Mueller J P, Smerdon M J
Department of Biochemistry and Biophysics, Washington State University, Pullman 99164-4660, USA.
Nucleic Acids Res. 1995 Sep 11;23(17):3457-64. doi: 10.1093/nar/23.17.3457.
Repair of UV-induced cyclobutane pyrimidine dimers (CPDs) was examined in a yeast plasmid of known chromatin structure and in genomic DNA in a radiation-sensitive deletion mutant of yeast, rad7 delta, and its isogenic wild-type strain. A whole plasmid repair assay revealed that only approximately 50% of the CPDs in plasmid DNA are repaired after 6 h in this mutant, compared with almost 90% repaired in wild-type. Using a site-specific repair assay on 44 individual CPD sites within the plasmid we found that repair in the rad7 delta mutant occurred primarily in the transcribed regions of each strand of the plasmid, however, the rate of repair at nearly all sites measured was less than in the wild-type. There was no apparent correlation between repair rate and nucleosome position. In addition, approximately 55% of the CPDs in genomic DNA of the mutant are repaired during the 6 h period, compared with > 80% in the wild-type.
在已知染色质结构的酵母质粒以及酵母辐射敏感缺失突变体rad7δ及其同基因野生型菌株的基因组DNA中,对紫外线诱导的环丁烷嘧啶二聚体(CPD)的修复进行了检测。全质粒修复试验表明,在该突变体中,质粒DNA中只有约50%的CPD在6小时后得到修复,而野生型中这一比例接近90%。通过对质粒内44个单个CPD位点进行位点特异性修复试验,我们发现rad7δ突变体中的修复主要发生在质粒每条链的转录区域,然而,几乎所有检测位点的修复率都低于野生型。修复率与核小体位置之间没有明显的相关性。此外,突变体基因组DNA中约55%的CPD在6小时内得到修复,而野生型中这一比例大于80%。