Dodd I B, Reed M R, Egan J B
Department of Biochemistry, University of Adelaide, Australia.
Mol Microbiol. 1993 Dec;10(5):1139-50. doi: 10.1111/j.1365-2958.1993.tb00983.x.
The Apl protein of the temperature coliphage 186 represses transcription of the immunity repressor gene and down-regulates lytic transcription. It is shown here that an apl- mutant is competent for lytic development and establishes lysogeny normally but is defective in excision of the prophage. The Apl protein binds between the lytic and lysogenic promoters and also near the phage attachment site, suggesting that its role in excision is direct. Apl thus appears to act as an excisionase as well as a repressor. The pattern of Apl-induced DNase I enhancements indicates that the DNA is bent by Apl. Potential Apl recognition sequences are identified; these sequences are directly repeated several times across each binding region and are spaced 10 or 11 bases apart, suggesting that Apl binds to one face of the DNA helix.
温度型大肠杆菌噬菌体186的Apl蛋白可抑制免疫抑制基因的转录并下调裂解转录。本文表明,apl突变体具有裂解发育能力,能正常建立溶原状态,但在原噬菌体切除方面存在缺陷。Apl蛋白结合在裂解启动子和溶原启动子之间以及噬菌体附着位点附近,这表明其在切除过程中的作用是直接的。因此,Apl似乎既作为一种切除酶又作为一种阻遏物发挥作用。Apl诱导的DNase I增强模式表明DNA被Apl弯曲。确定了潜在的Apl识别序列;这些序列在每个结合区域直接重复几次,间隔为10或11个碱基,这表明Apl结合在DNA螺旋的一个面上。