Kanoh J, Sugimoto A, Yamamoto M
Department of Biophysics and Biochemistry, School of Science, University of Tokyo, Japan.
Mol Biol Cell. 1995 Sep;6(9):1185-95. doi: 10.1091/mbc.6.9.1185.
We isolated the Schizosaccharomyces pombe zfs1 gene as a multicopy suppressor of the sterility caused by overexpression of a double-stranded RNase. The deduced zfs1 gene product of 404 amino acids showed similarity to a mouse growth factor-inducible nuclear protein Nup475. Its C-terminal region carried two putative zinc-fingers, both of which should be intact for the protein to be functional as the suppressor. This protein appeared to localize in nuclei. Disruption of zfs1 was not lethal but conferred deficiency in mating and sporulation. Activation of transcription in response to the mating pheromone signaling was greatly reduced in the zfs1-disrupted cells. The mating deficiency of the zfs1-disruptant was suppressed partially by overexpression of either gpa1, ras1, byr1, or byr2, which are involved in the transmission of the pheromone signal. Disruption of zfs1 reduced both hypersensitivity of the ras1Val17 mutant to the mating pheromone and uncontrolled mating response caused by mutational activation of Gpa1, the G protein alpha subunit coupled to the mating pheromone receptors. However, overexpression of zfs1 could not bypass complete loss of function of either gpa1, ras1, byr1, or byr2. These observations indicate that the function of zfs1 is involved in the mating pheromone signaling pathway, and are consistent with its function being required to fully activate a factor in this pathway, either directly or indirectly.
我们分离出粟酒裂殖酵母zfs1基因,作为由双链核糖核酸酶过表达导致的不育的多拷贝抑制因子。推导的由404个氨基酸组成的zfs1基因产物与小鼠生长因子诱导型核蛋白Nup475具有相似性。其C端区域带有两个推定的锌指结构,两者对于该蛋白发挥抑制因子功能均应保持完整。该蛋白似乎定位于细胞核中。zfs1基因的破坏并非致死性的,但导致交配和孢子形成缺陷。在zfs1基因破坏的细胞中,对交配信息素信号作出反应的转录激活大幅降低。zfs1基因破坏菌株的交配缺陷被gpa1、ras1、byr1或byr2的过表达部分抑制,这些基因参与信息素信号的传递。zfs1基因的破坏降低了ras1Val17突变体对交配信息素的超敏感性以及由与交配信息素受体偶联的G蛋白α亚基Gpa1的突变激活所导致的失控交配反应。然而,zfs1基因的过表达不能绕过gpa1、ras1、byr1或byr2功能的完全丧失。这些观察结果表明,zfs1的功能参与交配信息素信号通路,并且与其功能是直接或间接完全激活该通路中的一个因子所必需的这一观点一致。