The ascomycete Penicillium marneffei is an opportunistic human pathogen exhibiting a temperature-dependent dimorphic switch. At 25°C, P. marneffei grows as filamentous multinucleate hyphae and undergoes asexual development, producing uninucleate spores. At 37°C, it forms uninucleate yeast cells which divide by fission. We have cloned a gene encoding a G␣ subunit of a heterotrimeric G protein from P. marneffei named gasA with high similarity to fadA in Aspergillus nidulans. Through the characterization of a ⌬gasA strain and mutants carrying a dominant activating or a dominant interfering gasA allele, we show that GasA is a key regulator of asexual development but seems to play no role in the regulation of growth. A dominant activating gasA mutant whose mutation results in a G42-to-R change (gasA G42R ) does not express brlA, the conidiation-specific regulatory gene, and is locked in vegetative growth, while a dominant interfering gasA G203R mutant shows inappropriate brlA expression and conidiation. Interestingly, the gasA mutants have no apparent defect in dimorphic switching or yeast-like growth at 37°C. Growth tests on dibutyryl cyclic AMP (dbcAMP) and theophylline suggest that a cAMP-protein kinase A cascade may be involved in the GasA signaling pathway.Environmental signals leading to a variety of developmental processes and physiological responses are sensed and transduced to the cell interior through complex interactions at the cell membrane. Heterotrimeric guanine nucleotide-binding proteins (G proteins) act as signal transducers that couple cell surface receptors to cytoplasmic effector proteins in eukaryotes. Upon binding of the agonist with the corresponding serpentine transmembrane receptor, the G␣ subunit becomes activated, exchanging GDP for GTP and dissociating from the ␥ complex. G␣ and G␥ subunits can then interact with appropriate targets such as phosphodiesterases, protein kinases, adenylyl cyclases, phospholipases, and ion channels to trigger downstream signaling pathways (20,27,37,44).In fungi, G proteins affect a number of developmental and morphogenic processes and play essential roles during pathogenic and sexual development programs (4). The best-characterized fungal G␣ proteins are Saccharomyces cerevisiae Gpa1 and Gpa2. Gpa1 is linked to cell-type-specific pheromone receptors encoded by the STE2 and STE3 genes and plays a negative role in the mitogen-activated protein kinase pheromone signaling pathway that leads to mating (32). Gpa2 is required for the induction of pseudohyphal growth in diploid yeast cells under nitrogen starvation and signals through a cyclic AMP (cAMP)-dependent protein kinase A (PKA) pathway (30, 35). Interestingly, Gpa2 is coupled to a G-proteincoupled receptor, Gpr1, which appears to be a glucose sensor (28,33,36). G␣ subunits from other fungi with high homology to Gpa2 have also been implicated in morphogenesis through cAMP-PKA signaling. The corn smut fungus Ustilago maydis displays a dimorphic switch between a haploid yeast-like form and a pathogenic filamen...