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Genomic organization and expression of Campylobacter flagellin genes.

机译:弯曲杆菌鞭毛蛋白基因的基因组组织和表达。

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摘要

Campylobacter coli VC167, which undergoes an antigenic flagellar variation, contains two full-length flagellin genes, flaA and flaB, that are located adjacent to one another in a tandem orientation and are 91.5% homologous. The gene product of flaB, which has an Mr of 58,946, has 93% sequence homology to the gene product of flaA, which has an Mr of 58,916 (S. M. Logan, T. J. Trust, and P. Guerry, J. Bacteriol. 171:3031-3038, 1989). Mutational analyses and primer extension experiments indicated that the two genes are transcribed under the control of distinct promoters but that they are expressed concomitantly in the same cell, regardless of the antigenic phase of flagella being produced. The flaA gene, which was expressed at higher levels than the flaB gene in both phases, was transcribed from a typical sigma 28-type promoter, whereas the flaB promoter was unusual. A mutant producing only the flaB gene product did not synthesize a flagellar filament and was nonmotile. Southern blot analysis indicated that flagellar antigenic variation involves a rearrangement of flagellin sequence information rather than the alternate expression of the two distinct genes.
机译:经历抗原性鞭毛变异的弯曲杆菌VC167包含两个全长鞭毛蛋白基因flaA和flaB,它们以串联方向彼此相邻,并且具有91.5%的同源性。 flaB的基因产物的Mr为58,946,与flaA的基因产物的Mr.为58,916具有93%的序列同源性(SM Logan,TJ Trust和P. Guerry,J. Bacteriol。171:3031 -3038,1989)。突变分析和引物延伸实验表明,这两个基因在不同启动子的控制下转录,但无论鞭毛的抗原相如何,它们都在同一细胞中同时表达。从一个典型的sigma 28型启动子转录了在两个阶段均比flaB基因更高水平表达的flaA基因,而flaB启动子则是异常的。仅产生flaB基因产物的突变体不合成鞭毛丝并且不活动。 Southern印迹分析表明鞭毛抗原变异涉及鞭毛蛋白序列信息的重排,而不是两个不同基因的交替表达。

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