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真核生物DNA复制起点双向前导链合成建立的机制

Mechanism of Bidirectional Leading-Strand Synthesis Establishment at Eukaryotic DNA Replication Origins.

作者信息

Aria Valentina, Yeeles Joseph T P

机构信息

Division of Protein and Nucleic Acid Chemistry, Medical Research Council Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK.

Division of Protein and Nucleic Acid Chemistry, Medical Research Council Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK.

出版信息

Mol Cell. 2018 Nov 16;73(2):199-211.e10. doi: 10.1016/j.molcel.2018.10.019.

Abstract

DNA replication commences at eukaryotic replication origins following assembly and activation of bidirectional CMG helicases. Once activated, CMG unwinds the parental DNA duplex and DNA polymerase α-primase initiates synthesis on both template strands. By utilizing an origin-dependent replication system using purified yeast proteins, we have mapped start sites for leading-strand replication. Synthesis is mostly initiated outside the origin sequence. Strikingly, rightward leading strands are primed left of the origin and vice versa. We show that each leading strand is established from a lagging-strand primer synthesized by the replisome on the opposite side of the origin. Preventing elongation of primers synthesized left of the origin blocked rightward leading strands, demonstrating that replisomes are interdependent for leading-strand synthesis establishment. The mechanism we reveal negates the need for dedicated leading-strand priming and necessitates a crucial role for the lagging-strand polymerase Pol δ in connecting the nascent leading strand with the advancing replisome.

摘要

在双向CMG解旋酶组装并激活后,DNA复制在真核生物复制起点开始。一旦被激活,CMG解开亲本DNA双链,DNA聚合酶α-引发酶在两条模板链上启动合成。通过使用纯化的酵母蛋白构建依赖于起点的复制系统,我们绘制了前导链复制的起始位点。合成大多在起点序列之外起始。引人注目的是,向右的前导链在起点左侧起始引发,反之亦然。我们表明,每条前导链都由复制体在起点另一侧合成的滞后链引物建立。阻止在起点左侧合成的引物延伸会阻断向右的前导链,这表明复制体在前导链合成建立过程中相互依赖。我们揭示的机制消除了对专用前导链引发的需求,并且滞后链聚合酶Pol δ在将新生前导链与前进的复制体连接起来方面起着关键作用。

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