Genes (Dec 2020)

Mutations Affecting HVO_1357 or HVO_2248 Cause Hypermotility in <i>Haloferax volcanii</i>, Suggesting Roles in Motility Regulation

  • Michiyah Collins,
  • Simisola Afolayan,
  • Aime B. Igiraneza,
  • Heather Schiller,
  • Elise Krespan,
  • Daniel P. Beiting,
  • Mike Dyall-Smith,
  • Friedhelm Pfeiffer,
  • Mechthild Pohlschroder

DOI
https://doi.org/10.3390/genes12010058
Journal volume & issue
Vol. 12, no. 1
p. 58

Abstract

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Motility regulation plays a key role in prokaryotic responses to environmental stimuli. Here, we used a motility screen and selection to isolate hypermotile Haloferax volcanii mutants from a transposon insertion library. Whole genome sequencing revealed that hypermotile mutants were predominantly affected in two genes that encode HVO_1357 and HVO_2248. Alterations of these genes comprised not only transposon insertions but also secondary genome alterations. HVO_1357 contains a domain that was previously identified in the regulation of bacteriorhodopsin transcription, as well as other domains frequently found in two-component regulatory systems. The genes adjacent to hvo_1357 encode a sensor box histidine kinase and a response regulator, key players of a two-component regulatory system. None of the homologues of HVO_2248 have been characterized, nor does it contain any of the assigned InterPro domains. However, in a significant number of Haloferax species, the adjacent gene codes for a chemotaxis receptor/transducer. Our results provide a foundation for characterizing the root causes underlying Hfx. volcanii hypermotility.

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