Literature DB >> 35047558

The Mysterious Multitude: Structural Perspective on the Accessory Subunits of Respiratory Complex I.

Abhilash Padavannil1, Maria G Ayala-Hernandez1, Eimy A Castellanos-Silva1, James A Letts1.   

Abstract

Complex I (CI) is the largest protein complex in the mitochondrial oxidative phosphorylation electron transport chain of the inner mitochondrial membrane and plays a key role in the transport of electrons from reduced substrates to molecular oxygen. CI is composed of 14 core subunits that are conserved across species and an increasing number of accessory subunits from bacteria to mammals. The fact that adding accessory subunits incurs costs of protein production and import suggests that these subunits play important physiological roles. Accordingly, knockout studies have demonstrated that accessory subunits are essential for CI assembly and function. Furthermore, clinical studies have shown that amino acid substitutions in accessory subunits lead to several debilitating and fatal CI deficiencies. Nevertheless, the specific roles of CI's accessory subunits have remained mysterious. In this review, we explore the possible roles of each of mammalian CI's 31 accessory subunits by integrating recent high-resolution CI structures with knockout, assembly, and clinical studies. Thus, we develop a framework of experimentally testable hypotheses for the function of the accessory subunits. We believe that this framework will provide inroads towards the complete understanding of mitochondrial CI physiology and help to develop strategies for the treatment of CI deficiencies.
Copyright © 2022 Padavannil, Ayala-Hernandez, Castellanos-Silva and Letts.

Entities:  

Keywords:  accessory subunits; electron transport chain; mitochondrial complex I; mitochondrial diseases; oxidative phosphorylation (OXPHOS)

Year:  2022        PMID: 35047558      PMCID: PMC8762328          DOI: 10.3389/fmolb.2021.798353

Source DB:  PubMed          Journal:  Front Mol Biosci        ISSN: 2296-889X


  134 in total

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Journal:  Biochim Biophys Acta       Date:  2016-04-01

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5.  X-linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy.

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6.  The mechanism of alternative splicing of the X-linked NDUFB11 gene of the respiratory chain complex I, impact of rotenone treatment in neuroblastoma cells.

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7.  NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect.

Authors:  F Baertling; L Sánchez-Caballero; M A M van den Brand; C-W Fung; S H-S Chan; V C-N Wong; D M E Hellebrekers; I F M de Coo; J A M Smeitink; R J T Rodenburg; L G J Nijtmans
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8.  Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome.

Authors:  Vanessa A van Rahden; Erika Fernandez-Vizarra; Malik Alawi; Kristina Brand; Florence Fellmann; Denise Horn; Massimo Zeviani; Kerstin Kutsche
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Review 10.  Accessory Subunits of the Matrix Arm of Mitochondrial Complex I with a Focus on Subunit NDUFS4 and Its Role in Complex I Function and Assembly.

Authors:  Flora Kahlhöfer; Max Gansen; Volker Zickermann
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4.  Human clinical mutations in mitochondrially encoded subunits of Complex I can be successfully modeled in E. coli.

Authors:  Fang Zhang; Quynh-Chi L Dang; Steven B Vik
Journal:  Mitochondrion       Date:  2022-03-17       Impact factor: 4.534

5.  cAMP/PKA Signaling Modulates Mitochondrial Supercomplex Organization.

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