Complex I (NADH:ubiquinone oxidoreductase) is active in but non-essential for procyclic Trypanosoma brucei

Mol Biochem Parasitol. 2011 Feb;175(2):196-200. doi: 10.1016/j.molbiopara.2010.11.003. Epub 2010 Nov 11.

Abstract

The requirement of complex I (NADH:ubiquionone oxidoreductase) for respiration in Trypanosoma brucei is controversial. Recent identification of homologues of its subunits in mitochondrial proteome resolved a question of its presence or absence. However, with one exception, no data have been available concerning the function(s) of complex I or its subunits. Here we present a functional RNAi study of three (NUBM, NUKM, NUEM) putative subunits of this complex. Although no changes were detected in growth, mitochondrial membrane potential or reactive oxygen species production in cell lines depleted for target transcript, the NUBM and NUKM RNAi knock-downs showed decreased specific NADH:ubiquinone oxidoreductase activity. Moreover, glycerol gradients of all cell lines revealed the presence of two distinct peaks of NADH dehydrogenase activity, with shifted sensitivity to inhibitors of complex I upon RNAi induction. Thus complex I is not only present in the procyclic stage of T. brucei 29-13 strain, but it does participate in electron transport chain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Respiration
  • Electron Transport Complex I / genetics
  • Electron Transport Complex I / metabolism*
  • Gene Knockdown Techniques
  • Microbial Viability*
  • Protein Subunits / genetics
  • Protein Subunits / metabolism
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Reactive Oxygen Species / metabolism
  • Trypanosoma brucei brucei / enzymology*
  • Trypanosoma brucei brucei / growth & development
  • Trypanosoma brucei brucei / metabolism
  • Trypanosoma brucei brucei / physiology*

Substances

  • Protein Subunits
  • RNA, Small Interfering
  • Reactive Oxygen Species
  • Electron Transport Complex I