Wu J H, Ippen-Ihler K
Department of Medical Microbiology and Immunology, Texas A&M University, College Station 77843.
J Bacteriol. 1989 Jan;171(1):213-21. doi: 10.1128/jb.171.1.213-221.1989.
The F tra operon region that includes genes trbA, traQ, and trbB was analyzed. Determination of the DNA sequence showed that on the tra operon strand, the trbA gene begins 19 nucleotides (nt) distal to traF and encodes a 115-amino-acid, Mr-12,946 protein. The traQ gene begins 399 nt distal to trbA and encodes a 94-amino-acid, Mr-10,867 protein. The trbB gene, which encodes a 179-amino-acid, Mr-19,507 protein, was found to overlap slightly with traQ; its start codon begins 11 nt before the traQ stop codon. Protein analysis and subcellular fractionation of the products expressed by these genes indicated that the trbB product was processed and that the mature form of this protein accumulated in the periplasm. In contrast, the protein products of trbA and traQ appeared to be unprocessed, membrane-associated proteins. The DNA sequence also revealed the presence of a previously unsuspected locus, artA, in the region between trbA and traQ. The artA open reading frame was found to lie on the DNA strand complementary to that of the F tra operon and could encode a 104-amino-acid, 12,132-dalton polypeptide. Since this sequence would not be expressed as part of the tra operon, the activity of a potential artA promoter region was assessed in a galK fusion vector system. In vivo utilization of the artA promoter and translational start sites was also examined by testing expression of an artA-beta-galactosidase fusion protein. These results indicated that the artA gene is expressed from its own promoter.
对包含trbA、traQ和trbB基因的F质粒转移操纵子区域进行了分析。DNA序列测定表明,在转移操纵子链上,trbA基因起始于traF下游19个核苷酸(nt)处,编码一个含115个氨基酸、分子量为12,946的蛋白质。traQ基因起始于trbA下游399 nt处,编码一个含94个氨基酸、分子量为10,867的蛋白质。发现编码含179个氨基酸、分子量为19,507蛋白质的trbB基因与traQ略有重叠;其起始密码子在traQ终止密码子前11 nt处开始。对这些基因表达产物的蛋白质分析和亚细胞分级分离表明,trbB产物经过了加工,该蛋白质的成熟形式积累在周质中。相比之下,trbA和traQ的蛋白质产物似乎未经过加工,是与膜相关的蛋白质。DNA序列还揭示了在trbA和traQ之间的区域存在一个先前未被怀疑的位点artA。发现artA开放阅读框位于与F质粒转移操纵子互补的DNA链上,可编码一个含104个氨基酸、12,132道尔顿的多肽。由于该序列不会作为转移操纵子的一部分表达,因此在galK融合载体系统中评估了潜在artA启动子区域的活性。还通过检测artA-β-半乳糖苷酶融合蛋白的表达来研究artA启动子和翻译起始位点在体内的利用情况。这些结果表明,artA基因是从其自身的启动子表达的。