Alt-Mörbe J, Stryker J L, Fuqua C, Li P L, Farrand S K, Winans S C
Institut für Biologie III, Universität Freiburg, Germany.
J Bacteriol. 1996 Jul;178(14):4248-57. doi: 10.1128/jb.178.14.4248-4257.1996.
We have determined the DNA sequences of two unlinked regions of octopine-type Ti plasmids that contain genes required for conjugal transfer. Both regions previously were shown to contain sequences that hybridize with tra genes of the nopaline-type Ti plasmid pTiC58. One gene cluster (designated tra) contains a functional oriT site and is probably required for conjugal DNA processing, while the other gene cluster (designated trb) probably directs the synthesis of a conjugal pilus and mating pore. Most predicted Tra and Trb proteins show relatively strong sequence similarity (30 to 50% identity) to the Tra and Trb proteins of the broad-host-range IncP plasmid RP4 and show significantly weaker sequence similarity to Vir proteins found elsewhere on the Ti plasmid. An exception is found in the Ti plasmid TraA protein, which is predicted to be a bifunctional nickase-helicase that has no counterpart in IncP plasmids or among Vir proteins but has homologs in at least six other self-transmissible and mobilizable plasmids. We conclude that this Ti plasmid tra system evolved by acquiring genes from two or three different sources. A similar analysis of the Ti plasmid vir region indicates that it also evolved by appropriating genes from at least two conjugal transfer systems. The widely studied plasmid pTiA6NC previously was found to be nonconjugal and to have a 12.65-kb deletion of DNA relative to other octopine-type Ti plasmids. We show that this deletion removes the promoter-distal gene of the trb region and probably accounts for the inability of this plasmid to conjugate.
我们已经确定了章鱼碱型Ti质粒两个不连锁区域的DNA序列,这两个区域包含接合转移所需的基因。先前已表明这两个区域都含有与胭脂碱型Ti质粒pTiC58的tra基因杂交的序列。一个基因簇(命名为tra)含有一个功能性的oriT位点,可能是接合DNA加工所必需的,而另一个基因簇(命名为trb)可能指导接合菌毛和交配孔的合成。大多数预测的Tra和Trb蛋白与广泛宿主范围的IncP质粒RP4的Tra和Trb蛋白显示出相对较强的序列相似性(30%至50%的同一性),与Ti质粒其他位置发现的Vir蛋白的序列相似性明显较弱。Ti质粒TraA蛋白是个例外,它被预测为一种双功能切口酶-解旋酶,在IncP质粒或Vir蛋白中没有对应物,但在至少其他六种自我传递和可移动质粒中有同源物。我们得出结论,这个Ti质粒tra系统是通过从两三个不同来源获取基因而进化的。对Ti质粒vir区域的类似分析表明,它也是通过从至少两个接合转移系统获取基因而进化的。先前发现广泛研究的质粒pTiA6NC是非接合性的,相对于其他章鱼碱型Ti质粒有一个12.65 kb的DNA缺失。我们表明,这个缺失去除了trb区域的启动子远端基因,这可能是该质粒无法进行接合的原因。