Smerdon M J, Lieberman M W
Proc Natl Acad Sci U S A. 1978 Sep;75(9):4238-41. doi: 10.1073/pnas.75.9.4238.
The distribution of UV-induced DNA repair synthesis within chromatin was measured in confluent human fibroblasts that were pulse-labeled with [3H]dThd (10 or 90 min) immediately after irradiation and chased in nonradioactive medium for different time periods. Initially (i.e., at the end of the pulse period), most of the repair synthesis occurs in staphylococcal nuclease-sensitive regions. With increasing chase times the nucleotides inserted during repair synthesis become progressively more nuclease resistant. Gel electrophoresis data indicate that nuclease resistance is conferred on these nucleotides by their appearance in core DNA. The kinetics of this rearrangement process are biphasic: greater than 85% of the repair synthesis sites undergo rapid rearrangement (4--5 hr); the remaining sites ( less than 15%) rearrange much more slowly, if at all. The time courses of nucleosome rearrangement and repair synthesis are similar, suggesting that nucleosome rearrangement may be induced by the repair process or that the rate of repair synthesis may be regulated by nucleosome rearrangement.
在汇合的人成纤维细胞中测量了紫外线诱导的染色质内DNA修复合成的分布情况。这些细胞在照射后立即用[³H]dThd进行脉冲标记(10或90分钟),然后在无放射性培养基中追踪不同时间段。最初(即脉冲期结束时),大部分修复合成发生在对葡萄球菌核酸酶敏感的区域。随着追踪时间的增加,修复合成过程中插入的核苷酸对核酸酶的抗性逐渐增强。凝胶电泳数据表明,这些核苷酸因出现在核心DNA中而具有核酸酶抗性。这种重排过程的动力学是双相的:超过85%的修复合成位点经历快速重排(4 - 5小时);其余位点(少于15%)重排得非常缓慢,甚至根本不重排。核小体重排和修复合成的时间进程相似,这表明核小体重排可能是由修复过程诱导的,或者修复合成的速率可能受核小体重排调节。