Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hirano, Tomonari, Takagi, Keiichi, Hoshino, Yoichiro, Abe, Tomoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
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
_version_ 1782260762987724800
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
work_keys_str_mv AT hiranotomonari dnadamageresponseinmalegametesofcyrtanthusmackeniiduringpollentubegrowth
AT takagikeiichi dnadamageresponseinmalegametesofcyrtanthusmackeniiduringpollentubegrowth
AT hoshinoyoichiro dnadamageresponseinmalegametesofcyrtanthusmackeniiduringpollentubegrowth
AT abetomoko dnadamageresponseinmalegametesofcyrtanthusmackeniiduringpollentubegrowth