Lane M E, Sauer K, Wallace K, Jan Y N, Lehner C F, Vaessin H
Friedrich-Miescher-Laboratorium der Max-Planck-Gesellschaft, Tübingen,Federal Republic of Germany.
Cell. 1996 Dec 27;87(7):1225-35. doi: 10.1016/s0092-8674(00)81818-8.
Most cell types in multicellular eukaryotes exit from the mitotic cell cycle before terminal differentiation. We show that the dacapo gene is required to arrest the epidermal cell proliferation at the correct developmental stage during Drosophila embryogenesis. dacapo encodes an inhibitor of cyclin E/cdk2 complexes with similarity to the vertebrate Cip/Kip inhibitors. dacapo is transiently expressed beginning late in the G2 phase preceding the terminal division (mitosis 16). Mutants unable to express the inhibitor fail to arrest cell proliferation after mitosis 16 and progress through an extra division cycle. Conversely, premature dacapo expression in transgenic embryos results in a precocious G1 arrest.
多细胞真核生物中的大多数细胞类型在终末分化之前就退出有丝分裂细胞周期。我们发现,dacapo基因对于在果蝇胚胎发育的正确发育阶段阻止表皮细胞增殖是必需的。dacapo编码一种与脊椎动物Cip/Kip抑制剂相似的细胞周期蛋白E/细胞周期蛋白依赖性激酶2(cyclin E/cdk2)复合物的抑制剂。dacapo在终末分裂(有丝分裂16)之前的G2期晚期开始短暂表达。无法表达该抑制剂的突变体在有丝分裂16之后无法阻止细胞增殖,并进入额外的分裂周期。相反,在转基因胚胎中过早表达dacapo会导致过早的G1期停滞。