Watanabe Y, Shinozaki-Yabana S, Chikashige Y, Hiraoka Y, Yamamoto M
Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Japan.
Nature. 1997 Mar 13;386(6621):187-90. doi: 10.1038/386187a0.
Meiosis generates haploid gametes from diploid cells and is an almost universal feature of eukaryotic organisms. But little is known about how the switch from mitotic to meiotic cell cycles is molecularly controlled. In the fission yeast Schizosaccharomyces pombe, inactivation of the protein kinase Pat1(Ran1) upon nutrient deprivation triggers entry into the meiotic cell cycle. Here we show that the RNA-binding protein Mei2 is a substrate of Pat1 kinase and that dephosphorylation of Mei2 is sufficient to switch cells from the mitotic cell cycle into meiosis. Mei2 is localized mainly in the cytoplasm of proliferating cells but is seen as a single spot close to the microtubule organizing centre in prophase nuclei during meiosis. Our results, and others from a metazoan, emphasize the crucial role of RNA-binding proteins in the initiation and execution of meiosis.
减数分裂从二倍体细胞产生单倍体配子,是真核生物几乎普遍具有的特征。但是,关于从有丝分裂细胞周期向减数分裂细胞周期的转变是如何在分子水平上受到控制的,人们了解得很少。在裂殖酵母粟酒裂殖酵母中,营养剥夺时蛋白激酶Pat1(Ran1)的失活会触发进入减数分裂细胞周期。在这里,我们表明RNA结合蛋白Mei2是Pat1激酶的底物,并且Mei2的去磷酸化足以使细胞从有丝分裂细胞周期转变为减数分裂。Mei2主要定位于增殖细胞的细胞质中,但在减数分裂前期核中,它在靠近微管组织中心的位置呈现为一个单点。我们的结果以及来自后生动物的其他结果强调了RNA结合蛋白在减数分裂起始和执行中的关键作用。