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通过引物延伸分析对酵母端粒酶进行分析。

Analysis of yeast telomerase by primer extension assays.

作者信息

Hsu Min, Lue Neal F

机构信息

Department of Microbiology & Immunology, W.R. Hearst Microbiology Research Center, Weill Medical College of Cornell University, New York, NY, USA.

出版信息

Methods Mol Biol. 2011;735:97-106. doi: 10.1007/978-1-61779-092-8_9.

Abstract

Telomeres are specialized nucleoprotein structures located at eukaryotic chromosomal termini, which are required for chromosome stability and are maintained by a reverse transcriptase named telomerase. Budding yeast has served as an extremely useful model system for analyzing telomere maintenance because the organism offers a wide range of genetic and biochemical tools. Several milestones in telomerase research were reached through investigation of the yeast system. For example, the consequence of telomerase loss was first characterized in the budding yeast Saccharomyces cerevisiae (Lundblad and Szostak, Cell 57:633-643, 1989). The catalytic component of telomerase (telomerase reverse transcriptase; TERT) was likewise initially cloned from this organism (Lendvay et al., Genetics 144:1399-1412, 1996). Moreover, much of the current understanding of the structure and function of the telomerase complex was derived from yeast studies (Autexier and Lue, Annu Rev Biochem 75:493-517, 2006). In this chapter, we discuss one of the most useful tools for investigating yeast telomerase mechanisms and regulation: the primer extension assay. This assay can be used to examine the overall activity as well as the processivity of telomerase, which represents a unique aspect of telomerase enzymology (Lue et al., Mol Cell Biol 23:8440-8449, 2003; Bosoy and Lue, Nucleic Acids Res 32:93-101, 2004). It can also be employed to analyze the mechanisms of telomerase regulatory proteins (Zappulla et al., Nucleic Acids Res 37:354-367, 2009; DeZwaan and Freeman, Proc Natl Acad Sci USA 106, 17337-17342, 2009).

摘要

端粒是位于真核染色体末端的特殊核蛋白结构,对于染色体稳定性而言是必需的,并由一种名为端粒酶的逆转录酶维持。芽殖酵母已成为分析端粒维持的极为有用的模型系统,因为该生物体提供了广泛的遗传和生化工具。通过对酵母系统的研究,端粒酶研究取得了几个里程碑式的成果。例如,端粒酶缺失的后果首先在芽殖酵母酿酒酵母中得到表征(伦德布拉德和绍斯塔克,《细胞》57:633 - 643,1989年)。端粒酶的催化成分(端粒酶逆转录酶;TERT)同样最初是从这种生物体中克隆出来的(伦德维等人,《遗传学》144:1399 - 1412,1996年)。此外,目前对端粒酶复合物结构和功能的许多理解都源自酵母研究(奥特克西尔和卢,《生物化学年度评论》75:493 - 517,2006年)。在本章中,我们讨论用于研究酵母端粒酶机制和调控的最有用工具之一:引物延伸测定法。该测定法可用于检测端粒酶的总体活性以及持续性,这代表了端粒酶酶学的一个独特方面(卢等人,《分子细胞生物学》23:8440 - 8449,2003年;博索伊和卢,《核酸研究》32:93 - 101,2004年)。它还可用于分析端粒酶调节蛋白的机制(扎普拉等人,《核酸研究》37:354 - 367,2009年;德兹万和弗里曼,《美国国家科学院院刊》106, 17337 - 17342,2009年)。

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