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Meiotic chromosome mobility in fission yeast is resistant to environmental stress

The formation of healthy gametes requires pairing of homologous chromosomes (homologs) as a prerequisite for their correct segregation during meiosis. Initially, homolog alignment is promoted by meiotic chromosome movements feeding into intimate homolog pairing by homologous recombination and/or syn...

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Autores principales: Illner, Doris, Lorenz, Alexander, Scherthan, Harry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831013/
https://www.ncbi.nlm.nih.gov/pubmed/27074839
http://dx.doi.org/10.1038/srep24222
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author Illner, Doris
Lorenz, Alexander
Scherthan, Harry
author_facet Illner, Doris
Lorenz, Alexander
Scherthan, Harry
author_sort Illner, Doris
collection PubMed
description The formation of healthy gametes requires pairing of homologous chromosomes (homologs) as a prerequisite for their correct segregation during meiosis. Initially, homolog alignment is promoted by meiotic chromosome movements feeding into intimate homolog pairing by homologous recombination and/or synaptonemal complex formation. Meiotic chromosome movements in the fission yeast, Schizosaccharomyces pombe, depend on astral microtubule dynamics that drag the nucleus through the zygote; known as horsetail movement. The response of microtubule-led meiotic chromosome movements to environmental stresses such as ionizing irradiation (IR) and associated reactive oxygen species (ROS) is not known. Here, we show that, in contrast to budding yeast, the horsetail movement is largely radiation-resistant, which is likely mediated by a potent antioxidant defense. IR exposure of sporulating S. pombe cells induced misrepair and irreparable DNA double strand breaks causing chromosome fragmentation, missegregation and gamete death. Comparing radiation outcome in fission and budding yeast, and studying meiosis with poisoned microtubules indicates that the increased gamete death after IR is innate to fission yeast. Inhibition of meiotic chromosome mobility in the face of IR failed to influence the course of DSB repair, indicating that paralysis of meiotic chromosome mobility in a genotoxic environment is not a universal response among species.
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spelling pubmed-48310132016-04-19 Meiotic chromosome mobility in fission yeast is resistant to environmental stress Illner, Doris Lorenz, Alexander Scherthan, Harry Sci Rep Article The formation of healthy gametes requires pairing of homologous chromosomes (homologs) as a prerequisite for their correct segregation during meiosis. Initially, homolog alignment is promoted by meiotic chromosome movements feeding into intimate homolog pairing by homologous recombination and/or synaptonemal complex formation. Meiotic chromosome movements in the fission yeast, Schizosaccharomyces pombe, depend on astral microtubule dynamics that drag the nucleus through the zygote; known as horsetail movement. The response of microtubule-led meiotic chromosome movements to environmental stresses such as ionizing irradiation (IR) and associated reactive oxygen species (ROS) is not known. Here, we show that, in contrast to budding yeast, the horsetail movement is largely radiation-resistant, which is likely mediated by a potent antioxidant defense. IR exposure of sporulating S. pombe cells induced misrepair and irreparable DNA double strand breaks causing chromosome fragmentation, missegregation and gamete death. Comparing radiation outcome in fission and budding yeast, and studying meiosis with poisoned microtubules indicates that the increased gamete death after IR is innate to fission yeast. Inhibition of meiotic chromosome mobility in the face of IR failed to influence the course of DSB repair, indicating that paralysis of meiotic chromosome mobility in a genotoxic environment is not a universal response among species. Nature Publishing Group 2016-04-14 /pmc/articles/PMC4831013/ /pubmed/27074839 http://dx.doi.org/10.1038/srep24222 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Illner, Doris
Lorenz, Alexander
Scherthan, Harry
Meiotic chromosome mobility in fission yeast is resistant to environmental stress
title Meiotic chromosome mobility in fission yeast is resistant to environmental stress
title_full Meiotic chromosome mobility in fission yeast is resistant to environmental stress
title_fullStr Meiotic chromosome mobility in fission yeast is resistant to environmental stress
title_full_unstemmed Meiotic chromosome mobility in fission yeast is resistant to environmental stress
title_short Meiotic chromosome mobility in fission yeast is resistant to environmental stress
title_sort meiotic chromosome mobility in fission yeast is resistant to environmental stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4831013/
https://www.ncbi.nlm.nih.gov/pubmed/27074839
http://dx.doi.org/10.1038/srep24222
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