The rate and extent of a cell's response to an extracellular stimulus is in
fluenced by regulators that act on the intracellular signalling machinery.
Although not directly involved in propagating the intracellular signal, reg
ulators control the activity of the proteins that transmit the signals. To
understand this aspect of cell signalling, we have studied the pheromone re
sponse pathway in the fission yeast Schizosaccharomyces pombe, a relatively
simple signalling system in a genetically tractable organism. We demonstra
te this approach by investigating the role of Rgs1, a member of the Regulat
or of G protein Signalling (RGS) family of proteins. The rgs1 gene was iden
tified through the St. pombe genome sequencing project (accession number Q0
9777) and recognized as having similarity to RGS proteins [Tesmer ef al. (1
997) Cell 89: 251-261], but this is the first report concerning the activit
y of the protein. Strains lacking rgs1 (Delta rgs1) are hypersensitive to p
heromone stimulation and unable to conjugate with a mating partner. Inhibit
ion of mating occurs at a relative late stage in the process as Delta rgs1
strains exhibit pheromone-dependent transcription and form shmoos. Expressi
on of SST2 (an RGS protein that regulates pheromone signalling in the buddi
ng yeast Saccharomyces cerevisiae) overcomes the hypersensitivity of the De
lta rgs1 strains but fails to rescue their mating defect.