Skip to main content
Log in

Mitochondrial genome diversity in soybean: repeats and rearrangements

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

Mitochondrial (mt) genome organization in soybean was examined at the molecular level. This study builds upon previous reports that four soybean cytoplasmic groups, Bedford, Arksoy, Lincoln, and soja-forage, are differentiated by polymorphisms detected with a 2.3 kb Hind III mtDNA probe [12]. The variation detected results from DNA alterations in a region within and around a 4.8 kb repeat. The Bedford-type cytoplasm is the only cytoplasm that contains copies of a 4.8 kb repeat in four different genomic environments, evidence that it is recombinationally active. The Lincoln- and Arksoy-type cytoplasms each contain two copies of the repeat, as well as unique fragments that appear to result from rare recombination events outside, but near, the repeat. The soja-forage-type cytoplasm contains no complete copies of the repeat, but does contain a unique truncated version of the repeat. Sequence analysis indicates that the truncation is a result of recombination across a 9 bp repeated sequence, CCCCTCCCC. The structural rearrangements that have occurred in the region surrounding the 4.8 kb repeat may provide a means to dissect species relationships and evolution within the subgenus soja.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Almasan A, Mishra N: Recombination by sequence repeats with formation of suppressive or residual mitochondrial DNA in Neurospora. Proc Natl Acad Sci USA 88: 7684–7688 (1991).

    Google Scholar 

  2. Bailey-Serres J, Leroy P, Jones SS, Wahleithner JA, Wolstenholme DR: Size distribution of circular molecules in plant mitochondrial DNAs. Curr Genet 12: 49–53 (1987).

    Google Scholar 

  3. Bendich A: Reaching for the ring: the study of mitochondrial genome structure. Curr Genet 24: 279–290 (1993).

    Google Scholar 

  4. Bone L, Brown G: Genetic plasticity and its consequences: perspectives on gene organization and expression in plant mitochondria. Can J Bot 71: 645–660 (1993).

    Google Scholar 

  5. Chanut FA, Grabau EA, Gesteland RF: Complex organization of the soybean mitochondrial genome: recombination repeats and multiple transcripts at the atpA loci. Curr Genet 23: 234–247 (1993).

    Google Scholar 

  6. Conklin PL, Hanson MR: A truncated recombination repeat in the mitochondrial genome of a petunia cms line. Curr Genet 23: 477–482 (1993).

    Google Scholar 

  7. Conklin PL, Hanson MR: Recombination of plant mitochondrial genomes. In: Paszkowski J (ed) Homologous Recombination and Gene Silencing in Plants, pp. 61–81. Kluwer Academic Publishers, Dordrecht, Netherlands (1994).

    Google Scholar 

  8. Dewey RE, Levings III CS, Timothy DH: Novel recombinations in the maize mitochondrial genome produce a unique transcriptional unit in the Texas male-sterile cytoplasm. Cell 44: 439–449 (1986).

    Google Scholar 

  9. Fauron CMR, Havlik M, Brettell RIS: The mitochondrial genome orgaization of a maize fertile cmsT revertant line is generated through recombination between two sets of repeats. Genetics 124: 423–428 (1990).

    Google Scholar 

  10. Feinberg A, Vogelstein B: A technique for radio-labeling DNA restriction endonuclease fragments to a high specific activity. Anal Biochem 132: 6–13 (1983).

    Google Scholar 

  11. Grabau E, Davis WH, Gengenbach BG: Restriction fragment length polymorphism in a subclass of the mandarin soybean. Crop Sci 29: 1554–1559 (1989).

    Google Scholar 

  12. Grabau EA, Davis WH, Phelps ND, Gengenbach BG: Classification of soybean cultivars based on mitochondrial DNA restriction fragment length polymorphisms. Crop Sci 32: 271–274 (1992).

    Google Scholar 

  13. Grabau E, Havlik M, Gestland R: Chimeric organization of two genes for the soybean mitochondrial ATPase subunit 6. Curr Genet 13: 83–89 (1988).

    Google Scholar 

  14. Gray MW: Origin and evolution of mitochondrial DNA. Annu Rev Cell Biol 5: 25–50 (1989).

    Google Scholar 

  15. Hartman C, Recipon H, Jubier MF, Valon C, Delcher-Besin E, Henry Y, De Buyser J, Lejeune B, Rode A: Mitochondrial DNA variability detected in a single wheat regenerant involves a rare recombination event across a short repeat. Curr Genet 25: 456–464 (1994).

    Google Scholar 

  16. Hunt MD, Newton KJ: The NCS3 mutation: genetic evidence for the expression of the ribosomal protein genes in Zea mays mitochondria. EMBO J 10: 1045–1052 (1991).

    Google Scholar 

  17. Hymowitz T, Singh RJ: Taxonomy and speciation. In: Wilcox JR (ed) Soybean: Improvement, Production, and Uses, pp. 23–45. American Society of Agronomy/Crop Science Society of America/Soil Science Society of America; Madison, WI (1987).

    Google Scholar 

  18. Janska H, Mackenzie SA: Unusual mitochondrial genome organization in cytoplasmic male sterile common bean and the nature of cytoplasmic reversion to fertility. Genetics 135: 869–879 (1993).

    Google Scholar 

  19. Johns C, Lu M, Lyznik A, Mackenzie S: A mitochondrial DNA sequence is associated with abnormal pollen development in cytoplasmic male sterile bean plants. Plant Cell 4: 435–449 (1992).

    Google Scholar 

  20. Kanazawa A, Tsutsumi N, Hirai A: Reversible changes in the composition of mtDNAs during dedifferentation and regeneration in tobacco. Genetics 134: 865–870 (1994).

    Google Scholar 

  21. Laver HK, Reynolds SJ, Moneger F, Leaver CJ: Mitochondrial genome organization and expression associated with cytoplasmic male sterility in sunflower (Helianthus annuus). Plant J 1: 185–193 (1991).

    Google Scholar 

  22. Lee DJ, Caha CA, Specht JE, Graef GL: Analysis of cytoplasmic diversity in an outcrossing population of soybean. Crop Sci 34: 46–50 (1994).

    Google Scholar 

  23. Levings III CS, Pring DR: Mitochondrial DNA of Higher Plants and Genetic Engineering, vol 1. Plenum Press, New York (1979).

    Google Scholar 

  24. Lonsdale D, Brears T, Hodge T, Melville S, Rottmann T: The plant mitochondrial genome: homologous recombinations as a mechanism for generating heterogeneity. Phil Trans R Soc Lond B 319: 149–163 (1988).

    Google Scholar 

  25. Martinez-Zapater JM, Gil P, Capel J, Somerville CR: Mutations at the Arabidopsis CHM locus promote rear-rangements of the mitochondrial genome. Plant Cell 4: 889–899 (1992).

    Google Scholar 

  26. Manna E, Brennicke A: Site-specific circularisation at an intragenic sequence in Oenothera mitochondria. Mol Gen Genet. 203: 377–381 (1986).

    Google Scholar 

  27. Muhawish SM: Nuclear genetic transformation and a restriction fragment length polymorphism analysis of soybean (Glycine max L. Merr.) mitochondrial genetics. Ph.D. dissertation, Iowa State University Ames Iowa (1992).

    Google Scholar 

  28. Newton K, Knudsen C, Gabay-Laughnan S, Laughnan J: An abnormal growth mutant in maize has a defective mitochondrial cytochrome oxidase gene. Plant Cell 2: 107–113 (1990).

    Google Scholar 

  29. Palmer JD: Contrasting modes and tempos of genome evolution in land plant organelles. Trends Genet 6: 115–120 (1990).

    Google Scholar 

  30. Palmer JD, Shields CR: Tripartite structure of the Brassica campestris mitochondrial genome. Nature 307: 437–440 (1984).

    Google Scholar 

  31. Palmer J, Thompson W: Chloroplast DNA rearrangements are more frequent when a large inverted repeat sequence is lost. Cell 29: 573–550 (1982).

    Google Scholar 

  32. Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning: A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (1989).

    Google Scholar 

  33. Shoemaker RC, Hatfield PM, Palmer RG, Atherly AG: Chloroplast DNA variation in the genus Glycine subgenus Soja. J Hered 77: 26–30 (1986).

    Google Scholar 

  34. Sisson VA, Brim CA, Levings III CS: Characterization of cytoplasmic diversity in soybeans by restriction endonuclease analysis. Crop Sci 18: 991–996 (1978).

    Google Scholar 

  35. Synenki RM, Levings III CS, Shah DM: Physicochemical characterization of mitochondrial DNA from soybean. Plant Physiol 61: 460–464 (1978).

    Google Scholar 

  36. Wissinger B, Brennicke A, Schuster W: Regenerating good sense: RNA editing and trans-splicing in plant mitochondria. Trends Genet 8: 322–328 (1992).

    Google Scholar 

  37. Young EG, Hanson MR: A fused mitochondrial gene associated with cytoplasmic male sterility is developmentally regulated. Cell 50: 41–49 (1987).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Moeykens, C.A., Mackenzie, S.A. & Shoemaker, R.C. Mitochondrial genome diversity in soybean: repeats and rearrangements. Plant Mol Biol 29, 245–254 (1995). https://doi.org/10.1007/BF00043649

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00043649

Key words

Navigation