Complex I function and supercomplex formation are preserved in liver mitochondria despite progressive complex III deficiency

• Published in: PloS one 2014-01, Vol.9 (1), p.e86767-e86767
• Main Authors: Davoudi, Mina, Kotarsky, Heike, Hansson, Eva, Fellman, Vineta
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Assembly; ATPases Associated with Diverse Cellular Activities; Biology; Biosynthesis; Blotting, Western; Catalysis; Cell culture; Clinical Medicine; Cytochrome b; Electron Transport; Electron transport chain; Electron Transport Complex I - metabolism; Electron Transport Complex III - deficiency; Electron Transport Complex III - metabolism; Electrophoresis, Gel, Two-Dimensional; Electrophoresis, Polyacrylamide Gel; Free form; Gel electrophoresis; Homozygotes; Iron; Klinisk medicin; Liver; Liver diseases; Medical and Health Sciences; Medicin och hälsovetenskap; Medicine; Mice; Mice, Transgenic; Mitochondria; Mitochondria, Liver - metabolism; Mitochondrial DNA; Molecular Chaperones - genetics; Molecular Chaperones - metabolism; mRNA; Mutation; Oxidative phosphorylation; Oxygen; Oxygen consumption; Oxygen Consumption - physiology; Pediatrics; Pediatrik; Permeability; Phosphorylation; Physiology; Respirometry; Rieske iron-sulfur protein; RNA; Rodents; Stability analysis; Sulfur; Sulfur compounds; Transgenic mice
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0086767

Functional oxidative phosphorylation requires appropriately assembled mitochondrial respiratory complexes and their supercomplexes formed mainly of complexes I, III and IV. BCS1L is the chaperone needed to incorporate the catalytic subunit, Rieske iron-sulfur protein, into complex III at the final stage of its assembly. In cell culture studies, this subunit has been considered necessary for supercomplex formation and for maintaining the stability of complex I. Our aim was to assess the importance of fully assembled complex III for supercomplex formation in intact liver tissue. We used our transgenic mouse model with a homozygous c.232A>G mutation in Bcs1l leading to decreased expression of BCS1L and progressive decrease of Rieske iron-sulfur protein in complex III, resulting in hepatopathy. We studied supercomplex formation at different ages using blue native gel electrophoresis and complex activity using high-resolution respirometry. In isolated liver mitochondria of young and healthy homozygous mutant mice, we found similar supercomplexes as in wild type. In homozygotes aged 27-29 days with liver disorder, complex III was predominantly a pre-complex lacking Rieske iron-sulfur protein. However, the main supercomplex was clearly detected and contained complex III mainly in the pre-complex form. Oxygen consumption of complex IV was similar and that of complex I was twofold compared with controls. These complexes in free form were more abundant in homozygotes than in controls, and the mRNA of complex I subunits were upregulated. In conclusion, when complex III assembly is deficient, the pre-complex without Rieske iron-sulfur protein can participate with available fully assembled complex III in supercomplex formation, complex I function is preserved, and respiratory chain stability is maintained.