Chu Y, Huang T S, Hsu M T
Department of Microbiology, Mt Sinai Medical Center, New York, NY 10029.
Nucleic Acids Res. 1990 Jul 11;18(13):3705-11. doi: 10.1093/nar/18.13.3705.
Under exhaustive digestion conditions P1 nuclease was found to cleave a subpopulation of intracellular SV40 chromatin only once. The major P1 cleavage site in SV40 DNA was mapped at the origin of DNA replication, and the two minor sites at the SV40 enhancers. The P1-sensitive SV40 chromatin subpopulation was found to have higher superhelical density than the bulk of the intracellular SV40 chromatin. Furthermore, pulse labeled SV40 DNA which had higher superhelical density than that of the steady state viral DNA (S.S. Chen and M.T.Hsu, J. Virol 51:14-19, 1984) was also found to be preferentially cleaved by P1 nuclease. These results are consistent with a supercoil-dependent alteration of chromatin conformation near the regulatory region of the viral genome that can be recognized by P1 nuclease. Since P1 nuclease cleaves the subpopulation of SV40 chromatin only once without further degradation, this nuclease can be used as a general tool to define viral or cellular chromatin fraction with altered chromatin conformation and to map nuclease hypersensitive sites. Preliminary studies indicate that P1 makes limited double stranded cleavages in cellular chromatin to generate large DNA fragments.
在彻底消化的条件下,发现P1核酸酶仅能切割细胞内SV40染色质的一个亚群一次。SV40 DNA中的主要P1切割位点定位于DNA复制起点,两个次要位点位于SV40增强子处。已发现对P1敏感的SV40染色质亚群比细胞内大部分SV40染色质具有更高的超螺旋密度。此外,还发现脉冲标记的、超螺旋密度高于稳态病毒DNA(S.S.陈和M.T.许,《病毒学杂志》51:14 - 19,1984)的SV40 DNA也优先被P1核酸酶切割。这些结果与病毒基因组调控区域附近染色质构象的超螺旋依赖性改变一致,这种改变可被P1核酸酶识别。由于P1核酸酶仅切割SV40染色质亚群一次而无进一步降解,该核酸酶可作为一种通用工具,用于定义染色质构象改变的病毒或细胞染色质组分,并绘制核酸酶超敏位点图谱。初步研究表明,P1在细胞染色质中进行有限次数的双链切割以产生大的DNA片段。