Jeong Hee Tae, Oowatari Yasuo, Abe Michiyo, Tanaka Katsunori, Matsuda Hideyuki, Kawamukai Makoto
Department of Life Science and Biotechnology, Faculty of Life and Environmental Science, Shimane University, 1060 Nishikawatsu, Matsue 690-8504, Japan.
Biosci Biotechnol Biochem. 2004 Jul;68(7):1621-6. doi: 10.1271/bbb.68.1621.
The sexual differentiation of Schizosaccharomyces pombe is controlled by many cellular components which have not been fully characterized. We isolated a gene called msa2 as a multi-copy suppressor of a sporulation abnormal mutant (sam1). Msa2p is identical with Nrd1p which has been characterized as a factor that blocks the onset of sexual differentiation. The yeast two-hybrid system was used to identify Cpc2p, a fission yeast homolog of the RACK1 protein, that interacted with Msa2p/Nrd1p. We confirmed that Msa2p/Nrd1p interacted with Cpc2p in S. pombe cells. An epistatic analysis of msa2/nrd1 and cpc2 suggests that Msa2p/Nrd1p was an upstream regulator for Cpc2p. A localization analysis of Cpc2p and Msa2p/Nrd1p indicates that both proteins were predominantly localized in the cytoplasm. The interaction of negative regulator Msa2p/Nrd1p with positive regulator Cpc2p suggests a new regulatory circuit in the sexual differentiation of S. pombe.
粟酒裂殖酵母的性别分化受许多尚未完全表征的细胞成分控制。我们分离出一个名为msa2的基因,作为孢子形成异常突变体(sam1)的多拷贝抑制子。Msa2p与Nrd1p相同,Nrd1p已被表征为一种阻止性别分化起始的因子。利用酵母双杂交系统鉴定出与Msa2p/Nrd1p相互作用的Cpc2p,它是RACK1蛋白在裂殖酵母中的同源物。我们证实在粟酒裂殖酵母细胞中Msa2p/Nrd1p与Cpc2p相互作用。对msa2/nrd1和cpc2进行上位性分析表明,Msa2p/Nrd1p是Cpc2p的上游调节因子。对Cpc2p和Msa2p/Nrd1p的定位分析表明,这两种蛋白主要定位于细胞质中。负调节因子Msa2p/Nrd1p与正调节因子Cpc2p的相互作用提示了粟酒裂殖酵母性别分化中的一种新的调节回路。