Sundin G W, Mayfield C T, Zhao Y, Gunasekera T S, Foster G L, Ullrich M S
Department of Plant Pathology and Center for Microbial Ecology, Michigan State University, 103 Center for Integrated Plant Systems, East Lansing, MI 48824, USA.
Mol Genet Genomics. 2004 Jan;270(6):462-76. doi: 10.1007/s00438-003-0945-9. Epub 2003 Nov 21.
Plasmid pPSR1 is a conjugative plasmid originally isolated from Pseudomonas syringae pv. syringae A2, and is a member of the recently described pPT23A plasmid family. We have determined the complete sequence of pPSR1 and found the plasmid to be 72,601 bp in length, encoding 55 ORFs. Putative functions were assigned to 49 ORFs; of these, 24 (49.0%) are involved in plasmid replication, maintenance or conjugation, 17 (34.7%) have roles in virulence or ecological fitness, and eight (16.3%) encode transposase functions as part of mobile elements. pPSR1 carries the effector gene orf34, the mutagenic DNA repair operon rulAB which confers tolerance to ultraviolet radiation, and two genes for methyl-accepting chemotaxis proteins, one of which was located within the novel transposon Tn 5395. The streptomycin resistance transposon Tn 5393a, which carries a strA-strB determinant, was found inserted immediately downstream of the pPSR1 repA gene. Functional analysis of the replication region of pPSR1 indicated that the repA gene and flanking upstream and downstream sequences are required for autonomous replication in P. syringae. Hybridization analyses of the distribution of 11 of the pPSR1 ORFs indicated that many of the ecologically important ORFs were confined to the pathovar P. syringae pv. syringae -either to strains from the local population from which pPSR1 was originally isolated, or strains from a worldwide collection. Conjugative transfer genes and a gene encoding a transcriptional regulator were more widely distributed among several P. syringae pathovars. The sequence analysis of pPSR1 suggests that pPT23A-family plasmids evolve by accumulating genes that are important for host-pathogen interactions or growth on plant hosts, which are incorporated onto a conserved backbone encoding conjugation and stability determinants.
质粒pPSR1是一种接合质粒,最初从丁香假单胞菌丁香致病变种A2中分离得到,是最近描述的pPT23A质粒家族的成员。我们已经确定了pPSR1的完整序列,发现该质粒长度为72,601 bp,编码55个开放阅读框(ORF)。已为49个ORF指定了推定功能;其中,24个(49.0%)参与质粒复制、维持或接合,17个(34.7%)在毒力或生态适应性方面起作用,8个(16.3%)编码作为移动元件一部分的转座酶功能。pPSR1携带效应基因orf34、赋予对紫外线耐受性的诱变DNA修复操纵子rulAB以及两个甲基接受趋化蛋白基因,其中一个位于新型转座子Tn 5395内。携带strA-strB决定簇的链霉素抗性转座子Tn 5393a被发现插入在pPSR1 repA基因的紧邻下游。pPSR1复制区域的功能分析表明,repA基因及其上下游侧翼序列是在丁香假单胞菌中自主复制所必需的。对pPSR1的11个ORF分布的杂交分析表明,许多具有生态重要性的ORF局限于丁香假单胞菌丁香致病变种——要么局限于最初分离出pPSR1的当地种群的菌株,要么局限于来自全球收集的菌株。接合转移基因和一个编码转录调节因子的基因在几个丁香假单胞菌致病变种中分布更广泛。pPSR1的序列分析表明,pPT23A家族质粒通过积累对宿主-病原体相互作用或在植物宿主上生长重要的基因而进化,这些基因被整合到一个编码接合和稳定性决定因素的保守主链上。