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SQSTM1/p62 mediates crosstalk between autophagy and the UPS in DNA repair
SQSTM1/p62 (sequestosome 1) selectively targets polyubiquitinated proteins for degradation via macroautophagy and the proteasome. Additionally, SQSTM1 shuttles between the cytoplasmic and nuclear compartments, although its role in the nucleus is relatively unknown. Here, we report that SQSTM1 dynami...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5391493/ https://www.ncbi.nlm.nih.gov/pubmed/27391408 http://dx.doi.org/10.1080/15548627.2016.1210368 |
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author | Hewitt, Graeme Carroll, Bernadette Sarallah, Rezazadeh Correia-Melo, Clara Ogrodnik, Mikołaj Nelson, Glyn Otten, Elsje G. Manni, Diego Antrobus, Robin Morgan, Brian A. von Zglinicki, Thomas Jurk, Diana Seluanov, Andrei Gorbunova, Vera Johansen, Terje Passos, João F. Korolchuk, Viktor I. |
author_facet | Hewitt, Graeme Carroll, Bernadette Sarallah, Rezazadeh Correia-Melo, Clara Ogrodnik, Mikołaj Nelson, Glyn Otten, Elsje G. Manni, Diego Antrobus, Robin Morgan, Brian A. von Zglinicki, Thomas Jurk, Diana Seluanov, Andrei Gorbunova, Vera Johansen, Terje Passos, João F. Korolchuk, Viktor I. |
author_sort | Hewitt, Graeme |
collection | PubMed |
description | SQSTM1/p62 (sequestosome 1) selectively targets polyubiquitinated proteins for degradation via macroautophagy and the proteasome. Additionally, SQSTM1 shuttles between the cytoplasmic and nuclear compartments, although its role in the nucleus is relatively unknown. Here, we report that SQSTM1 dynamically associates with DNA damage foci (DDF) and regulates DNA repair. Upon induction of DNA damage SQSTM1 interacts with FLNA (filamin A), which has previously been shown to recruit DNA repair protein RAD51 (RAD51 recombinase) to double-strand breaks and facilitate homologous recombination (HR). SQSTM1 promotes proteasomal degradation of FLNA and RAD51 within the nucleus, resulting in reduced levels of nuclear RAD51 and slower DNA repair. SQSTM1 regulates the ratio between HR and nonhomologous end joining (NHEJ) by promoting the latter at the expense of the former. This SQSTM1-dependent mechanism mediates the effect of macroautophagy on DNA repair. Moreover, nuclear localization of SQSTM1 and its association with DDF increase with aging and are prevented by life-span-extending dietary restriction, suggesting that an imbalance in the mechanism identified here may contribute to aging and age-related diseases. |
format | Online Article Text |
id | pubmed-5391493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-53914932017-04-24 SQSTM1/p62 mediates crosstalk between autophagy and the UPS in DNA repair Hewitt, Graeme Carroll, Bernadette Sarallah, Rezazadeh Correia-Melo, Clara Ogrodnik, Mikołaj Nelson, Glyn Otten, Elsje G. Manni, Diego Antrobus, Robin Morgan, Brian A. von Zglinicki, Thomas Jurk, Diana Seluanov, Andrei Gorbunova, Vera Johansen, Terje Passos, João F. Korolchuk, Viktor I. Autophagy Basic Research Papers SQSTM1/p62 (sequestosome 1) selectively targets polyubiquitinated proteins for degradation via macroautophagy and the proteasome. Additionally, SQSTM1 shuttles between the cytoplasmic and nuclear compartments, although its role in the nucleus is relatively unknown. Here, we report that SQSTM1 dynamically associates with DNA damage foci (DDF) and regulates DNA repair. Upon induction of DNA damage SQSTM1 interacts with FLNA (filamin A), which has previously been shown to recruit DNA repair protein RAD51 (RAD51 recombinase) to double-strand breaks and facilitate homologous recombination (HR). SQSTM1 promotes proteasomal degradation of FLNA and RAD51 within the nucleus, resulting in reduced levels of nuclear RAD51 and slower DNA repair. SQSTM1 regulates the ratio between HR and nonhomologous end joining (NHEJ) by promoting the latter at the expense of the former. This SQSTM1-dependent mechanism mediates the effect of macroautophagy on DNA repair. Moreover, nuclear localization of SQSTM1 and its association with DDF increase with aging and are prevented by life-span-extending dietary restriction, suggesting that an imbalance in the mechanism identified here may contribute to aging and age-related diseases. Taylor & Francis 2016-07-08 /pmc/articles/PMC5391493/ /pubmed/27391408 http://dx.doi.org/10.1080/15548627.2016.1210368 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC 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. The moral rights of the named author(s) have been asserted. |
spellingShingle | Basic Research Papers Hewitt, Graeme Carroll, Bernadette Sarallah, Rezazadeh Correia-Melo, Clara Ogrodnik, Mikołaj Nelson, Glyn Otten, Elsje G. Manni, Diego Antrobus, Robin Morgan, Brian A. von Zglinicki, Thomas Jurk, Diana Seluanov, Andrei Gorbunova, Vera Johansen, Terje Passos, João F. Korolchuk, Viktor I. SQSTM1/p62 mediates crosstalk between autophagy and the UPS in DNA repair |
title | SQSTM1/p62 mediates crosstalk between autophagy and the UPS in DNA repair |
title_full | SQSTM1/p62 mediates crosstalk between autophagy and the UPS in DNA repair |
title_fullStr | SQSTM1/p62 mediates crosstalk between autophagy and the UPS in DNA repair |
title_full_unstemmed | SQSTM1/p62 mediates crosstalk between autophagy and the UPS in DNA repair |
title_short | SQSTM1/p62 mediates crosstalk between autophagy and the UPS in DNA repair |
title_sort | sqstm1/p62 mediates crosstalk between autophagy and the ups in dna repair |
topic | Basic Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5391493/ https://www.ncbi.nlm.nih.gov/pubmed/27391408 http://dx.doi.org/10.1080/15548627.2016.1210368 |
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