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噬菌体T4基因41蛋白是合成RNA引物所必需的,它也是一种DNA解旋酶。

Bacteriophage T4 gene 41 protein, required for the synthesis of RNA primers, is also a DNA helicase.

作者信息

Venkatesan M, Silver L L, Nossal N G

出版信息

J Biol Chem. 1982 Oct 25;257(20):12426-34.

PMID:6288720
Abstract

Bacteriophage T4 gene 41 protein is one of the two phage proteins previously shown to be required for the synthesis of the pentaribonucleotide primers which initiate the synthesis of new chains in the T4 DNA replication system. We now show that a DNA helicase activity which can unwind short fragments annealed to complementary single-stranded DNA copurifies with the gene 41 priming protein. T4 gene 41 is essential for both the priming and helicase activities, since both are absent after infection by T4 phage with an amber mutation in gene 41. A complete gene 41 product is also required for two other activities previously found in purified preparations of the priming activity: a single-stranded DNA-dependent GTPase (ATPase) and an activity which stimulates strand displacement synthesis catalyzed by T4 DNA polymerase, the T4 gene 44/62 and 45 polymerase accessory proteins, and the T4 gene 32 helix-destabilizing protein (five-protein reaction). The 41 protein helicase requires a single-stranded DNA region adjoining the duplex region and begins unwinding at the 3' terminus of the fragment. There is a sigmoidal dependence on both nucleotide (rGTP, rATP) and protein concentration for this reaction. 41 Protein helicase activity is stimulated by our purest preparation of the T4 gene 61 priming protein, and by the T4 gene 44/62 and 45 polymerase accessory proteins. The direction of unwinding is consistent with the idea that 41 protein facilitates DNA synthesis on duplex templates by destabilizing the helix as it moves 5' to 3' on the displaced strand.

摘要

噬菌体T4基因41蛋白是之前已证明的两种噬菌体蛋白之一,这两种蛋白是在T4 DNA复制系统中起始新链合成的五核糖核苷酸引物合成所必需的。我们现在表明,一种能够解开与互补单链DNA退火的短片段的DNA解旋酶活性与基因41引发蛋白共纯化。T4基因41对于引发活性和解旋酶活性都是必不可少的,因为在用基因41中具有琥珀突变的T4噬菌体感染后,这两种活性都不存在。完整的基因41产物对于之前在引发活性的纯化制剂中发现的另外两种活性也是必需的:一种单链DNA依赖性GTP酶(ATP酶)和一种刺激由T4 DNA聚合酶、T4基因44/62和45聚合酶辅助蛋白以及T4基因32解链蛋白催化的链置换合成的活性(五蛋白反应)。41蛋白解旋酶需要一个与双链区域相邻的单链DNA区域,并从片段的3'末端开始解旋。该反应对核苷酸(rGTP、rATP)和蛋白质浓度均呈S形依赖性。41蛋白解旋酶活性受到我们最纯的T4基因61引发蛋白制剂以及T4基因44/62和45聚合酶辅助蛋白的刺激。解旋方向与以下观点一致,即41蛋白通过在被置换链上从5'向3'移动时使螺旋不稳定,从而促进双链模板上的DNA合成。

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