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端粒复制的大终场 CST。

CST for the grand finale of telomere replication.

机构信息

Swiss Institute for Experimental Cancer Research (ISREC); School of Life Sciences; Frontiers in Genetics National Center of Competence in Research; Ecole Polytechnique Fédérale de Lausanne (EPFL); Lausanne, Switzerland.

出版信息

Nucleus. 2013 Jul-Aug;4(4):277-82. doi: 10.4161/nucl.25701. Epub 2013 Jul 10.

Abstract

Telomeric DNA at eukaryotic chromosome ends terminates with single stranded 3' G-rich overhangs. The overhang is generated by the interplay of several dynamic processes including semiconservative DNA replication, 3' end elongation by telomerase, C-strand fill-in synthesis and nucleolytic processing. The mammalian CST (CTC1-STN1-TEN1) complex is directly involved at several stages of telomere end formation. Elucidation of its structural organization and identification of interaction partners support the notion that mammalian CST is, as its yeast counterpart, a RPA-like complex. CST binding at mammalian telomere 3' overhangs increases upon their elongation by telomerase. Formation of a trimeric CST complex at telomeric 3'overhangs leads to telomerase inhibition and at the same time mediates a physical interaction with DNA polymerase-α. Thus CST seems to play critical roles in coordinating telomerase elongation and fill-in synthesis to complete telomere replication.

摘要

真核染色体末端的端粒 DNA 以单链 3' G 丰富的突出端终止。这种突出端是由几个动态过程相互作用产生的,包括半保守性 DNA 复制、端粒酶介导的 3' 端延伸、C 链填充合成和核酸酶加工。哺乳动物 CST(CTC1-STN1-TEN1)复合物直接参与端粒末端形成的几个阶段。阐明其结构组织并鉴定相互作用伙伴支持哺乳动物 CST 是一种与酵母 CST 类似的 RPA 样复合物的观点。端粒酶延长哺乳动物端粒 3' 突出端时,CST 结合增加。在端粒 3' 突出端形成三聚体 CST 复合物会抑制端粒酶,并同时介导与 DNA 聚合酶-α 的物理相互作用。因此,CST 似乎在协调端粒酶延伸和填充合成以完成端粒复制方面发挥着关键作用。

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