Impact of mutations affecting ND mitochondria-encoded subunits on the activity and assembly of complex I in Chlamydomonas. Implication for the structural …

P Cardol, RF Matagne, C Remacle - Journal of molecular biology, 2002 - Elsevier
P Cardol, RF Matagne, C Remacle
Journal of molecular biology, 2002Elsevier
The mitochondrial rotenone-sensitive NADH: ubiquinone oxidoreductase (complex I)
comprises more than 35 subunits, the majority of which are encoded by the nucleus. In
Chlamydomonas reinhardtii, only five components (ND1, ND2, ND4, ND5 and ND6) are
coded for by the mitochondrial genome. Here, we characterize two mitochondrial mutants
(dum5 and dum17) showing strong reduction or inactivation of complex I activity: dum5 is a
1T deletion in the 3′ UTR of nd5 whereas dum17 is a 1T deletion in the coding sequence …
The mitochondrial rotenone-sensitive NADH:ubiquinone oxidoreductase (complex I) comprises more than 35 subunits, the majority of which are encoded by the nucleus. In Chlamydomonas reinhardtii, only five components (ND1, ND2, ND4, ND5 and ND6) are coded for by the mitochondrial genome. Here, we characterize two mitochondrial mutants (dum5 and dum17) showing strong reduction or inactivation of complex I activity: dum5 is a 1T deletion in the 3′ UTR of nd5 whereas dum17 is a 1T deletion in the coding sequence of nd6. The impact of these mutations and of mutations affecting nd1, nd4 and nd4/nd5 genes on the assembly of complex I is investigated. After separation of the respiratory complexes by blue native (BN)-PAGE or sucrose gradient centrifugation, we demonstrate that the absence of intact ND1 or ND6 subunit prevents the assembly of the 850kDa whole complex, whereas the loss of ND4 or ND4/ND5 leads to the formation of a subcomplex of 650kDa present in reduced amount. The implications of our findings for the possible role of these ND subunits on the activity of complex I and for the structural organization of the membrane arm of the enzyme are discussed. In mitochondria from all the strains analyzed, we moreover detected a 160–210kDa fragment comprising the hydrophilic 49kDa and 76kDa subunits of the complex I peripheral arm and showing NADH dehydrogenase activity.
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