Degradation of the mitochondrial complex I assembly factor TMEM126B under chronic hypoxia

Cell Mol Life Sci. 2018 Aug;75(16):3051-3067. doi: 10.1007/s00018-018-2779-y. Epub 2018 Feb 20.


Cell stress such as hypoxia elicits adaptive responses, also on the level of mitochondria, and in part is mediated by the hypoxia-inducible factor (HIF) 1α. Adaptation of mitochondria towards acute hypoxic conditions is reasonably well understood, while regulatory mechanisms, especially of respiratory chain assembly factors, under chronic hypoxia remains elusive. One of these assembly factors is transmembrane protein 126B (TMEM126B). This protein is part of the mitochondrial complex I assembly machinery. We identified changes in complex I abundance under chronic hypoxia, in association with impaired substrate-specific mitochondrial respiration. Complexome profiling of isolated mitochondria of the human leukemia monocytic cell line THP-1 revealed HIF-1α-dependent deficits in complex I assembly and mitochondrial complex I assembly complex (MCIA) abundance. Of all mitochondrial MCIA members, we proved a selective HIF-1-dependent decrease of TMEM126B under chronic hypoxia. Mechanistically, HIF-1α induces the E3-ubiquitin ligase F-box/WD repeat-containing protein 1A (β-TrCP1), which in turn facilitates the proteolytic degradation of TMEM126B. Attenuating a functional complex I assembly appears critical for cellular adaptation towards chronic hypoxia and is linked to destruction of the mitochondrial assembly factor TMEM126B.

Keywords: AKT; Complexome profiling; Hypoxia-inducible factor (HIF); MCIA; Mitochondrial respiration; β-TrCP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cell Hypoxia
  • Cell Line, Tumor
  • Electron Transport Complex I / genetics
  • Electron Transport Complex I / metabolism*
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mitochondria / genetics
  • Mitochondria / metabolism*
  • Oxygen Consumption*
  • Proteolysis
  • RNA Interference
  • THP-1 Cells


  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Membrane Proteins
  • TMEM126B protein, human
  • Electron Transport Complex I