Perkus M E, Shub D A
J Virol. 1985 Oct;56(1):40-8. doi: 10.1128/JVI.56.1.40-48.1985.
Although most early transcription from SPO1, a lytic DNA bacteriophage of Bacillus subtilis, is specified by the 12.6-kilobase region of the terminal redundancy, early genes from this region have not been identified by standard genetic means. We mapped genes to DNA regions of the SPO1 terminal redundancy by analyzing in vitro protein synthesis from isolated SPO1 restriction fragments in an Escherichia coli-coupled transcription-translation cell-free system. DNA from the terminal redundancy directs the synthesis in vitro of eleven proteins, e3, e4, e6, e7, e9, e12, e15, e16, e18, e20, and e21, which correspond in mobility on sodium dodecyl sulfate-polyacrylamide gels with authentic SPO1 early proteins. From their mapped positions on the DNA, genes were positioned downstream from most, but not all, of the twelve early promoter regions identified in vitro in the terminal redundancy. The temporal patterns of early protein synthesis in vivo suggest a differential turning on and off of early promoters in the terminal redundancy. Both in vivo and in vitro evidence suggests the existence of previously unidentified early promoter regions upstream from the genes for e6 and e4 as well as a middle promoter region upstream from the gene for e16.
虽然枯草芽孢杆菌的裂解性DNA噬菌体SPO1的大多数早期转录由末端冗余的12.6千碱基区域指定,但该区域的早期基因尚未通过标准遗传学方法鉴定出来。我们通过在大肠杆菌偶联转录-翻译无细胞系统中分析从分离的SPO1限制性片段进行的体外蛋白质合成,将基因定位到SPO1末端冗余的DNA区域。来自末端冗余的DNA在体外指导合成11种蛋白质,即e3、e4、e6、e7、e9、e12、e15、e16、e18、e20和e21,它们在十二烷基硫酸钠-聚丙烯酰胺凝胶上的迁移率与真正的SPO1早期蛋白质相对应。根据它们在DNA上的定位,基因位于末端冗余中体外鉴定出的12个早期启动子区域中的大多数(但不是全部)的下游。体内早期蛋白质合成的时间模式表明末端冗余中早期启动子存在差异开启和关闭。体内和体外证据均表明,在e6和e4基因上游存在先前未鉴定的早期启动子区域,以及在e16基因上游存在一个中间启动子区域。