Heisig A, Riedel H D, Dobrinski B, Lurz R, Schuster H
Max-Planck-Institut für Molekulare Genetik, Berlin, FRG.
J Mol Biol. 1989 Oct 20;209(4):525-38. doi: 10.1016/0022-2836(89)90591-3.
The immI region of bacteriophage P1 includes the ant/reb gene, which encodes the antirepressor protein, and the c4 gene, which encodes a repressor molecule that negatively regulates antirepressor synthesis. The antirepressor interferes with the activity of the P1 repressor of lytic function, the product of the c1 gene. We have determined the DNA sequences of the immI region of P1 wild-type and the mutants virs, ant16, ant17, and reb22. Using suitable P1 immI DNA subfragments cloned into a vector of the T7 bacteriophage RNA polymerase expression system the antirepressor protein(s) was overproduced. On the basis of positions of immI mutations and the sizes of ant gene products, the following organizational feature of the P1 immI region is suggested: (1) the genes c4 and ant are cotranscribed in that order from the same promoter in the clockwise direction of the P1 genetic map; (2) an open reading frame for an unknown gene is located in between c4 and ant; (3) the site at which the c4 repressor acts is located within the c4 structural gene; (4) two antirepressor proteins of molecular weights 42,000 and 32,000 are encoded by a single open reading frame, with the smaller protein initiating at an in-frame start codon; (5) transcription of immI is regulated via a c1-controlled operator, Op51, indicating a communication between the immunity systems immC and immI.
噬菌体P1的immI区域包括编码抗阻遏蛋白的ant/reb基因和编码对抗阻遏蛋白合成起负调控作用的阻遏分子的c4基因。抗阻遏蛋白会干扰裂解功能的P1阻遏蛋白(c1基因的产物)的活性。我们已经测定了P1野生型以及突变体virs、ant16、ant17和reb22的immI区域的DNA序列。通过将合适的P1 immI DNA亚片段克隆到T7噬菌体RNA聚合酶表达系统的载体中,过量产生了抗阻遏蛋白。根据immI突变的位置和ant基因产物的大小,提出了P1 immI区域的以下组织特征:(1)c4和ant基因从P1遗传图谱顺时针方向的同一个启动子以该顺序共转录;(2)c4和ant之间存在一个未知基因的开放阅读框;(3)c4阻遏蛋白作用的位点位于c4结构基因内;(4)一个单一的开放阅读框编码分子量为42,000和分子量为32,000的两种抗阻遏蛋白,较小的蛋白从框内起始密码子开始;(5)immI的转录通过c1控制的操纵子Op51进行调控,这表明免疫系统immC和immI之间存在联系。