Gallie D R, Kado C I
Department of Plant Pathology, University of California, Davis 95616.
J Bacteriol. 1988 Jul;170(7):3170-6. doi: 10.1128/jb.170.7.3170-3176.1988.
The native 44-kilobase-pair plasmid pTAR, discovered in a grapevine strain of Agrobacterium tumefaciens, contains a single origin of DNA replication confined to a 1.0-kilobase-pair region of the macromolecule. This region (ori) confers functions sufficient for replication in Agrobacterium and Rhizobium species but not in Pseudomonas solanacearum, Pseudomonas glumae, Pseudomonas syringae pv. savastanoi, Xanthomonas campestris pv. campestris, and Escherichia coli. ori contains a repA gene that encodes a 28,000-dalton protein required for replication. Nucleotide sequencing of repA and its promoter region revealed four 8-base-pair palindromic repeats upstream of the repA coding region. Deletion of these repeats alters repA expression and plasmid copy number. Downstream of repA are three additional repeats in a region essential for replication. A locus responsible for plasmid partitioning (parA) and a putative second locus regulating plasmid copy number are part of the origin region and are required for stable plasmid maintenance.
在根癌土壤杆菌的一株葡萄菌株中发现的天然44千碱基对质粒pTAR,含有一个单一的DNA复制起点,该起点局限于该大分子的一个1.0千碱基对区域。这个区域(ori)赋予了在土壤杆菌属和根瘤菌属物种中进行复制所需的功能,但在青枯假单胞菌、颖枯假单胞菌、丁香假单胞菌番茄致病变种、野油菜黄单胞菌野油菜致病变种和大肠杆菌中则不具备。ori含有一个repA基因,该基因编码复制所需的一种28,000道尔顿的蛋白质。repA及其启动子区域的核苷酸测序显示,在repA编码区域上游有四个8碱基对的回文重复序列。这些重复序列的缺失会改变repA的表达和质粒拷贝数。在repA下游的一个对复制至关重要的区域还有另外三个重复序列。一个负责质粒分配的位点(parA)和一个推测的调节质粒拷贝数的第二个位点是起始区域的一部分,是稳定质粒维持所必需的。