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枯草芽孢杆菌中的双趋化信号通路:一个依赖于σD的基因编码一种具有CheW和CheY同源结构域的新型蛋白质。

Dual chemotaxis signaling pathways in Bacillus subtilis: a sigma D-dependent gene encodes a novel protein with both CheW and CheY homologous domains.

作者信息

Fredrick K L, Helmann J D

机构信息

Section of Microbiology, Cornell University, Ithaca, New York 14853.

出版信息

J Bacteriol. 1994 May;176(9):2727-35. doi: 10.1128/jb.176.9.2727-2735.1994.

Abstract

The alternative sigma factor, sigma D, activates the expression of genes required for chemotaxis and motility in Bacillus subtilis, including those encoding flagellin, hook-associated proteins, and the motor proteins. The sigma D protein is encoded in a large operon which also encodes the structural proteins for the basal body and homologs of the enteric CheW, CheY, CheA, and CheB chemotaxis proteins. We report the identification and molecular characterization of a novel chemotaxis gene, cheV. The predicted CheV gene product contains an amino-terminal CheW homologous domain linked to a response regulator domain of the CheY family, suggesting that either or both of these functions are duplicated. Transcription of cheV initiates from a sigma D-dependent promoter element both in vivo and in vitro, and expression of a cheV-lacZ fusion is completely dependent on sigD. Expression is repressed by nonpolar mutations in structural genes for the basal body, fliM or fliP, indicating that cheV belongs to class III in the B. subtilis flagellar hierarchy. The cheV locus is monocistronic and is located at 123 degrees on the B. subtilis genetic map near the previously defined cheX locus. A cheV mutant strain is motile but impaired in chemotaxis on swarm plates. Surprisingly, an insertion in the CheW homologous domain leads to a more severe defect than an insertion in the CheY homologous domain. The presence of dual pathways for chemotactic signal transduction is consistent with the residual signaling observed in previous studies of cheW mutants (D. W. Hanlon, L. Márques-Magaña, P. B. Carpenter, M. J. Chamberlin, and G. W. Ordal, J. Biol. Chem. 267:12055-12060, 1992).

摘要

替代σ因子σD可激活枯草芽孢杆菌中趋化性和运动性所需基因的表达,包括那些编码鞭毛蛋白、钩相关蛋白和运动蛋白的基因。σD蛋白由一个大操纵子编码,该操纵子还编码基体的结构蛋白以及肠道趋化蛋白CheW、CheY、CheA和CheB的同源物。我们报告了一个新的趋化性基因cheV的鉴定和分子特征。预测的CheV基因产物包含一个与CheY家族响应调节结构域相连的氨基末端CheW同源结构域,这表明这些功能中的一个或两个都被重复。cheV的转录在体内和体外均从一个依赖于σD的启动子元件起始,并且cheV-lacZ融合蛋白的表达完全依赖于sigD。基体结构基因fliM或fliP中的非极性突变会抑制表达,这表明cheV属于枯草芽孢杆菌鞭毛层级中的III类。cheV基因座是单顺反子的,位于枯草芽孢杆菌遗传图谱上123°处,靠近先前定义的cheX基因座。cheV突变株具有运动能力,但在群体平板上的趋化性受损。令人惊讶的是,在CheW同源结构域中的插入导致的缺陷比在CheY同源结构域中的插入更严重。趋化信号转导双重途径的存在与先前对cheW突变体研究中观察到的残留信号一致(D. W. Hanlon、L. Márques-Magaña、P. B. Carpenter、M. J. Chamberlin和G. W. Ordal,《生物化学杂志》267:12055 - 12060,1992)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11be/205414/7e87da087f67/jbacter00027-0266-a.jpg

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