Mitochondrial contact site and cristae organizing system promotes modular assembly of cytochrome c oxidase

Cell Rep. 2026 Jan 27;45(1):116727. doi: 10.1016/j.celrep.2025.116727. Epub 2025 Dec 18.

Abstract

Mitochondrial cytochrome c oxidase, complex IV (CIV) of the respiratory chain, is assembled in a modular fashion from mitochondrial as well as nuclear-encoded subunits, guided by numerous assembly factors. This intricate process is further complicated by the characteristic architecture of the inner mitochondrial membrane. The mitochondrial contact site and cristae organizing system (MICOS) maintains the stability of crista junctions that connect the cristae, the site of mitochondrial respiration, with the inner boundary membrane, where newly imported respiratory subunits first arrive. Here, we report that MICOS facilitates specific assembly steps of CIV and associates with intermediates of the Cox1 and Cox3 modules. Moreover, MICOS recruits a variety of assembly factors even in the absence of ongoing CIV biogenesis, directly or via the mitochondrial multifunctional assembly (MIMAS). Our results establish MICOS as an important agent in efficient respiratory chain assembly that promotes CIV biogenesis within the compartmentalized inner membrane architecture.

Keywords: CP: Cell biology; CP: Metabolism; MICOS; MIMAS; Mic60; cristae; cytochrome c oxidase; mitochondria; protein assembly; respiratory chain.

MeSH terms

  • Animals
  • Electron Transport Complex IV* / metabolism
  • Humans
  • Mitochondria Associated Membranes
  • Mitochondria* / metabolism
  • Mitochondrial Membranes* / metabolism
  • Mitochondrial Proteins / metabolism

Substances

  • Electron Transport Complex IV
  • Mitochondrial Proteins