之下,我们最近发现,在微型染色体中,光解酶优先修复URA3和HIS3基因的非转录链(NTS)。为了测试光复活作用是否依赖于转录,我们在一个缺乏NER的酵母菌株[AMY3(rad1Δ)]的转录调控GAL10基因中研究了CPD的修复情况。在活跃基因(在半乳糖中生长的细胞)中,NTS上的光复活作用很快,而TS上的则很慢,这表明NTS优先被修复。在非活跃基因(在葡萄糖中生长的细胞)中,两条链以相似的速率被修复。这表明在CPD处受阻的RNA聚合酶II会抑制CPD对光解酶的可及性。在一个两种途径都起作用的菌株[W303-1a(RAD1)]中,无论是在活跃基因还是非活跃基因中都未观察到链偏向性,这表明NTS的光复活作用补偿了NER对TS的优先修复。此外,活跃基因中NTS的修复比受抑制基因中的更快,这表明转录依赖性的染色质破坏促进了活跃基因的修复。