Cornelis G R, Sluiters C, Delor I, Geib D, Kaniga K, Lambert de Rouvroit C, Sory M P, Vanooteghem J C, Michiels T
Microbiol Pathogenesis Unit, International Institute of Cellular and Molecular Pathology, Brussels, Belgium.
Mol Microbiol. 1991 May;5(5):1023-34. doi: 10.1111/j.1365-2958.1991.tb01875.x.
The virulence functions of Yersinia enterocolitica include the pYV-encoded Yop proteins and YadA adhesin as well as the chromosome-encoded enterotoxin, Yst. The yop and yadA genes form a temperature-activated regulon controlled by the transcriptional activator VirF. Gene virF, also localized on pYV, is itself thermoinduced in the absence of other pYV genes. The enterotoxin yst gene is silent in some collection strains including strain W22703. This paper describes two Tn5-Tc1 chromosomal insertion mutants of W22703 transcribing virF, and hence the yop and yadA genes, at low temperature. These mutants also resumed their production of Yst, with its typical temperature dependence. Both mutations were insertions in the same gene called ymoA for 'Yersinia modulator'. The cloned ymoA gene fully complemented the two mutations. Several properties of the mutants suggest that ymoA encodes a histone-like protein. According to the nucleic acid sequence, the product of ymoA is an 8064 Da protein rich in aspartic acid (9%), glutamic acid (9%) and lysine (10.5%), but the predicted amino acid sequence shows no similarity with any described histone-like protein. This work supports recent reports which propose a role for DNA topology and bacterial chromatin structure in thermoregulation of virulence functions.
小肠结肠炎耶尔森菌的毒力功能包括由毒力质粒(pYV)编码的Yop蛋白和YadA黏附素,以及由染色体编码的肠毒素Yst。yop和yadA基因形成一个受转录激活因子VirF控制的温度激活调节子。基因virF也位于pYV上,在没有其他pYV基因的情况下,它自身受热诱导。肠毒素yst基因在包括W22703菌株在内的一些菌株中是沉默的。本文描述了W22703的两个Tn5-Tc1染色体插入突变体,它们在低温下转录virF,进而转录yop和yadA基因。这些突变体还恢复了Yst的产生,且具有典型的温度依赖性。两个突变均插入到同一个名为ymoA(“耶尔森菌调节子”)的基因中。克隆的ymoA基因完全互补了这两个突变。突变体的几个特性表明ymoA编码一种类组蛋白。根据核酸序列,ymoA的产物是一种8064 Da的蛋白质,富含天冬氨酸(9%)、谷氨酸(9%)和赖氨酸(10.5%),但预测的氨基酸序列与任何已描述的类组蛋白均无相似性。这项工作支持了最近的一些报道,这些报道提出DNA拓扑结构和细菌染色质结构在毒力功能的温度调节中起作用。