ArticleJournal of bacteriology2000
Developmental aggregation of Myxococcus xanthus requires frgA, an frz-related gene.
Article in Journal of bacteriology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 17 citations in OpenAlex.
- A miniTurbo-based proximity labeling protocol to identify conditional protein interactomes in vivo in Myxococcus xanthus.STAR protocols · 2023Article
- ProfilingJournal of bacteriology · 2021Article
- Nucleotide binding by the widespread high-affinity cyclic di-GMP receptor MshEN domain.Nature communications · 2016Article
- Specificity residues determine binding affinity for two-component signal transduction systems.mBio · 2013Article
- Intra- and interprotein phosphorylation between two-hybrid histidine kinases controls Myxococcus xanthus developmental progression.The Journal of biological chemistry · 2012Article
- Comparative analyses imply that the enigmatic Sigma factor 54 is a central controller of the bacterial exterior.BMC genomics · 2011Article
- Bacterial community dynamics during the application of a Myxococcus xanthus-inoculated culture medium used for consolidation of ornamental limestone.Microbial ecology · 2010Article
- SigF, a new sigma factor required for a motility system of Myxococcus xanthus.Journal of bacteriology · 2005Article
- Sigma54 enhancer binding proteins and Myxococcus xanthus fruiting body development.Journal of bacteriology · 2004Article
- Genetic studies of mrp, a locus essential for cellular aggregation and sporulation of Myxococcus xanthus.Journal of bacteriology · 2001Article
- Light regulation of type IV pilus-dependent motility by chemosensor-like elements in Synechocystis PCC6803.Proceedings of the National Academy of Sciences of the United States of America · 2001Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
Abstract
Myxococcus xanthus is a gram-negative bacterium which has a complex life cycle that includes multicellular fruiting body formation. Frizzy mutants are characterized by the formation of tangled filaments instead of hemispherical fruiting bodies on fruiting agar. Mutations in the frz genes have been shown to cause defects in directed motility, which is essential for both vegetative swarming and fruiting body formation. In this paper, we report the discovery of a new gene, called frgA (for frz-related gene), which confers a subset of the frizzy phenotype when mutated. The frgA null mutant showed reduced swarming and the formation of frizzy aggregates on fruiting agar. However, this mutant still displayed directed motility in a spatial chemotaxis assay, whereas the majority of frz mutants fail to show directed movements in this assay. Furthermore, the frizzy phenotype of the frgA mutant could be complemented extracellularly by wild-type cells or strains carrying non-frz mutations. The phenotype of the frgA mutant is similar to that of the abcA mutant and suggests that both of these mutants could be defective in the production or export of extracellular signals required for fruiting body formation rather than in the sensing of such extracellular signals. The frgA gene encodes a large protein of 883 amino acids which lacks homologues in the databases. The frgA gene is part of an operon which includes two additional genes, frgB and frgC. The frgB gene encodes a putative histidine protein kinase, and the frgC gene encodes a putative response regulator. The frgB and frgC null mutants, however, formed wild-type fruiting bodies.
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