Dacapo, a cyclin-dependent kinase inhibitor, stops cell proliferation during Drosophila development

被引:281
作者
Lane, ME
Sauer, K
Wallace, K
Jan, YN
Lehner, CF
Vaessin, H
机构
[1] MAX PLANCK GESELL,FRIEDRICH MIESCHER LAB,D-72076 TUBINGEN,GERMANY
[2] OHIO STATE UNIV,DEPT MOL GENET,CTR NEUROBIOTECHNOL,COLUMBUS,OH 43210
[3] UNIV CALIF SAN FRANCISCO,HOWARD HUGHES MED INST,DEPT PHYSIOL,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,HOWARD HUGHES MED INST,DEPT BIOCHEM,SAN FRANCISCO,CA 94143
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0092-8674(00)81818-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1225 / 1235
页数:11
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