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Journal of Bacteriology, December 2000, p. 6614-6621, Vol. 182, No. 23
Department of Molecular and Cell Biology,
University of California, Berkeley, California 94720-3204
Received 9 June 2000/Accepted 8 September 2000
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.
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Developmental Aggregation of Myxococcus
xanthus Requires frgA, an
frz-Related Gene
*
Corresponding author. Mailing address: University of
California, Department of Molecular and Cell Biology, 401 Barker Hall, Berkeley, CA 94720-3204. Phone: (510) 642-2293. Fax: (510) 643-6334. E-mail: zusman{at}uclink4.berkeley.edu.
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