Kim Jun Hyun, Gurumurthy Channabasavaiah Basavaraju, Naramura Mayumi, Zhang Ying, Dudley Andrew T, Doglio Lynn, Band Hamid, Band Vimla
Department of Genetics, College of Medicine, University of Nebraska Medical Center, Omaha, Nebraska 68198-5805, USA.
J Biol Chem. 2009 Sep 25;284(39):26402-10. doi: 10.1074/jbc.M109.030551. Epub 2009 Jul 29.
The Ecdysoneless (Ecd) protein is required for cell-autonomous roles in development and oogenesis in Drosophila, but the function of its evolutionarily conserved mammalian orthologs is not clear. To study the cellular function of Ecd in mammalian cells, we generated Ecd(lox/lox) mouse embryonic fibroblast cells from Ecd floxed mouse embryos. Cre-mediated deletion of Ecd in Ecd(lox/lox) mouse embryonic fibroblasts led to a proliferative block due to a delay in G(1)-S cell cycle progression; this defect was reversed by the introduction of human Ecd. Loss of Ecd led to marked down-regulation of E2F target gene expression. Furthermore, Ecd directly bound to Rb at the pocket domain and competed with E2F for binding to hypophosphorylated Rb. Our results demonstrate that mammalian Ecd plays a role in cell cycle progression via the Rb-E2F pathway.
无蜕皮激素蛋白(Ecd)在果蝇的发育和卵子发生中具有细胞自主功能,但与其进化上保守的哺乳动物直系同源物的功能尚不清楚。为了研究Ecd在哺乳动物细胞中的细胞功能,我们从Ecd基因敲除小鼠胚胎中生成了Ecd(lox/lox)小鼠胚胎成纤维细胞。在Ecd(lox/lox)小鼠胚胎成纤维细胞中,Cre介导的Ecd缺失由于G(1)-S细胞周期进程延迟而导致增殖阻滞;引入人Ecd可逆转此缺陷。Ecd的缺失导致E2F靶基因表达显著下调。此外,Ecd在口袋结构域直接与Rb结合,并与E2F竞争结合低磷酸化的Rb。我们的结果表明,哺乳动物Ecd通过Rb-E2F途径在细胞周期进程中发挥作用。