Division of Cellular and Developmental Biology, MCB Department, University of California, Berkeley, Berkeley, CA 94720, USA.
Department of Genetics, Edison Family Center for Genome Science and System Biology, McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO 63110, USA.
Cell. 2021 Oct 28;184(22):5541-5558.e22. doi: 10.1016/j.cell.2021.09.021. Epub 2021 Oct 12.
Retrotransposons mediate gene regulation in important developmental and pathological processes. Here, we characterized the transient retrotransposon induction during preimplantation development of eight mammals. Induced retrotransposons exhibit similar preimplantation profiles across species, conferring gene regulatory activities, particularly through long terminal repeat (LTR) retrotransposon promoters. A mouse-specific MT2B2 retrotransposon promoter generates an N-terminally truncated Cdk2ap1 that peaks in preimplantation embryos and promotes proliferation. In contrast, the canonical Cdk2ap1 peaks in mid-gestation and represses cell proliferation. This MT2B2 promoter, whose deletion abolishes Cdk2ap1 production, reduces cell proliferation and impairs embryo implantation, is developmentally essential. Intriguingly, Cdk2ap1 is evolutionarily conserved in sequence and function yet is driven by different promoters across mammals. The distinct preimplantation Cdk2ap1 expression in each mammalian species correlates with the duration of its preimplantation development. Hence, species-specific transposon promoters can yield evolutionarily conserved, alternative protein isoforms, bestowing them with new functions and species-specific expression to govern essential biological divergence.
逆转录转座子在重要的发育和病理过程中调节基因表达。在这里,我们描述了八种哺乳动物着床前发育过程中逆转录转座子的瞬时诱导。诱导的逆转录转座子在物种间表现出相似的着床前特征,赋予基因调控活性,特别是通过长末端重复(LTR)逆转录转座子启动子。一个鼠特异性的 MT2B2 逆转录转座子启动子产生一个 N 端截断的 Cdk2ap1,在着床前胚胎中达到峰值,并促进增殖。相比之下,经典的 Cdk2ap1 在妊娠中期达到峰值,抑制细胞增殖。这个 MT2B2 启动子,其缺失会消除 Cdk2ap1 的产生,减少细胞增殖并损害胚胎着床,在发育上是必需的。有趣的是,Cdk2ap1 在序列和功能上在进化上是保守的,但在哺乳动物中却由不同的启动子驱动。每种哺乳动物中独特的着床前 Cdk2ap1 表达与它们的着床前发育时间相关。因此,特异性转座子启动子可以产生进化上保守的、替代的蛋白质同工型,赋予它们新的功能和物种特异性表达,以控制重要的生物学分歧。