van Die I, Bergmans H
Gene. 1984 Dec;32(1-2):83-90. doi: 10.1016/0378-1119(84)90035-0.
The cloned DNA fragment encoding the F72 fimbrial subunit from the uropathogenic Escherichia coli strain AD110 has been identified. The nucleotide sequence of the structural gene and of 196 bp of the noncoding region preceding the gene was determined. The structural gene codes for a polypeptide of 188 amino acid residues, including a 21-residue N-terminal signal sequence. The nucleotide sequence and the deduced amino acid sequence of the F72 gene were compared with the reported sequences of the papA gene (Båga et al., 1984). Both genes code for subunits of fimbriae that are involved in mannose-resistant hemagglutination (MRHA) of human erythrocytes. The available data show that there is absolute homology between the noncoding regions preceding both genes over 129 bp. The two proteins are homologous at the N terminus and C terminus; there is less, but significant, homology in the region between the N and C termini.
已鉴定出编码来自尿路致病性大肠杆菌菌株AD110的F72菌毛亚基的克隆DNA片段。确定了结构基因及其之前196 bp非编码区的核苷酸序列。该结构基因编码一个由188个氨基酸残基组成的多肽,包括一个21个残基的N端信号序列。将F72基因的核苷酸序列和推导的氨基酸序列与已报道的papA基因序列(Båga等人,1984年)进行了比较。这两个基因都编码参与人红细胞甘露糖抗性血凝(MRHA)的菌毛亚基。现有数据表明,两个基因之前的非编码区在129 bp以上存在绝对同源性。这两种蛋白质在N端和C端是同源的;在N端和C端之间的区域同源性较低,但很显著。