Cargando…
The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair
EXD2 is a recently identified exonuclease that has been implicated in nuclear double-strand break repair. Given our long standing interest in mitochondrial DNA maintenance and indications that EXD2 could also be a mitochondrial protein we sought to determine its cellular localization and possible mi...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876329/ https://www.ncbi.nlm.nih.gov/pubmed/29599527 http://dx.doi.org/10.1038/s41598-018-23690-y |
_version_ | 1783310489836584960 |
---|---|
author | Hensen, Fenna Moretton, Amandine van Esveld, Selma Farge, Géraldine Spelbrink, Johannes N. |
author_facet | Hensen, Fenna Moretton, Amandine van Esveld, Selma Farge, Géraldine Spelbrink, Johannes N. |
author_sort | Hensen, Fenna |
collection | PubMed |
description | EXD2 is a recently identified exonuclease that has been implicated in nuclear double-strand break repair. Given our long standing interest in mitochondrial DNA maintenance and indications that EXD2 could also be a mitochondrial protein we sought to determine its cellular localization and possible mitochondrial associated functions. Our results show that EXD2 indeed shows mitochondrial localization, but, surprisingly, is found predominantly associated with the mitochondrial outer-membrane. Gradient purified nuclei show only the faintest hint of EXD2 presence while overexpression of the predicted full-length protein shows exclusive mitochondrial localization. Importantly, induction of double-strand DNA breaks via X-irradiation or Zeocin treatment does not support the notion that EXD2 re-locates to the nucleus following double-strand breaks and thus is unlikely to have a direct role in nuclear DNA repair. Knockdown or overexpression of EXD2 affects the cellular distribution of mitochondria. These results suggest that the reported defects in nuclear DNA repair following EXD2 depletion are likely an indirect consequence of altered mitochondrial dynamics and/or function. |
format | Online Article Text |
id | pubmed-5876329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58763292018-04-02 The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair Hensen, Fenna Moretton, Amandine van Esveld, Selma Farge, Géraldine Spelbrink, Johannes N. Sci Rep Article EXD2 is a recently identified exonuclease that has been implicated in nuclear double-strand break repair. Given our long standing interest in mitochondrial DNA maintenance and indications that EXD2 could also be a mitochondrial protein we sought to determine its cellular localization and possible mitochondrial associated functions. Our results show that EXD2 indeed shows mitochondrial localization, but, surprisingly, is found predominantly associated with the mitochondrial outer-membrane. Gradient purified nuclei show only the faintest hint of EXD2 presence while overexpression of the predicted full-length protein shows exclusive mitochondrial localization. Importantly, induction of double-strand DNA breaks via X-irradiation or Zeocin treatment does not support the notion that EXD2 re-locates to the nucleus following double-strand breaks and thus is unlikely to have a direct role in nuclear DNA repair. Knockdown or overexpression of EXD2 affects the cellular distribution of mitochondria. These results suggest that the reported defects in nuclear DNA repair following EXD2 depletion are likely an indirect consequence of altered mitochondrial dynamics and/or function. Nature Publishing Group UK 2018-03-29 /pmc/articles/PMC5876329/ /pubmed/29599527 http://dx.doi.org/10.1038/s41598-018-23690-y Text en © The Author(s) 2018 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 Hensen, Fenna Moretton, Amandine van Esveld, Selma Farge, Géraldine Spelbrink, Johannes N. The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair |
title | The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair |
title_full | The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair |
title_fullStr | The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair |
title_full_unstemmed | The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair |
title_short | The mitochondrial outer-membrane location of the EXD2 exonuclease contradicts its direct role in nuclear DNA repair |
title_sort | mitochondrial outer-membrane location of the exd2 exonuclease contradicts its direct role in nuclear dna repair |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876329/ https://www.ncbi.nlm.nih.gov/pubmed/29599527 http://dx.doi.org/10.1038/s41598-018-23690-y |
work_keys_str_mv | AT hensenfenna themitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT morettonamandine themitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT vanesveldselma themitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT fargegeraldine themitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT spelbrinkjohannesn themitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT hensenfenna mitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT morettonamandine mitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT vanesveldselma mitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT fargegeraldine mitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair AT spelbrinkjohannesn mitochondrialoutermembranelocationoftheexd2exonucleasecontradictsitsdirectroleinnucleardnarepair |