Department of Life Science and Biotechnology, Faculty of Life and Environmental Science, Shimane University, 1060 Nishikawatsu, Matsue, 690-8504, Japan.
Curr Genet. 2011 Jun;57(3):191-200. doi: 10.1007/s00294-011-0335-5. Epub 2011 Mar 16.
The msa2/nrd1 gene encodes an RNA-binding protein that negatively regulates sexual differentiation of fission yeast Schizosaccharomyces pombe by repressing the Ste11-regulated genes. However, it is not known how Msa2 regulates sexual differentiation, and to characterize its role, we altered the msa2 gene by inducing point mutations and tested the resulting mutants for their ability to inhibit sexual differentiation and their suppressive effect on a temperature sensitive pat1 mutant. Several amino acids were found to be important, including three phenylalanine residues (F153, F245 and F453) in the three consensus RNA recognition motifs (RRMs) and a threonine residue (T126) that normally functions as a phosphorylation site. Results indicated that Msa2 was negatively regulated by phosphorylation that arose from Spk1-mediated pheromone signaling. Msa2 also regulated the Ste11 protein level coordinating with Cpc2, a ribosomal-associated protein. In addition, Msa2 was detected in stress granules that co-localized with Pabp in the cytosol under conditions of glucose starvation. Msa2 may regulate the translation of Ste11, be a component of stress granules that form in response to glucose starvation, and regulate the sexual differentiation of S. pombe.
msa2/nrd1 基因编码一种 RNA 结合蛋白,通过抑制 Ste11 调控基因,负调控裂殖酵母 Schizosaccharomyces pombe 的性别分化。然而,目前尚不清楚 Msa2 如何调节性别分化,为了表征其作用,我们通过诱导点突变改变了 msa2 基因,并测试了由此产生的突变体抑制性别分化的能力及其对温度敏感型 pat1 突变体的抑制作用。发现几个氨基酸很重要,包括三个苯丙氨酸残基(F153、F245 和 F453)在三个公认的 RNA 识别基序(RRMs)中,以及一个苏氨酸残基(T126),该残基通常作为磷酸化位点发挥作用。结果表明,Msa2 受到 Spk1 介导的信息素信号转导引起的磷酸化的负调控。Msa2 还调节 Ste11 蛋白水平,与核糖体相关蛋白 Cpc2 协调。此外,在葡萄糖饥饿条件下,Msa2 检测到在细胞质中与 Pabp 共定位的应激颗粒中。Msa2 可能调节 Ste11 的翻译,作为应激颗粒的组成部分,应激颗粒是对葡萄糖饥饿的反应而形成的,并且调节 S. pombe 的性别分化。