Mutants of Chlamydomonas reinhardtii deficient in mitochondrial complex I: characterization of two mutations affecting the nd1 coding sequence

Genetics. 2001 Jul;158(3):1051-60. doi: 10.1093/genetics/158.3.1051.

Abstract

The mitochondrial rotenone-sensitive NADH:ubiquinone oxidoreductase (complex I) comprises more than 30 subunits, the majority of which are encoded by the nucleus. In Chlamydomonas reinhardtii, only five components of complex I are coded for by mitochondrial genes. Three mutants deprived of complex I activity and displaying slow growth in the dark were isolated after mutagenic treatment with acriflavine. A genetical analysis demonstrated that two mutations (dum20 and dum25) affect the mitochondrial genome whereas the third mutation (dn26) is of nuclear origin. Recombinational analyses showed that dum20 and dum25 are closely linked on the genetic map of the mitochondrial genome and could affect the nd1 gene. A sequencing analysis confirmed this conclusion: dum20 is a deletion of one T at codon 243 of nd1; dum25 corresponds to a 6-bp deletion that eliminates two amino acids located in a very conserved hydrophilic segment of the protein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics*
  • Chlamydomonas reinhardtii / genetics*
  • Electron Transport Complex I
  • Genes, Plant
  • Humans
  • Mitochondria / genetics
  • Molecular Sequence Data
  • Mutation*
  • NADH, NADPH Oxidoreductases / genetics*
  • Phenotype
  • Recombination, Genetic
  • Sequence Homology, Amino Acid

Substances

  • Carrier Proteins
  • nd1 protein, Rhodobacter capsulatus
  • NADH, NADPH Oxidoreductases
  • Electron Transport Complex I