端粒 C 链填充机制:人类 CST-DNA 聚合酶 Alpha-Primase 结构和功能的新见解。

Q1 Biochemistry, Genetics and Molecular Biology
Ci Ji Lim
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引用次数: 0

摘要

真核生物染色体末端的端粒是由一组专门的酶和端粒相关蛋白延长的,在这里统称为端粒 "复制体"。端粒复制体作用于端粒每个染色体末端的独特复制子,即 3' DNA 悬垂。端粒复制过程与复制人类基因组的复制体机制不同。在填充互补的 C 链之前,富含 G 的悬垂首先被延伸。这种悬垂是由端粒酶、一种特殊的核糖核蛋白和逆转录酶延伸的。当端粒酶被单链 DNA 结合蛋白复合物 CTC1-STN1-TEN1 (CST) 取代时,悬垂延伸过程终止。然后,CST 招募 DNA 聚合酶 α-primase,通过填充互补的 C 链来完成端粒复制过程。本章将讨论人类端粒C链填充机制(DNA聚合酶α-primase和CST)的最新结构-功能研究成果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Telomere C-Strand Fill-In Machinery: New Insights into the Human CST-DNA Polymerase Alpha-Primase Structures and Functions.

Telomeres at the end of eukaryotic chromosomes are extended by a specialized set of enzymes and telomere-associated proteins, collectively termed here the telomere "replisome." The telomere replisome acts on a unique replicon at each chromosomal end of the telomeres, the 3' DNA overhang. This telomere replication process is distinct from the replisome mechanism deployed to duplicate the human genome. The G-rich overhang is first extended before the complementary C-strand is filled in. This overhang is extended by telomerase, a specialized ribonucleoprotein and reverse transcriptase. The overhang extension process is terminated when telomerase is displaced by CTC1-STN1-TEN1 (CST), a single-stranded DNA-binding protein complex. CST then recruits DNA polymerase α-primase to complete the telomere replication process by filling in the complementary C-strand. In this chapter, the recent structure-function insights into the human telomere C-strand fill-in machinery (DNA polymerase α-primase and CST) will be discussed.

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来源期刊
Sub-cellular biochemistry
Sub-cellular biochemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
5.90
自引率
0.00%
发文量
33
期刊介绍: The book series SUBCELLULAR BIOCHEMISTRY is a renowned and well recognized forum for disseminating advances of emerging topics in Cell Biology and related subjects. All volumes are edited by established scientists and the individual chapters are written by experts on the relevant topic. The individual chapters of each volume are fully citable and indexed in Medline/Pubmed to ensure maximum visibility of the work.
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