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RUFY4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages
We report here that RUFY4, a newly characterized member of the ‘RUN and FYVE domain-containing’ family of proteins previously associated with autophagy enhancement, is highly expressed in alveolar macrophages (AM). We show that RUFY4 interacts with mitochondria upon stimulation by microbial-associat...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278043/ https://www.ncbi.nlm.nih.gov/pubmed/34295519 http://dx.doi.org/10.1098/rsos.202333 |
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author | Valečka, Jan Camosseto, Voahirana McEwan, David G. Terawaki, Seigo Liu, Zhuangzhuang Strock, Eva Almeida, Catarina R. Su, Bing Dikic, Ivan Liang, Yinming Gatti, Evelina Pierre, Philippe |
author_facet | Valečka, Jan Camosseto, Voahirana McEwan, David G. Terawaki, Seigo Liu, Zhuangzhuang Strock, Eva Almeida, Catarina R. Su, Bing Dikic, Ivan Liang, Yinming Gatti, Evelina Pierre, Philippe |
author_sort | Valečka, Jan |
collection | PubMed |
description | We report here that RUFY4, a newly characterized member of the ‘RUN and FYVE domain-containing’ family of proteins previously associated with autophagy enhancement, is highly expressed in alveolar macrophages (AM). We show that RUFY4 interacts with mitochondria upon stimulation by microbial-associated molecular patterns of AM and dendritic cells. RUFY4 interaction with mitochondria and other organelles is dependent on a previously uncharacterized OmpH domain located immediately upstream of its C-terminal FYVE domain. Further, we demonstrate that rufy4 messenger RNA can be translated from an alternative translation initiation codon, giving rise to a N-terminally truncated form of the molecule lacking most of its RUN domain and with enhanced potential for its interaction with mitochondria. Our observations point towards a role of RUFY4 in selective mitochondria clearance in activated phagocytes. |
format | Online Article Text |
id | pubmed-8278043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82780432021-07-21 RUFY4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages Valečka, Jan Camosseto, Voahirana McEwan, David G. Terawaki, Seigo Liu, Zhuangzhuang Strock, Eva Almeida, Catarina R. Su, Bing Dikic, Ivan Liang, Yinming Gatti, Evelina Pierre, Philippe R Soc Open Sci Biochemistry, Cellular and Molecular Biology We report here that RUFY4, a newly characterized member of the ‘RUN and FYVE domain-containing’ family of proteins previously associated with autophagy enhancement, is highly expressed in alveolar macrophages (AM). We show that RUFY4 interacts with mitochondria upon stimulation by microbial-associated molecular patterns of AM and dendritic cells. RUFY4 interaction with mitochondria and other organelles is dependent on a previously uncharacterized OmpH domain located immediately upstream of its C-terminal FYVE domain. Further, we demonstrate that rufy4 messenger RNA can be translated from an alternative translation initiation codon, giving rise to a N-terminally truncated form of the molecule lacking most of its RUN domain and with enhanced potential for its interaction with mitochondria. Our observations point towards a role of RUFY4 in selective mitochondria clearance in activated phagocytes. The Royal Society 2021-07-14 /pmc/articles/PMC8278043/ /pubmed/34295519 http://dx.doi.org/10.1098/rsos.202333 Text en © 2021 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Biochemistry, Cellular and Molecular Biology Valečka, Jan Camosseto, Voahirana McEwan, David G. Terawaki, Seigo Liu, Zhuangzhuang Strock, Eva Almeida, Catarina R. Su, Bing Dikic, Ivan Liang, Yinming Gatti, Evelina Pierre, Philippe RUFY4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages |
title | RUFY4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages |
title_full | RUFY4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages |
title_fullStr | RUFY4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages |
title_full_unstemmed | RUFY4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages |
title_short | RUFY4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages |
title_sort | rufy4 exists as two translationally regulated isoforms, that localize to the mitochondrion in activated macrophages |
topic | Biochemistry, Cellular and Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278043/ https://www.ncbi.nlm.nih.gov/pubmed/34295519 http://dx.doi.org/10.1098/rsos.202333 |
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