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Extended chromatin fibers and chromatin organization.

机译:扩展的染色质纤维和染色质组织。

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Studies of chromatin extensibility have revealed the flow of chromatin and DNA from cell nuclei and chromosomes in response to gravity or mechanical stretch following lysis by hypertonic saline and detergent solutions. Since this phenomenon was first reported, the technical methods by which extended chromatin fibers (ECFs) may be analyzed have been improved. These methods include topochemical assays, fluorescence in situ hybridization, immunofluorescence, electron microscopy, and polarization microscopy. Chromatin and DNA "halos" also have been studied in materials subjected to lysis, especially in a horizontal position or after cytocentrifugation. The analysis of ECF formation is useful not only as a tool for detecting the positioning of certain DNA signals on chromatin filaments, but also for describing diverse DNA-protein associations that may be related to varying transcriptional activities and chromatin supraorganization. A brief review of the methods and applications of ECF formation is presented here. We focus on light microscopy studies of ECF formation in mouse hepatocytes under different chromatin supraorganization and physiological conditions and in sperm cells with different DNA-protein complexes.
机译:染色质可扩展性的研究表明,在高渗盐溶液和去污剂溶液裂解后,响应于重力或机械拉伸,细胞核和染色体中的染色质和DNA流动。自从首次报道这种现象以来,用于分析扩展染色质纤维(ECF)的技术方法已得到改进。这些方法包括拓扑化学分析,荧光原位杂交,免疫荧光,电子显微镜和偏振显微镜。在已经裂解的材料中,尤其是在水平位置或细胞离心后,也已经研究了染色质和DNA“晕”。 ECF形成的分析不仅可用作检测染色质丝上某些DNA信号定位的工具,而且还可用于描述可能与转录活性和染色质超组织变化有关的各种DNA-蛋白质缔合。此处简要介绍ECF的形成方法和应用。我们专注于在不同染色质超组织和生理条件下小鼠肝细胞和具有不同DNA-蛋白质复合物的精细胞中ECF形成的光学显微镜研究。

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