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Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis
The Apoptosis-Inducing Factor (AIF) is a moonlighting flavoenzyme involved in the assembly of mitochondrial respiratory complexes in healthy cells, but also able to trigger DNA cleavage and parthanatos. Upon apoptotic-stimuli, AIF redistributes from the mitochondria to the nucleus, where upon associ...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944232/ https://www.ncbi.nlm.nih.gov/pubmed/36845352 http://dx.doi.org/10.1093/pnasnexus/pgac312 |
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author | Novo, Nerea Romero-Tamayo, Silvia Marcuello, Carlos Boneta, Sergio Blasco-Machin, Irene Velázquez-Campoy, Adrián Villanueva, Raquel Moreno-Loshuertos, Raquel Lostao, Anabel Medina, Milagros Ferreira, Patricia |
author_facet | Novo, Nerea Romero-Tamayo, Silvia Marcuello, Carlos Boneta, Sergio Blasco-Machin, Irene Velázquez-Campoy, Adrián Villanueva, Raquel Moreno-Loshuertos, Raquel Lostao, Anabel Medina, Milagros Ferreira, Patricia |
author_sort | Novo, Nerea |
collection | PubMed |
description | The Apoptosis-Inducing Factor (AIF) is a moonlighting flavoenzyme involved in the assembly of mitochondrial respiratory complexes in healthy cells, but also able to trigger DNA cleavage and parthanatos. Upon apoptotic-stimuli, AIF redistributes from the mitochondria to the nucleus, where upon association with other proteins such as endonuclease CypA and histone H2AX, it is proposed to organize a DNA–degradosome complex. In this work, we provide evidence for the molecular assembly of this complex as well as for the cooperative effects among its protein components to degrade genomic DNA into large fragments. We have also uncovered that AIF has nuclease activity that is stimulated in the presence of either Mg(2+) or Ca(2+). Such activity allows AIF by itself and in cooperation with CypA to efficiently degrade genomic DNA. Finally, we have identified TopIB and DEK motifs in AIF as responsible for its nuclease activity. These new findings point, for the first time, to AIF as a nuclease able to digest nuclear dsDNA in dying cells, improving our understanding of its role in promoting apoptosis and opening paths for the development of new therapeutic strategies. |
format | Online Article Text |
id | pubmed-9944232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-99442322023-02-23 Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis Novo, Nerea Romero-Tamayo, Silvia Marcuello, Carlos Boneta, Sergio Blasco-Machin, Irene Velázquez-Campoy, Adrián Villanueva, Raquel Moreno-Loshuertos, Raquel Lostao, Anabel Medina, Milagros Ferreira, Patricia PNAS Nexus Research Report The Apoptosis-Inducing Factor (AIF) is a moonlighting flavoenzyme involved in the assembly of mitochondrial respiratory complexes in healthy cells, but also able to trigger DNA cleavage and parthanatos. Upon apoptotic-stimuli, AIF redistributes from the mitochondria to the nucleus, where upon association with other proteins such as endonuclease CypA and histone H2AX, it is proposed to organize a DNA–degradosome complex. In this work, we provide evidence for the molecular assembly of this complex as well as for the cooperative effects among its protein components to degrade genomic DNA into large fragments. We have also uncovered that AIF has nuclease activity that is stimulated in the presence of either Mg(2+) or Ca(2+). Such activity allows AIF by itself and in cooperation with CypA to efficiently degrade genomic DNA. Finally, we have identified TopIB and DEK motifs in AIF as responsible for its nuclease activity. These new findings point, for the first time, to AIF as a nuclease able to digest nuclear dsDNA in dying cells, improving our understanding of its role in promoting apoptosis and opening paths for the development of new therapeutic strategies. Oxford University Press 2022-12-26 /pmc/articles/PMC9944232/ /pubmed/36845352 http://dx.doi.org/10.1093/pnasnexus/pgac312 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of National Academy of Sciences. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Report Novo, Nerea Romero-Tamayo, Silvia Marcuello, Carlos Boneta, Sergio Blasco-Machin, Irene Velázquez-Campoy, Adrián Villanueva, Raquel Moreno-Loshuertos, Raquel Lostao, Anabel Medina, Milagros Ferreira, Patricia Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis |
title | Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis |
title_full | Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis |
title_fullStr | Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis |
title_full_unstemmed | Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis |
title_short | Beyond a platform protein for the degradosome assembly: The Apoptosis-Inducing Factor as an efficient nuclease involved in chromatinolysis |
title_sort | beyond a platform protein for the degradosome assembly: the apoptosis-inducing factor as an efficient nuclease involved in chromatinolysis |
topic | Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944232/ https://www.ncbi.nlm.nih.gov/pubmed/36845352 http://dx.doi.org/10.1093/pnasnexus/pgac312 |
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