Abstract

A putative seven transmembrane protein gene, stm1(+), which is required for proper recognition of nitrogen starvation signals, was isolated as a multicopy suppressor of a ras1 synthetic lethal mutant in Schizosaccharomyces pombe. Under nitrogen-deficient conditions, transcription of the stm1 gene was induced; deletion of stm1 was associated with early entry into G(1) arrest. Under nutritionally sufficient conditions, overexpression of Stm1 inhibited vegetative cell growth, resulted in decreased intracellular cAMP levels, increased the expression of the meiosis-specific genes ste11, mei2, and mam2, and facilitated sexual development in homothallic cells. However inhibition of vegetative cell growth and reduction of cAMP levels were not observed in a deletion mutant of the heterotrimeric G protein Galpha2 gene, gpa2, that is responsible for regulating intracellular cAMP levels, a key factor in determining the sexual development in S. pombe. Stm1 protein was shown to interact with Gpa2 through its C-terminal transmembrane domains 5-7. Mutation at Lys(199) in the C-terminal domain (stm1(K199A)) abolished the Stm1 overexpression effect on lowering cAMP levels. Induction of ste11, a meiosis-specific gene transcription factor, by Stm1 overexpression was enhanced in gpa2-deleted cells but was absent in a deletion mutant of sty1, a key protein kinase that links mitotic control with environmental signals and induces stress-responsive genes. Moreover, deletion of both stm1 and ras1 caused delayed entry into G(1) arrest in S. pombe when the cells were grown in a nitrogen-deficient medium. Thus we consider that the stm1 gene can function through Gpa2-dependent and/or -independent pathways and may play a role in providing the prerequisite state for entering the pheromone-dependent differentiation cycle in which heterotrimeric Galpha1 protein, Gpa1, and Ras1 play major roles. Stm1 could function as a sentinel molecule sensing the nutritional state of the cells, stopping the proliferative cell cycle, and preparing the cell to enter meiosis under nutritionally deficient conditions.

Highlights

  • Ceptors relay signals to the interior of the cell using several different classes of heterotrimeric G proteins: Gs, Gi, Go, Gq, G12, and G13

  • Gpa1 is responsible for pheromone-responsive sexual development, and Gpa2 relays the nutritional status information necessary to initiate the sexual differentiation of S. pombe

  • Isolation of the stm1ϩ Gene, Which Suppressed a Synthetic Lethal Mutant of ras1—In an attempt to identify the elements that function in association with Ras1 in terms of delivering cell surface signals into the cell interior for the differentiation of S. pombe, we looked for novel genes that might function in linking poor nutritional status and pheromone signals with activated Ras1

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Summary

Introduction

Ceptors relay signals to the interior of the cell using several different classes of heterotrimeric G proteins: Gs, Gi, Go, Gq, G12, and G13. It has been observed that in S. pombe, when the nitrogen source is depleted, cell growth is arrested at G1 first (30 –33), and the heterotrimeric G protein ␣-subunit, Gpa, which regulates adenylate cyclase in accordance with nutritional state of the cells [19], lowers the intracellular cAMP levels. This in turn triggers the induction of expression of genes such as mam, ste, and mei, which are required in the initial stage of meiosis [22]. This interaction may provide the initiating signal that links signals triggered by nutritional deficiency and pheromone-dependent sexual differentiation, to allow Ras to activate sexual differentiation in S. pombe

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