Yoshimura Shige H, Kim Joongbaek, Takeyasu Kunio
Laboratory of Plasma Membrane and Nuclear Signaling, Graduate School of Biostudies, Kyoto University, Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan.
J Electron Microsc (Tokyo). 2003;52(4):415-23. doi: 10.1093/jmicro/52.4.415.
The proper function of the genome largely depends on the higher-order architecture of the chromosome. To understand the detailed chromosome structure in a native state, we developed an on-substrate procedure of subcellular fractionation suitable for the observation by atomic force microscopy (AFM). HeLa cells on a coverslip were successively treated with a detergent and a high-salt solution to remove the cytoplasmic and nucleoplasmic materials. A closer observation of the nucleus by AFM revealed that the interphase chromosome is composed of a granular unit of approximately 80 nm in diameter. Subsequent mild treatment with deoxyribonuclease I (10 U ml(-1)) exposed these units more clearly, which enabled us to uncover the 80-nm granules forming a fibre of approximately 80 nm width. In the cytoplasmic regions, cytoskeletal fibres with varying widths (10-70 nm) were observed. These observations suggest that the 80 nm granular fibre is a fundamental structural unit of the interphase chromosome. This on-substrate procedure was also applied to Escherichia coli. Cells attached on a coverslip were successively treated with lysozyme and detergent to partially release the nucleoid onto the substrate. The AFM observation revealed that the approximately 80 nm fundamental structural unit forms a granular fibre similar to that of HeLa cells. These results suggest that the fundamental mechanism of chromosome packing is common in both prokaryotes and eukaryotes.
基因组的正常功能很大程度上取决于染色体的高级结构。为了了解天然状态下详细的染色体结构,我们开发了一种适用于原子力显微镜(AFM)观察的亚细胞分级分离的底物上操作方法。将盖玻片上的HeLa细胞先后用去污剂和高盐溶液处理,以去除细胞质和核质物质。通过AFM对细胞核进行更仔细的观察发现,间期染色体由直径约80 nm的颗粒单元组成。随后用脱氧核糖核酸酶I(10 U ml(-1))进行温和处理,更清楚地显示了这些单元,这使我们能够揭示80 nm的颗粒形成了宽度约80 nm的纤维。在细胞质区域,观察到宽度不同(10 - 70 nm)的细胞骨架纤维。这些观察结果表明,80 nm颗粒纤维是间期染色体的基本结构单元。这种底物上操作方法也应用于大肠杆菌。将附着在盖玻片上的细胞先后用溶菌酶和去污剂处理,以将类核部分释放到底物上。AFM观察显示,大约80 nm的基本结构单元形成了与HeLa细胞类似的颗粒纤维。这些结果表明,染色体包装的基本机制在原核生物和真核生物中是共同的。