Ouhammouch M, Orsini G, Brody E N
Department of Biological Sciences, State University of New York at Buffalo 14260.
J Bacteriol. 1994 Jul;176(13):3956-65. doi: 10.1128/jb.176.13.3956-3965.1994.
The asiA gene of bacteriophage T4 encodes a 10-kDa peptide which binds strongly in vitro to the sigma 70 subunit of Escherichia coli RNA polymerase, thereby weakening sigma 70-core interactions and inhibiting sigma 70-dependent transcription. To assess the physiological role of this protein, we have introduced an amber mutation into the proximal portion of the asiA gene. On suppressor-deficient hosts, this mutant phage (amS22) produces minute plaques and exhibits a pronounced delay in phage production. During these mutant infections, T4 DNA synthesis is strongly delayed, suggesting that the AsiA protein plays an important role during the prereplicative period of phage T4 development. The kinetics of protein synthesis show clearly that while T4 early proteins are synthesized normally, those expressed primarily via the middle mode exhibit a marked inhibition. In fact, the pattern of protein synthesis after amS22 infection resembles greatly that seen after infection by amG1, an amber mutant in motA, a T4 gene whose product is known to control middle mode RNA synthesis. The amber mutations in the motA and asiA genes complement, both for phage growth and for normal kinetics of middle mode protein synthesis. Furthermore, primer extension analyses show that three different MotA-dependent T4 middle promoters are not recognized after infection by the asiA mutant phage. Thus, in conjunction with the MotA protein, the AsiA protein is required for transcription activation at T4 middle mode promoters.
噬菌体T4的asiA基因编码一种10 kDa的肽,该肽在体外能与大肠杆菌RNA聚合酶的σ70亚基紧密结合,从而削弱σ70与核心酶的相互作用并抑制依赖σ70的转录。为了评估这种蛋白质的生理作用,我们在asiA基因的近端引入了一个琥珀突变。在缺乏抑制基因的宿主上,这种突变噬菌体(amS22)产生微小噬菌斑,并在噬菌体产生过程中表现出明显延迟。在这些突变感染期间,T4 DNA合成强烈延迟,这表明AsiA蛋白在噬菌体T4发育的复制前期发挥重要作用。蛋白质合成动力学清楚地表明,虽然T4早期蛋白质正常合成,但主要通过中期模式表达的蛋白质表现出明显抑制。事实上,amS22感染后的蛋白质合成模式与motA基因(其产物已知控制中期模式RNA合成的一个T4基因)的琥珀突变体amG1感染后的模式非常相似。motA和asiA基因中的琥珀突变在噬菌体生长和中期模式蛋白质合成的正常动力学方面相互补充。此外,引物延伸分析表明,asiA突变噬菌体感染后,三种不同的依赖MotA的T4中期启动子未被识别。因此,与MotA蛋白一起,AsiA蛋白是T4中期模式启动子转录激活所必需的。