Recombination: Effects on Structure and Function of the Mitochondrial Genome

  • Wolfgang Friedt
  • Renate Horn
  • Volker Hahn
Part of the Progress in Botany/Fortschritte der Botanik book series (BOTANY, volume 55)


Three decades ago, it was shown for the first time that mitochondria contain DNA (Luck and Reich 1964, cited in Lonsdale and Grienenberger 1992). In the meantime, the mitochondrial DNA (mtDNA) of eukaryotes has been studied in detail and some of the mitochondrial genomes have already been sequenced. In many cases, mtDNAs are small (approx. 16 kb) and circular. Furthermore, it can now be generalized for all vertebrates and invertebrates that the genetic information of mitochondria is compactly organized and predominantly on one strand of the mtDNA (for ref. cf. review of Lonsdale and Grienenberger 1992).


Mitochondrial Genome Cytoplasmic Male Sterility Somatic Hybrid Restorer Gene Plant Mitochondrial Genome 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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  1. Bears T, Curtis GJ, Lonsdale DM (1989) A specific rearrangement of mitochondrial DNA induced by tissue culture. Theor Appl Genet 77:620–624.Google Scholar
  2. Begu D, Graves PV, Domec C, Arselin G, Litvak S, Araya A (1990) RNA editing of wheat mitochondrial ATP synthase subunit 9: direct protein and cDNA sequencing. Plant Cell 2:1283–1290.PubMedCrossRefGoogle Scholar
  3. Bendich AJ, Loretz C, Monnat J (1993) The structure of the plant mitochondrial genome. In: Kück U, Brennicke A (eds) Plant mitochondria. Springer, Berlin Heidelberg New York.Google Scholar
  4. Bonhomme S, Budar F, Lancelin D, Small I, Defrance MD, Pelletier G (1992) Sequence and transcript analysis of the Nco 2.5 Ogura-specific fragment correlated with cytoplasmic male sterility in Brassica cybrids. Mol Gen Genet 235:340–348.PubMedCrossRefGoogle Scholar
  5. Bonnett HT, Djurberg I, Fajardo M, Glimelius K (1993) A mutation causing variegation and abnormal development in tobacco is associated with an altered mitochondrial DNA. Plant J 3:519–525.CrossRefGoogle Scholar
  6. Braun CJ, Brown GG, Levings CS III (1992) Cytoplasmic male sterility. In: Herrmann RG (ed) Cell organelles. Springer, Berlin Heidelberg New York, pp 219–245.Google Scholar
  7. Brown GG (1993) Regulation of mitochondrial gene expression. In: Verma DP (ed) Control of plant gene expression. CRC, Boca Raton, pp 175–198.Google Scholar
  8. Chase CD, Ortega VM (1992) Organization of atpA coding and 3’-flanking sequences associated with cytoplasmic male sterility in Phaseolus vulgaris L. Curr Genet 22:147–153.PubMedCrossRefGoogle Scholar
  9. Chetrit P, Rios R, Paepe R, Vitart V, Gutierres S, Vedel F (1992) Cytoplasmic male sterility is associated with large deletions in the mitochondrial DNA of twoNicotiana sylvestris protoclones. Curr Genet 21:131–137.PubMedCrossRefGoogle Scholar
  10. Conklin PL, Hanson MR (1991) Ribosomal protein S19 is encoded by the mitochondrial genome in Petunia hybrida. Nucleic Acids Res 19:2701–2705.PubMedCrossRefGoogle Scholar
  11. Conklin PL, Hanson MR (1993) A truncated recombination repeat in the mitochondrial genome of a Petunia CMS line. Curr Genet 23:477–482.PubMedCrossRefGoogle Scholar
  12. Conklin PL, Wilson RK, Hanson MR (1991) Multiple trans-splicing events are required to produce a mature nad1 transcript in a plant mitochondrion. Genes & Dev 5:1407–1415.CrossRefGoogle Scholar
  13. Crouzillat D, Leroy P, Perrault A, Ledoigt G (1987) Molecular analysis of the mitochondrial genome of Helianthus annuus in relation to cytoplasmic male sterility and phylogeny. Theor Appl Genet 74:773–780.CrossRefGoogle Scholar
  14. Crouzillat D, Gentzbittel L, De La Canal L, Vaury C, Perrault A, Nicolas P, Ledoigt G (1989) Properties and nucleotide sequence of a mitochondrial plasmid from sunflower. Curr Genet 15:283–289.PubMedCrossRefGoogle Scholar
  15. De La Canal L, Crouzillat D, Flamand MC, Perrault A, Boutry M, Ledoigt G (1991) Nucleotide sequence and transcriptional analysis of a mitochondrial plasmid from a cytoplasmic male-sterile line of sunflower. Theor Appl Genet 81:812–818.CrossRefGoogle Scholar
  16. Dewey RE, Levings CS III, Timothy DH (1986) Novel recombinations in the maize mitochondrial genome produce a unique transcriptional unit in the Texas male-sterile cytoplasm. Cell 44:439–449.PubMedCrossRefGoogle Scholar
  17. Fauron CM, Havlik M, Lonsdale D, Nichols L (1989) Mitochondrial genome organization of the maize cytoplasmic male-sterile type T. Mol Gen Genet 216:395–401.CrossRefGoogle Scholar
  18. Fauron CM, Havlik M, Brettell RI (1990) The mitochondrial genome organization of a maize fertile CMS-T revertant line is generated through recombination between two sets of repeats. Genetics 124:423–428.PubMedGoogle Scholar
  19. Fauron CM, Havlik M, Casper M (1991) Organization and evolution of the maize mitochondrial genome. In: Herrmann RG, Larkins BA (eds) NATO ASI A, Life science, plant molecular biology 2. Plenum, New York, pp 345–363.CrossRefGoogle Scholar
  20. Fauron CM, Casper M, Gesteland R, Albertsen M (1992) A multi-recombination model for the mtDNA rearrangements seen in maize CMS-T regenerated plants. Plant J 2(6):949–958.CrossRefGoogle Scholar
  21. Flamand MC, Goblet JP, Due G, Briquet M, Boutry M (1992) Sequence and transcription analysis of mitochondrial plasmids isolated from cytoplasmic male-sterile lines of Vicia faba. Plant Mol Biol 19(6):913–923.PubMedCrossRefGoogle Scholar
  22. Folkerts O, Hanson MR (1989) Three copies of a recombination repeat occur on the 443 kb mastercircle of Petunia hybrida 3704 mitochondrial genome. Nucleic Acids Res 17:7345–7357.PubMedCrossRefGoogle Scholar
  23. Folkerts O, Hanson MR (1991) The male sterility-associated pcf gene and the normal atp9–1 gene in petunia are located on different mitochondrial DNA molecules. Genetics 129:885–895.PubMedGoogle Scholar
  24. Fox TD, Leaver CJ (1981) The Zea mays mitochondrial gene coding cytochrome oxidase subunit II has an intervening sequence and does not contain TGA codons. Cell 26:315–323.PubMedCrossRefGoogle Scholar
  25. Fukuchi M, Shikanai T, Kossykh VG, Yamada Y (1991) Analysis of nuclear sequences homologous to the B4 plasmid-like DNA of rice mitochondria, evidence for sequence transfer from mitochondria to nuclei. Curr Genet 20:487–494.PubMedCrossRefGoogle Scholar
  26. Gass DA, Makaroff CA, Palmer JD (1992) Variable intron content of the NADH dehydrogenase subunit 4 gene of plant mitochondria. Curr Genet 21:423–430.PubMedCrossRefGoogle Scholar
  27. Gasser CS, Farley RT (1989) Genetically engineering plant for crop improvement. Science 244:1293–1299.PubMedCrossRefGoogle Scholar
  28. Graves PV, Begu D, Velours J, Neau E, Belloc F (1990) Direct protein sequencing of wheat mitochondrial ATP synthase subunit 9 confirms RNA editing in plants. J Mol Biol 214:1–6.PubMedCrossRefGoogle Scholar
  29. Gray MW, Hanice-Joyce PJ, Covello PS (1992) Transcription, processing and editing in plant mitochondria. Annu Rev Plant Physiol Plant Mol Biol 43:145–175.CrossRefGoogle Scholar
  30. Hagimori M, Nagaoka M, Kato N, Yoshikawa H (1992) Production and characterization of somatic hybrids between the Japanese radish and cauliflower. Theor Appl Genet 84:819–824.CrossRefGoogle Scholar
  31. Hahn V (1993) Molekulargenetische Untersuchungen über die Ursachen cytoplasmatischer Pollensterilität bei der Sonnenblume. Thesis Univ Gießen.Google Scholar
  32. Hahn V, Friedt W (1992) Nutzung von Helianthus- Wildformen zur Entwicklung neuer “Plasmen” für die Sonnenblumenzüchtung. Vortr Pflanzenzucht 22:145–151.Google Scholar
  33. Handa H, Nakajima K (1992) Different organization and altered transcription of the mitochondrial atp6 gene in the male-sterile cytoplasm of rapeseed (Brassica napus L.). Curr Genet 21:153–159.PubMedCrossRefGoogle Scholar
  34. Hanice-Joyce PJ, Gray MW (1990) Processing of transfer RNA precursors in a wheat mitochondrial extract. J Biol Chem 265:13782–13792.Google Scholar
  35. Hanson MR (1984) Stability, variation and recombination in plant mitochondrial genomes via tissue culture and somatic hybridization. Oxford Surv Plant Mol Cell Biol 1:33–52.Google Scholar
  36. Hanson MR, Folkerts O (1992) Structure and function of the higher plant mitochondrial genomes. Int Rev Cytol 141:129–172.CrossRefGoogle Scholar
  37. Hanson MR, Pruitt KD, Nivison HT (1989) Male sterility loci in plant mitochondrial genomes. Oxford Surv Plant Mol Cell Biol 6:61–85.Google Scholar
  38. Hayakawa T, Zhu Y, Itoh K, Kimura Y, Iwaza T, Shimamoto, Toriyama S (1992) Genetically engineered rice resistant to rice stripe vims, an insect-transmitted virus. Proc Natl Sei USA 89:9865–9869.CrossRefGoogle Scholar
  39. Hernould M, Suharsono S, Litvak S, Araya A, Mouras A (1993) Male-sterility induction in transgenic tobacco plants with an unedited atp9 mitochondrial gene from wheat. Proc Natl Acad Sei USA 90:2370–2374.CrossRefGoogle Scholar
  40. Hiesel R, Wissinger B, Brennicke A (1990) Cytochrome oxidase subunit II mRNA Oenothera mitochondria are edited at 24 sites. Curr Genet 18:371–375.PubMedCrossRefGoogle Scholar
  41. Holford P, Croft J, Newbury HJ (1991) Stmctural studies of microsporogenesis in fertile and male-sterile onions (Allium cepa L.) containing the CMS-S cytoplasm. Theor Appl Genet 82:745–755.Google Scholar
  42. Honda H, Hirai A (1992) The gene for the alpha-subunit of ATPase: a site of homologous recombination in plant mitochondrial DNA also functions in somatic hybrid cells. Theor Appl Genet 84:33–38.CrossRefGoogle Scholar
  43. Horn R, Köhler RH, Zetsche K (1991) A mitochondrial 16 kDa protein is associated with cytoplasmic male sterility in sunflower. Plant Mol Biol 17:29–36.PubMedCrossRefGoogle Scholar
  44. Hunt M, Newton KJ (1991) the NCS3 mutation: genetic evidence for the expression of ribosomal protein genes in Zea mays mitochondria. EMBO J 10:1045–1052.PubMedGoogle Scholar
  45. Iwabuchi M, Kyozuka J, Shimamoto K (1993) Processing followed by complete editing of an altered mitochondrial atp6 RNA restores fertility of cytoplasmic male sterile rice. EMBO J 12:1437–1446.PubMedGoogle Scholar
  46. Izuchi S, Terachi T, Sakamoto M, Mikami T, Sugita M (1990) Structure and expression of tomato mitochondrial genes coding for tRNACys (GCA), tRNAAsn (GUU) and tRNA-Tyr (GUA): a native tRNACys gene is present in dicot plants but absent in monocot plants. Curr Genet 18:239–243.PubMedCrossRefGoogle Scholar
  47. Johns C, Lu M, Lyznik A, Mackenzie S (1992) A mitochondrial DNA sequence is associated with abnormal pollen development in cytoplasmic male sterile bean plants. Plant Cell 4:435–449.PubMedCrossRefGoogle Scholar
  48. Joyce PB, Gray MW (1989) Chloroplast-like transfer RNA genes expressed in wheat mitochondria. Nucleic Acids Res 17:5461–5476.PubMedCrossRefGoogle Scholar
  49. Kane EJ, Wilson AJ, Chourey PS (1992) Mitochondrial genome variability in sorghum cell culture protoclones. Theor Appl Genet 83:799–806.CrossRefGoogle Scholar
  50. Kao HM, Keller WA, Gleddie S, Brown GG (1992) Synthesis of Brassica oleracea/Brassica napus somatic hybrid plants with novel organelle DNA compositions. Theor Appl Genet 83:313–320.CrossRefGoogle Scholar
  51. Kofer W, Glimelius K, Bonnett HT (1991) Modifications of the mitochondrial DNA cause changes in floral development in homeotic-like mutants of tobacco. Plant Cell 3(8):759–769.PubMedCrossRefGoogle Scholar
  52. Köhler RH, Horn R, Lössl A, Zetsche K (1991) Cytoplasmic male sterility in sunflower is correlated with the co-transcription of a new open reading frame with the atpk gene. Mol Gen Genet 227:369–376.PubMedCrossRefGoogle Scholar
  53. Kool AJ, de Haas JM, Mol JN, Van Marrewijk GA (1985) Isolation and physicochemical characterization of mitochondrial DNA from cultured cells of Petunia hybrida. Theor Appl Genet 69:223–233.CrossRefGoogle Scholar
  54. Kräuter R, Steinmetz A, Friedt W (1991) Efficient interspecific hybridization in the genus Helianthus via “embryo rescue” and characterization of the hybrids. Theor Appl Genet 82:521–525.CrossRefGoogle Scholar
  55. Laser KD, Lersten NR (1972) Anatomy and cytology of microsporogenesis in cytoplasmic male sterile angiosperms. Bot Rev 38:425–454.CrossRefGoogle Scholar
  56. Lauer M, Knudsen C, Newton KJ, Gabay-Laughnan S, Laughnan JR (1990) A partially deleted mitochondrial cytochrome oxidase gene in the NCS6 abnormal growth mutant of maize. New Biol 2:179–186.PubMedGoogle Scholar
  57. Laver HK, Reynolds SJ, Moneger F, Leaver CJ (1991) Mitochondrial genome organization and expression associated with cytoplasmic male sterility in sunflower(Helianthus annuus). Plant J 1:185–193.PubMedCrossRefGoogle Scholar
  58. Leon P, Walbot V, Bedinger P (1989) Molecular analysis of the linear 2.3 kb plasmid of maize mitochondria: apparent capture of tRNA genes. Nucleic Acids Res 17:4089–4099.PubMedCrossRefGoogle Scholar
  59. Lippok B, Brennicke A, Wissinger B (1992) The coxll gene in carrot mitochondria contains two introns. Mol Gen Genet 232(2):322–327.PubMedGoogle Scholar
  60. Lonsdale DM (1989) The plant mitochondrial genome. In: Stump PK, Conn EE (eds) The biochemistry of plant: a comprehensive treatise, vol 15. Academic Press, New York, pp 229–295.Google Scholar
  61. Lonsdale DM, Grienenberger JM (1992) The mitochondrial genome of plants. In: Herrmann RG (ed) Cell organelles. Springer, Vienna New York, pp 183–218.Google Scholar
  62. Macfarlane SA, Davies J (1992) Plants transformed with region of the 201-kilodalton replicase gene from pea early browning virus RNA1 are resistant to virus infection. Proc Natl Acad Sei USA 89:5829–5833.CrossRefGoogle Scholar
  63. Malone R, Horvath GV, Cseplo A, Buzas B, Dix PJ, Medgyesy P (1992) Impact of the stringency of cell selection on plastid segregation in protoplast fusion-derived Nicotiana regenerates. Theor Appl Genet 84:866–873.CrossRefGoogle Scholar
  64. Mann V, Ekstein I, Nissen H, Hiser C, Mclntosch L, Hirschberg J (1991) The cytochrome oxidase II gene in mitochondria of the sugar-beet Beta vulgaris L. Plant Mol Biol 17(3):559–566.PubMedCrossRefGoogle Scholar
  65. Mariani C, de Beuckeleer M, Treuttner J, Leemans J, Goldberg RB (1990) Induction of male sterility in plants by a chimaeric ribonuclease gene. Nature 347:737–741.CrossRefGoogle Scholar
  66. Mariani C, Goselle V, de Beuckeleer M, de Block M, Goldberg RB, de Greef W, Leemans J (1992) A chimaeric ribonuclease-inhibitor gene restores fertility to male sterile plants. Nature 357:384–387.CrossRefGoogle Scholar
  67. Melchers G, Mohri Y, Watanabe K, Wakabayashi S, Harada K (1992) One- step generation of cytoplasmic male sterility by fusion of mitochondrial-inactivated tomato protoplasts with nuclear-inactivated Solanum protoplasts. Proc Natl Acad Sci USA 89:6832–6836.PubMedCrossRefGoogle Scholar
  68. Michel F, Dujon B (1983) Conservation of RNA secondary structure features in two intron families including mitochondrial-, chloroplast-, and nuclear-encoded members. EMBO J 2:33–38.PubMedGoogle Scholar
  69. Michel F, Umesono K, Ozeki H (1989) Comparative and functional anatomy of group II catalytic introns — a review. Gene 82:5–30.PubMedCrossRefGoogle Scholar
  70. Moon E, Kao TH, Wu R (1985) Pea cytochrome oxidase subunit II gene has no intron and generates two mRNA transcripts with different 5’-termini. Nucleic Acids Res 13:3195–3212PubMedCrossRefGoogle Scholar
  71. Mukhopadhyay A, Pradhan AK, Pentel D (1991) Mitochondrial DNA patterns are similar in gametosomatic and somatic hybrids of two Nicotiana species. Plant Cell Rep 10(10):522–524.CrossRefGoogle Scholar
  72. Newton KJ, Coe EH (1986) Mitochondrial DNA changes in abnormal growth (nonchromosomal stripe) mutants in maize. Proc Natl Acad Sci USA 83:7363–7366.PubMedCrossRefGoogle Scholar
  73. Newton KJ, Knudsen C, Gabay-Laughnan S, Laughnan J (1990) An abnormal growth mutant in maize has a defective mitochondrial cytochrome oxidase gene. Plant Cell 2:107–113.PubMedCrossRefGoogle Scholar
  74. Nivison HT, Hanson MR (1989) Identification of a mitochondrial protein associated with cytoplasmic male sterility in Petunia. Plant Cell 1:1121–1130.PubMedCrossRefGoogle Scholar
  75. Nugent JM, Palmer JD (1988) Location, identity, amount and serial entry of chloroplast DNA sequences in crucifer mitochondrial DNAs. Curr Genet 14:501–509.PubMedCrossRefGoogle Scholar
  76. Oda K, Yamato K, Ohta E, Nakamura Y, Takemura M, Nozato N, Akashi K, Kanegae T, Ogur Y, Kohchi T, Ohyama K (1992) Gene organization from the complete sequence of liverwort Marchantía polymorpha mitochondrial DNA. J Mol Biol 223:1–7.PubMedCrossRefGoogle Scholar
  77. Orellano EG, Carrillo N, Calcaterra NB (1992) Evaluation of the extent of homologous chloroplast DNA sequences in the mitochondrial genome of cowpea (Vigna unguiculata L.) Plant Physiol 98(2):525–529.PubMedGoogle Scholar
  78. Palmer JD (1992) Comparison of chloroplast and mitochondrial genome evolution in plants. In: Herrmann RG (ed) Cell organelles. Springer, Berlin Heidelberg New York, pp 99–133.Google Scholar
  79. Palmer JD, Herbom LA (1986) Tricircular mitochondrial genomes of Brassica and Raphanus: reversal of repeat configurations by inversion. Nucleic Acids Res 14:9755–9764.PubMedCrossRefGoogle Scholar
  80. Palmer JD, Herbom LA (1987) Unicircular structure of the Brassica hirta mitochondrial genome. Curr Genet 11:565–570.PubMedCrossRefGoogle Scholar
  81. Palmer JD, Shields CR, Cohen DG, Orton TJ (1983) An unusual mitochondrial DNA plasmid in the genus Brassica. Nature 301:725–728.CrossRefGoogle Scholar
  82. Sakamoto W, Kadowaki K, Kishimoto N, Yano M, Saito A, Tano S (1991) RFLP analysis of nuclear DNAs homologous with mitochondrial plasmid-like DNAs in cultivated rice. Theor Appl Genet 82:179–184.CrossRefGoogle Scholar
  83. Sangare A, Weil JH, Grienenberger JM, Fauron C, Lonsdale D (1990) Localization and organization of tRNA genes on the mitochondrial genomes of fertile and male-sterile lines of maize. Mol Gen Genet 223:224–232.PubMedCrossRefGoogle Scholar
  84. Schardl CL, Lonsdale DM, Pring DR, Rose KR (1984) Linearization of maize mitochondrial chromosomes by recombination with linear episomes. Nature 310:292–296.CrossRefGoogle Scholar
  85. Schuster W, Brennicke A (1986) Pseudocopies of the ATPase a-subunit gene in Oenothera mitochondria are present on different circular molecules. Mol Gen Genet 204:29–35.CrossRefGoogle Scholar
  86. Shirzadegan M, Christey M, Earle ED, Palmer JD (1989) Rearrangement, amplification and assortment of mitochondrial DNA molecules in cultured cells of Brassica campestris. Theor Appl Genet 77:17–25.CrossRefGoogle Scholar
  87. Shirzadegan M, Christey M, Earle ED, Palmer JD (1991) Patterns of mitochondrial DNA instability in Brassica campestris cultured cells. Plant Mol Biol 16:21–37.PubMedCrossRefGoogle Scholar
  88. Siculella L, Palmer JD (1988) Physical and gene organization of mitochondrial DNA in fertile and male sterile sunflower CMS-associated alterations in structure and transcription of the atpk gene. Nucleic Acids Res 16:3787–3799.PubMedCrossRefGoogle Scholar
  89. Singh M, Brown GG (1991) Suppression of cytoplasmic male sterility by nuclear genes alters expression of a novel mitochondrial gene region. Plant Cell 3:1349–1362.PubMedCrossRefGoogle Scholar
  90. Small I, Isaac PG, Leaver CJ (1987) Stoichiometric differences in DNA molecules containing the atpk gene suggest mechanisms for the generation of mitochondrial genome diversity in maize. EMBO J 6:865–869.PubMedGoogle Scholar
  91. Small I, Marechal-Drouard L, Masson J, Pelletier G, Cosset A, Weil JH, Dietrich A (1992) In vivo import of a normal or mutagenized heterologous transfer RNA into the mitochondria of transgenic plants: towards novel ways of influencing mitochondrial gene expression. EMBO J 11 (4): 1291–1296.PubMedGoogle Scholar
  92. Smith RL, Chowdhury MKU (1991) Characterization of pearl millet DNA fragments rearranged by reversion from cytoplasmic male sterility to fertility. Theor Appl Genet 81:793–799.CrossRefGoogle Scholar
  93. Souza AP, Jubier MF, Deicher E, Lancelin D, Lejeune B (1991) A trans-splicing model for the expression of the Tripartite nad5 gene in wheat and maize mitochondria. Plant Cell 3(12):1363–1378.CrossRefGoogle Scholar
  94. Spassova M, Christov M, Bohorova N, Petrov P, Dudov K, Atanassov A, Nijkamp HJJ, Hille J (1992) Molecular analysis of a new cytoplasmic male sterile genotype in sunflower. FEBS Lett 297:159–163.PubMedCrossRefGoogle Scholar
  95. Sproule A, Donaldson P, Dijak M, Bevis E, Pandeya R, Keller WA, Gleddie S (1991) Fertile somatic hybrids between transgenicNicotiana tabacum and transgenic N. debneyi selected by dual-antibiotic resistance. Theor Appl Genet 82:450–456.CrossRefGoogle Scholar
  96. Stern DB, Lonsdale DM (1982) Mitochondrial and chloroplast genomes of maize have a 12-kilobase DNA sequence in common. Nature 299:698–702.PubMedCrossRefGoogle Scholar
  97. Stern DB, Palmer JD (1984) Extensive and widespread homologies between mitochondrial DNA and chloroplast DNA in higher plants. Proc Natl Acad Sei USA 81:1946–1950.CrossRefGoogle Scholar
  98. Stern DB, Palmer JD (1986) Tripartite mitochondrial genome of spinach: physical structure, mitochondrial gene mapping, and locations of transposed chloroplast DNA sequences. Nucleic Acids Res 14:5651–5666.PubMedCrossRefGoogle Scholar
  99. Sutton CA, Conklin PL, Pruitt KD, Hanson MR (1991) Editing of pre-mRNA can occur before cis- and trans-splicing in Petunia mitochondria. Mol Cell Biol 11:4274–4277.PubMedGoogle Scholar
  100. Sutton CA, Conklin PR, Pruitt KD, Calfee AJ, Cobb AG, Hanson MR (1993) Editing of rps3/rpl16 trancripts creates a premature truncation of the rpl16 open reading frame. Curr Genet 23:472–476.PubMedCrossRefGoogle Scholar
  101. Takamizo T, Spangenberg G, Suginobu KI, Potrykus I (1991) Intergeneric somatic hybridization in Gramineae: somatic hybrid plants between tall fescue (Festuca arundinacea Schreb.) and Italian ryegrass (Lolium multiflorum Lam.). Mol Gen Genet 231:1–6.PubMedCrossRefGoogle Scholar
  102. van der Meer IM, Stam Me, Zunen JA, Mol JN, Stuitje AR (1992) Antisense inhibition of flavo- noid biosynthesis in petunia anthers results in male sterility. Plant Cell 4(3):253–262.PubMedCrossRefGoogle Scholar
  103. Verhoeven HA, Blaas J (1992) Direct cell to cell transfer of organelles by microinjection. Plant Cell Rep 10(12):613–616.CrossRefGoogle Scholar
  104. Vitart V, Paepe R, Mathieu C, Chetrit P, Vedel F (1992) Amplification of sub-stoichiometric recombinant mitochondrial DNA sequences in a nuclear, male sterile mutant regenerated from protoplast culture in Nicotiana sylvestris. Mol Gen Genet 233:193–200.PubMedCrossRefGoogle Scholar
  105. Von-Allem JM, Rottmann WH, Gengenbach BG, Harvey AJ, Lonsdale DM (1991) Transfer of methomyl and HmT-toxin sensitivity from T-cytoplasm maize to tobacco. Mol Gen Genet 229:405–412.CrossRefGoogle Scholar
  106. Wahleithner JA, Wolstenholme DR (1987) Mitochondrial plasmid DNAs of broad bean mitochondrial DNA. Curr Genet 12:55–67.PubMedCrossRefGoogle Scholar
  107. Wahleithner JA, Macfarlane JL, Wolstenholme DR (1990) A sequence encoding a maturase-related protein in a group II intron of a plant mitochondrialnad\ gene. Proc Natl Acad Sei USA 87:548–552.CrossRefGoogle Scholar
  108. Warmke HE, Lee SL (1977) Mitochondrial degeneration in T cytoplasmic male-sterile com anthers. J Hered 68:213–222.Google Scholar
  109. Warmke HE, Lee SL (1978) Pollen abortion in T cytoplasmic male sterility com (Zea mays): a suggested mechanism. Science 200:561–563.PubMedCrossRefGoogle Scholar
  110. Williams ME, Levings CS (1992) Molecular biology of cytoplasmic male sterility. Plant Breed Rev 10:23–51.Google Scholar
  111. Wintz H, Grienenberger JR, Weie HJ, Lonsdale DR (1988) Location and nucleotide sequence of two tRNA genes and a tRNA pseudogene in the maize mitochondrial genome: evidence for the transcription of a chloroplast gene in mitochondria. Curr Genet 13:247–254.PubMedCrossRefGoogle Scholar
  112. Wissinger B, Hiesel R, Schuster W, Brennicke A (1988) The NADH-dehydrogenase subunit 5 gene in Oenothera mitochondria contains two introns and is co-transcribed with the 5S rRNA gene. Mol Gen Genet 212:56–65.PubMedCrossRefGoogle Scholar
  113. Witt U, Hanson S, Albaum M, Abel WO (1991) Molecular analysis of the CMS-inducing “Polima” cytoplasm of Brassica napus L. Curr Genet 19:323–327.CrossRefGoogle Scholar
  114. Wolf-Litman O, Soferman O, Tabib Y, Izahr S (1992) Interaction of the mitochondrial S-Pcf locus for cytoplasmic male sterility in Petunia with multiple fertility-restoration genes in somatic hybrid plants. Theor Appl Genet 84:829–834.CrossRefGoogle Scholar
  115. Worrall D, Hird DL, Hodge R, Paul W, Draper J, Scott R (1992) Premature dissolution of the microsporocyte callose causes male sterility in transgenic tobacco. Plant Cell 4(7):759–771.PubMedCrossRefGoogle Scholar
  116. Young EG, Hanson MR (1987) A fused mitochondrial gene associated with cytoplasmic male sterility is developmentally regulated. Cell 50:41–49.PubMedCrossRefGoogle Scholar
  117. Zabala G, O’Brien-Vedder C, Walbot V (1987) S2 episome of maize mitochondria encodes a 130-kilodalton protein found in male sterile and fertile plants. Proc Natl Acad Sei USA 84:7861–7865.CrossRefGoogle Scholar
  118. Zetsche K, Horn R (1993) Molecular analysis of cytoplasmic male sterility in sunflower (Helianthus annuus). In: Kück U, Brennicke A (eds) Plant mitochondria. Springer, Berlin Heidelberg New York.Google Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 1994

Authors and Affiliations

  • Wolfgang Friedt
    • 1
  • Renate Horn
    • 1
  • Volker Hahn
    • 2
  1. 1.Institut für Pflanzenbau und Pflanzenzüchtung IJustus-Liebig-UniversitätGiessenGermany
  2. 2.Landessaatzuchtanstalt Versuchsstation EckartsweierUniversity HohenheimWillstättGermany

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