Tanaka K, Davey J, Imai Y, Yamamoto M
Department of Biophysics and Biochemistry, Faculty of Science, University of Tokyo, Japan.
Mol Cell Biol. 1993 Jan;13(1):80-8. doi: 10.1128/mcb.13.1.80-88.1993.
A defect in the map3 gene of the fission yeast Schizosaccharomyces pombe causes h+ mating-type-specific sterility. This gene was cloned by complementation. Nucleotide sequence analysis showed that it has a coding capacity of 365 amino acids. The deduced map3 gene product is a putative seven-transmembrane protein and has 20.0% amino acid identity with the a-factor receptor of Saccharomyces cerevisiae, encoded by STE3. It is also homologous with the Ustilago maydis mating pheromone receptors. The map3 gene is expressed in h+ cells but not in h- cells, and the transcripts are induced in response to nitrogen starvation. h+ cells defective in map3 do not respond to purified M-factor. When map3 is expressed ectopically in h- cells, they apparently acquire the ability to respond to the M-factor produced by themselves. The gpa1 gene, which encodes the alpha-subunit of a G-protein presumed to couple with the mating pheromone receptors, is essential for this function of map3. These observations strongly suggest that map3 encodes the M-factor receptor. Furthermore, this study provides strong support for the notion that pheromone signaling is essential for initiation of meiosis in S. pombe and that either M-factor signaling or P-factor signaling alone is sufficient.
粟酒裂殖酵母(Schizosaccharomyces pombe)的map3基因缺陷会导致h⁺交配型特异性不育。该基因通过互补作用被克隆。核苷酸序列分析表明,它具有编码365个氨基酸的能力。推导的map3基因产物是一种假定的七跨膜蛋白,与酿酒酵母(Saccharomyces cerevisiae)由STE3编码的a因子受体具有20.0%的氨基酸同一性。它也与玉米黑粉菌(Ustilago maydis)交配信息素受体同源。map3基因在h⁺细胞中表达,但在h⁻细胞中不表达,并且转录本在氮饥饿时被诱导。map3缺陷的h⁺细胞对纯化的M因子无反应。当map3在h⁻细胞中异位表达时,它们显然获得了对自身产生的M因子作出反应的能力。gpa1基因编码一种推测与交配信息素受体偶联的G蛋白的α亚基,对map3的这一功能至关重要。这些观察结果强烈表明map3编码M因子受体。此外,本研究为以下观点提供了有力支持:信息素信号传导对于粟酒裂殖酵母减数分裂的起始至关重要,并且单独的M因子信号传导或P因子信号传导就足够了。