Gamma-tubulin is required for bipolar spindle assembly and for proper kinetochore microtubule attachments during prometaphase I in Drosophila oocytes
In many animal species the meiosis I spindle in oocytes is anastral and lacks centrosomes. Previous studies of Drosophila oocytes failed to detect the native form of the germline-specific γ-tubulin (γTub37C) in meiosis I spindles, and genetic studies have yielded conflicting data regarding the role...
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Published in: | PLoS genetics Vol. 7; no. 8; p. e1002209 |
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Abstract | In many animal species the meiosis I spindle in oocytes is anastral and lacks centrosomes. Previous studies of Drosophila oocytes failed to detect the native form of the germline-specific γ-tubulin (γTub37C) in meiosis I spindles, and genetic studies have yielded conflicting data regarding the role of γTub37C in the formation of bipolar spindles at meiosis I. Our examination of living and fixed oocytes carrying either a null allele or strong missense mutation in the γtub37C gene demonstrates a role for γTub37C in the positioning of the oocyte nucleus during late prophase, as well as in the formation and maintenance of bipolar spindles in Drosophila oocytes. Prometaphase I spindles in γtub37C mutant oocytes showed wide, non-tapered spindle poles and disrupted positioning. Additionally, chromosomes failed to align properly on the spindle and showed morphological defects. The kinetochores failed to properly co-orient and often lacked proper attachments to the microtubule bundles, suggesting that γTub37C is required to stabilize kinetochore microtubule attachments in anastral spindles. Although spindle bipolarity was sometimes achieved by metaphase I in both γtub37C mutants, the resulting chromosome masses displayed highly disrupted chromosome alignment. Therefore, our data conclusively demonstrate a role for γTub37C in both the formation of the anastral meiosis I spindle and in the proper attachment of kinetochore microtubules. Finally, multispectral imaging demonstrates the presences of native γTub37C along the length of wild-type meiosis I spindles. |
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AbstractList | In many animal species the meiosis I spindle in oocytes is anastral and lacks centrosomes. Previous studies of Drosophila oocytes failed to detect the native form of the germline-specific γ-tubulin (γTub37C) in meiosis I spindles, and genetic studies have yielded conflicting data regarding the role of γTub37C in the formation of bipolar spindles at meiosis I. Our examination of living and fixed oocytes carrying either a null allele or strong missense mutation in the γtub37C gene demonstrates a role for γTub37C in the positioning of the oocyte nucleus during late prophase, as well as in the formation and maintenance of bipolar spindles in Drosophila oocytes. Prometaphase I spindles in γtub37C mutant oocytes showed wide, non-tapered spindle poles and disrupted positioning. Additionally, chromosomes failed to align properly on the spindle and showed morphological defects. The kinetochores failed to properly co-orient and often lacked proper attachments to the microtubule bundles, suggesting that γTub37C is required to stabilize kinetochore microtubule attachments in anastral spindles. Although spindle bipolarity was sometimes achieved by metaphase I in both γtub37C mutants, the resulting chromosome masses displayed highly disrupted chromosome alignment. Therefore, our data conclusively demonstrate a role for γTub37C in both the formation of the anastral meiosis I spindle and in the proper attachment of kinetochore microtubules. Finally, multispectral imaging demonstrates the presences of native γTub37C along the length of wild-type meiosis I spindles. In many animal species the meiosis I spindle in oocytes is anastral and lacks centrosomes. Previous studies of Drosophila oocytes failed to detect the native form of the germline-specific γ-tubulin (γTub37C) in meiosis I spindles, and genetic studies have yielded conflicting data regarding the role of γTub37C in the formation of bipolar spindles at meiosis I. Our examination of living and fixed oocytes carrying either a null allele or strong missense mutation in the γtub37C gene demonstrates a role for γTub37C in the positioning of the oocyte nucleus during late prophase, as well as in the formation and maintenance of bipolar spindles in Drosophila oocytes. Prometaphase I spindles in γtub37C mutant oocytes showed wide, non-tapered spindle poles and disrupted positioning. Additionally, chromosomes failed to align properly on the spindle and showed morphological defects. The kinetochores failed to properly co-orient and often lacked proper attachments to the microtubule bundles, suggesting that γTub37C is required to stabilize kinetochore microtubule attachments in anastral spindles. Although spindle bipolarity was sometimes achieved by metaphase I in both γtub37C mutants, the resulting chromosome masses displayed highly disrupted chromosome alignment. Therefore, our data conclusively demonstrate a role for γTub37C in both the formation of the anastral meiosis I spindle and in the proper attachment of kinetochore microtubules. Finally, multispectral imaging demonstrates the presences of native γTub37C along the length of wild-type meiosis I spindles. In many animal species the meiosis I spindle in oocytes is anastral and lacks centrosomes. Previous studies of Drosophila oocytes failed to detect the native form of the germline-specific γ -tubulin (γTub37C) in meiosis I spindles, and genetic studies have yielded conflicting data regarding the role of γTub37C in the formation of bipolar spindles at meiosis I. Our examination of living and fixed oocytes carrying either a null allele or strong missense mutation in the γtub37C gene demonstrates a role for γTub37C in the positioning of the oocyte nucleus during late prophase, as well as in the formation and maintenance of bipolar spindles in Drosophila oocytes. Prometaphase I spindles in γtub37C mutant oocytes showed wide, non-tapered spindle poles and disrupted positioning. Additionally, chromosomes failed to align properly on the spindle and showed morphological defects. The kinetochores failed to properly co-orient and often lacked proper attachments to the microtubule bundles, suggesting that γTub37C is required to stabilize kinetochore microtubule attachments in anastral spindles. Although spindle bipolarity was sometimes achieved by metaphase I in both γtub37C mutants, the resulting chromosome masses displayed highly disrupted chromosome alignment. Therefore, our data conclusively demonstrate a role for γTub37C in both the formation of the anastral meiosis I spindle and in the proper attachment of kinetochore microtubules. Finally, multispectral imaging demonstrates the presences of native γTub37C along the length of wild-type meiosis I spindles. Proper chromosome segregation during cell division is essential. Missegregation of mitotic chromosomes leads to cell death or cancer, and chromosome missegregation during meiosis leads to miscarriage and birth defects. Cells utilize a bipolar microtubule-based structure known as the meiotic or mitotic spindle to segregate chromosomes. Because proper bipolar spindle formation is critically important for chromosome segregation, cells have many redundant mechanisms to ensure that this structure is properly formed. In most animal cells, centrosomes containing γ-tubulin protein complexes help organize and shape the bipolar spindle. Since meiosis I spindles in oocytes lack centrosomes, the mechanisms by which a meiotic bipolar spindle is assembled are not fully understood. In Drosophila oocytes it was not clear whether γ-tubulin played a role in bipolar spindle assembly or if it was even present on the meiotic spindle. We demonstrate that γ-tubulin plays vital roles in bipolar spindle formation and maintenance, as well as in aligning the chromosomes on the oocyte spindle. Additionally, we show that γ-tubulin is present on the bipolar spindle in Drosophila oocytes. More importantly, we demonstrate that γ-tubulin plays a critical role in the formation of the kinetochore microtubules that are required to properly orient chromosomes on the meiotic spindle. |
Audience | Academic |
Author | Seat, Angela Hawley, R Scott Hughes, Stacie E Unruh, Jay R Bauerly, Elisabeth Beeler, J Scott Slaughter, Brian D Matthies, Heinrich J G |
AuthorAffiliation | 4 Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America 3 The University of Kansas, Overland Park, Kansas, United States of America 5 Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas, United States of America The University of North Carolina at Chapel Hill, United States of America 1 Stowers Institute for Medical Research, Kansas City, Missouri, United States of America 2 Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America |
AuthorAffiliation_xml | – name: 4 Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America – name: 5 Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas, United States of America – name: 3 The University of Kansas, Overland Park, Kansas, United States of America – name: The University of North Carolina at Chapel Hill, United States of America – name: 1 Stowers Institute for Medical Research, Kansas City, Missouri, United States of America – name: 2 Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America |
Author_xml | – sequence: 1 givenname: Stacie E surname: Hughes fullname: Hughes, Stacie E email: sfh@stowers.org organization: Stowers Institute for Medical Research, Kansas City, Missouri, United States of America. sfh@stowers.org – sequence: 2 givenname: J Scott surname: Beeler fullname: Beeler, J Scott – sequence: 3 givenname: Angela surname: Seat fullname: Seat, Angela – sequence: 4 givenname: Brian D surname: Slaughter fullname: Slaughter, Brian D – sequence: 5 givenname: Jay R surname: Unruh fullname: Unruh, Jay R – sequence: 6 givenname: Elisabeth surname: Bauerly fullname: Bauerly, Elisabeth – sequence: 7 givenname: Heinrich J G surname: Matthies fullname: Matthies, Heinrich J G – sequence: 8 givenname: R Scott surname: Hawley fullname: Hawley, R Scott |
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Copyright | COPYRIGHT 2011 Public Library of Science Hughes et al. 2011 2011 Hughes et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Hughes SE, Beeler JS, Seat A, Slaughter BD, Unruh JR, et al. (2011) Gamma-Tubulin Is Required for Bipolar Spindle Assembly and for Proper Kinetochore Microtubule Attachments during Prometaphase I in Drosophila Oocytes. PLoS Genet 7(8): e1002209. doi:10.1371/journal.pgen.1002209 |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Conceived and designed the experiments: SEH RSH HJGM BDS JRU. Performed the experiments: SEH JSB AS EB BDS JRU. Analyzed the data: SEH BDS JRU. Wrote the paper: SEH RSH BDS JRU. Designed figures and tables: AS. |
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Snippet | In many animal species the meiosis I spindle in oocytes is anastral and lacks centrosomes. Previous studies of Drosophila oocytes failed to detect the native... In many animal species the meiosis I spindle in oocytes is anastral and lacks centrosomes. Previous studies of Drosophila oocytes failed to detect the native... In many animal species the meiosis I spindle in oocytes is anastral and lacks centrosomes. Previous studies of Drosophila oocytes failed to detect the native... |
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SubjectTerms | Animals Biology Cell Cycle Checkpoints Cell division Cellular biology Chromosomes Chromosomes - metabolism Drosophila Drosophila melanogaster - cytology Drosophila melanogaster - genetics Drosophila melanogaster - physiology Drosophila Proteins - metabolism Female Genetic aspects Kinetochores - metabolism Male Meiosis Metaphase Microtubules Microtubules - metabolism Mutation, Missense Oocytes - metabolism Oocytes - physiology Physiological aspects Prometaphase Protein Binding Proteins Spindle Apparatus - metabolism Tubulin - genetics Tubulin - metabolism Tubulins |
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Title | Gamma-tubulin is required for bipolar spindle assembly and for proper kinetochore microtubule attachments during prometaphase I in Drosophila oocytes |
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