Institute of Genetic Medicine, Newcastle University, Newcastle, United Kingdom.
MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Elife. 2019 Jan 24;8:e39304. doi: 10.7554/eLife.39304.
Male germ cells of all placental mammals express an ancient nuclear RNA binding protein of unknown function called RBMXL2. Here we find that deletion of the retrogene encoding RBMXL2 blocks spermatogenesis. Transcriptome analyses of age-matched deletion mice show that RBMXL2 controls splicing patterns during meiosis. In particular, RBMXL2 represses the selection of aberrant splice sites and the insertion of cryptic and premature terminal exons. Our data suggest a retrogene has been conserved across mammals as part of a splicing control mechanism that is fundamentally important to germ cell biology. We propose that this mechanism is essential to meiosis because it buffers the high ambient concentrations of splicing activators, thereby preventing poisoning of key transcripts and disruption to gene expression by aberrant splice site selection.
所有胎盘哺乳动物的雄性生殖细胞都表达一种古老的核 RNA 结合蛋白,称为 RBMXL2,但它的功能未知。在这里,我们发现编码 RBMXL2 的反转录基因缺失会阻止精子发生。对年龄匹配的基因缺失小鼠的转录组分析表明,RBMXL2 控制减数分裂过程中的剪接模式。特别是,RBMXL2 抑制了异常剪接位点的选择以及隐藏和过早的末端外显子的插入。我们的数据表明,作为剪接控制机制的一部分,反转录基因在哺乳动物中被保守,这对于生殖细胞生物学至关重要。我们提出,这种机制对于减数分裂至关重要,因为它缓冲了高浓度的剪接激活剂,从而防止关键转录本中毒和异常剪接位点选择对基因表达的破坏。