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Spindle Self-organization and Cytokinesis During Male Meiosis in asterless Mutants of Drosophila melanogaster
While Drosophila female meiosis is anastral, both meiotic divisions in Drosophila males exhibit prominent asters. We have identified a gene we call asterless (asl) that is required for aster formation during male meiosis. Ultrastructural analysis showed that asl mutants have morphologically normal c...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148166/ https://www.ncbi.nlm.nih.gov/pubmed/9700163 |
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author | Bonaccorsi, Silvia Giansanti, Maria Grazia Gatti, Maurizio |
author_facet | Bonaccorsi, Silvia Giansanti, Maria Grazia Gatti, Maurizio |
author_sort | Bonaccorsi, Silvia |
collection | PubMed |
description | While Drosophila female meiosis is anastral, both meiotic divisions in Drosophila males exhibit prominent asters. We have identified a gene we call asterless (asl) that is required for aster formation during male meiosis. Ultrastructural analysis showed that asl mutants have morphologically normal centrioles. However, immunostaining with antibodies directed either to γ tubulin or centrosomin revealed that these proteins do not accumulate in the centrosomes, as occurs in wild-type. Thus, asl appears to specify a function required for the assembly of centrosomal material around the centrioles. Despite the absence of asters, meiotic cells of asl mutants manage to develop an anastral spindle. Microtubules grow from multiple sites around the chromosomes, and then focus into a peculiar bipolar spindle that mediates chromosome segregation, although in a highly irregular way. Surprisingly, asl spermatocytes eventually form a morphologically normal ana–telophase central spindle that has full ability to stimulate cytokinesis. These findings challenge the classical view on central spindle assembly, arguing for a self-organization of this structure from either preexisting or newly formed microtubules. In addition, these findings strongly suggest that the asters are not required for signaling cytokinesis. |
format | Text |
id | pubmed-2148166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21481662008-05-01 Spindle Self-organization and Cytokinesis During Male Meiosis in asterless Mutants of Drosophila melanogaster Bonaccorsi, Silvia Giansanti, Maria Grazia Gatti, Maurizio J Cell Biol Regular Articles While Drosophila female meiosis is anastral, both meiotic divisions in Drosophila males exhibit prominent asters. We have identified a gene we call asterless (asl) that is required for aster formation during male meiosis. Ultrastructural analysis showed that asl mutants have morphologically normal centrioles. However, immunostaining with antibodies directed either to γ tubulin or centrosomin revealed that these proteins do not accumulate in the centrosomes, as occurs in wild-type. Thus, asl appears to specify a function required for the assembly of centrosomal material around the centrioles. Despite the absence of asters, meiotic cells of asl mutants manage to develop an anastral spindle. Microtubules grow from multiple sites around the chromosomes, and then focus into a peculiar bipolar spindle that mediates chromosome segregation, although in a highly irregular way. Surprisingly, asl spermatocytes eventually form a morphologically normal ana–telophase central spindle that has full ability to stimulate cytokinesis. These findings challenge the classical view on central spindle assembly, arguing for a self-organization of this structure from either preexisting or newly formed microtubules. In addition, these findings strongly suggest that the asters are not required for signaling cytokinesis. The Rockefeller University Press 1998-08-10 /pmc/articles/PMC2148166/ /pubmed/9700163 Text en 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 | Regular Articles Bonaccorsi, Silvia Giansanti, Maria Grazia Gatti, Maurizio Spindle Self-organization and Cytokinesis During Male Meiosis in asterless Mutants of Drosophila melanogaster |
title | Spindle Self-organization and Cytokinesis During Male Meiosis in asterless Mutants of Drosophila melanogaster
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title_full | Spindle Self-organization and Cytokinesis During Male Meiosis in asterless Mutants of Drosophila melanogaster
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title_fullStr | Spindle Self-organization and Cytokinesis During Male Meiosis in asterless Mutants of Drosophila melanogaster
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title_full_unstemmed | Spindle Self-organization and Cytokinesis During Male Meiosis in asterless Mutants of Drosophila melanogaster
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title_short | Spindle Self-organization and Cytokinesis During Male Meiosis in asterless Mutants of Drosophila melanogaster
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title_sort | spindle self-organization and cytokinesis during male meiosis in asterless mutants of drosophila melanogaster |
topic | Regular Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2148166/ https://www.ncbi.nlm.nih.gov/pubmed/9700163 |
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