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接合性质粒RP4转移起始位点侧翼基因的核苷酸序列及基因组织

Nucleotide sequence and organization of genes flanking the transfer origin of promiscuous plasmid RP4.

作者信息

Ziegelin G, Pansegrau W, Strack B, Balzer D, Kröger M, Kruft V, Lanka E

机构信息

Max-Planck-Institut für Molekulare Genetik, Abteilung Schuster, Berlin, F.R.G.

出版信息

DNA Seq. 1991;1(5):303-27. doi: 10.3109/10425179109020786.

DOI:10.3109/10425179109020786
PMID:1665997
Abstract

The nucleotide sequence of the relaxase operon and the leader operon which are part of the Tra1 region of the promiscuous plasmid RP4 was determined. These two polycistronic operons are transcribed divergently from an intergenic region of about 360 bp containing the transfer origin and six close-packed genes. A seventh gene completely overlaps another one in a different reading frame. Conjugative DNA transfer proceeds unidirectionally from oriT with the leader operon heading the DNA to be transferred. The traI gene of the relaxase operon includes within its 3' terminal region a promoter controlling the 7.2-kb polycistronic primase operon. Comparative sequence analysis of the closely related IncP plasmid R751 revealed a similarity of 74% at the nucleotide sequence level, indicating that RP4 and R751 have evolved from a common ancestor. The gene organization of relaxase- and leader operons is conserved among the two IncP plasmids. The transfer origins and the genes traJ and traK exhibit greater sequence divergence than the other genes of the corresponding operons. This is conceivable, because traJ and traK are specificity determinants, the products of which can only recognize homologous oriT sequences. Surprisingly, the organization of the IncP relaxase operons resembles that of the virD operon of Agrobacterium tumefaciens plasmid pTiA6 that mediates DNA transfer to plant cells by a process analogous to bacterial conjugation. Furthermore, the IncP TraG proteins and the product of the virD4 gene share extended amino acid sequence similarity, suggesting a functional relationship.

摘要

测定了接合性质粒RP4的Tra1区域中松弛酶操纵子和前导操纵子的核苷酸序列。这两个多顺反子操纵子从一个约360 bp的基因间区域双向转录,该区域包含转移起始点和六个紧密排列的基因。第七个基因在不同的阅读框中与另一个基因完全重叠。接合性DNA转移从oriT单向进行,前导操纵子引导待转移的DNA。松弛酶操纵子的traI基因在其3'末端区域内包含一个控制7.2 kb多顺反子引发酶操纵子的启动子。对密切相关的IncP质粒R751的比较序列分析显示,核苷酸序列水平上的相似性为74%,表明RP4和R751是由一个共同祖先进化而来的。松弛酶操纵子和前导操纵子的基因组织在这两个IncP质粒中是保守的。转移起始点以及traJ和traK基因比相应操纵子的其他基因表现出更大的序列差异。这是可以想象的,因为traJ和traK是特异性决定因素,其产物只能识别同源oriT序列。令人惊讶的是,IncP松弛酶操纵子的组织类似于根癌土壤杆菌质粒pTiA6的virD操纵子,后者通过类似于细菌接合的过程介导DNA转移到植物细胞中。此外,IncP TraG蛋白和virD4基因的产物具有广泛的氨基酸序列相似性,表明它们之间存在功能关系。

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