Cell and molecular biology of spindle poles and NuMA

被引:44
作者
Fant, X
Merdes, A
Haren, L
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[2] CNRS Pierre Fabre, Ctr Rech Pharmacol Sante, UMR 2587, F-31400 Toulouse, France
来源
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL. 238 | 2004年 / 238卷
关键词
spindle; mitosis; meiosis; microtubules; motor proteins; NuMA;
D O I
10.1016/S0074-7696(04)38001-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitotic and meiotic cells contain a bipolar spindle apparatus of microtubules and associated proteins. To arrange microtubules into focused spindle poles, different mechanisms are used by various organisms. Principally, two major pathways have been characterized: nucleation and anchorage of microtubules at preexisting centers such as centrosomes or spindle pole bodies, or microtubule growth off the surface of chromosomes, followed by sorting and focusing into spindle poles. These two mechanisms can even be found in cells of the same organism: whereas most somatic animal cells utilize the centrosome as an organizing center for spindle microtubules, female meiotic cells build an acentriolar spindle apparatus. Most interestingly, the molecular components that drive acentriolar spindle pole formation are also present in cells containing centrosomes. They include microtubule-dependent motor proteins and a variety of structural proteins that regulate microtubule orientation, anchoring, and stability. The first of these spindle pole proteins, NuMA, had already been identified more than 20 years ago. In addition, several new proteins have been characterized more recently. This review discusses their role during spindle formation and their regulation in the cell cycle.
引用
收藏
页码:1 / 57
页数:57
相关论文
共 252 条
[1]   Spindle pole body duplication: a model for centrosome duplication? [J].
Adams, IR ;
Kilmartin, JV .
TRENDS IN CELL BIOLOGY, 2000, 10 (08) :329-335
[2]  
ANDO A, 1994, IMMUNOGENETICS, V39, P194
[3]   Abnormal spindle protein, asp, and the integrity of mitotic centrosomal microtubule organizing centers [J].
Avides, MD ;
Glover, DM .
SCIENCE, 1999, 283 (5408) :1733-1735
[4]   Polo kinase and Asp are needed to promote the mitotic organizing activity of centrosomes [J].
Avides, MD ;
Tavares, A ;
Glover, DM .
NATURE CELL BIOLOGY, 2001, 3 (04) :421-424
[5]   Unraveling the organization of the internal nuclear matrix: RNA-dependent anchoring of NuMA to a lamin scaffold [J].
Barboro, P ;
D'Arrigo, C ;
Diaspro, A ;
Mormino, M ;
Alberti, I ;
Parodi, S ;
Patrone, E ;
Balbi, C .
EXPERIMENTAL CELL RESEARCH, 2002, 279 (02) :202-218
[6]   Structural basis of Aurora-A activation by TPX2 at the mitotic spindle [J].
Bayliss, R ;
Sardon, T ;
Vernos, I ;
Conti, E .
MOLECULAR CELL, 2003, 12 (04) :851-862
[7]   TAC-1 and ZYG-9 form a complex that promotes microtubule assembly in C-elegans embryos [J].
Bellanger, JM ;
Gönczy, P .
CURRENT BIOLOGY, 2003, 13 (17) :1488-1498
[8]   Drosophila aurora-A is required for centrosome maturation and actin-dependent asymmetric protein localization during mitosis [J].
Berdnik, D ;
Knoblich, JA .
CURRENT BIOLOGY, 2002, 12 (08) :640-647
[9]   Pim-1 associates with protein complexes necessary for mitosis [J].
Bhattacharya, N ;
Wang, ZP ;
Davitt, C ;
McKenzie, IFC ;
Xing, PX ;
Magnuson, NS .
CHROMOSOMA, 2002, 111 (02) :80-95
[10]   Phosphorylation by p34(cdc2) protein kinase regulates binding of the kinesin-related motor HsEg5 to the dynactin subunit p150(Glued) [J].
Blangy, A ;
Arnaud, L ;
Nigg, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (31) :19418-19424