共 127 条
Targeting of γ-tubulin complexes to microtubule organizing centers: conservation and divergence
被引:89
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Neuner, Annett
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机构:
Heidelberg Univ, Zentrum Mol Biol, ZMBH, DKFZ ZMBH Allianz, D-69120 Heidelberg, Germany Heidelberg Univ, Zentrum Mol Biol, ZMBH, DKFZ ZMBH Allianz, D-69120 Heidelberg, Germany

Schiebel, Elmar
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Heidelberg Univ, Zentrum Mol Biol, ZMBH, DKFZ ZMBH Allianz, D-69120 Heidelberg, Germany Heidelberg Univ, Zentrum Mol Biol, ZMBH, DKFZ ZMBH Allianz, D-69120 Heidelberg, Germany
机构:
[1] Heidelberg Univ, Zentrum Mol Biol, ZMBH, DKFZ ZMBH Allianz, D-69120 Heidelberg, Germany
关键词:
microtubule;
gamma-tubulin complex;
mitotic spindle;
centrosome;
spindle pole body;
SPINDLE-POLE-BODY;
FISSION YEAST;
RING COMPLEX;
MITOTIC SPINDLE;
CG-NAP;
SCHIZOSACCHAROMYCES-POMBE;
SACCHAROMYCES-CEREVISIAE;
CHROMOSOME SEGREGATION;
CENTROSOMAL PROTEINS;
ASPERGILLUS-NIDULANS;
D O I:
10.1016/j.tcb.2014.12.002
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Organisms with closed or open mitosis have differentially evolved various gamma-tubulin complex (gamma-TuC) recruiting factors to organize diverse cellular microtubule (MT) arrays, including the mitotic spindle. gamma-TuC recruiting factors not only target the gamma-TuC to MT nucleation sites, but also regulate MT nucleation activity by generating the template for MT nucleation or promoting the MT nucleation activity of pre-existing gamma-tubulin ring complexes (gamma-TuRCs). Here we outline the current understanding of MT nucleator assembly and its regulation by gamma-tubulin small complex (gamma-TuSC) receptors. Moreover, we discuss the emergence of gamma-TuC recruiting factors through evolution with augmented complexity and diversity and propose a hypothesis to account for the evolution of these factors in cooperative spindle assembly.
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页码:296 / 307
页数:12
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