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噬菌体P22 DNA包装系列的起始。对改变包装装置DNA靶标特异性的突变体的分析。

Initiation of bacteriophage P22 DNA packaging series. Analysis of a mutant that alters the DNA target specificity of the packaging apparatus.

作者信息

Casjens S, Huang W M, Hayden M, Parr R

出版信息

J Mol Biol. 1987 Apr 5;194(3):411-22. doi: 10.1016/0022-2836(87)90671-1.

Abstract

Bacteriophage P22 is thought to package its double-stranded DNA chromosome from concatemeric replicating DNA in a "processive" sequential fashion. According to this model, during the initial packaging event in such a series the packaging apparatus recognizes a nucleotide sequence, called pac, on the DNA, and then condenses DNA within the coat protein shell unidirectionally from that point. DNA ends are generated near the pac site before or during the condensation reaction. The opposite end of the mature chromosome is created by a cut made in the DNA after a complete chromosome is condensed within the phage head. Subsequent packaging events on that concatemeric DNA begin at the end generated by the headful cut of the previous event and proceed in the same direction as the previous event. We report here the identification of a consensus nucleotide sequence for the pac site, and present evidence that supports the idea that the gene 3 protein is a central participant in this recognition event. In addition, we tentatively locate the portion of the gene 3 protein that contacts the pac site during the initiation of packaging.

摘要

噬菌体P22被认为是以“连续”的顺序方式从串联复制的DNA中包装其双链DNA染色体。根据这个模型,在这样一系列的初始包装事件中,包装装置识别DNA上一个叫做pac的核苷酸序列,然后从该点开始单向地在衣壳蛋白壳内浓缩DNA。在浓缩反应之前或期间,在pac位点附近产生DNA末端。成熟染色体的另一端是在完整的染色体在噬菌体头部内浓缩后,通过在DNA上进行切割而形成的。在该串联DNA上的后续包装事件从前一事件的满头部切割产生的末端开始,并以前一事件相同的方向进行。我们在此报告pac位点共有核苷酸序列的鉴定,并提供证据支持基因3蛋白是这一识别事件的核心参与者这一观点。此外,我们初步定位了基因3蛋白在包装起始过程中与pac位点接触的部分。

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