Cargando…

DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age

In mammalian oocytes DNA damage can cause chromosomal abnormalities that potentially lead to infertility and developmental disorders. However, there is little known about the response of oocytes to DNA damage. Here we find that oocytes with DNA damage arrest at metaphase of the first meiosis (MI). T...

Descripción completa

Detalles Bibliográficos
Autores principales: Marangos, Petros, Stevense, Michelle, Niaka, Konstantina, Lagoudaki, Michaela, Nabti, Ibtissem, Jessberger, Rolf, Carroll, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667640/
https://www.ncbi.nlm.nih.gov/pubmed/26522734
http://dx.doi.org/10.1038/ncomms9706
_version_ 1782403867076460544
author Marangos, Petros
Stevense, Michelle
Niaka, Konstantina
Lagoudaki, Michaela
Nabti, Ibtissem
Jessberger, Rolf
Carroll, John
author_facet Marangos, Petros
Stevense, Michelle
Niaka, Konstantina
Lagoudaki, Michaela
Nabti, Ibtissem
Jessberger, Rolf
Carroll, John
author_sort Marangos, Petros
collection PubMed
description In mammalian oocytes DNA damage can cause chromosomal abnormalities that potentially lead to infertility and developmental disorders. However, there is little known about the response of oocytes to DNA damage. Here we find that oocytes with DNA damage arrest at metaphase of the first meiosis (MI). The MI arrest is induced by the spindle assembly checkpoint (SAC) because inhibiting the SAC overrides the DNA damage-induced MI arrest. Furthermore, this MI checkpoint is compromised in oocytes from aged mice. These data lead us to propose that the SAC is a major gatekeeper preventing the progression of oocytes harbouring DNA damage. The SAC therefore acts to integrate protection against both aneuploidy and DNA damage by preventing production of abnormal mature oocytes and subsequent embryos. Finally, we suggest escaping this DNA damage checkpoint in maternal ageing may be one of the causes of increased chromosome anomalies in oocytes and embryos from older mothers.
format Online
Article
Text
id pubmed-4667640
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Nature Pub. Group
record_format MEDLINE/PubMed
spelling pubmed-46676402015-12-10 DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age Marangos, Petros Stevense, Michelle Niaka, Konstantina Lagoudaki, Michaela Nabti, Ibtissem Jessberger, Rolf Carroll, John Nat Commun Article In mammalian oocytes DNA damage can cause chromosomal abnormalities that potentially lead to infertility and developmental disorders. However, there is little known about the response of oocytes to DNA damage. Here we find that oocytes with DNA damage arrest at metaphase of the first meiosis (MI). The MI arrest is induced by the spindle assembly checkpoint (SAC) because inhibiting the SAC overrides the DNA damage-induced MI arrest. Furthermore, this MI checkpoint is compromised in oocytes from aged mice. These data lead us to propose that the SAC is a major gatekeeper preventing the progression of oocytes harbouring DNA damage. The SAC therefore acts to integrate protection against both aneuploidy and DNA damage by preventing production of abnormal mature oocytes and subsequent embryos. Finally, we suggest escaping this DNA damage checkpoint in maternal ageing may be one of the causes of increased chromosome anomalies in oocytes and embryos from older mothers. Nature Pub. Group 2015-11-02 /pmc/articles/PMC4667640/ /pubmed/26522734 http://dx.doi.org/10.1038/ncomms9706 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. 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
Marangos, Petros
Stevense, Michelle
Niaka, Konstantina
Lagoudaki, Michaela
Nabti, Ibtissem
Jessberger, Rolf
Carroll, John
DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age
title DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age
title_full DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age
title_fullStr DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age
title_full_unstemmed DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age
title_short DNA damage-induced metaphase I arrest is mediated by the spindle assembly checkpoint and maternal age
title_sort dna damage-induced metaphase i arrest is mediated by the spindle assembly checkpoint and maternal age
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667640/
https://www.ncbi.nlm.nih.gov/pubmed/26522734
http://dx.doi.org/10.1038/ncomms9706
work_keys_str_mv AT marangospetros dnadamageinducedmetaphaseiarrestismediatedbythespindleassemblycheckpointandmaternalage
AT stevensemichelle dnadamageinducedmetaphaseiarrestismediatedbythespindleassemblycheckpointandmaternalage
AT niakakonstantina dnadamageinducedmetaphaseiarrestismediatedbythespindleassemblycheckpointandmaternalage
AT lagoudakimichaela dnadamageinducedmetaphaseiarrestismediatedbythespindleassemblycheckpointandmaternalage
AT nabtiibtissem dnadamageinducedmetaphaseiarrestismediatedbythespindleassemblycheckpointandmaternalage
AT jessbergerrolf dnadamageinducedmetaphaseiarrestismediatedbythespindleassemblycheckpointandmaternalage
AT carrolljohn dnadamageinducedmetaphaseiarrestismediatedbythespindleassemblycheckpointandmaternalage