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STAT6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting MFN2 dimerization

Although it is reported that mitochondria-localized nuclear transcription factors (TFs) regulate mitochondrial processes such as apoptosis and mitochondrial transcription/respiration, the functions and mechanisms of mitochondrial dynamics regulated by mitochondria-localized nuclear TFs are yet to be...

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Detalles Bibliográficos
Autores principales: Kim, Hyunmi, Park, Soo Jung, Jou, Ilo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440285/
https://www.ncbi.nlm.nih.gov/pubmed/36065189
http://dx.doi.org/10.1016/j.isci.2022.104923
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author Kim, Hyunmi
Park, Soo Jung
Jou, Ilo
author_facet Kim, Hyunmi
Park, Soo Jung
Jou, Ilo
author_sort Kim, Hyunmi
collection PubMed
description Although it is reported that mitochondria-localized nuclear transcription factors (TFs) regulate mitochondrial processes such as apoptosis and mitochondrial transcription/respiration, the functions and mechanisms of mitochondrial dynamics regulated by mitochondria-localized nuclear TFs are yet to be fully characterized. Here, we identify STAT6 as a mitochondrial protein that is localized in the outer membrane of mitochondria (OMM). STAT6 in OMM inhibits mitochondrial fusion by blocking MFN2 dimerization. This implies that STAT6 has a critical role in mitochondrial dynamics. Moreover, mitochondrial accumulation of STAT6 in response to hypoxic conditions reveals that STAT6 is a regulator of mitochondrial processes including fusion/fission mechanisms.
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spelling pubmed-94402852022-09-04 STAT6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting MFN2 dimerization Kim, Hyunmi Park, Soo Jung Jou, Ilo iScience Article Although it is reported that mitochondria-localized nuclear transcription factors (TFs) regulate mitochondrial processes such as apoptosis and mitochondrial transcription/respiration, the functions and mechanisms of mitochondrial dynamics regulated by mitochondria-localized nuclear TFs are yet to be fully characterized. Here, we identify STAT6 as a mitochondrial protein that is localized in the outer membrane of mitochondria (OMM). STAT6 in OMM inhibits mitochondrial fusion by blocking MFN2 dimerization. This implies that STAT6 has a critical role in mitochondrial dynamics. Moreover, mitochondrial accumulation of STAT6 in response to hypoxic conditions reveals that STAT6 is a regulator of mitochondrial processes including fusion/fission mechanisms. Elsevier 2022-08-13 /pmc/articles/PMC9440285/ /pubmed/36065189 http://dx.doi.org/10.1016/j.isci.2022.104923 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Kim, Hyunmi
Park, Soo Jung
Jou, Ilo
STAT6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting MFN2 dimerization
title STAT6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting MFN2 dimerization
title_full STAT6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting MFN2 dimerization
title_fullStr STAT6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting MFN2 dimerization
title_full_unstemmed STAT6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting MFN2 dimerization
title_short STAT6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting MFN2 dimerization
title_sort stat6 in mitochondrial outer membrane impairs mitochondrial fusion by inhibiting mfn2 dimerization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9440285/
https://www.ncbi.nlm.nih.gov/pubmed/36065189
http://dx.doi.org/10.1016/j.isci.2022.104923
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