Lutter L C
Nucleic Acids Res. 1979 Jan;6(1):41-56. doi: 10.1093/nar/6.1.41.
The precise locations of the DNase I cutting sites in the nucleosome core have been determined by analysis of the DNA products of a DNase I digestion of 32P end-labelled mucleosome cores on a high resolution gel electrophoresis system. This system is capable of resolving fragments of mixed sequence DNA differing by one base into the region of 160 bases in length. The DNase I cutting sites in the core are found to be spaced at multiples of about 10.4 (i.e. clearly different from 10.0) bases along the DNA, but show significant variations about this value. In addition to the location of the sites, the stagger between individual sites on opposite strands has been determined and is found to be inconsistent with at least one proposed mechanism for nuclease cleavage of chromatin DNA. Finally, a calculated distribution of fragment lengths in a DNase I digest of nuclei has been determined from the data obtained from the nucleosome core and found to be in reasonable agreement with the observed distribution. The periodicity of 10.4 is discussed with respect to the number of base pairs per turn of chromatin DNA and the number of superhelical turns of DNA per nucleosome.
通过在高分辨率凝胶电泳系统上对32P末端标记的核小体核心进行DNA酶I消化的DNA产物进行分析,已确定了核小体核心中DNA酶I切割位点的精确位置。该系统能够将相差一个碱基的混合序列DNA片段分辨到长度为160个碱基的区域。发现核心中的DNA酶I切割位点沿DNA以约10.4(即明显不同于10.0)个碱基的倍数间隔排列,但围绕该值存在显著变化。除了位点的位置,还确定了相反链上各个位点之间的错开情况,发现其与至少一种提出的染色质DNA核酸酶切割机制不一致。最后,根据从核小体核心获得的数据确定了细胞核DNA酶I消化中片段长度的计算分布,发现其与观察到的分布合理一致。关于染色质DNA每圈的碱基对数和每个核小体的DNA超螺旋圈数,讨论了10.4的周期性。