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首页> 外文期刊>Molecular Microbiology >Rv1675c (cmr) regulates intramacrophage and cyclic AMP-induced gene expression in Mycobacterium tuberculosis-complex mycobacteria.
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Rv1675c (cmr) regulates intramacrophage and cyclic AMP-induced gene expression in Mycobacterium tuberculosis-complex mycobacteria.

机译:Rv1675c(cmr)调节结核分枝杆菌-复杂分枝杆菌中的巨噬细胞内和环AMP诱导的基因表达。

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Cyclic AMP (cAMP) has recently been shown to be a global regulator of gene expression in Mycobacterium tuberculosis (Mtb). In this study we identified a new cAMP-associated regulon in Mtb and Mycobacterium bovis BCG, which is distinct from the previously described CRP(Mt) regulon. Proteomic comparison of wild-type M. bovis BCG with a Rv1675c (cmr) knockout strain showed dysregulated expression of four previously identified proteins encoded by the cAMP-induced genes (cAIGs) mdh, groEL2, Rv1265 and PE_PGRS6a. Regulated expression of these four cAIGs also occurred during macrophage infection, and this regulation required cmr in both Mtb and M. bovis BCG. Purified His-Cmr bound to the DNA sequences upstream of three cAIGs (mdh, groEL2, Rv1265) in electrophoretic mobility shift assays, suggesting direct regulation of these genes by Cmr. We also found that low pH stimulated cAMP production in both Mtb and M. bovis BCG, but broadly affected cAIG regulation only in M. bovis BCG. These studies identify Cmr as atranscription factor that regulates cAIGs within macrophages, and suggest that multiple factors affect cAMP-associated gene regulation in tuberculosis-complex mycobacteria. cAMP signalling and Cmr-mediated gene regulation during Mtb infection of macrophages may have implications for TB pathogenesis.
机译:循环AMP(cAMP)最近已被证明是结核分枝杆菌(Mtb)中基因表达的全球调节者。在这项研究中,我们在Mtb和牛分枝杆菌BCG中鉴定了一种新的与cAMP相关的调节子,这与先前描述的CRP(Mt)调节子不同。野生型牛分枝杆菌BCG与Rv1675c(cmr)敲除菌株的蛋白质组学比较显示,四个先前鉴定的由cAMP诱导基因(cAIGs)mdh,groEL2,Rv1265和PE_PGRS6a编码的蛋白表达失调。在巨噬细胞感染期间,这四个cAIGs的表达也发生了调节,这种调节在Mtb和牛分枝杆菌BCG中都需要cmr。在电泳迁移率变动分析中,纯化的His-Cmr与三个cAIG(mdh,groEL2,Rv1265)上游的DNA序列结合,表明Cmr可直接调控这些基因。我们还发现低pH值刺激Mtb和牛分枝杆菌BCG中的cAMP产生,但仅在牛分枝杆菌BCG中广泛影响cAIG调节。这些研究确定Cmr是调节巨噬细胞内cAIG的转录因子,并表明多种因素影响结核病复杂分枝杆菌中与cAMP相关的基因调节。巨噬细胞Mtb感染过程中的cAMP信号传导和Cmr介导的基因调控可能与结核病发病机制有关。

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