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肠炎沙门氏菌中tRNA(精氨酸)(fimU)以及SEF14和SEF21的表达

tRNA(Arg) (fimU) and expression of SEF14 and SEF21 in Salmonella enteritidis.

作者信息

Clouthier S C, Collinson S K, White A P, Banser P A, Kay W W

机构信息

Department of Biochemistry and Microbiology, University of Victoria, British Columbia, Canada.

出版信息

J Bacteriol. 1998 Feb;180(4):840-5. doi: 10.1128/JB.180.4.840-845.1998.

Abstract

A Tn10 insertion affecting SEF14 fimbrial synthesis in Salmonella enteritidis was located 13 bp upstream of a gene designated fimU. The 77-bp DNA sequence of fimU from S. enteritidis was identical to that of fimU encoding tRNA(Arg) (UCU) from Salmonella typhimurium and 96% identical to that of the Escherichia coli argU homolog. Furthermore, the open reading frame adjacent to and overlapping the 3' end of fimU was similar to the prophage DLP12 integrase gene. The fimU-encoded transcript comigrated with total cellular tRNA and was predicted to form a tRNA-like cloverleaf structure containing the arginine anticodon UCU. Thus, fimU encoded a tRNA(Arg) specific for the rare codon AGA. fimU mapped to the SEF21 fim operon located 15 C's from the sef14 gene cluster. Although fimU was located within the SEF21 fim gene cluster, the fimU Tn10 insertion mutant of S. enteritidis was found to be defective in SEF14 as well as SEF21 (type 1) fimbria production. SEF17 and SEF18 fimbria production was not affected. Complementation of this mutant with plasmid-borne fimU restored normal production of the fimbrins SefA and FimA as well as their respective fimbriae SEF14 and SEF21. This is the first description of tRNA simultaneously controlling the production of two distinct fimbriae.

摘要

一个影响肠炎沙门氏菌SEF14菌毛合成的Tn10插入序列位于一个名为fimU的基因上游13 bp处。肠炎沙门氏菌fimU的77 bp DNA序列与鼠伤寒沙门氏菌编码tRNA(Arg)(UCU)的fimU序列相同,与大肠杆菌argU同源物的序列有96%的同一性。此外,与fimU 3'端相邻并重叠的开放阅读框与噬菌体DLP12整合酶基因相似。fimU编码的转录本与总细胞tRNA一起迁移,并预计形成一个类似tRNA的三叶草结构,其中包含精氨酸反密码子UCU。因此,fimU编码一种对稀有密码子AGA特异的tRNA(Arg)。fimU定位于距sef14基因簇15个C处的SEF21菌毛操纵子。虽然fimU位于SEF21菌毛基因簇内,但肠炎沙门氏菌的fimU Tn10插入突变体被发现不仅在SEF21(1型)菌毛产生方面有缺陷,在SEF14菌毛产生方面也有缺陷。SEF17和SEF18菌毛的产生不受影响。用质粒携带的fimU对该突变体进行互补,可恢复菌毛蛋白SefA和FimA及其各自菌毛SEF14和SEF21的正常产生。这是tRNA同时控制两种不同菌毛产生的首次描述。

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