Orbit, a novel microtubule-associated protein essential for mitosis in Drosophila melanogaster

被引:110
|
作者
Inoue, YH
Avides, MD
Shiraki, M
Deak, P
Yamaguchi, M
Nishimoto, Y
Matsukage, A
Glover, DM
机构
[1] Aichi Canc Ctr, Res Inst, Cell Biol Lab, Nagoya, Aichi 4648681, Japan
[2] Univ Dundee, Inst Med Sci, Cell Cycle Genet Res Grp, Dundee DD1 4HN, Scotland
[3] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
来源
JOURNAL OF CELL BIOLOGY | 2000年 / 149卷 / 01期
关键词
mitosis; microtubule-associated protein; Drosophila melanogaster; mitotic spindle; centrosome;
D O I
10.1083/jcb.149.1.153
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We describe a Drosophila gene, orbit, that encodes a conserved 165-kD microtubule-associated protein (MAP) with GTP binding motifs, Hypomorphic mutations in orbit lead to a maternal effect resulting in branched and bent mitotic spindles in the syncytial embryo. In the larval central nervous system, such mutants have an elevated mitotic index with some mitotic cells showing an increase in ploidy. Amorphic alleles show late lethality and greater frequencies of hyperploid mitotic cells. The presence of cells in the hypomorphic mutant in which the chromosomes can be arranged, either in a circular metaphase or an anaphase-like configuration on monopolar spindles, suggests that polyploidy arises through spindle and chromosome segregation defects rather than defects in cytokinesis. A role for the Orbit protein in regulating microtubule behavior in mitosis is suggested by its association with microtubules throughout the spindle at all mitotic stages, by its copurification with microtubules from embryonic extracts, and by the finding that the Orbit protein directly binds to MAP-free microtubules in a GTP-dependent manner.
引用
收藏
页码:153 / 165
页数:13
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