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Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster
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,...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175100/ https://www.ncbi.nlm.nih.gov/pubmed/10747094 |
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author | Inoue, Yoshihiro H. do Carmo Avides, Maria Shiraki, Michina Deak, Peter Yamaguchi, Masamitsu Nishimoto, Yoshio Matsukage, Akio Glover, David M. |
author_facet | Inoue, Yoshihiro H. do Carmo Avides, Maria Shiraki, Michina Deak, Peter Yamaguchi, Masamitsu Nishimoto, Yoshio Matsukage, Akio Glover, David M. |
author_sort | Inoue, Yoshihiro H. |
collection | PubMed |
description | 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. |
format | Text |
id | pubmed-2175100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21751002008-05-01 Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster Inoue, Yoshihiro H. do Carmo Avides, Maria Shiraki, Michina Deak, Peter Yamaguchi, Masamitsu Nishimoto, Yoshio Matsukage, Akio Glover, David M. J Cell Biol Original Article 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. The Rockefeller University Press 2000-04-03 /pmc/articles/PMC2175100/ /pubmed/10747094 Text en © 2000 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Original Article Inoue, Yoshihiro H. do Carmo Avides, Maria Shiraki, Michina Deak, Peter Yamaguchi, Masamitsu Nishimoto, Yoshio Matsukage, Akio Glover, David M. Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster |
title | Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster
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title_full | Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster
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title_fullStr | Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster
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title_full_unstemmed | Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster
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title_short | Orbit, a Novel Microtubule-Associated Protein Essential for Mitosis in Drosophila melanogaster
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title_sort | orbit, a novel microtubule-associated protein essential for mitosis in drosophila melanogaster |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175100/ https://www.ncbi.nlm.nih.gov/pubmed/10747094 |
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