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lcrE基因是小肠结肠炎耶尔森氏菌O:3的lcr区域中一个操纵子的一部分。

The lcrE gene is part of an operon in the lcr region of Yersinia enterocolitica O:3.

作者信息

Viitanen A M, Toivanen P, Skurnik M

机构信息

Department of Medical Microbiology, Turku University, Finland.

出版信息

J Bacteriol. 1990 Jun;172(6):3152-62. doi: 10.1128/jb.172.6.3152-3162.1990.

Abstract

The low-calcium response (lcr) region of the virulence plasmid of Yersinia pestis, Yersinia pseudotuberculosis, and Yersinia enterocolitica has been associated with calcium-dependent growth of bacteria. Mutations in the previously identified lcrE locus within the lcr region lack the repressor control of production of the lcr specific proteins, Yersinia outer membrane proteins (Yops) and V and W antigens. We sequenced a 3.3-kilobase-pair BamHI-ClaI fragment of the lcrE locus of pYVO3, the virulence plasmid of Y. enterocolitica O:3. The sequence of lcrE locus revealed six tightly packed open reading frames (ORFs), one of which was identified as the structural gene, lcrE, of the 32.9-kilodalton outer membrane protein LcrE (formerly known as Yop4b or YopN). Detection of large (greater than 2.3-kilobase-pair) transcripts strongly supports the conclusion that the lcrE gene and ORF1 to -5 function as an operon. Transcription of the lcrE-containing operon and the adjacent lcrB locus was found to be divergent, and the corresponding transcripts overlapped about 1,200 nucleotides. This extremely long overlap of the 5' ends of the transcripts produced from face-to-face promoters is a new finding; the longest overlap thus far found has been a few hundred nucleotides. Temperature was found to play the major role in regulation of transcription of the lcrE-containing operon of pYVO3, whereas Ca2+ concentration seemed to affect it only moderately.

摘要

鼠疫耶尔森菌、假结核耶尔森菌和小肠结肠炎耶尔森菌毒力质粒的低钙反应(lcr)区域与细菌的钙依赖性生长有关。lcr区域内先前确定的lcrE位点发生突变后,缺乏对lcr特异性蛋白(耶尔森菌外膜蛋白(Yops)以及V和W抗原)产生的阻遏控制。我们对小肠结肠炎耶尔森菌O:3毒力质粒pYVO3的lcrE位点的一个3.3千碱基对的BamHI-ClaI片段进行了测序。lcrE位点的序列揭示了6个紧密排列的开放阅读框(ORF),其中一个被鉴定为32.9千道尔顿外膜蛋白LcrE(以前称为Yop4b或YopN)的结构基因lcrE。检测到较大(大于2.3千碱基对)的转录本有力地支持了lcrE基因以及ORF1至 -5作为一个操纵子发挥功能的结论。发现含lcrE的操纵子和相邻的lcrB位点的转录是反向的,并且相应的转录本重叠约1200个核苷酸。由面对面启动子产生的转录本5'端的这种极长重叠是一个新发现;迄今为止发现的最长重叠为几百个核苷酸。发现温度在pYVO3含lcrE操纵子的转录调控中起主要作用,而Ca2+浓度似乎仅对其有适度影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bd8/209120/c85c34536c4e/jbacter00160-0349-a.jpg

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