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端粒酶通过使用相邻的RNA基序来识别其模板。

Telomerase recognizes its template by using an adjacent RNA motif.

作者信息

Miller Michael C, Collins Kathleen

机构信息

Department of Molecular and Cell Biology, University of California, 401 Barker Hall, Berkeley, CA 94720-3204, USA.

出版信息

Proc Natl Acad Sci U S A. 2002 May 14;99(10):6585-90. doi: 10.1073/pnas.102024699. Epub 2002 May 7.

Abstract

Telomerase adds telomeric repeats to chromosome 3' ends, forestalling the cellular senescence, apoptosis, and genomic instability that result from telomere loss caused by incomplete DNA replication. The telomerase ribonucleoprotein is dedicated to synthesis of tandem, simple-sequence repeats by virtue of its specialization for copying only a specific template region within the integral RNA. Here, using circularly permuted variants of Tetrahymena thermophila telomerase RNA, we identify the features that allow recognition of the template region within the RNA. We engineered a template-less telomerase ribonucleoprotein that can position and reverse transcribe an exchangeable RNA oligonucleotide template accurately. Only a short "template-recognition" element sequence tag is required to direct efficient use of adjacent 5' residues as a template for telomeric repeat synthesis. Our findings reveal molecular requirements for template selection by telomerase and physically resolve templating from other RNA functions in catalysis.

摘要

端粒酶将端粒重复序列添加到染色体的3'末端,防止因DNA复制不完全导致端粒丢失而引起的细胞衰老、凋亡和基因组不稳定。端粒酶核糖核蛋白专门用于合成串联的简单序列重复序列,因为它仅对整合RNA内的特定模板区域进行复制。在这里,我们使用嗜热四膜虫端粒酶RNA的环状排列变体,确定了能够识别RNA内模板区域的特征。我们设计了一种无模板的端粒酶核糖核蛋白,它可以准确地定位并逆转录一个可交换的RNA寡核苷酸模板。只需要一个短的“模板识别”元件序列标签,就能指导有效地将相邻的5'残基用作端粒重复序列合成的模板。我们的研究结果揭示了端粒酶选择模板的分子要求,并从催化中的其他RNA功能中物理解析了模板化过程。

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本文引用的文献

2
RNA binding domain of telomerase reverse transcriptase.端粒酶逆转录酶的RNA结合结构域
Mol Cell Biol. 2001 Feb;21(4):990-1000. doi: 10.1128/MCB.21.4.990-1000.2001.
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The end of the (DNA) line.(DNA)序列的末端。
Nat Struct Biol. 2000 Oct;7(10):847-50. doi: 10.1038/79594.
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Ciliate telomerase biochemistry.纤毛虫端粒酶生物化学
Annu Rev Biochem. 1999;68:187-218. doi: 10.1146/annurev.biochem.68.1.187.

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