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Selective elimination of messenger RNA prevents an incidence of untimely meiosis

机译:选择性消除信使RNA可防止发生不适当的减数分裂

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Much remains unknown about the molecular regulation of meiosis. Here we show that meiosis-specific transcripts are selectively removed if expressed during vegetative growth in fission yeast. These messenger RNAs contain a cis-acting region-which we call the DSR-that confers this removal via binding to a YTH-family protein Mmi1. Loss of Mmi1 function severely impairs cell growth owing to the untimely expression of meiotic transcripts. Microarray analysis reveals that at least a dozen such meiosis-specific transcripts are eliminated by the DSR-Mmi1 system. Mmi1 remains in the form of multiple nuclear foci during vegetative growth. At meiotic prophase these foci precipitate to a single focus, which coincides with the dot formed by the master meiosis-regulator Mei2. A meiotic arrest due to the loss of the Mei2 dot is released by a reduction in Mmi1 activity. We propose that Mei2 turns off the DSR-Mmi1 system by sequestering Mmi1 to the dot and thereby secures stable expression of meiosis-specific transcripts.
机译:关于减数分裂的分子调控尚不清楚。在这里,我们显示,如果在裂殖酵母的营养生长过程中表达,减数分裂特异的转录本会被选择性去除。这些信使RNA包含一个顺式作用区(我们称为DSR),该区域通过与YTH家族蛋白Mmi1结合而赋予这种去除作用。由于减数分裂转录物的过时表达,Mmi1功能的丧失严重损害了细胞的生长。微阵列分析显示,DSR-Mmi1系统消除了至少十二种此类减数分裂特异的转录本。 Mmi1在营养生长过程中仍以多个核病灶的形式存在。在减数分裂前期,这些病灶沉淀到一个单一的焦点,这与主要的减数分裂调节因子Mei2形成的点重合。通过减少Mmi1活性释放由于Mei2点丢失而引起的减数分裂停滞。我们建议Mei2通过将Mmi1隔离到点上来关闭DSR-Mmi1系统,从而确保减数分裂特异转录本的稳定表达。

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