Identification of small RNAs in Mycobacterium smegmatis using heterologous Hfq

  1. Terrence Chi-Kong Lau1,6
  1. 1Department of Biology and Chemistry, City University of Hong Kong, Hong Kong SAR
  2. 2School of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR
  3. 3School of Life Sciences, The Chinese University of Hong Kong, Hong Kong SAR
    1. 4 These authors contributed equally to this work.

    • 5 Present address: Department of Systems Biology, The University of Texas, MD Anderson Cancer Center, Houston, TX 77030, USA

    Abstract

    Gene regulation by small RNAs (sRNAs) has been extensively studied in various bacteria. However, the presence and roles of sRNAs in mycobacteria remain largely unclear. Immunoprecipitation of RNA chaperone Hfq to enrich for sRNAs is one of the effective methods to isolate sRNAs. However, the lack of an identified mycobacterial hfq restricts the feasibility of this approach. We developed a novel method that takes advantage of the conserved inherent sRNAs-binding capability of heterologous Hfq from Escherichia coli to enrich sRNAs from Mycobacterium smegmatis, a model organism for studying Mycobacterium tuberculosis. We validated 12 trans-encoded and 12 cis-encoded novel sRNAs in M. smegmatis. Many of these sRNAs are differentially expressed at exponential phase compared with stationary phase, suggesting that sRNAs are involved in the growth of mycobacteria. Intriguingly, five of the cis-encoded novel sRNAs target known transposases. Phylogenetic conservation analysis shows that these sRNAs are pathogenicity dependent. We believe that our findings will serve as an important reference for future analysis of sRNAs regulation in mycobacteria and will contribute significantly to the development of sRNAs prediction programs. Moreover, this novel method of using heterologous Hfq for sRNAs enrichment can be of general use for the discovery of bacterial sRNAs in which no endogenous Hfq is identified.

    Keywords

    Footnotes

    • Received April 29, 2012.
    • Accepted October 22, 2012.
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