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人类DNA聚合酶的结构与功能关系

Structural and functional relationships of human DNA polymerases.

作者信息

Hao H, Jiang Y, Zhang S J, Zhang P, Zeng R X, Lee M Y

机构信息

Department of Medicine and Biochemistry & Molecular Biology, University of Miami, FL 33101.

出版信息

Chromosoma. 1992;102(1 Suppl):S121-7. doi: 10.1007/BF02451795.

Abstract

A continuing theme of our laboratory has been the understanding of human DNA polymerases at the structural level. We have purified DNA polymerases delta, epsilon and alpha from human placenta. Monoclonal antibodies to these polymerases were isolated and used as tools to study their immunochemical relationships. These studies have shown that while DNA polymerases delta, epsilon and alpha are discrete proteins, they must share common structural features by virtue of the ability of several of our monoclonal antibodies to exhibit cross-reactivity. A second approach we have taken is the molecular cloning of human DNA polymerase delta and epsilon. We have cloned the DNA polymerase delta cDNA, and this has allowed us to compare its primary structure to those of human polymerase alpha and other members of this polymerase family. Multiple sequence alignments have revealed that human DNA polymerase delta is also closely related to the herpes virus family of DNA polymerases. In situ hybridization has shown that the human DNA polymerase delta gene is localized to chromosome 19 q13.3-q13.4. In order to further determine the functional regions of the DNA polymerase delta structure we are currently expressing human pol delta in E. coli and baculovirus systems. Other work in our laboratory is directed toward examining the expression of DNA polymerase delta during the cell cycle.

摘要

我们实验室的一个持续研究主题是在结构层面理解人类DNA聚合酶。我们从人胎盘中纯化了DNA聚合酶δ、ε和α。分离出针对这些聚合酶的单克隆抗体,并将其用作研究它们免疫化学关系的工具。这些研究表明,虽然DNA聚合酶δ、ε和α是不同的蛋白质,但由于我们的几种单克隆抗体具有交叉反应能力,它们必定具有共同的结构特征。我们采取的第二种方法是对人类DNA聚合酶δ和ε进行分子克隆。我们已经克隆了DNA聚合酶δ的cDNA,这使我们能够将其一级结构与人类聚合酶α以及该聚合酶家族的其他成员进行比较。多序列比对显示,人类DNA聚合酶δ也与疱疹病毒DNA聚合酶家族密切相关。原位杂交表明,人类DNA聚合酶δ基因定位于19号染色体q13.3 - q13.4区域。为了进一步确定DNA聚合酶δ结构的功能区域,我们目前正在大肠杆菌和杆状病毒系统中表达人类聚合酶δ。我们实验室的其他工作旨在研究细胞周期中DNA聚合酶δ的表达情况。

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