| Literature DB >> 34644528 |
Andrew J Modzelewski1, Wanqing Shao2, Jingqi Chen1, Angus Lee1, Xin Qi1, Mackenzie Noon1, Kristy Tjokro1, Gabriele Sales3, Anne Biton4, Aparna Anand2, Terence P Speed5, Zhenyu Xuan6, Ting Wang7, Davide Risso8, Lin He9.
Abstract
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 Cdk2ap1ΔN 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 Cdk2ap1ΔN production, reduces cell proliferation and impairs embryo implantation, is developmentally essential. Intriguingly, Cdk2ap1ΔN is evolutionarily conserved in sequence and function yet is driven by different promoters across mammals. The distinct preimplantation Cdk2ap1ΔN 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.Entities:
Keywords: Cdk2; Cdk2ap1; cell proliferation; implantation; mammals; mouse; preimplantation embryos; promoters; retrotransposons; transposons
Mesh:
Substances:
Year: 2021 PMID: 34644528 PMCID: PMC8787082 DOI: 10.1016/j.cell.2021.09.021
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582