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Mutations affecting the mitochondrial genes encoding the cytochrome oxidase subunit I and apocytochrome b of Chlamydomonas reinhardtii

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Abstract

Mitochondrial mutants of the green alga Chlamydomonas reinhardtii that are inactivated in the cytochrome pathway of respiration have previously been isolated. Despite the fact that the alternative oxidase pathway is still active the mutants have lost the capacity to grow heterotrophically (dark + acetate) and display reduced growth under mixotrophic conditions (light + acetate). In crosses between wild-type and mutant cells, the meiotic progeny only inherit the character transmitted by the mt parent, which indicates that the mutations are located in the 15.8 kb linear mitochondrial genome. Two new mutants (dum-18 and dum-19) have now been isolated and characterized genetically, biochemically and at the molecular level. In addition, two previously isolated mutants (dum-11 and dum-15) were characterized in more detail. dum-11 contains two types of deleted mitochondrial DNA molecules: 15.1 kb monomers lacking the subterminal part of the genome, downstream of codon 147 of the apocytochrome b (COB) gene, and dimers resulting from head-to-head fusion of asymmetrically deleted monomers (15.1 and 9.5 kb DNA molecules, respectively). As in the wild type, the three other mutants contain only 15.8 kb mitochondrial DNA molecules. dum-15 is mutated at codon 140 of the COB gene, a serine (TCT) being changed into a tyrosine (TAC). dum-18 and dum-19 both inactivate cytochrome c oxidase, as a result of frameshift mutations (addition or deletion of 1 bp) at codons 145 and 152, respectively, of the COX1 gene encoding subunit I of cytochrome c oxidase. In a total of ten respiratory deficient mitochondrial mutants characterized thus far, only mutations located in COB or COXI have been isolated. The possibility that the inactivation of the other mitochondrial genes is lethal for the cells is discussed.

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References

  • Beckers M-C, Munaut C, Minet A, Matagne RF (1991) The fate of mitochondrial DNAs of mt + and mt origin in gametes and zygotes of Chlamydomonas. Curr Genet 20:239–243

    Google Scholar 

  • Bennoun P, Delosme M, Kuck U (1991) Mitochondrial genetics of Chlamydomonas reinhardtii: resistance mutations marking the cytochrome b gene. Genetics 127:335–343

    Google Scholar 

  • Bennoun P, Delosme M, Godehardt I, Kück U (1992) New tools for mitochondrial genetics of Chlamydomonas reinhardtii: manganese mutagenesis and cytoduction. Mol Gen Genet 234:147–154

    Google Scholar 

  • Boer PH, Gray MW (1986) Nucleotide sequence of a protein coding region in Chlamydomonas reinhardtii mitochondrial DNA. Nucleic Acids Res 14:7506–7507

    Google Scholar 

  • Boynton JE, Harris EH, Burkhart BD, Lamerson PM, Gillham NW (1987) Transmission of mitochondrial and chloroplast genomes in crosses of Chlamydomonas. Proc Natl Acad Sci USA 84:2391–2395

    Google Scholar 

  • Brasseur R (1988) Calculation of the three-dimensional structure of Saccharomyces cerevisiae cytochrome b inserted in a lipid matrix. J Biol Chem 263:12571–12575

    Google Scholar 

  • Colleaux L, Michel-Wolwertz M-R, Matagne RF, Dujon B (1990) The apocytochrome b gene of Chlamydomonas smithii contains a mobile intron related to both Saccharomyces and Neurospora introns. Mol Gen Genet 223:288–296

    Google Scholar 

  • di Rago J-P, Colson A-M (1988) Molecular basis for resistance to antimycin and diuron, Q cycle inhibitors acting at the Qi site in the mitochondrial ubiquinol-cytochrome c reductase in Saccharomyces cerevisiae. J Biol Chem 263:12564–12570

    Google Scholar 

  • di Rago J-P, Coppée J-Y, Colson A-M (1989) Molecular basis for resistance to myxothiazol, mucidin (strobilurin A), and stigmatellin. J Biol Chem 264:14543–14548

    Google Scholar 

  • Dorthu M-P, Remy S, Michel-Wolwertz M-R, Colleaux L, Breyer D, Beckers M-C, Englebert S, Duyckaerts C, Sluse FE, Matagne RF (1992) Biochemical, genetic and molecular characterization of new respiratory-deficient mutants in Chlamydomonas reinhardtii. Plant Mol Biol 18:759–772

    Google Scholar 

  • Gillham NW, Boynton JE, Harris EH (1987) Specific elimination of mitochondrial DNA from Chlamydomonas by intercalating dyes. Curr Genet 12:41–48

    Google Scholar 

  • Gorman DS, Levine RP (1965) Cytochrome f and plastocyanin: their sequence in the photosynthetic electron transport chain of Chlamydomonas reinhardtii. Proc Natl Acad Sci USA 54:1665–1669

    Google Scholar 

  • Harris EH (1989) The Chlamydomonas sourcebook. Academic Press, San Diego

    Google Scholar 

  • Kück U, Neuhaus H (1986) Universal genetic code evidenced in mitochondria of Chlamydomonas reinhardtii. Appl Microbiol Biotechnol 23:462–469

    Google Scholar 

  • Laties GG (1982) The cyanide-resistant, alternative pathway in higher plant respiration. Annu Rev Plant Physiol 24:445–466

    Google Scholar 

  • Ma DP, Yang YW, King YT, Hasnain SE (1990) The mitochondrial apocytochrome b gene from Chlamydomonas reinhardtii. Plant Mol Biol 15:357–359

    Google Scholar 

  • Matagne RF, Michel-Wolwertz M-R, Munaut C, Duyckaerts C, Sluse F (1989) Induction and characterization of mitochondrial DNA mutants in Chlamydomonas reinhardtii. J Cell Biol 108:1221–1226

    Google Scholar 

  • Michaelis G, Vahrenholz C, Pratje E (1990) Mitochondrial DNA of Chlamydomonas reinhardtii: the gene for apocytochrome b and the complete functional map of the 15.8 kb DNA. Mol Gen Genet 223:211–216

    Google Scholar 

  • Randolph-Anderson BL, Boynton JE, Gillham NW, Harris EH, Johnson AM, Dorthu M-P, Matagne RF (1993) Further characterization of the respiratory deficient dum-1 mutation of Chlamydomonas reinhardtii and its use as a recipient for mitochondrial transformation. Mol Gen Genet 236:235–244

    Google Scholar 

  • Remacle C, Colin M, Matagne RF (1995) Genetic mapping of mitochondrial markers by recombination analysis in Chlamydomonas reinhardtii. Mol Gen Genet 249:185–190

    Google Scholar 

  • Sanger F, Nicklen S, Coulson AR (1977) DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74:5463–5467

    Google Scholar 

  • Vahrenholz C, Riemen G, Pratje E, Dujon B, Michaelis G (1993) Mitochondrial DNA of Chlamydomonas reinhardtii: the structure of the ends of the linear 15.8 kb genome suggests mechanisms for DNA replication. Curr Genet 24:241–247

    Google Scholar 

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Communicated by R. Herrmann

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Colin, M., Dorthu, M.P., Duby, F. et al. Mutations affecting the mitochondrial genes encoding the cytochrome oxidase subunit I and apocytochrome b of Chlamydomonas reinhardtii . Molec. Gen. Genet. 249, 179–184 (1995). https://doi.org/10.1007/BF00290364

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  • DOI: https://doi.org/10.1007/BF00290364

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