Sherman A, Shefer M, Sagee S, Kassir Y
Department of Genetics, Hebrew University, Jerusalem, Israel.
Mol Gen Genet. 1993 Mar;237(3):375-84. doi: 10.1007/BF00279441.
The IME1 gene of Saccharomyces cerevisiae is required for initiation of meiosis. Transcription of IME1 is detected under conditions which are known to induce initiation of meiosis, namely starvation for nitrogen and glucose, and the presence of MATa1 and MAT alpha 2 gene products. In this paper we show that IME1 is also subject to translational regulation. Translation of IME1 mRNA is achieved either upon nitrogen starvation, or upon G1 arrest. In the presence of nutrients, constitutively elevated transcription of IME1 is also sufficient for the translation of IME1 RNA. Four different conditions were found to cause expression of Ime1 protein in vegetative cultures: elevated transcription levels due to the presence of IME1 on a multicopy plasmid; elevated transcription provided by a Gal-IME1 construct; G1 arrest due to alpha-factor treatment; G1 arrest following mild heat-shock treatment of cdc28 diploids. Using these conditions, we obtained evidence that starvation is required not only for transcription and efficient translation of IME1, but also for either the activation of Ime1 protein or for the induction/activation of another factor that, either alone or in combination with Ime1, induces meiosis.
酿酒酵母的IME1基因是减数分裂起始所必需的。在已知可诱导减数分裂起始的条件下,即氮和葡萄糖饥饿以及MATa1和MATα2基因产物存在时,可检测到IME1的转录。在本文中,我们表明IME1也受到翻译调控。IME1 mRNA的翻译可在氮饥饿时或G1期停滞时实现。在有营养物质存在的情况下,IME1组成型升高的转录对于IME1 RNA的翻译也是足够的。发现有四种不同的条件可导致营养细胞培养物中Ime1蛋白的表达:由于多拷贝质粒上存在IME1而导致转录水平升高;由Gal-IME1构建体提供的转录升高;α因子处理导致的G1期停滞;对cdc28二倍体进行轻度热休克处理后的G1期停滞。利用这些条件,我们获得了证据,表明饥饿不仅是IME1转录和有效翻译所必需的,而且对于Ime1蛋白的激活或另一种因子的诱导/激活也是必需的,该因子单独或与Ime1结合可诱导减数分裂。