RIKEN SPring-8 Center, Hyogo, Japan.
EMBO J. 2012 Apr 4;31(7):1644-53. doi: 10.1038/emboj.2012.35. Epub 2012 Feb 17.
How a long strand of genomic DNA is compacted into a mitotic chromosome remains one of the basic questions in biology. The nucleosome fibre, in which DNA is wrapped around core histones, has long been assumed to be folded into a 30-nm chromatin fibre and further hierarchical regular structures to form mitotic chromosomes, although the actual existence of these regular structures is controversial. Here, we show that human mitotic HeLa chromosomes are mainly composed of irregularly folded nucleosome fibres rather than 30-nm chromatin fibres. Our comprehensive and quantitative study using cryo-electron microscopy and synchrotron X-ray scattering resolved the long-standing contradictions regarding the existence of 30-nm chromatin structures and detected no regular structure >11 nm. Our finding suggests that the mitotic chromosome consists of irregularly arranged nucleosome fibres, with a fractal nature, which permits a more dynamic and flexible genome organization than would be allowed by static regular structures.
基因组 DNA 长链如何压缩成有丝分裂染色体仍然是生物学中的基本问题之一。核小体纤维,即 DNA 缠绕在核心组蛋白周围,长期以来一直被认为折叠成 30nm 的染色质纤维,并进一步形成有丝分裂染色体的层次有序结构,尽管这些规则结构的实际存在存在争议。在这里,我们表明,人类有丝分裂 HeLa 染色体主要由不规则折叠的核小体纤维组成,而不是 30nm 的染色质纤维。我们使用冷冻电子显微镜和同步加速器 X 射线散射进行的全面和定量研究解决了关于 30nm 染色质结构存在的长期矛盾,并检测到没有>11nm 的规则结构。我们的发现表明,有丝分裂染色体由不规则排列的核小体纤维组成,具有分形性质,这使得基因组组织比静态规则结构允许的更具动态和灵活性。