Wu Chenyi, Bassett Andrew, Travers Andrew
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK.
EMBO Rep. 2007 Dec;8(12):1129-34. doi: 10.1038/sj.embor.7401115.
The structure of the 30-nm chromatin fibre is an important determinant of the regulation of eukaryotic transcription. A fundamental issue is whether the stacking of nucleosomes in this fibre is organized as a one-start or two-start helix. We argue that all recent experimental data are compatible with a two-start helix and propose that the topology of the fibre, but not the mode of stacking the nucleosomes, is dependent on the length of the linker DNA. This arrangement conserves nucleosome stacking and thus the external morphology of the fibre, and also ensures that the fibre adopts the highest available packing density.
30纳米染色质纤维的结构是真核转录调控的一个重要决定因素。一个基本问题是,该纤维中核小体的堆积是呈单起始螺旋还是双起始螺旋排列。我们认为,所有最新实验数据都与双起始螺旋相符,并提出纤维的拓扑结构(而非核小体的堆积方式)取决于连接DNA的长度。这种排列方式保留了核小体堆积,从而维持了纤维的外部形态,还确保纤维采用了最高的可用堆积密度。