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On a Stake-out: Small RNA Identification and Regulation

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Date 2020 Feb 22
PMID 32083232
Citations 11
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Abstract

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 .

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References
1.
Houghton J, Cortes T, Schubert O, Rose G, Rodgers A, De Ste Croix M . A small RNA encoded in the Rv2660c locus of Mycobacterium tuberculosis is induced during starvation and infection. PLoS One. 2013; 8(12):e80047. PMC: 3861185. DOI: 10.1371/journal.pone.0080047. View

2.
Lucchetti-Miganeh C, Burrowes E, Baysse C, Ermel G . The post-transcriptional regulator CsrA plays a central role in the adaptation of bacterial pathogens to different stages of infection in animal hosts. Microbiology (Reading). 2008; 154(Pt 1):16-29. DOI: 10.1099/mic.0.2007/012286-0. View

3.
Wayne L, Sohaskey C . Nonreplicating persistence of mycobacterium tuberculosis. Annu Rev Microbiol. 2001; 55:139-63. DOI: 10.1146/annurev.micro.55.1.139. View

4.
Chao Y, Li L, Girodat D, Forstner K, Said N, Corcoran C . In Vivo Cleavage Map Illuminates the Central Role of RNase E in Coding and Non-coding RNA Pathways. Mol Cell. 2017; 65(1):39-51. PMC: 5222698. DOI: 10.1016/j.molcel.2016.11.002. View

5.
Zhou Y, Xie J . The roles of pathogen small RNAs. J Cell Physiol. 2010; 226(4):968-73. DOI: 10.1002/jcp.22483. View