Saïd-Salim Battouli, Mostowy Serge, Kristof Arnold S, Behr Marcel A
McGill University Health Centre, Montreal, QC, Canada.
Mol Microbiol. 2006 Dec;62(5):1251-63. doi: 10.1111/j.1365-2958.2006.05455.x. Epub 2006 Oct 25.
It has recently been advanced that Mycobacterium tuberculosis sigma factor K (SigK) positively regulates expression of the antigenic proteins MPB70 and MPB83. As expression of these proteins differs between M. tuberculosis (low) and Mycobacterium bovis (high), this study set out to determine whether M. bovis lacks a functional SigK repressor (anti-SigK). By comparing genes near sigK in M. tuberculosis H37Rv and M. bovis AF2122/97, we observed that Rv0444c, annotated as unknown function, had variable sequence in M. bovis. Analysis of in vitro mpt70/mpt83 expression and Rv0444c sequencing across M. tuberculosis complex (MTC) members revealed that high-level expression was associated with a mutated Rv0444c. Complementation of M. bovis bacillus Calmette-Guerin Russia, a high producer of MPB70/MPB83, with wild-type Rv0444c resulted in a significant decrease in mpb70/mpb83 expression. Conversely, a M. tuberculosis H37Rv mutant which expressed sigK but not Rv0444c manifested the M. bovis phenotype of high-level MPB70/MPB83 expression. Further support that Rv0444c encodes the anti-SigK was obtained by yeast two-hybrid studies, where the N-terminal region of Rv0444c-encoded protein interacted with SigK. Together these findings indicate that Rv0444c encodes the regulator of SigK (RskA) and mutations in this gene explain high-level MPT70/MPT83 expression by certain MTC members.
最近有研究提出,结核分枝杆菌σ因子K(SigK)正向调节抗原蛋白MPB70和MPB83的表达。由于这些蛋白在结核分枝杆菌(低表达)和牛分枝杆菌(高表达)之间的表达存在差异,本研究旨在确定牛分枝杆菌是否缺乏功能性的SigK阻遏物(抗SigK)。通过比较结核分枝杆菌H37Rv和牛分枝杆菌AF2122/97中sigK附近的基因,我们观察到注释为功能未知的Rv0444c在牛分枝杆菌中具有可变序列。对结核分枝杆菌复合群(MTC)成员的体外mpt70/mpt83表达和Rv0444c测序分析表明,高水平表达与Rv0444c突变有关。用野生型Rv0444c对MPB70/MPB83高产的俄罗斯卡介苗牛分枝杆菌进行互补,导致mpb70/mpb83表达显著降低。相反,一个表达sigK但不表达Rv0444c的结核分枝杆菌H37Rv突变体表现出牛分枝杆菌高水平MPB70/MPB83表达的表型。酵母双杂交研究进一步支持Rv0444c编码抗SigK,其中Rv0444c编码蛋白的N端区域与SigK相互作用。这些发现共同表明,Rv0444c编码SigK的调节因子(RskA),该基因的突变解释了某些MTC成员高水平的MPT70/MPT83表达。