Skip to main content
Log in

A mitochondrial 16 kDa protein is associated with cytoplasmic male sterility in sunflower

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

Cytoplasmic male-sterile lines CMS89 and CMSBaso of sunflower (Helianthus annuus) differ from the fertile lines HA89 and Baso in a mitochondrial DNA sequence in the vicinity of theatpA gene. In addition, the transcriptional pattern of theatpA gene is changed in male-sterile lines compared to fertile ones. Besides one main transcript in the fertile lines, the male-sterile lines additionally show larger transcripts. Investigation of Baso and CMSBaso revealed that the two fertility-restored lines of CMS89 have the same transcripts as CMSBaso or a combination of CMSBaso and CMS89. Comparing the mitochondrialin organello translation products we observed a unique 16 kDa protein, which is expressed in male-sterile lines carrying theH. petiolaris cytoplasm but is not detectable in fertile lines withH. annuus cytoplasm. The 16 kDa protein can also be observed in restored lines but not inH. petiolaris. As the expression of the 16 kDa polypeptide seems to be linked to the interspecific cross betweenH. petiolaris andH. annuus it may play a role in CMS. By different criteria such as molecular mass, isoelectric point and peptide fingerprinting the α subunit of the F1-ATPase of male-sterile and fertile lines is very similar if not identical.

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.

Institutional subscriptions

Similar content being viewed by others

References

  1. Bailey-Serres JD, Hanson MR, Fox TD, Leaver CJ: Mitochondrial genome rearrangement leads to extension and relocation of the cytochrome c oxidase subunit I gene inSorghum. Cell 47: 567–576 (1986).

    Google Scholar 

  2. Boeshore ML, Hanson MR and Izhar S: A variant mitochondrial DNA arrangement specific toPetunia stable sterile somatic hybrids. Plant Mol Biol 4: 125–132 (1985).

    Google Scholar 

  3. Bonner WM, Laskey RA: A film detection method for tritium-labelled proteins and nucleic acids in poly-acrylamide gels. Eur J Biochem 46: 83–88 (1974).

    Google Scholar 

  4. Boutry M, Briquet M: Mitochondrial modifications associated with the cytoplasmic male sterility in faba beans. Eur J Biochem 127: 129–139 (1982).

    Google Scholar 

  5. Braun CJ, Siedow JN, Williams ME, LevingsIII CS: Mutations in the maize mitochondrial T-urf13 gene eliminate sensitivity to a fungal pathotoxin. Proc Natl Acad Sci USA 86: 4435–4439 (1989).

    Google Scholar 

  6. Brown GG, Bussey H, Desrosiers LJ: Analysis of mitochondrial DNA, chloroplast DNA, and double-stranded RNA in fertile and cytoplasmic male-sterile sunflower (Helianthus annuus). Can J Genet Cytol 28: 121–129 (1986).

    Google Scholar 

  7. Cleveland DW, Stuart GF, Kirschner MW, Laemmli UK: Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis. J Biol Chem 252: 1102–1106 (1977).

    Google Scholar 

  8. Crouzillat D, Leroy P, Perrault A, Ledoigt G: Molecular analysis of the mitochondrial genome ofHelianthus annuus in relation to cytoplasmic male sterility and phylogeny. Theor Appl Genet 74: 773–780 (1987).

    Google Scholar 

  9. Dewey RE, LevingsIII 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 

  10. Dewey RE, Timothy DH, LevingsIII CS: A mitochondrial protein associated with cytoplasmic male sterility in the T cytoplasm of maize. Proc Natl Acad Sci USA 84: 5374–5378 (1987).

    Google Scholar 

  11. Forde BG, Oliver RJC, Leaver CJ: Variation in mitochondrial translation products associated with male-sterile cytoplasms in maize. Proc Natl Acad Sci USA 75: 3841–3845 (1978).

    Google Scholar 

  12. Forde GB, Leaver CJ: Nuclear and cytoplasmic genes controlling synthesis of variant mitochondrial poly-peptides in male-sterile maize. Proc Natl Acad Sci USA 77: 418–422 (1980).

    Google Scholar 

  13. Köhler RH, Horn R, Lössl A, Zetsche K: Cytoplasmic male sterility in sunflower is correlated with the contranscription of a new open reading frame with theatpA gene. Mol Gen Genet (in press 1991).

  14. Laemmli UK: Cleavage of structural proteins during the assembly of the head of bacteriophage T 4. Nature 227: 680–685 (1970).

    Google Scholar 

  15. Leaver CJ, Gray MW: Mitochondrial genome organization and expression in higher plants. Ann Rev Plant Physiol 33: 373–402 (1982).

    Google Scholar 

  16. Leaver CJ, Hack E, Forde BG: Protein synthesis by isolated plant mitochondria. Meth Enzymol 97: 476–484 (1983).

    Google Scholar 

  17. Leclercq P: Une sterilité mâle chez le tournesol. Ann Amélior Plantes 19: 99–106 (1969).

    Google Scholar 

  18. Leclercq CP: Identification de gènes de restauration de fertilité sur cytoplasmes stérilisants chez le tournesol. Agronomie 4: 573–576 (1984).

    Google Scholar 

  19. Makaroff CA, Palmer JD: Mitochondrial DNA rearrangements and transcriptional alterations in the male-sterile cytoplasm of Ogura radish. Mol Cell Biol 8: 1474–1480 (1988).

    Google Scholar 

  20. Makaroff CA, Apel IJ, Palmer JD: The atp6 coding region has been disrupted and a novel reading frame generated in the mitochondrial genome of cytoplasmic male-sterile radish. J Biol Chem 264: 11706–11713 (1989).

    Google Scholar 

  21. Maniatis T, Fritsch EF, Sambrook J: Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1982).

    Google Scholar 

  22. Newton KJ: Plant mitochondrial genomes: Organization, expression and variation. Ann Rev Plant Physiol Plant Mol Biol 39: 503–532 (1988).

    Google Scholar 

  23. Nivison HT, Hanson MR: Identification of a mitochondrial protein associated with cytoplasmic male sterility inPetunia. Plant Cell 1: 1121–1130 (1989).

    Google Scholar 

  24. O'Farrell PH: High resolution two-dimensional electrophoresis of proteins. J Biol Chem 250: 4007–4021 (1975).

    Google Scholar 

  25. Pring DR, Levings CS: Heterogeneity of maize cytoplasmic genomes among male-sterile cytoplasms. Genetics 89: 121–136 (1978).

    Google Scholar 

  26. Schuster W, Brennicke A: Pseudocopies of the ATPase α-subunit gene inOenothera mitochondria are present on different circular molecules. Mol Gen Genet 204: 29–35 (1986).

    Google Scholar 

  27. Siculella L, Palmer JD: Physical and gene organization of mitochondrial DNA in fertile and male sterile sunflower. CMS-associated alterations in structure and transcription of theatpA gene. Nucl Acids Res 16: 3787–3799 (1988).

    Google Scholar 

  28. Taylor B, Powell A: Isolation of plant DNA and RNA. Bethesda Research Laboratory, Focus 4(3): 4–6 (1982).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Horn, R., Köhler, R.H. & Zetsche, K. A mitochondrial 16 kDa protein is associated with cytoplasmic male sterility in sunflower. Plant Mol Biol 17, 29–36 (1991). https://doi.org/10.1007/BF00036803

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00036803

Key words

Navigation