Petrov Vasiliy M, Ng San-San, Karam Jim D
Department of Biochemistry, Tulane University Health Sciences Center, New Orleans, Louisiana 70112, USA.
J Biol Chem. 2002 Sep 6;277(36):33041-8. doi: 10.1074/jbc.M204754200. Epub 2002 Jun 26.
DNA polymerase (gp43) of phage T4 plays two biological roles, one as an essential DNA binding replication enzyme and the other as an mRNA-specific autogenous translational repressor. Binding of T4 gp43 to its mRNA target (translational operator RNA) interferes with gp43-DNA interactions, but it is unclear how the protein determinants for binding DNA are affected by the dynamics of gp43-mRNA interactions. We have used RB69 gp43, a natural variant of the T4 enzyme whose crystal structure has been determined to identify protein sites that respond to the interaction with specific RNA. We used protein phosphorylation markers, photocross-linking studies, protease sensitivity assays, and mutational analyses to examine the effects of operator RNA on the enzyme's five structural domains (N, exo, palm, fingers, and thumb). Our studies suggest that this RNA affects gp43-DNA interactions through global effects on protein structure that occlude DNA-binding sites but leave the enzyme accessible to interactions with the sliding clamp (RB69 gp45) and possibly other polymerase accessory proteins. We discuss the possible biological significance of putative RNA-binding motifs in the N and palm domains of RB69 gp43.
噬菌体T4的DNA聚合酶(gp43)具有两种生物学功能,一种是作为必不可少的DNA结合复制酶,另一种是作为mRNA特异性的自体翻译阻遏物。T4 gp43与其mRNA靶标(翻译操纵子RNA)的结合会干扰gp43与DNA的相互作用,但尚不清楚DNA结合的蛋白质决定因素如何受到gp43与mRNA相互作用动力学的影响。我们使用了RB69 gp43,它是T4酶的天然变体,其晶体结构已被确定,以识别与特定RNA相互作用时发生响应的蛋白质位点。我们使用蛋白质磷酸化标记、光交联研究、蛋白酶敏感性分析和突变分析来研究操纵子RNA对该酶五个结构域(N、外切酶、手掌、手指和拇指)的影响。我们的研究表明,这种RNA通过对蛋白质结构的全局影响来影响gp43与DNA的相互作用,这些影响会封闭DNA结合位点,但使该酶仍可与滑动夹钳(RB69 gp45)以及可能的其他聚合酶辅助蛋白相互作用。我们讨论了RB69 gp43的N和手掌结构域中假定的RNA结合基序可能具有的生物学意义。