Yamaguchi K, Yamaguchi M
Gene. 1984 Jul-Aug;29(1-2):211-9. doi: 10.1016/0378-1119(84)90181-1.
The nucleotide sequence of a 770-bp ori region of plasmid pSC101 is presented. The sequence shows homologies to some parts of Escherichia coli oriC and phage G4 ori. Several other features are an 80-bp A + T-rich region overlapping a part of the region homologous to oriC, three direct repeats of an 18-bp sequence adjacent to the A + T-rich region, a typical promoter sequence just upstream of the longest open reading frame (ORF) and a long inverted repeat sequence overlapping the putative promoter region. Analysis of successive deletions by BAL31 exonuclease demonstrated that one of the regions homologous to oriC along with the A + T-rich region are essential for autonomous replication of the plasmid. The three 18-bp repeats are responsible for incompatibility phenotype. The region containing the promoter-like sequence is required for expression of a trans-acting function.
本文给出了质粒pSC101 770碱基对ori区域的核苷酸序列。该序列与大肠杆菌oriC和噬菌体G4 ori的某些部分具有同源性。其他几个特征包括一个80碱基对的富含A+T的区域,它与oriC同源区域的一部分重叠;在富含A+T的区域相邻处有18碱基对序列的三个直接重复;在最长开放阅读框(ORF)上游有一个典型的启动子序列;以及一个与推定启动子区域重叠的长反向重复序列。用BAL31核酸外切酶对连续缺失进行分析表明,与oriC同源的区域之一以及富含A+T的区域对质粒的自主复制至关重要。这三个18碱基对的重复序列决定了不相容表型。含有启动子样序列的区域是反式作用功能表达所必需的。