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通过荧光显微镜技术对人端粒酶定位进行可视化观察。

Visualization of human telomerase localization by fluorescence microscopy techniques.

作者信息

Abreu Eladio, Terns Rebecca M, Terns Michael P

机构信息

Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA, USA.

出版信息

Methods Mol Biol. 2011;735:125-37. doi: 10.1007/978-1-61779-092-8_12.

Abstract

Human telomerase is a ribonucleoprotein (RNP) that synthesizes DNA repeats at the ends of chromosomes and maintains telomere length and genome stability. The enzyme comprises telomerase RNA (hTR) (which provides the template for telomere addition) and several protein subunits, including telomerase reverse transcriptase (hTERT) (the catalytic component). Intracellular trafficking of the enzyme has emerged as an important factor in the regulation of telomerase activity. Telomerase trafficking between nuclear Cajal bodies (proposed sites of telomerase biogenesis and regulation) and telomeres (sites of action) is regulated by the cell cycle in concordance with telomere synthesis during S phase. Here, we describe fluorescence microscopy approaches to visualize the subcellular localization of the essential RNA component of hTR relative to Cajal bodies and telomeres in cultured human cells. These methods include fluorescence in situ hybridization (to detect hTR and telomeric DNA) and immunofluorescence (IF) (to detect Cajal bodies and telomere-binding proteins). Because telomerase localization to telomeres is normally restricted to S phase, we also describe methods to synchronize and analyze cells within this phase of the cell cycle.

摘要

人端粒酶是一种核糖核蛋白(RNP),它在染色体末端合成DNA重复序列,维持端粒长度和基因组稳定性。该酶由端粒酶RNA(hTR)(为端粒添加提供模板)和几个蛋白质亚基组成,包括端粒酶逆转录酶(hTERT)(催化成分)。酶的细胞内运输已成为端粒酶活性调节的一个重要因素。端粒酶在核卡哈尔体(端粒酶生物发生和调节的假定位点)和端粒(作用位点)之间的运输受细胞周期调节,与S期的端粒合成一致。在这里,我们描述了荧光显微镜方法,以可视化培养的人类细胞中hTR的必需RNA成分相对于卡哈尔体和端粒的亚细胞定位。这些方法包括荧光原位杂交(用于检测hTR和端粒DNA)和免疫荧光(IF)(用于检测卡哈尔体和端粒结合蛋白)。由于端粒酶定位于端粒通常仅限于S期,我们还描述了在细胞周期的这个阶段同步和分析细胞的方法。

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