Affiliation:
1. School of Molecular Biosciences, Washington State University, Pullman, Washington 99164-4234
2. Department of Biochemistry, Stanford University School of Medicine, Stanford, California 94305-5329
3. Cereon Genomics, Monsanto Protein Technologies, Middleton, Wisconsin 53562-0999
Abstract
ABSTRACT
The multicellular developmental cycle of
Myxococcus xanthus
requires large-scale changes in gene transcription, and recent findings indicate that NtrC-like activators play a prominent role in regulating these changes. In this study, we made insertions in 28 uncharacterized
ntrC
-like activator (
nla
) genes and found that eight of these insertions cause developmental defects. Hence, these results are consistent with the idea that
M. xanthus
uses a series of different NtrC-like activators during fruiting body development. Four of the eight developmental mutants we identified have motility defects. The
nla1
,
nla19
, and
nla23
mutants show S-motility defects, while the
nla24
mutant shows defects in both S-motility and A-motility. During development, aggregation of the
nla1
,
nla19
, and
nla23
mutants is delayed slightly and the
nla24
mutant shows no signs of aggregation or sporulation. The
nla4
,
nla6
,
nla18
, and
nla28
mutants have no appreciable loss in motility, but they fail to aggregate and to sporulate normally. The
nla18
mutant belongs to a special class of developmental mutants whose defects can be rescued when they are codeveloped with wild-type cells, suggesting that
nla18
fails to produce a cell-cell signal required for development. The three remaining activator mutants,
nla4
,
nla6
, and
nla28
, appear to have complex developmental phenotypes that include deficiencies in cell-cell developmental signals.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
87 articles.
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