The Qo site of the mitochondrial complex III is required for the transduction of hypoxic signaling via reactive oxygen species production.

Abstract

Mammalian cells increase transcription of genes for adaptation to hypoxia through the stabilization of hypoxia-inducible factor 1alpha (HIF-1alpha) protein. How cells transduce hypoxic signals to stabilize the HIF-1alpha protein remains unresolved. We demonstrate that cells deficient in the complex III subunit cytochrome b, which are respiratory incompetent, increase ROS levels and stabilize the HIF-1alpha protein during hypoxia. RNA interference of the complex III subunit Rieske iron sulfur protein in the cytochrome b-null cells and treatment of wild-type cells with stigmatellin abolished reactive oxygen species (ROS) generation at the Qo site of complex III. These interventions maintained hydroxylation of HIF-1alpha protein and prevented stabilization of HIF-1alpha protein during hypoxia. Antioxidants maintained hydroxylation of HIF-1alpha protein and prevented stabilization of HIF-1alpha protein during hypoxia. Exogenous hydrogen peroxide under normoxia prevented hydroxylation of HIF-1alpha protein and stabilized HIF-1alpha protein. These results provide genetic and pharmacologic evidence that the Qo site of complex III is required for the transduction of hypoxic signal by releasing ROS to stabilize the HIF-1alpha protein.

• Authors: Eric L Bell, Tatyana A Klimova, James Eisenbart, Carlos T Moraes, Michael P Murphy, G R Scott Budinger, Navdeep S Chandel
• Journal: The Journal of cell biology (J Cell Biol) Vol. 177 Issue 6 Pg. 1029-36 (Jun 18 2007) ISSN: 0021-9525 [Print] United States
• PMID: 17562787 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Hypoxia-Inducible Factor 1, alpha Subunit
• Mitochondrial Proteins
• Reactive Oxygen Species
• Cytochromes b
• Electron Transport Complex III

Topics

• Animals
• Cell Hypoxia
• Cytochromes b
• Electron Transport Complex III (metabolism)
• Hypoxia-Inducible Factor 1, alpha Subunit (metabolism)
• Mitochondrial Proteins (metabolism)
• Reactive Oxygen Species (metabolism)
• Signal Transduction