Identification of a mutant locus that bypasses the BsgA protease requirement for social development in Myxococcus xanthus. Issue 1 (29th January 2015)

• Record Type: Journal Article
• Authors: Cusick, John K.; Hager, Elizabeth; Gill, Ronald E.
• Editors: Garbeva, Paolina
• Is Part Of: FEMS microbiology letters. Volume 362:Issue 1(2015:Jan.)
• Page Start: 1
• Page End: 8
• Publication Date: 2015-01-29
• Subjects: cell communication -- biofilm -- genetic bypass suppressor; Microbiology -- Periodicals; 579
• DOI: 10.1093/femsle/fnu028
• Languages: English
• ISSNs: 0378-1097

Abstract

Abstract : The BsgA protease is required for the earliest morphological changes observed in Myxococcus xanthus development. We hypothesize that the BsgA protease is required to cleave an inhibitor of the developmental program, and isolation of genetic bypass suppressors of a bsgA mutant was used to identify signaling components controlling development downstream of the BsgA protease. Strain M955 was created by transposon mutagenesis of a bsgA mutant followed by screening for strains that could develop despite the absence of the BsgA protease. Strain M955 was able to aggregate, form fruiting bodies, and partially restored the production of viable spores in comparison to the parental bsgA mutant. The bsgA Tn 5 Ω955 strain partially restored developmental expression to a subset of genes normally induced during development, and expressed one developmentally induced fusion at higher amounts during vegetative growth in comparison to wild-type cells. The transposon in strain M955 was localized to a Ribonuclease D homolog that appears to exist in an operon with a downstream aminopeptidase-encoding gene. The identification of a third distinct bypass suppressor of the BsgA protease suggests that the BsgA protease may regulate a potentially complex pathway during the initiation of the M. xanthus developmental program. Abstract : This work identifies a third distinct locus in which mutations that bypasses bypass the requirement for a protease essential for fruiting body and spore formation in the social bacterium Myxococcus xanthus . Abstract :