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端粒酶引物特异性与染色体修复。

Telomerase primer specificity and chromosome healing.

作者信息

Harrington L A, Greider C W

机构信息

Cold Spring Harbor Laboratory, New York 11724.

出版信息

Nature. 1991 Oct 3;353(6343):451-4. doi: 10.1038/353451a0.

Abstract

Chromosome healing by de novo telomere addition at nontelomeric sites has been well characterized in several organisms. The Tetrahymena telomerase ribonucleoprotein uses an internal RNA template to catalyse d(TTGGGG)n telomere addition to the 3' end of telomeric sequence in vitro and in vivo. Studies of telomerase RNA indicated that hybridization of the RNA template region, 5'-CAACCCCAA-3', to the 3' end of single-stranded telomeric oligonucleotides might be important for primer recognition and utilization. The apparent requirement of telomerase for pre-existing telomeric sequence has raised questions regarding its role in chromosome healing. We report here that Tetrahymena telomerase can specifically elongate single-stranded DNA oligonucleotides whose termini are not complementary to the RNA template sequence 5'-CAACCCCAA-3'. These data suggest that telomerase may be able to heal chromosomes directly in vivo.

摘要

在几种生物体中,通过在非端粒位点从头添加端粒来修复染色体的现象已得到充分表征。嗜热四膜虫端粒酶核糖核蛋白利用内部RNA模板在体外和体内催化d(TTGGGG)n端粒添加到端粒序列的3'末端。对端粒酶RNA的研究表明,RNA模板区域5'-CAACCCCAA-3'与单链端粒寡核苷酸3'末端的杂交可能对引物识别和利用很重要。端粒酶对预先存在的端粒序列的明显需求引发了关于其在染色体修复中作用的问题。我们在此报告,嗜热四膜虫端粒酶可以特异性地延长其末端与RNA模板序列5'-CAACCCCAA-3'不互补的单链DNA寡核苷酸。这些数据表明,端粒酶可能能够在体内直接修复染色体。

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