1. Academic Validation
  2. Human mitochondrial complex I assembly is mediated by NDUFAF1

Human mitochondrial complex I assembly is mediated by NDUFAF1

  • FEBS J. 2005 Oct;272(20):5317-26. doi: 10.1111/j.1742-4658.2005.04928.x.
Rutger O Vogel 1 Rolf J R J Janssen Cristina Ugalde Melissa Grovenstein Richard J Huijbens Henk-Jan Visch Lambert P van den Heuvel Peter H Willems Massimo Zeviani Jan A M Smeitink Leo G J Nijtmans
Affiliations

Affiliation

  • 1 Department of Paediatrics, Radboud University Nijmegen Medical Centre, Netherlands.
Abstract

Complex I (NADH:ubiquinone oxidoreductase) is the largest multiprotein Enzyme of the Oxidative Phosphorylation system. Its assembly in human cells is poorly understood and no proteins assisting this process have yet been described. A good candidate is NDUFAF1, the human homologue of Neurospora crassa complex I chaperone CIA30. Here, we demonstrate that NDUFAF1 is a mitochondrial protein that is involved in the complex I assembly process. Modulating the intramitochondrial amount of NDUFAF1 by knocking down its expression using RNA interference leads to a reduced amount and activity of complex I. NDUFAF1 is associated to two complexes of 600 and 700 kDa in size of which the relative distribution is altered in two complex I deficient patients. Analysis of NDUFAF1 expression in a conditional complex I assembly system shows that the 700 kDa complex may represent a key step in the complex I assembly process. Based on these data, we propose that NDUFAF1 is an important protein for the assembly/stability of complex I.

Figures