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1.
Mol Genet Genomics ; 270(3): 225-33, 2003 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-13680367

RESUMO

Yeast mat alpha2 mutants express both mating pheromones and both mating pheromone receptors. They show modest signaling in the pheromone response pathway, as revealed by increased levels of FUS1 transcript, yet are resistant to pheromone treatment. Together, these phenotypes suggest that alpha2- cells undergo autocrine activation of the pheromone response pathway, which is subsequently attenuated. We constructed a regulatable version of the alpha2 gene (GALalpha2) and showed that, upon loss of alpha2 activity, cells exhibit an initial robust response to pheromone that is attenuated within 3 h. We reasoned that the viability of alpha2- cells might be due to attenuation, and therefore performed a genome-wide synthetic lethal screen to identify potential adaptation components. We identified two genes, SST2 and ASG7. Loss of either of these attenuation components results in activation of the pheromone pathway in alpha2- cells. Loss of both proteins causes a more severe phenotype. Sst2 functions as a GTPase activating protein (GAP) for the Galpha subunit of the trimeric G protein. Asg7 is an a -cell specific protein that acts in concert with the alpha-cell specific a -factor receptor, Ste3, to inhibit signaling by Gbetagamma. Hence, our results suggest that mat alpha2 mutants mimic the intracellular signaling events that occur in newly fused zygotes.


Assuntos
Proteínas Ativadoras de GTPase/genética , Deleção de Genes , Regulação Fúngica da Expressão Gênica/genética , Proteínas de Homeodomínio/genética , Proteínas de Membrana/genética , Feromônios/fisiologia , Proteínas Repressoras/genética , Proteínas de Saccharomyces cerevisiae/genética , Saccharomyces cerevisiae/genética , Sequência de Bases , Primers do DNA , Genes Fúngicos , Genótipo , Dados de Sequência Molecular , Mutagênese , Reação em Cadeia da Polimerase
2.
J Neurosci ; 18(18): 7244-55, 1998 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-9736646

RESUMO

The nitric oxide (NO)-cGMP signaling system is thought to play important roles in the function of the olfactory system in both vertebrates and invertebrates. One way of studying the role of NO in the nervous system is to study the distribution and properties of NO synthase (NOS), as well as the soluble guanylyl cyclases (sGCs), which are the best characterized targets of NO. We study NOS and sGC in the relatively simple and well characterized insect olfactory system of the hawkmoth, Manduca sexta. We have cloned Manduca sexta nitric oxide synthase (MsNOS) and two sGCs (MsGCalpha1 and MsGCbeta1), characterized their basic biochemical properties, and studied their expression in the olfactory system. The sequences of the Manduca genes are highly similar to their mammalian homologs and show similar biochemical properties when expressed in COS-7 cells. In particular, we find that MsGC functions as an obligate heterodimer that is stimulated significantly by NO. We also find that MsNOS has a Ca2+-sensitive NO-producing activity similar to that of mammalian neuronal NOS. Northern and in situ hybridization analyses show that MsNOS and the MsGCs are expressed in a complementary pattern, with MsNOS expressed at high levels in the antennae and the MsGCs expressed at high levels in a subset of antennal lobe neurons. The expression patterns of these genes suggest that the NO-sGC signaling system may play a role in mediating communication between olfactory receptor neurons and projection neurons in the glomeruli of the antennal lobe.


Assuntos
Comunicação Celular/fisiologia , GMP Cíclico/metabolismo , Neurônios Aferentes/citologia , Óxido Nítrico/metabolismo , Estruturas Animais/inervação , Animais , Clonagem Molecular , Dimerização , Gânglios dos Invertebrados/química , Gânglios dos Invertebrados/enzimologia , Regulação Enzimológica da Expressão Gênica , Guanilato Ciclase/genética , Guanilato Ciclase/metabolismo , Isoenzimas/genética , Isoenzimas/metabolismo , Mamíferos , Manduca , Dados de Sequência Molecular , Neurônios Aferentes/enzimologia , Óxido Nítrico Sintase/genética , Óxido Nítrico Sintase/metabolismo , Homologia de Sequência de Aminoácidos , Olfato/fisiologia
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