Styrkársdóttir U, Egel R, Nielsen O
Institute of Genetics, University of Copenhagen, Denmark.
Mol Gen Genet. 1992 Oct;235(1):122-30. doi: 10.1007/BF00286189.
In fission yeast (Schizosaccharomyces pombe), the mat1-Pm gene, which is required for entry into meiosis, is expressed in response to a pheromone signal. Cells carrying a mutation in the ste8 gene are unable to induce transcription of mat1-Pm in response to pheromone, suggesting that the ste8 gene product functions in the signal transduction pathway. The ste8+ gene encodes a 659 amino acid putative protein kinase, which is identical to the previously identified byr2 suppressor of the ras1 defect. Furthermore, ste8+ is highly homologous to the Saccharomyces cerevisiae STE11 gene, which functions in signal transduction in budding yeast. Expression of the S. cerevisiae STE11 gene in S. pombe ste8 mutants restores the ability to transcribe mat1-Pm in response to pheromone. Also, such cells become capable of conjugation and sporulation. When mat1-Pm is artifically expressed from a heterologous promoter, ste8 mutant cells will enter meiosis. This demonstrates that the meiotic defect of ste8 mutants is due to the absence of the mat1-Pm gene product.
在裂殖酵母(粟酒裂殖酵母)中,进入减数分裂所必需的mat1 - Pm基因会响应信息素信号而表达。携带ste8基因突变的细胞无法响应信息素诱导mat1 - Pm的转录,这表明ste8基因产物在信号转导途径中发挥作用。ste8⁺基因编码一种含659个氨基酸的假定蛋白激酶,它与先前鉴定的ras1缺陷的byr2抑制子相同。此外,ste8⁺与酿酒酵母的STE11基因高度同源,STE11基因在芽殖酵母的信号转导中起作用。在粟酒裂殖酵母ste8突变体中表达酿酒酵母的STE11基因可恢复其响应信息素转录mat1 - Pm的能力。而且,这类细胞能够进行接合和孢子形成。当mat1 - Pm从异源启动子人工表达时,ste8突变体细胞将进入减数分裂。这表明ste8突变体的减数分裂缺陷是由于缺乏mat1 - Pm基因产物所致。