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N端缺失DNA引导蛋白的表达抑制了φX174复制的早期阶段。

The expression of N-terminal deletion DNA pilot proteins inhibits the early stages of phiX174 replication.

作者信息

Ruboyianes Mark V, Chen Min, Dubrava Mathew S, Cherwa James E, Fane Bentley A

机构信息

Department of Plant Sciences and The BIO5 Institute, University of Arizona, Tucson, Arizona 85719, USA.

出版信息

J Virol. 2009 Oct;83(19):9952-6. doi: 10.1128/JVI.01077-09. Epub 2009 Jul 29.

Abstract

The phiX174 DNA pilot protein H contains four predicted C-terminal coiled-coil domains. The region of the gene encoding these structures was cloned, expressed in vivo, and found to strongly inhibit wild-type replication. DNA and protein synthesis was investigated in the absence of de novo H protein synthesis and in wild-type-infected cells expressing the inhibitory proteins (DeltaH). The expression of the DeltaH proteins interfered with early stages of DNA replication, which did not require de novo H protein synthesis, suggesting that the inhibitory proteins interfere with the wild-type H protein that enters the cell with the penetrating DNA. As transcription and protein synthesis are dependent on DNA replication in positive single-stranded DNA life cycles, viral protein synthesis was also reduced. However, unlike DNA synthesis, efficient viral protein synthesis required de novo H protein synthesis, a novel function for this protein. A single amino acid change in the C terminus of protein H was both necessary and sufficient to confer resistance to the inhibitory DeltaH proteins, restoring both DNA and protein synthesis to wild-type levels. DeltaH proteins derived from the resistant mutant did not inhibit wild-type or resistant mutant replication. The inhibitory effects of the DeltaH proteins were lessened by the coexpression of the internal scaffolding protein, which may suppress H-H protein interactions. While coexpression relieved the block in DNA biosynthesis, viral protein synthesis remained suppressed. These data indicate that protein H's role in DNA replication and stimulating viral protein synthesis can be uncoupled.

摘要

噬菌体φX174 DNA引导蛋白H含有四个预测的C端卷曲螺旋结构域。编码这些结构的基因区域被克隆,在体内表达,并发现其强烈抑制野生型复制。在缺乏从头合成H蛋白的情况下以及在表达抑制蛋白(ΔH)的野生型感染细胞中研究了DNA和蛋白质合成。ΔH蛋白的表达干扰了DNA复制的早期阶段,这并不需要从头合成H蛋白,这表明抑制蛋白干扰了与穿透性DNA一起进入细胞的野生型H蛋白。由于转录和蛋白质合成在正链单链DNA生命周期中依赖于DNA复制,病毒蛋白质合成也减少了。然而,与DNA合成不同,高效的病毒蛋白质合成需要从头合成H蛋白,这是该蛋白的一种新功能。蛋白H的C端单个氨基酸变化对于赋予对抑制性ΔH蛋白的抗性既是必要的也是充分的,可将DNA和蛋白质合成恢复到野生型水平。来自抗性突变体的ΔH蛋白不抑制野生型或抗性突变体的复制。内部支架蛋白的共表达减轻了ΔH蛋白的抑制作用,这可能抑制了H-H蛋白相互作用。虽然共表达缓解了DNA生物合成中的阻滞,但病毒蛋白质合成仍然受到抑制。这些数据表明,蛋白H在DNA复制和刺激病毒蛋白质合成中的作用可以分开。

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