The OXPHOS supercomplex assembly factor HIG2A responds to changes in energetic metabolism and cell cycle

J Cell Physiol. 2019 Aug;234(10):17405-17419. doi: 10.1002/jcp.28362. Epub 2019 Feb 18.

Abstract

HIG2A promotes cell survival under hypoxia and mediates the assembly of complex III and complex IV into respiratory chain supercomplexes. In the present study, we show that human HIGD2A and mouse Higd2a gene expressions are regulated by hypoxia, glucose, and the cell cycle-related transcription factor E2F1. The latter was found to bind the promoter region of HIGD2A. Differential expression of the HIGD2A gene was found in C57BL/6 mice in relation to tissue and age. Besides, the silencing of HIGD2A evidenced the modulation of mitochondrial dynamics proteins namely, OPA1 as a fusion protein increases, while FIS1, a fission protein, decreases. Besides, the mitochondrial membrane potential (ΔΨm) increased. The protein HIG2A is localized in the mitochondria and nucleus. Moreover, we observed that the HIG2A protein interacts with OPA1. Changes in oxygen concentration, glucose availability, and cell cycle regulate HIGD2A expression. Alterations in HIGD2A expression are associated with changes in mitochondrial physiology.

Keywords: E2F1; HIG2A; OPA1; OXPHOS supercomplexes; cell cycle; hypoxia; mitochondrial dynamics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle / physiology*
  • Electron Transport Complex I / genetics
  • Humans
  • Membrane Potential, Mitochondrial / physiology*
  • Mice, Inbred C57BL
  • Mitochondrial Dynamics / physiology*
  • Mitochondrial Membranes / metabolism*
  • Mitochondrial Proteins / metabolism
  • Neoplasm Proteins / metabolism

Substances

  • HIG2 protein, mouse
  • HILPDA protein, human
  • Mitochondrial Proteins
  • Neoplasm Proteins
  • Electron Transport Complex I