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底物上裂解处理与扫描探针显微镜相结合揭示了真核生物和原核生物中的染色体结构。

On-substrate lysis treatment combined with scanning probe microscopy revealed chromosome structures in eukaryotes and prokaryotes.

作者信息

Yoshimura Shige H, Kim Joongbaek, Takeyasu Kunio

机构信息

Laboratory of Plasma Membrane and Nuclear Signaling, Graduate School of Biostudies, Kyoto University, Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan.

出版信息

J Electron Microsc (Tokyo). 2003;52(4):415-23. doi: 10.1093/jmicro/52.4.415.

Abstract

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.

摘要

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。

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