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Environmental and genetic determinants of colony morphology in yeast.
Abstract
Nutrient stresses trigger a variety of developmental switches in the budding yeast
Saccharomyces cerevisiae. One of the least understood of such responses is the development
of complex colony morphology, characterized by intricate, organized, and strain-specific
patterns of colony growth and architecture. The genetic bases of this phenotype and
the key environmental signals involved in its induction have heretofore remained poorly
understood. By surveying multiple strain backgrounds and a large number of growth
conditions, we show that limitation for fermentable carbon sources coupled with a
rich nitrogen source is the primary trigger for the colony morphology response in
budding yeast. Using knockout mutants and transposon-mediated mutagenesis, we demonstrate
that two key signaling networks regulating this response are the filamentous growth
MAP kinase cascade and the Ras-cAMP-PKA pathway. We further show synergistic epistasis
between Rim15, a kinase involved in integration of nutrient signals, and other genes
in these pathways. Ploidy, mating-type, and genotype-by-environment interactions also
appear to play a role in the controlling colony morphology. Our study highlights the
high degree of network reuse in this model eukaryote; yeast use the same core signaling
pathways in multiple contexts to integrate information about environmental and physiological
states and generate diverse developmental outputs.
Type
Journal articleSubject
CarbonCyclic AMP-Dependent Protein Kinases
Mutation
Nitrogen
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
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https://hdl.handle.net/10161/4461Published Version (Please cite this version)
10.1371/journal.pgen.1000823Publication Info
Granek, JA; & Magwene, PM (2010). Environmental and genetic determinants of colony morphology in yeast. PLoS Genet, 6(1). pp. e1000823. 10.1371/journal.pgen.1000823. Retrieved from https://hdl.handle.net/10161/4461.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Joshua Aaron Granek
Assistant Professor in Biostatistics & Bioinformatics
We have broad interests in using microbial genomics to understand how microbes interact
with each other and their hosts. This interest includes the roles played by both beneficial
and harmful bacteria, fungi, and viruses and how they interact with the immune system.
We study single microbes and microbial communities, primarily using high-throughput
sequencing methods. We have a particular interest in developing new experimental and
analytical methods that leverage the power of high-throughput
Paul Mitaari Magwene
Professor of Biology
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