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DNA damage response in male gametes of Cyrtanthus mackenii during pollen tube growth
Male gametophytes of plants are exposed to environmental stress and mutagenic agents during the double fertilization process and therefore need to repair the DNA damage in order to transmit the genomic information to the next generation. However, the DNA damage response in male gametes is still uncl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583183/ https://www.ncbi.nlm.nih.gov/pubmed/23550213 http://dx.doi.org/10.1093/aobpla/plt004 |
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author | Hirano, Tomonari Takagi, Keiichi Hoshino, Yoichiro Abe, Tomoko |
author_facet | Hirano, Tomonari Takagi, Keiichi Hoshino, Yoichiro Abe, Tomoko |
author_sort | Hirano, Tomonari |
collection | PubMed |
description | Male gametophytes of plants are exposed to environmental stress and mutagenic agents during the double fertilization process and therefore need to repair the DNA damage in order to transmit the genomic information to the next generation. However, the DNA damage response in male gametes is still unclear. In the present study, we analysed the response to DNA damage in the generative cells of Cyrtanthus mackenii during pollen tube growth. A carbon ion beam, which can induce DNA double-strand breaks (DSBs), was used to irradiate the bicellular pollen, and then the irradiated pollen grains were cultured in a liquid culture medium. The male gametes were isolated from the cultured pollen tubes and used for immunofluorescence analysis. Although inhibitory effects on pollen tube growth were not observed after irradiation, sperm cell formation decreased significantly after high-dose irradiation. After high-dose irradiation, the cell cycle progression of generative cells was arrested at metaphase in pollen mitosis II, and phosphorylated H2AX (γH2AX) foci, an indicator of DSBs, were detected in the majority of the arrested cells. However, these foci were not detected in cells that were past metaphase. Cell cycle progression in irradiated generative cells is regulated by the spindle assembly checkpoint, and modification of the histones surrounding the DSBs was confirmed. These results indicate that during pollen tube growth generative cells can recognize and manage genomic lesions using DNA damage response pathways. In addition, the number of generative cells with γH2AX foci decreased with culture prolongation, suggesting that the DSBs in the generative cells are repaired. |
format | Online Article Text |
id | pubmed-3583183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35831832013-02-27 DNA damage response in male gametes of Cyrtanthus mackenii during pollen tube growth Hirano, Tomonari Takagi, Keiichi Hoshino, Yoichiro Abe, Tomoko AoB Plants Research Articles Male gametophytes of plants are exposed to environmental stress and mutagenic agents during the double fertilization process and therefore need to repair the DNA damage in order to transmit the genomic information to the next generation. However, the DNA damage response in male gametes is still unclear. In the present study, we analysed the response to DNA damage in the generative cells of Cyrtanthus mackenii during pollen tube growth. A carbon ion beam, which can induce DNA double-strand breaks (DSBs), was used to irradiate the bicellular pollen, and then the irradiated pollen grains were cultured in a liquid culture medium. The male gametes were isolated from the cultured pollen tubes and used for immunofluorescence analysis. Although inhibitory effects on pollen tube growth were not observed after irradiation, sperm cell formation decreased significantly after high-dose irradiation. After high-dose irradiation, the cell cycle progression of generative cells was arrested at metaphase in pollen mitosis II, and phosphorylated H2AX (γH2AX) foci, an indicator of DSBs, were detected in the majority of the arrested cells. However, these foci were not detected in cells that were past metaphase. Cell cycle progression in irradiated generative cells is regulated by the spindle assembly checkpoint, and modification of the histones surrounding the DSBs was confirmed. These results indicate that during pollen tube growth generative cells can recognize and manage genomic lesions using DNA damage response pathways. In addition, the number of generative cells with γH2AX foci decreased with culture prolongation, suggesting that the DSBs in the generative cells are repaired. Oxford University Press 2013-01-23 /pmc/articles/PMC3583183/ /pubmed/23550213 http://dx.doi.org/10.1093/aobpla/plt004 Text en Published by Oxford University Press on behalf of the Annals of Botany Company. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Hirano, Tomonari Takagi, Keiichi Hoshino, Yoichiro Abe, Tomoko DNA damage response in male gametes of Cyrtanthus mackenii during pollen tube growth |
title | DNA damage response in male gametes of Cyrtanthus mackenii during pollen tube growth |
title_full | DNA damage response in male gametes of Cyrtanthus mackenii during pollen tube growth |
title_fullStr | DNA damage response in male gametes of Cyrtanthus mackenii during pollen tube growth |
title_full_unstemmed | DNA damage response in male gametes of Cyrtanthus mackenii during pollen tube growth |
title_short | DNA damage response in male gametes of Cyrtanthus mackenii during pollen tube growth |
title_sort | dna damage response in male gametes of cyrtanthus mackenii during pollen tube growth |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583183/ https://www.ncbi.nlm.nih.gov/pubmed/23550213 http://dx.doi.org/10.1093/aobpla/plt004 |
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