Taneja Sagarika, Dutta Tanmay
RNA Biology Laboratory, Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, 110016, India.
Noncoding RNA Res. 2019 May 16;4(3):86-95. doi: 10.1016/j.ncrna.2019.05.001. eCollection 2019 Sep.
Persistence of mycobacteria in the hostile environment of human macrophage is pivotal for its successful pathogenesis. Rapid adaptation to diverse stresses is the key aspect for their survival in the host cells. A range of heterogeneous mechanisms operate in bacteria to retaliate stress conditions. Small RNAs (sRNA) have been implicated in many of those mechanisms in either a single or multiple regulatory networks to post-transcriptionally modulate bacterial gene expression. Although small RNA profiling in mycobacteria by advanced technologies like deep sequencing, tilling microarray etc. have identified hundreds of sRNA, however, a handful of those small RNAs have been unearthed with precise regulatory mechanism. Extensive investigations on sRNA-mediated gene regulations in eubacteria like revealed the existence of a plethora of distinctive sRNA mechanisms e.g. base pairing, protein sequestration, RNA decoy etc. Increasing studies on mycobacterial sRNA also discovered several eccentric mechanisms where sRNAs act at the posttranscriptional stage to either activate or repress target gene expression that lead to promote mycobacterial survival in stresses. Several intrinsic features like high GC content, absence of any homologue of abundant RNA chaperones, Hfq and ProQ, isolate sRNA mechanisms of mycobacteria from that of other bacteria. An insightful approach has been taken in this review to describe sRNA identification and its regulations in mycobacterial species especially in .
分枝杆菌在人类巨噬细胞的恶劣环境中持续存在对其成功致病至关重要。快速适应各种应激是它们在宿主细胞中存活的关键方面。细菌中存在一系列不同的机制来应对应激条件。小RNA(sRNA)在许多这些机制中通过单一或多个调控网络参与转录后调节细菌基因表达。尽管通过深度测序、tiling微阵列等先进技术对分枝杆菌中的小RNA进行分析已鉴定出数百种sRNA,然而,只有少数小RNA的精确调控机制被揭示。对真细菌中sRNA介导的基因调控的广泛研究揭示了大量独特的sRNA机制,例如碱基配对、蛋白质隔离、RNA诱饵等。对分枝杆菌sRNA的研究不断增加,也发现了几种奇特的机制,其中sRNA在转录后阶段发挥作用,激活或抑制靶基因表达,从而促进分枝杆菌在应激中的存活。分枝杆菌的一些内在特征,如高GC含量、缺乏丰富的RNA伴侣Hfq和ProQ的任何同源物,使其sRNA机制与其他细菌不同。本综述采用了一种有见地的方法来描述分枝杆菌物种中sRNA的鉴定及其调控,特别是在……