Gober J W, Boyd C H, Jarvis M, Mangan E K, Rizzo M F, Wingrove J A
Department of Chemistry and Biochemistry, University of California, Los Angeles 90095-1569, USA.
J Bacteriol. 1995 Jul;177(13):3656-67. doi: 10.1128/jb.177.13.3656-3667.1995.
In Caulobacter crescentus, the genes encoding a single polar flagellum are expressed under cell cycle control. In this report, we describe the characterization of two early class II flagellar genes contained in the orfX-fliP locus. Strains containing mutations in this locus exhibit a filamentous growth phenotype and fail to express class III and IV flagellar genes. A complementing DNA fragment was sequenced and found to contain two potential open reading frames. The first, orfX, is predicted to encode a 105-amino-acid polypeptide that is similar to MopB, a protein which is required for both motility and virulence in Erwinia carotovora. The deduced amino acid sequence of the second open reading frame, fliP, is 264 amino acids in length and shows significant sequence identity with the FliP protein of Escherichia coli as well as virulence proteins of several plant and mammalian pathogens. The FliP homolog in pathogenic organisms has been implicated in the secretion of virulence factors, suggesting that the export of virulence proteins and some flagellar proteins share a common mechanism. The 5' end of orfX-fliP mRNA was determined and revealed an upstream promoter sequence that shares few conserved features with that of other early Caulobacter flagellar genes, suggesting that transcription of orfX-fliP may require a different complement of trans-acting factors. In C. crescentus, orfX-fliP is transcribed under cell cycle control, with a peak of transcriptional activity in the middle portion of the cell cycle. Later in the cell cycle, orfX-fliP expression occurs in both poles of the predivisional cell. Protein fusions to a lacZ reporter gene indicate that FliP is specifically targeted to the swarmer compartment of the predivisional cell.
在新月柄杆菌中,编码单一极鞭毛的基因在细胞周期控制下表达。在本报告中,我们描述了orfX-fliP基因座中两个早期II类鞭毛基因的特征。该基因座发生突变的菌株表现出丝状生长表型,且无法表达III类和IV类鞭毛基因。对一个互补DNA片段进行测序后发现它含有两个潜在的开放阅读框。第一个是orfX,预计编码一个105个氨基酸的多肽,该多肽与胡萝卜软腐欧文氏菌运动性和毒力所需的MopB蛋白相似。第二个开放阅读框fliP推导的氨基酸序列长度为264个氨基酸,与大肠杆菌的FliP蛋白以及几种植物和哺乳动物病原体的毒力蛋白具有显著的序列同一性。致病生物中的FliP同源物与毒力因子分泌有关,这表明毒力蛋白和一些鞭毛蛋白的输出共享一种共同机制。确定了orfX-fliP mRNA的5'端,发现其上游启动子序列与其他早期新月柄杆菌鞭毛基因的启动子序列几乎没有保守特征,这表明orfX-fliP的转录可能需要不同的反式作用因子组合。在新月柄杆菌中,orfX-fliP在细胞周期控制下转录,转录活性在细胞周期中部达到峰值。在细胞周期后期,orfX-fliP表达出现在分裂前细胞的两极。与lacZ报告基因的蛋白质融合表明FliP特异性定位于分裂前细胞的游动细胞区室。