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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >A developmentally regulated translational control pathway establishes the meiotic chromosome segregation pattern
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A developmentally regulated translational control pathway establishes the meiotic chromosome segregation pattern

机译:发育调控的翻译控制途径建立了减数分裂染色体分离模式

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摘要

Production of haploid gametes from diploid progenitor cells is mediated by a specialized cell division, meiosis, where two divisions, meiosis I and II, follow a single S phase. Errors in progression from meiosis I to meiosis II lead to aneuploid and polyploid gametes, but the regulatory mechanisms controlling this transition are poorly understood. Here, we demonstrate that the conserved kinase Ime2 regulates the timing and order of the meiotic divisions by controlling translation. Ime2 coordinates translational activation of a cluster of genes at the meiosis I-meiosis II transition, including the critical determinant of the meiotic chromosome segregation pattern CLB3. We further show that Ime2 mediates translational control through the meiosis-specific RNA-binding protein Rim4. Rim4 inhibits translation of CLB3 during meiosis I by interacting with the 59 untranslated region (UTR) of CLB3. At the onset of meiosis II, Ime2 kinase activity rises and triggers a decrease in Rim4 protein levels, thereby alleviating translational repression. Our results elucidate a novel developmentally regulated translational control pathway that establishes the meiotic chromosome segregation pattern.
机译:由二倍体祖细胞产生单倍体配子是由专门的细胞分裂减数分裂介导的,减数分裂I和II的两个分裂遵循一个S期。从减数分裂I到减数分裂II的进行过程中的错误导致非整倍体和多倍体配子,但控制这种转变的调控机制了解甚少。在这里,我们证明了保守的激酶Ime2通过控制翻译来调节减数分裂分裂的时间和顺序。 Ime2协调减数分裂I-减数分裂II转换时一组基因的翻译激活,包括减数分裂染色体分离模式CLB3的关键决定因素。我们进一步显示Ime2通过减数分裂特异性RNA结合蛋白Rim4介导翻译控制。 Rim4通过与CLB3的59个非翻译区(UTR)相互作用来抑制减数分裂I期间CLB3的翻译。在减数分裂II发作时,Ime2激酶活性升高并触发Rim4蛋白水平降低,从而减轻翻译抑制。我们的结果阐明了建立减数分裂染色体分离模式的新型发育调控翻译控制途径。

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