Transcription initiation in mycobacteria: a biophysical perspective.

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Transcription-Austin Pub Date : 2020-04-01 Epub Date: 2019-12-27 DOI:10.1080/21541264.2019.1707612
Hande Boyaci, Ruth M Saecker, Elizabeth A Campbell
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引用次数: 12

Abstract

Recent biophysical studies of mycobacterial transcription have shed new light on this fundamental process in a group of bacteria that includes deadly pathogens such as Mycobacterium tuberculosis (Mtb), Mycobacterium abscessus (Mab), Mycobacterium leprae (Mlp), as well as the nonpathogenic Mycobacterium smegmatis (Msm). Most of the research has focused on Mtb, the causative agent of tuberculosis (TB), which remains one of the top ten causes of death globally. The enzyme RNA polymerase (RNAP) is responsible for all bacterial transcription and is a target for one of the crucial antibiotics used for TB treatment, rifampicin (Rif). Here, we summarize recent biophysical studies of mycobacterial RNAP that have advanced our understanding of the basic process of transcription, have revealed novel paradigms for regulation, and thus have provided critical information required for developing new antibiotics against this deadly disease.

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分枝杆菌的转录起始:生物物理学的观点。
最近对分枝杆菌转录的生物物理学研究揭示了一组细菌的这一基本过程,这些细菌包括致命的病原体,如结核分枝杆菌(Mtb)、脓肿分枝杆菌(Mab)、麻风分枝杆菌(Mlp)以及非致病性耻垢分枝杆菌(Msm)。大多数研究都集中在结核分枝杆菌上,结核仍然是全球十大死亡原因之一。RNA聚合酶(RNAP)负责所有细菌转录,并且是用于结核病治疗的关键抗生素之一利福平(Rif)的靶标。在这里,我们总结了最近关于分枝杆菌RNAP的生物物理学研究,这些研究提高了我们对转录基本过程的理解,揭示了新的调控模式,从而为开发针对这种致命疾病的新抗生素提供了关键信息。
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来源期刊
Transcription-Austin
Transcription-Austin BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
6.50
自引率
5.60%
发文量
9
期刊最新文献
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