Nissen K A, Lan S Y, Smerdon M J
J Biol Chem. 1986 Jul 5;261(19):8585-8.
Rearrangements of chromatin structure during excision repair of UV-damaged DNA appear to involve unfolding of nucleosomal DNA while repair is taking place, followed by refolding of this DNA into a native nucleosome structure. Recently, we found that repair patches are not distributed uniformly along the DNA in nucleosome core particles immediately following their refolding into nucleosomes (Lan, S. Y., and Smerdon, M. J. (1985) Biochemistry, 24,7771). Therefore, the distribution of repair patches in nucleosome core DNA was used to monitor the stability of nucleosome placement in these regions. Our results indicate that in nondividing human cells undergoing excision repair there is a slow change in the positioning of nucleosomes in newly repaired regions of chromatin, resulting in the eventual randomization of repair patches in nucleosome core DNA. Furthermore, the nonrandom placement of nucleosomes observed just after the refolding event is not re-established during DNA replication. Possible mechanisms for this change in nucleosome placement along the DNA are discussed.
在紫外线损伤的DNA切除修复过程中,染色质结构的重排似乎涉及到在修复发生时核小体DNA的解折叠,随后该DNA重新折叠成天然核小体结构。最近,我们发现修复片段在重新折叠成核小体后,不会立即沿着核小体核心颗粒中的DNA均匀分布(Lan, S. Y., and Smerdon, M. J. (1985) Biochemistry, 24,7771)。因此,核小体核心DNA中修复片段的分布被用于监测这些区域核小体定位的稳定性。我们的结果表明,在进行切除修复的非分裂人类细胞中,染色质新修复区域的核小体定位存在缓慢变化,最终导致核小体核心DNA中修复片段的随机化。此外,在重新折叠事件后立即观察到的核小体非随机定位在DNA复制过程中不会重新建立。本文讨论了沿DNA的核小体定位发生这种变化的可能机制。