Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways

The assembly of mitochondrial oxidative phosphorylation (OXPHOS) complexes is an intricate process, which—given their dual-genetic control—requires tight co-regulation of two evolutionarily distinct gene expression machineries. Moreover, fine-tuning protein synthesis to the nascent assembly of OXPHO...

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Main Authors: Jia Xin Tang, Kyle Thompson, Robert W. Taylor, Monika Oláhová
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/21/11/3820
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author Jia Xin Tang
Kyle Thompson
Robert W. Taylor
Monika Oláhová
author_facet Jia Xin Tang
Kyle Thompson
Robert W. Taylor
Monika Oláhová
author_sort Jia Xin Tang
collection DOAJ
description The assembly of mitochondrial oxidative phosphorylation (OXPHOS) complexes is an intricate process, which—given their dual-genetic control—requires tight co-regulation of two evolutionarily distinct gene expression machineries. Moreover, fine-tuning protein synthesis to the nascent assembly of OXPHOS complexes requires regulatory mechanisms such as translational plasticity and translational activators that can coordinate mitochondrial translation with the import of nuclear-encoded mitochondrial proteins. The intricacy of OXPHOS complex biogenesis is further evidenced by the requirement of many tightly orchestrated steps and ancillary factors. Early-stage ancillary chaperones have essential roles in coordinating OXPHOS assembly, whilst late-stage assembly factors—also known as the LYRM (leucine–tyrosine–arginine motif) proteins—together with the mitochondrial acyl carrier protein (ACP)—regulate the incorporation and activation of late-incorporating OXPHOS subunits and/or co-factors. In this review, we describe recent discoveries providing insights into the mechanisms required for optimal OXPHOS biogenesis, including the coordination of mitochondrial gene expression with the availability of nuclear-encoded factors entering via mitochondrial protein import systems.
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spelling doaj.art-f0af452b624344d4a2903013e63ff7882023-11-20T01:59:02ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-05-012111382010.3390/ijms21113820Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly PathwaysJia Xin Tang0Kyle Thompson1Robert W. Taylor2Monika Oláhová3Wellcome Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne NE2 4HH, UKWellcome Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne NE2 4HH, UKWellcome Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne NE2 4HH, UKWellcome Centre for Mitochondrial Research, Newcastle University, Newcastle upon Tyne NE2 4HH, UKThe assembly of mitochondrial oxidative phosphorylation (OXPHOS) complexes is an intricate process, which—given their dual-genetic control—requires tight co-regulation of two evolutionarily distinct gene expression machineries. Moreover, fine-tuning protein synthesis to the nascent assembly of OXPHOS complexes requires regulatory mechanisms such as translational plasticity and translational activators that can coordinate mitochondrial translation with the import of nuclear-encoded mitochondrial proteins. The intricacy of OXPHOS complex biogenesis is further evidenced by the requirement of many tightly orchestrated steps and ancillary factors. Early-stage ancillary chaperones have essential roles in coordinating OXPHOS assembly, whilst late-stage assembly factors—also known as the LYRM (leucine–tyrosine–arginine motif) proteins—together with the mitochondrial acyl carrier protein (ACP)—regulate the incorporation and activation of late-incorporating OXPHOS subunits and/or co-factors. In this review, we describe recent discoveries providing insights into the mechanisms required for optimal OXPHOS biogenesis, including the coordination of mitochondrial gene expression with the availability of nuclear-encoded factors entering via mitochondrial protein import systems.https://www.mdpi.com/1422-0067/21/11/3820OXPHOS biogenesismitochondrial gene expressionmitochondrial importOXPHOS assembly factorsmitochondrial ACPLYRM proteins
spellingShingle Jia Xin Tang
Kyle Thompson
Robert W. Taylor
Monika Oláhová
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
International Journal of Molecular Sciences
OXPHOS biogenesis
mitochondrial gene expression
mitochondrial import
OXPHOS assembly factors
mitochondrial ACP
LYRM proteins
title Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
title_full Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
title_fullStr Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
title_full_unstemmed Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
title_short Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
title_sort mitochondrial oxphos biogenesis co regulation of protein synthesis import and assembly pathways
topic OXPHOS biogenesis
mitochondrial gene expression
mitochondrial import
OXPHOS assembly factors
mitochondrial ACP
LYRM proteins
url https://www.mdpi.com/1422-0067/21/11/3820
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AT kylethompson mitochondrialoxphosbiogenesiscoregulationofproteinsynthesisimportandassemblypathways
AT robertwtaylor mitochondrialoxphosbiogenesiscoregulationofproteinsynthesisimportandassemblypathways
AT monikaolahova mitochondrialoxphosbiogenesiscoregulationofproteinsynthesisimportandassemblypathways