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Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level

Mammalian oocytes are arrested in the dictyate stage of meiotic prophase I for long periods of time, during which the high concentration of the p53 family member TAp63α sensitizes them to DNA damage-induced apoptosis. TAp63α is kept in an inactive and exclusively dimeric state but undergoes rapid ph...

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Autores principales: Coutandin, Daniel, Osterburg, Christian, Srivastav, Ratnesh Kumar, Sumyk, Manuela, Kehrloesser, Sebastian, Gebel, Jakob, Tuppi, Marcel, Hannewald, Jens, Schäfer, Birgit, Salah, Eidarus, Mathea, Sebastian, Müller-Kuller, Uta, Doutch, James, Grez, Manuel, Knapp, Stefan, Dötsch, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876613/
https://www.ncbi.nlm.nih.gov/pubmed/27021569
http://dx.doi.org/10.7554/eLife.13909
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author Coutandin, Daniel
Osterburg, Christian
Srivastav, Ratnesh Kumar
Sumyk, Manuela
Kehrloesser, Sebastian
Gebel, Jakob
Tuppi, Marcel
Hannewald, Jens
Schäfer, Birgit
Salah, Eidarus
Mathea, Sebastian
Müller-Kuller, Uta
Doutch, James
Grez, Manuel
Knapp, Stefan
Dötsch, Volker
author_facet Coutandin, Daniel
Osterburg, Christian
Srivastav, Ratnesh Kumar
Sumyk, Manuela
Kehrloesser, Sebastian
Gebel, Jakob
Tuppi, Marcel
Hannewald, Jens
Schäfer, Birgit
Salah, Eidarus
Mathea, Sebastian
Müller-Kuller, Uta
Doutch, James
Grez, Manuel
Knapp, Stefan
Dötsch, Volker
author_sort Coutandin, Daniel
collection PubMed
description Mammalian oocytes are arrested in the dictyate stage of meiotic prophase I for long periods of time, during which the high concentration of the p53 family member TAp63α sensitizes them to DNA damage-induced apoptosis. TAp63α is kept in an inactive and exclusively dimeric state but undergoes rapid phosphorylation-induced tetramerization and concomitant activation upon detection of DNA damage. Here we show that the TAp63α dimer is a kinetically trapped state. Activation follows a spring-loaded mechanism not requiring further translation of other cellular factors in oocytes and is associated with unfolding of the inhibitory structure that blocks the tetramerization interface. Using a combination of biophysical methods as well as cell and ovary culture experiments we explain how TAp63α is kept inactive in the absence of DNA damage but causes rapid oocyte elimination in response to a few DNA double strand breaks thereby acting as the key quality control factor in maternal reproduction. DOI: http://dx.doi.org/10.7554/eLife.13909.001
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spelling pubmed-48766132016-05-27 Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level Coutandin, Daniel Osterburg, Christian Srivastav, Ratnesh Kumar Sumyk, Manuela Kehrloesser, Sebastian Gebel, Jakob Tuppi, Marcel Hannewald, Jens Schäfer, Birgit Salah, Eidarus Mathea, Sebastian Müller-Kuller, Uta Doutch, James Grez, Manuel Knapp, Stefan Dötsch, Volker eLife Biophysics and Structural Biology Mammalian oocytes are arrested in the dictyate stage of meiotic prophase I for long periods of time, during which the high concentration of the p53 family member TAp63α sensitizes them to DNA damage-induced apoptosis. TAp63α is kept in an inactive and exclusively dimeric state but undergoes rapid phosphorylation-induced tetramerization and concomitant activation upon detection of DNA damage. Here we show that the TAp63α dimer is a kinetically trapped state. Activation follows a spring-loaded mechanism not requiring further translation of other cellular factors in oocytes and is associated with unfolding of the inhibitory structure that blocks the tetramerization interface. Using a combination of biophysical methods as well as cell and ovary culture experiments we explain how TAp63α is kept inactive in the absence of DNA damage but causes rapid oocyte elimination in response to a few DNA double strand breaks thereby acting as the key quality control factor in maternal reproduction. DOI: http://dx.doi.org/10.7554/eLife.13909.001 eLife Sciences Publications, Ltd 2016-03-14 /pmc/articles/PMC4876613/ /pubmed/27021569 http://dx.doi.org/10.7554/eLife.13909 Text en © 2016, Coutandin et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Biophysics and Structural Biology
Coutandin, Daniel
Osterburg, Christian
Srivastav, Ratnesh Kumar
Sumyk, Manuela
Kehrloesser, Sebastian
Gebel, Jakob
Tuppi, Marcel
Hannewald, Jens
Schäfer, Birgit
Salah, Eidarus
Mathea, Sebastian
Müller-Kuller, Uta
Doutch, James
Grez, Manuel
Knapp, Stefan
Dötsch, Volker
Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level
title Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level
title_full Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level
title_fullStr Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level
title_full_unstemmed Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level
title_short Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level
title_sort quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level
topic Biophysics and Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876613/
https://www.ncbi.nlm.nih.gov/pubmed/27021569
http://dx.doi.org/10.7554/eLife.13909
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