Cargando…

Frame-shifted APOBEC3A encodes two alternative proapoptotic proteins that target the mitochondrial network

The human APOBEC3A (A3A) cytidine deaminase is a powerful DNA mutator enzyme recognized as a major source of somatic mutations in tumor cell genomes. However, there is a discrepancy between APOBEC3A mRNA levels after interferon stimulation in myeloid cells and A3A detection at the protein level. To...

Descripción completa

Detalles Bibliográficos
Autores principales: Caval, Vincent, Suspène, Rodolphe, Khalfi, Pierre, Gaillard, Julien, Caignard, Grégory, Vitour, Damien, Roingeard, Philippe, Vartanian, Jean-Pierre, Wain-Hobson, Simon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424220/
https://www.ncbi.nlm.nih.gov/pubmed/34403699
http://dx.doi.org/10.1016/j.jbc.2021.101081
_version_ 1783749629866672128
author Caval, Vincent
Suspène, Rodolphe
Khalfi, Pierre
Gaillard, Julien
Caignard, Grégory
Vitour, Damien
Roingeard, Philippe
Vartanian, Jean-Pierre
Wain-Hobson, Simon
author_facet Caval, Vincent
Suspène, Rodolphe
Khalfi, Pierre
Gaillard, Julien
Caignard, Grégory
Vitour, Damien
Roingeard, Philippe
Vartanian, Jean-Pierre
Wain-Hobson, Simon
author_sort Caval, Vincent
collection PubMed
description The human APOBEC3A (A3A) cytidine deaminase is a powerful DNA mutator enzyme recognized as a major source of somatic mutations in tumor cell genomes. However, there is a discrepancy between APOBEC3A mRNA levels after interferon stimulation in myeloid cells and A3A detection at the protein level. To understand this difference, we investigated the expression of two novel alternative “A3Alt” proteins encoded in the +1-shifted reading frame of the APOBEC3A gene. A3Alt-L and its shorter isoform A3Alt-S appear to be transmembrane proteins targeted to the mitochondrial compartment that induce membrane depolarization and apoptosis. Thus, the APOBEC3A gene represents a new example wherein a single gene encodes two proapoptotic proteins, A3A cytidine deaminases that target the genome and A3Alt proteins that target mitochondria.
format Online
Article
Text
id pubmed-8424220
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher American Society for Biochemistry and Molecular Biology
record_format MEDLINE/PubMed
spelling pubmed-84242202021-09-13 Frame-shifted APOBEC3A encodes two alternative proapoptotic proteins that target the mitochondrial network Caval, Vincent Suspène, Rodolphe Khalfi, Pierre Gaillard, Julien Caignard, Grégory Vitour, Damien Roingeard, Philippe Vartanian, Jean-Pierre Wain-Hobson, Simon J Biol Chem Research Article The human APOBEC3A (A3A) cytidine deaminase is a powerful DNA mutator enzyme recognized as a major source of somatic mutations in tumor cell genomes. However, there is a discrepancy between APOBEC3A mRNA levels after interferon stimulation in myeloid cells and A3A detection at the protein level. To understand this difference, we investigated the expression of two novel alternative “A3Alt” proteins encoded in the +1-shifted reading frame of the APOBEC3A gene. A3Alt-L and its shorter isoform A3Alt-S appear to be transmembrane proteins targeted to the mitochondrial compartment that induce membrane depolarization and apoptosis. Thus, the APOBEC3A gene represents a new example wherein a single gene encodes two proapoptotic proteins, A3A cytidine deaminases that target the genome and A3Alt proteins that target mitochondria. American Society for Biochemistry and Molecular Biology 2021-08-14 /pmc/articles/PMC8424220/ /pubmed/34403699 http://dx.doi.org/10.1016/j.jbc.2021.101081 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Caval, Vincent
Suspène, Rodolphe
Khalfi, Pierre
Gaillard, Julien
Caignard, Grégory
Vitour, Damien
Roingeard, Philippe
Vartanian, Jean-Pierre
Wain-Hobson, Simon
Frame-shifted APOBEC3A encodes two alternative proapoptotic proteins that target the mitochondrial network
title Frame-shifted APOBEC3A encodes two alternative proapoptotic proteins that target the mitochondrial network
title_full Frame-shifted APOBEC3A encodes two alternative proapoptotic proteins that target the mitochondrial network
title_fullStr Frame-shifted APOBEC3A encodes two alternative proapoptotic proteins that target the mitochondrial network
title_full_unstemmed Frame-shifted APOBEC3A encodes two alternative proapoptotic proteins that target the mitochondrial network
title_short Frame-shifted APOBEC3A encodes two alternative proapoptotic proteins that target the mitochondrial network
title_sort frame-shifted apobec3a encodes two alternative proapoptotic proteins that target the mitochondrial network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424220/
https://www.ncbi.nlm.nih.gov/pubmed/34403699
http://dx.doi.org/10.1016/j.jbc.2021.101081
work_keys_str_mv AT cavalvincent frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork
AT suspenerodolphe frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork
AT khalfipierre frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork
AT gaillardjulien frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork
AT caignardgregory frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork
AT vitourdamien frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork
AT roingeardphilippe frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork
AT vartanianjeanpierre frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork
AT wainhobsonsimon frameshiftedapobec3aencodestwoalternativeproapoptoticproteinsthattargetthemitochondrialnetwork