The cytochrome c oxidase subunit COX6B1 is required for redox-sensitive early assembly and late stabilization of complex IV

COX6B1 is a nuclear-encoded subunit of the human mitochondrial cytochrome c oxidase (cIV) located in its intermembrane space-facing region. The relevance of COX6B1 in mitochondrial physiopathology was highlighted by the missense pathogenic variants associated with cIV deficiency. Despite the assigned COX6B1 role as a late incorporation subunit, the COX6B1 human cell line KO exhibited a total loss of cIV. To get a deeper insight into the mechanisms driving the lack of cIV assembly or destabilization in the absence of COX6B1, we used the COX6B1 KO cell background to express alternative oxidase and COX6B1 pathogenic variants. These analyses uncovered that the COX6B1 subunit is indispensable for redox-sensitive early cIV assembly steps, besides its contribution to the stabilization of cIV in the late assembly stages. In addition, we have evidenced the incorporation of partially assembled cIV modules directly into supercomplex structures, supporting the "cooperative assembly" model for respiratory chain biogenesis.

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Journal
Journal of Biological Chemistry
Published
2025-12-17
DOI
https://doi.org/10.1016/j.jbc.2025.111070
Primary Topic
Mitochondrial Function and Pathology
Type
article
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article

The cytochrome c oxidase subunit COX6B1 is required for redox-sensitive early assembly and late stabilization of complex IV

Tomáš Mráček, Michal Knězů, Marek Vrbacký, Lukáš Alán et al.
Journal of Biological Chemistry
Mitochondrial Function and Pathology
article

The cytochrome c oxidase subunit COX6B1 is required for redox-sensitive early assembly and late stabilization of complex IV

Tomáš Mráček, Michal Knězů, Marek Vrbacký, Lukáš Alán, Erika Fernández‐Vizarra, Petr Pecina, Alena Pecinová, Kristýna Čunátová, J Houštěk
article en

Abstract

COX6B1 is a nuclear-encoded subunit of the human mitochondrial cytochrome c oxidase (cIV) located in its intermembrane space-facing region. The relevance of COX6B1 in mitochondrial physiopathology was highlighted by the missense pathogenic variants associated with cIV deficiency. Despite the assigned COX6B1 role as a late incorporation subunit, the COX6B1 human cell line KO exhibited a total loss of cIV. To get a deeper insight into the mechanisms driving the lack of cIV assembly or destabilization in the absence of COX6B1, we used the COX6B1 KO cell background to express alternative oxidase and COX6B1 pathogenic variants. These analyses uncovered that the COX6B1 subunit is indispensable for redox-sensitive early cIV assembly steps, besides its contribution to the stabilization of cIV in the late assembly stages. In addition, we have evidenced the incorporation of partially assembled cIV modules directly into supercomplex structures, supporting the "cooperative assembly" model for respiratory chain biogenesis.

Journal of Biological ChemistryVol. 302(2)
University of Padua (IT), Czech Academy of Sciences (CZ), Veneto Institute of Molecular Medicine (IT), BioEnergetics (United States) (US), Czech Academy of Sciences, Institute of Physiology (CZ)
Openalex Percentile: Top 63%
Mitochondrial Function and Pathology
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The cytochrome c oxidase subunit COX6B1 is required for redox-sensitive early assembly and late stabilization of complex IV — Tomáš Mráček, Michal Knězů, et al. · Journal of Biological Chemistry (2025) | TGRS Research Map | TGRS