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T4 噬菌体 DNA 复制的起始和复制叉动力学:在噬菌体 T4 及其相关病毒系列的病毒学期刊上的综述。

Initiation of bacteriophage T4 DNA replication and replication fork dynamics: a review in the Virology Journal series on bacteriophage T4 and its relatives.

机构信息

Department of Biochemistry, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Virol J. 2010 Dec 3;7:358. doi: 10.1186/1743-422X-7-358.

Abstract

Bacteriophage T4 initiates DNA replication from specialized structures that form in its genome. Immediately after infection, RNA-DNA hybrids (R-loops) occur on (at least some) replication origins, with the annealed RNA serving as a primer for leading-strand synthesis in one direction. As the infection progresses, replication initiation becomes dependent on recombination proteins in a process called recombination-dependent replication (RDR). RDR occurs when the replication machinery is assembled onto D-loop recombination intermediates, and in this case, the invading 3' DNA end is used as a primer for leading strand synthesis. Over the last 15 years, these two modes of T4 DNA replication initiation have been studied in vivo using a variety of approaches, including replication of plasmids with segments of the T4 genome, analysis of replication intermediates by two-dimensional gel electrophoresis, and genomic approaches that measure DNA copy number as the infection progresses. In addition, biochemical approaches have reconstituted replication from origin R-loop structures and have clarified some detailed roles of both replication and recombination proteins in the process of RDR and related pathways. We will also discuss the parallels between T4 DNA replication modes and similar events in cellular and eukaryotic organelle DNA replication, and close with some current questions of interest concerning the mechanisms of replication, recombination and repair in phage T4.

摘要

噬菌体 T4 从其基因组中形成的专门结构开始进行 DNA 复制。感染后立即,在(至少一些)复制起点处出现 RNA-DNA 杂交(R 环),退火的 RNA 作为一个引物,用于在一个方向上进行前导链合成。随着感染的进展,复制起始变得依赖于重组蛋白,这一过程称为重组依赖的复制(RDR)。当复制机制组装到 D 环重组中间体上时,就会发生 RDR,在这种情况下,入侵的 3' DNA 末端被用作前导链合成的引物。在过去的 15 年中,人们使用各种方法在体内研究了 T4 DNA 复制起始的这两种模式,包括用 T4 基因组的片段复制质粒、通过二维凝胶电泳分析复制中间体,以及通过基因组方法测量感染过程中 DNA 拷贝数。此外,生化方法已从起始 R 环结构中重建了复制,并阐明了复制和重组蛋白在 RDR 及相关途径中的一些详细作用。我们还将讨论 T4 DNA 复制模式与细胞和真核细胞器 DNA 复制中类似事件之间的平行关系,并以有关噬菌体 T4 复制、重组和修复机制的一些当前关注问题结束。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b61/3016281/f669af2cd852/1743-422X-7-358-1.jpg

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