Cycling through development in Drosophila and other metazoa

被引:34
作者
Vidwans, SJ [1 ]
Su, TT
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[2] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
关键词
D O I
10.1038/35050681
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The cell-division cycle is an orchestrated sequence of events that results in the duplication of a cell. In metazoa, cell proliferation is regulated in response to differentiation signals and body-size parameters, which either induce cell duplication or arrest the cell cycle, to ensure that organs develop to the correct size. In addition, the cell cycle may be altered to meet specialized requirements. This can be seen in the rapid cleavage cycles of vertebrates and insects that lack gap phases, in the nested S phases of Drosophila, and in the endocycles of nematodes, insects, plants and mammals that lack mitosis. Here we present the various modes of cell-cycle regulation in metazoa and discuss their possible generation by a combination of universally conserved molecules and new regulatory circuits.
引用
收藏
页码:E35 / E39
页数:5
相关论文
共 56 条
[1]  
Ambros V, 1999, DEVELOPMENT, V126, P1947
[2]   Cdc25A stability is controlled by the ubiquitin-proteasome pathway during cell cycle progression and terminal differentiation [J].
Bernardi, R ;
Liebermann, DA ;
Hoffman, B .
ONCOGENE, 2000, 19 (20) :2447-2454
[3]   Cell polarity in the early Caenorhabditis elegans embryo [J].
Bowerman, B ;
Shelton, CA .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1999, 9 (04) :390-395
[4]  
Britton JS, 1998, DEVELOPMENT, V125, P2149
[5]  
Brodsky MH, 2000, GENE DEV, V14, P666
[6]   p21 is a transcriptional target of HOXA10 in differentiating myelomonocytic cells [J].
Bromleigh, VC ;
Freedman, LP .
GENES & DEVELOPMENT, 2000, 14 (20) :2581-2586
[7]  
Brown EJ, 2000, GENE DEV, V14, P397
[8]   CLEAVAGE ORIENTATION AND THE ASYMMETRIC INHERITANCE OF NOTCH1 IMMUNOREACTIVITY IN MAMMALIAN NEUROGENESIS [J].
CHENN, A ;
MCCONNELL, SK .
CELL, 1995, 82 (04) :631-641
[9]   Turnover of cyclin E by the ubiquitin-proteasome pathway is regulated by cdk2 binding and cyclin phosphorylation [J].
Clurman, BE ;
Sheaff, RJ ;
Thress, K ;
Groudine, M ;
Roberts, JM .
GENES & DEVELOPMENT, 1996, 10 (16) :1979-1990
[10]  
CUI X, 1995, DEVELOPMENT, V121, P3233