Kamio Y, Tabuchi A, Itoh Y, Katagiri H, Terawaki Y
J Bacteriol. 1984 Apr;158(1):307-12. doi: 10.1128/jb.158.1.307-312.1984.
The nucleotide sequence of the whole mini-Rts1 genome consisting of 1,855 base pairs was determined. In addition to the cluster of five 24-base-pair direct repeats previously detected (Y. Kamio and Y. Terawaki, J. Bacteriol. 155:1185-1191, 1983), another cluster of three 21-base-pair direct repeats was found. All eight repeats were located in one direction and contained a consensus sequence TTCCCCPyPyPuPuCACACACC. Between the two clusters, a large open reading frame that could encode a 32,980-dalton polypeptide consisting of 288 amino acids was assigned. The molecular size predicted from the amino acid composition was close to the value of a unique mini-Rts1 product, the RepA protein, newly determined in minicells. A copy mutant of mini-Rts1 obtained in vitro by hydroxylamine treatment contained two-base-pair substitutions, one of which was located in the RepA protein coding region, and the other was close to the region where the oriC homologous sequences exist.
测定了由1855个碱基对组成的整个微小Rts1基因组的核苷酸序列。除了先前检测到的五个24碱基对直接重复序列簇(Y. Kamio和Y. Terawaki,《细菌学杂志》155:1185 - 1191,1983年)外,还发现了另一个由三个21碱基对直接重复序列组成的簇。所有八个重复序列都位于一个方向,并且包含共有序列TTCCCCPyPyPuPuCACACACC。在这两个簇之间,指定了一个大的开放阅读框,它可以编码一个由288个氨基酸组成的32,980道尔顿的多肽。根据氨基酸组成预测的分子大小接近于在微小细胞中新确定的独特微小Rts1产物RepA蛋白的值。通过羟胺处理在体外获得的微小Rts1的一个拷贝突变体包含两个碱基对的替换,其中一个位于RepA蛋白编码区,另一个靠近oriC同源序列存在的区域。