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rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2010-11-8
pubmed:abstractText
Regulation by signaling molecules of pathways involved in determining cell size and shape is fundamental to understand morphogenesis. In eukaryotic cells, Rho GTPases modulate cellular events by acting as molecular switches. GTPase Activating Proteins (GAPs) control the fine-tuning of Rho GTPase activity as downregulators that promote their inactive state. We use Schizosaccharomyces pombe as a model to unveil key mechanisms underlying processes of general significance. Rga4, one of the nine RhoGAPs present in the fission yeast, is a key factor in the control of cell polarity and morphogenesis by negatively regulating the activity of the essential Rho GTPase Cdc42. We have demonstrated that Rga4 is also a GAP for Rho2 GTPase, which acts upstream of the Pmk1 cell integrity MAP kinase pathway and positively regulates cell integrity and cell separation. Our findings suggest that Rga4 control of both Cdc42 and Rho2 function is rather independent, thus providing a good example of regulatory specificity. Additionally, we describe multiple GAPs that can downregulate Pmk1 activity in a Rho2-dependent and independent fashion. These studies corroborate the existence of a sophisticated regulatory network by which different RhoGAPs modulate differentially the activity of Rho GTPases, and the existence of different inputs for the Pmk1 cell integrity MAP kinase pathway.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Sep
pubmed:issn
1942-0889
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
3
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
436-9
pubmed:year
2010
pubmed:articleTitle
Rga4, a Rho-GAP from fission yeast: Finding specificity within promiscuity.
pubmed:affiliation
Yeast Physiology Group; Department of Genetics and Microbiology; Facultad de Biología; Universidad de Murcia; Murcia, Spain.
pubmed:publicationType
Journal Article