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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
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.
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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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