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T4相关噬菌体的DNA聚合酶。

DNA polymerase of the T4-related bacteriophages.

作者信息

Karam J D, Konigsberg W H

机构信息

Department of Biochemistry, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.

出版信息

Prog Nucleic Acid Res Mol Biol. 2000;64:65-96. doi: 10.1016/s0079-6603(00)64002-3.

Abstract

The DNA polymerase of bacteriophage T4, product of phage gene 43 (gp43), has served as a model replicative DNA polymerase in nucleic acids research for nearly 40 years. The base-selection (polymerase, or Pol) and editing (3'-exonuclease, or Exo) functions of this multifunctional protein, which have counterparts in the replicative polymerases of other organisms, are primary determinants of the high fidelity of DNA synthesis in phage DNA replication. T4 gp43 is considered to be a member of the "B family" of DNA-dependent DNA polymerases (those resembling eukaryotic Pol alpha) because it exhibits striking similarities in primary structure to these enzymes. It has been extensively analyzed at the genetic, physiological, and biochemical levels; however, relationships between the in vivo properties of this enzyme and its physical structure have not always been easy to explain due to a paucity of structural data on the intact molecule. However, gp43 from phage RB69, a phylogenetic relative of T4, was crystallized and its structure solved in a complex with single-stranded DNA occupying the Exo site, as well as in the unliganded form. Analyses with these crystals, and crystals of a T4 gp43 proteolytic fragment harboring the Exo function, are opening new avenues to interpret existing biological and biochemical data on the intact T4 enzyme and are revealing new aspects of the microanatomy of gp43 that can now be explored further for functional significance. We summarize our current understanding of gp43 structure and review the physiological roles of this protein as an essential DNA-binding component of the multiprotein T4 DNA replication complex and as a nucleotide-sequence-specific RNA-binding translational repressor that controls its own biosynthesis and activity in vivo. We also contrast the properties of the T4 DNA replication complex to the functionally analogous complexes of other organisms, particularly Escherichia coli, and point out some of the unanswered questions about gp43 and T4 DNA replication.

摘要

噬菌体T4的DNA聚合酶是噬菌体基因43(gp43)的产物,在核酸研究中作为一种复制性DNA聚合酶的模型已近40年。这种多功能蛋白质的碱基选择(聚合酶,或Pol)和编辑(3'-外切核酸酶,或Exo)功能在其他生物体的复制性聚合酶中也有对应功能,是噬菌体DNA复制中DNA合成高保真度的主要决定因素。T4 gp43被认为是依赖DNA的DNA聚合酶“B家族”(类似于真核生物Polα的那些酶)的成员,因为它在一级结构上与这些酶表现出显著的相似性。它已在遗传、生理和生化水平上进行了广泛分析;然而,由于缺乏完整分子的结构数据,这种酶的体内性质与其物理结构之间的关系并不总是容易解释。然而,来自噬菌体RB69(T4的系统发育亲缘种)的gp43被结晶,其结构在与占据Exo位点的单链DNA形成的复合物中以及未结合配体的形式下得到了解决。对这些晶体以及具有Exo功能的T4 gp43蛋白水解片段的晶体进行分析,正在为解释关于完整T4酶的现有生物学和生化数据开辟新途径,并揭示gp43微观结构的新方面,现在可以进一步探索其功能意义。我们总结了目前对gp43结构的理解,并回顾了这种蛋白质作为多蛋白T4 DNA复制复合物中必需的DNA结合成分以及作为控制其自身体内生物合成和活性的核苷酸序列特异性RNA结合翻译阻遏物的生理作用。我们还将T4 DNA复制复合物的性质与其他生物体(特别是大肠杆菌)的功能类似复合物进行了对比,并指出了一些关于gp43和T4 DNA复制尚未解决的问题。

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