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Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module
Sideroflexins (SFXNs) comprise a family of five paralogous proteins (SFXN1–5) in metazoan species. SFXN1/2/3 function as mitochondrial serine transporters and are required for efficient mitochondrial one-carbon (1C) metabolism. SFXN4 is evolutionarily divergent, and mutations in SFXN4 give rise to m...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060475/ https://www.ncbi.nlm.nih.gov/pubmed/35333655 http://dx.doi.org/10.1073/pnas.2115566119 |
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author | Jackson, Thomas D. Crameri, Jordan J. Muellner-Wong, Linden Frazier, Ann E. Palmer, Catherine S. Formosa, Luke E. Hock, Daniella H. Fujihara, Kenji M. Stait, Tegan Sharpe, Alice J. Thorburn, David R. Ryan, Michael T. Stroud, David A. Stojanovski, Diana |
author_facet | Jackson, Thomas D. Crameri, Jordan J. Muellner-Wong, Linden Frazier, Ann E. Palmer, Catherine S. Formosa, Luke E. Hock, Daniella H. Fujihara, Kenji M. Stait, Tegan Sharpe, Alice J. Thorburn, David R. Ryan, Michael T. Stroud, David A. Stojanovski, Diana |
author_sort | Jackson, Thomas D. |
collection | PubMed |
description | Sideroflexins (SFXNs) comprise a family of five paralogous proteins (SFXN1–5) in metazoan species. SFXN1/2/3 function as mitochondrial serine transporters and are required for efficient mitochondrial one-carbon (1C) metabolism. SFXN4 is evolutionarily divergent, and mutations in SFXN4 give rise to mitochondrial disease, pointing to a distinct function of this protein in mitochondrial biology. Using a combination of genome editing, interaction studies, and quantitative proteomics, we show that loss of SFXN4 leads to an isolated complex I assembly defect and that SFXN4 interacts with the core components of the mitochondrial complex I intermediate assembly (MCIA) complex. Our findings suggest that SFXN4 is required for the incorporation of the mtDNA-encoded ND6 subunit in the ND2 assembly module of complex I. These findings provide insights into the fundamental process of complex I assembly and functional insights into a disease-causing gene belonging to the SFXN family. |
format | Online Article Text |
id | pubmed-9060475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-90604752022-09-25 Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module Jackson, Thomas D. Crameri, Jordan J. Muellner-Wong, Linden Frazier, Ann E. Palmer, Catherine S. Formosa, Luke E. Hock, Daniella H. Fujihara, Kenji M. Stait, Tegan Sharpe, Alice J. Thorburn, David R. Ryan, Michael T. Stroud, David A. Stojanovski, Diana Proc Natl Acad Sci U S A Biological Sciences Sideroflexins (SFXNs) comprise a family of five paralogous proteins (SFXN1–5) in metazoan species. SFXN1/2/3 function as mitochondrial serine transporters and are required for efficient mitochondrial one-carbon (1C) metabolism. SFXN4 is evolutionarily divergent, and mutations in SFXN4 give rise to mitochondrial disease, pointing to a distinct function of this protein in mitochondrial biology. Using a combination of genome editing, interaction studies, and quantitative proteomics, we show that loss of SFXN4 leads to an isolated complex I assembly defect and that SFXN4 interacts with the core components of the mitochondrial complex I intermediate assembly (MCIA) complex. Our findings suggest that SFXN4 is required for the incorporation of the mtDNA-encoded ND6 subunit in the ND2 assembly module of complex I. These findings provide insights into the fundamental process of complex I assembly and functional insights into a disease-causing gene belonging to the SFXN family. National Academy of Sciences 2022-03-25 2022-03-29 /pmc/articles/PMC9060475/ /pubmed/35333655 http://dx.doi.org/10.1073/pnas.2115566119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Jackson, Thomas D. Crameri, Jordan J. Muellner-Wong, Linden Frazier, Ann E. Palmer, Catherine S. Formosa, Luke E. Hock, Daniella H. Fujihara, Kenji M. Stait, Tegan Sharpe, Alice J. Thorburn, David R. Ryan, Michael T. Stroud, David A. Stojanovski, Diana Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module |
title | Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module |
title_full | Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module |
title_fullStr | Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module |
title_full_unstemmed | Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module |
title_short | Sideroflexin 4 is a complex I assembly factor that interacts with the MCIA complex and is required for the assembly of the ND2 module |
title_sort | sideroflexin 4 is a complex i assembly factor that interacts with the mcia complex and is required for the assembly of the nd2 module |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060475/ https://www.ncbi.nlm.nih.gov/pubmed/35333655 http://dx.doi.org/10.1073/pnas.2115566119 |
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