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CarD Is an Essential Regulator of rRNA Transcription Required for Mycobacterium tuberculosis Persistence

机译:CarD是结核分枝杆菌持续性所需的rRNA转录的重要调节剂

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Mycobacterium tuberculosis is arguably the world's most successful infectious agent because of its ability to control its own cell growth within the host. Bacterial growth rate is closely coupled to rRNA transcription, which in E. coli is regulated through DksA and (p) ppGpp. The mechanisms of rRNA transcriptional control in mycobacteria, which lack DksA, are undefined. Here we identify CarD as an essential mycobacterial protein that controls rRNA transcription. Loss of CarD is lethal for mycobacteria in culture and during infection of mice. CarD depletion leads to sensitivity to killing by oxidative stress, starvation, and DNA damage, accompanied by failure to reduce rRNA transcription. CarD can functionally replace DksA for stringent control of rRNA transcription, even though CarD associates with a different site on RNA polymerase. These findings highlight a distinct molecular mechanism for regulating rRNA transcription in mycobacteria that is critical for M. tuberculosis pathogenesis.
机译:结核分枝杆菌可以说是世界上最成功的传染原,因为它能够控制宿主自身的细胞生长。细菌生长速率与rRNA转录密切相关,rRNA在大肠杆菌中是通过DksA和(p)ppGpp调控的。缺乏DksA的分枝杆菌中rRNA转录控制的机制尚不清楚。在这里,我们确定CarD为控制rRNA转录的必需分枝杆菌蛋白。 CarD的丢失对培养中的分枝杆菌和小鼠感染具有致命性。 CarD耗竭导致对氧化应激,饥饿和DNA损伤杀死的敏感性,并伴随着无法减少rRNA转录。即使CarD与RNA聚合酶上的另一个位点结合,CarD仍可以功能上替代DksA来严格控制rRNA转录。这些发现突出了分枝杆菌中调节rRNA转录的独特分子机制,这对于结核分枝杆菌的发病机理至关重要。

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