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p53 and cyclin G cooperate in mediating genome stability in somatic cells of Drosophila
One of the key players in genome surveillance is the tumour suppressor p53 mediating the adaptive response to a multitude of stress signals. Here we identify Cyclin G (CycG) as co-factor of p53-mediated genome stability. CycG has been shown before to be involved in double-strand break repair during...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738409/ https://www.ncbi.nlm.nih.gov/pubmed/29263364 http://dx.doi.org/10.1038/s41598-017-17973-z |
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author | Bayer, Fabienne E. Zimmermann, Mirjam Fischer, Patrick Gromoll, Christian Preiss, Anette Nagel, Anja C. |
author_facet | Bayer, Fabienne E. Zimmermann, Mirjam Fischer, Patrick Gromoll, Christian Preiss, Anette Nagel, Anja C. |
author_sort | Bayer, Fabienne E. |
collection | PubMed |
description | One of the key players in genome surveillance is the tumour suppressor p53 mediating the adaptive response to a multitude of stress signals. Here we identify Cyclin G (CycG) as co-factor of p53-mediated genome stability. CycG has been shown before to be involved in double-strand break repair during meiosis. Moreover, it is also important for mediating DNA damage response in somatic tissue. Here we find it in protein complexes together with p53, and show that the two proteins interact physically in vitro and in vivo in response to ionizing irradiation. In contrast to mammals, Drosophila Cyclin G is no transcriptional target of p53. Genetic interaction data reveal that p53 activity during DNA damage response requires the presence of CycG. Morphological defects caused by overexpression of p53 are ameliorated in cycG null mutants. Moreover, using a p53 biosensor we show that p53 activity is impeded in cycG mutants. As both p53 and CycG are likewise required for DNA damage repair and longevity we propose that CycG plays a positive role in mediating p53 function in genome surveillance of Drosophila. |
format | Online Article Text |
id | pubmed-5738409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57384092017-12-22 p53 and cyclin G cooperate in mediating genome stability in somatic cells of Drosophila Bayer, Fabienne E. Zimmermann, Mirjam Fischer, Patrick Gromoll, Christian Preiss, Anette Nagel, Anja C. Sci Rep Article One of the key players in genome surveillance is the tumour suppressor p53 mediating the adaptive response to a multitude of stress signals. Here we identify Cyclin G (CycG) as co-factor of p53-mediated genome stability. CycG has been shown before to be involved in double-strand break repair during meiosis. Moreover, it is also important for mediating DNA damage response in somatic tissue. Here we find it in protein complexes together with p53, and show that the two proteins interact physically in vitro and in vivo in response to ionizing irradiation. In contrast to mammals, Drosophila Cyclin G is no transcriptional target of p53. Genetic interaction data reveal that p53 activity during DNA damage response requires the presence of CycG. Morphological defects caused by overexpression of p53 are ameliorated in cycG null mutants. Moreover, using a p53 biosensor we show that p53 activity is impeded in cycG mutants. As both p53 and CycG are likewise required for DNA damage repair and longevity we propose that CycG plays a positive role in mediating p53 function in genome surveillance of Drosophila. Nature Publishing Group UK 2017-12-20 /pmc/articles/PMC5738409/ /pubmed/29263364 http://dx.doi.org/10.1038/s41598-017-17973-z Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Bayer, Fabienne E. Zimmermann, Mirjam Fischer, Patrick Gromoll, Christian Preiss, Anette Nagel, Anja C. p53 and cyclin G cooperate in mediating genome stability in somatic cells of Drosophila |
title | p53 and cyclin G cooperate in mediating genome stability in somatic cells of Drosophila |
title_full | p53 and cyclin G cooperate in mediating genome stability in somatic cells of Drosophila |
title_fullStr | p53 and cyclin G cooperate in mediating genome stability in somatic cells of Drosophila |
title_full_unstemmed | p53 and cyclin G cooperate in mediating genome stability in somatic cells of Drosophila |
title_short | p53 and cyclin G cooperate in mediating genome stability in somatic cells of Drosophila |
title_sort | p53 and cyclin g cooperate in mediating genome stability in somatic cells of drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738409/ https://www.ncbi.nlm.nih.gov/pubmed/29263364 http://dx.doi.org/10.1038/s41598-017-17973-z |
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