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癌症中端粒酶活性与端粒功能的分析

Analysis of telomerase activity and telomere function in cancer.

作者信息

Gordon Katrina E, Parkinson E Kenneth

机构信息

Beatson Institute for Cancer Research, Glasgow, Scotland.

出版信息

Methods Mol Biol. 2004;281:333-48. doi: 10.1385/1-59259-811-0:333.

Abstract

Telomeres are the structures at the ends of chromosomes, composed of repetitive sequences and associated proteins, which cap chromosome ends to maintain genomic stability. These structures are maintained by the enzyme complex telomerase in germ cells and some stem cells, but are absent in the majority of somatic cells. The consequence of this lack of telomerase in normal somatic cells is the shortening of the telomeric repeat, which results in a limited replicative life span. However, in cancer cells, which grow indefinitely, telomerase activity has been detected in a large number of different cancer cell types. This has lead to a great deal of interest in establishing techniques to measure telomerase activity, telomere length, and telomere function in both normal and cancer cells/tissue. Here we describe the TRAP (telomeric repeat amplification protocol) assay, a technique to measure telomerase activity in cells, TRF (terminal restriction fragment length) analysis to estimate telomere length, and both the anaphase bridge index and the frequency of dicentric chromosomes as indicators of telomere dysfunction.

摘要

端粒是染色体末端的结构,由重复序列和相关蛋白质组成,它覆盖染色体末端以维持基因组稳定性。这些结构在生殖细胞和一些干细胞中由端粒酶复合物维持,但在大多数体细胞中不存在。正常体细胞中端粒酶缺乏的结果是端粒重复序列缩短,这导致有限的复制寿命。然而,在无限生长的癌细胞中,已在大量不同类型的癌细胞中检测到端粒酶活性。这引发了人们对建立测量正常细胞和癌细胞/组织中端粒酶活性、端粒长度和端粒功能技术的极大兴趣。在这里,我们描述了TRAP(端粒重复序列扩增协议)分析,一种测量细胞中端粒酶活性的技术,TRF(末端限制片段长度)分析以估计端粒长度,以及后期桥接指数和双着丝粒染色体频率作为端粒功能障碍的指标。

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