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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
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.
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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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