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.
Skip Nav Destination
Article navigation
3 April 2000
Article|
April 03 2000
Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster
Yoshihiro H. Inoue,
Yoshihiro H. Inoue
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
bCell Cycle Genetics Research Group, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland
Search for other works by this author on:
Maria do Carmo Avides,
Maria do Carmo Avides
bCell Cycle Genetics Research Group, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland
cDepartment of Genetics, University of Cambridge, Cambridge CB2 3EH, England
Search for other works by this author on:
Michina Shiraki,
Michina Shiraki
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
Search for other works by this author on:
Peter Deak,
Peter Deak
bCell Cycle Genetics Research Group, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland
cDepartment of Genetics, University of Cambridge, Cambridge CB2 3EH, England
Search for other works by this author on:
Masamitsu Yamaguchi,
Masamitsu Yamaguchi
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
Search for other works by this author on:
Yoshio Nishimoto,
Yoshio Nishimoto
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
Search for other works by this author on:
Akio Matsukage,
Akio Matsukage
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
Search for other works by this author on:
David M. Glover
David M. Glover
bCell Cycle Genetics Research Group, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland
cDepartment of Genetics, University of Cambridge, Cambridge CB2 3EH, England
Search for other works by this author on:
Yoshihiro H. Inoue
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
bCell Cycle Genetics Research Group, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland
Maria do Carmo Avides
bCell Cycle Genetics Research Group, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland
cDepartment of Genetics, University of Cambridge, Cambridge CB2 3EH, England
Michina Shiraki
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
Peter Deak
bCell Cycle Genetics Research Group, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland
cDepartment of Genetics, University of Cambridge, Cambridge CB2 3EH, England
Masamitsu Yamaguchi
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
Yoshio Nishimoto
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
Akio Matsukage
aLaboratory of Cell Biology, Aichi Cancer Center, Research Institute, Nagoya 464-8681, Japan
David M. Glover
bCell Cycle Genetics Research Group, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, Scotland
cDepartment of Genetics, University of Cambridge, Cambridge CB2 3EH, England
Michina Shiraki's present address is Graduate School of Biological Sciences, Nara Institute of Science and Technology, Takayama-cho, lkoma, Nara 630-0101, Japan.
Abbreviations used in this paper: asp, abnormal spindle; aur, aurora; GST, glutathione S-transferase; MAP, microtubule-associated protein; mgr, merry-go-round.
Received:
August 24 1999
Revision Requested:
February 28 2000
Accepted:
February 29 2000
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 2000 The Rockefeller University Press
2000
The Rockefeller University Press
J Cell Biol (2000) 149 (1): 153–166.
Article history
Received:
August 24 1999
Revision Requested:
February 28 2000
Accepted:
February 29 2000
Citation
Yoshihiro H. Inoue, Maria do Carmo Avides, Michina Shiraki, Peter Deak, Masamitsu Yamaguchi, Yoshio Nishimoto, Akio Matsukage, David M. Glover; Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster. J Cell Biol 3 April 2000; 149 (1): 153–166. doi: https://doi.org/10.1083/jcb.149.1.153
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement