Characterization of ribonuclease III from Brucella.

Gene

State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China. Electronic address:

Published: April 2016

AI Article Synopsis

  • Bacterial ribonuclease III (RNase III) is crucial for RNA processing, specifically by cutting double-stranded RNA, and the study focused on RNase III from Brucella melitensis.
  • Researchers cloned the rncS gene, discovered the binding and cutting abilities of Bm-RNase III on Brucella-encoding small RNAs and miRNA precursors, and found that its activity requires specific metal ions and a certain pH.
  • Mutations showed that a specific residue is essential for its function, and differences in expression levels of RNase III between virulent and vaccine strains hint at its role in Brucella’s virulence regulation.

Article Abstract

Bacterial ribonuclease III (RNase III) is a highly conserved endonuclease, which plays pivotal roles in RNA maturation and decay pathways by cleaving double-stranded structure of RNAs. Here we cloned rncS gene from the genomic DNA of Brucella melitensis, and analyzed the cleavage properties of RNase III from Brucella. We identified Brucella-encoding small RNA (sRNA) by high-throughput sequencing and northern blot, and found that sRNA of Brucella and Homo miRNA precursor (pre-miRNA) can be bound and cleaved by B.melitensis ribonuclease III (Bm-RNase III). Cleavage activity of Bm-RNase III is bivalent metal cations- and alkaline buffer-dependent. We constructed several point mutations in Bm-RNase III, whose cleavage activity indicated that the 133th Glutamic acid residue was required for catalytic activity. Western blot revealed that Bm-RNase III was differently expressed in Brucella virulence strain 027 and vaccine strain M5-90. Collectively, our data suggest that Brucella RNase III can efficiently bind and cleave stem-loop structure of small RNA, and might participate in regulation of virulence in Brucella.

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Source
http://dx.doi.org/10.1016/j.gene.2015.12.068DOI Listing

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