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噬菌体f1的基因X是噬菌体DNA合成所必需的。框内重叠基因的诱变。

Gene X of bacteriophage f1 is required for phage DNA synthesis. Mutagenesis of in-frame overlapping genes.

作者信息

Fulford W, Model P

出版信息

J Mol Biol. 1984 Sep 15;178(2):137-53. doi: 10.1016/0022-2836(84)90136-0.

Abstract

The gene II protein of bacteriophage f1 is a site-specific endonuclease required for initiation of phage viral strand DNA synthesis. Within gene II is another gene, X, encoding a protein of unknown function identical to the C-terminal 27% of the gene II protein, and separately translated from codon 300 (AUG) of gene II. By oligonucleotide mutagenesis, we constructed phage mutants in which this codon has been changed to UAG (amber) or UUG (leucine), and propagated them on cells carrying a cloned copy of gene X on a plasmid. The amber mutant makes no gene X protein, and cannot grow in the absence of the complementing plasmid; the leucine-inserting mutant can make gene X protein, and grows normally without the plasmid. Without gene X protein, phage DNA synthesis (particularly viral strand synthesis) is impaired. We discuss this finding in the context of other known in-frame overlapping genes (particularly genes A and A* of phage phi X174), many of which are also involved in the specific initiation of DNA synthesis, and suggest applications for the mutagenic strategy we employed.

摘要

噬菌体f1的基因II蛋白是噬菌体病毒链DNA合成起始所需的位点特异性内切核酸酶。基因II内还有另一个基因X,它编码一种功能未知的蛋白质,该蛋白质与基因II蛋白的C端27%相同,并且从基因II的密码子300(AUG)开始单独翻译。通过寡核苷酸诱变,我们构建了噬菌体突变体,其中该密码子已变为UAG(琥珀)或UUG(亮氨酸),并在携带基因X克隆拷贝的质粒的细胞上繁殖它们。琥珀突变体不产生基因X蛋白,并且在没有互补质粒的情况下不能生长;插入亮氨酸的突变体可以产生基因X蛋白,并且在没有质粒的情况下正常生长。没有基因X蛋白,噬菌体DNA合成(特别是病毒链合成)会受到损害。我们在其他已知的框内重叠基因(特别是噬菌体phi X174的基因A和A*)的背景下讨论这一发现,其中许多基因也参与DNA合成的特异性起始,并提出了我们所采用诱变策略的应用。

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