Stoichiometric shifts in the common bean mitochondrial genome leading to male sterility and spontaneous reversion to fertility

Plant Cell

Volumn 10, Issue 7, 1998, Pages 1163-1180

  Janska, Hanna ^a   Sarria, Rodrigo ^b   Woloszynska, Magdalena ^a   Arrieta Montiel, Maria ^b   Mackenzie, Sally A ^b  

^a UNIVERSITY OF WROC AW   (Poland)

^b PURDUE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTORADIOGRAPHY; BEAN; DNA MOLECULE; FERTILIZATION; GEL BLOTTING; MALE STERILITY; MITOCHONDRIAL GENOME; PLANT DEVELOPMENT; PLANT GENOME; POLYMERASE CHAIN REACTION; STOICHIOMETRY; TRANSCRIPTION REGULATION;

EID: 0031767994     PISSN: 10404651     EISSN: None     Source Type: Journal    
DOI: 10.1105/tpc.10.7.1163     Document Type: Article

References (40)

1. Abad, A.R., Mehrtens, B.J., and Mackenzie, S.A. (1995). Specific expression in reproductive tissues and fate of a mitochondrial sterility-associated protein in cytoplasmic male-sterile bean. Plant Cell 7, 271-285.
2. Albert, B., Godelle, B., Atlan, A., De Paepe, R., and Gouyon, P.H. (1996). Dynamics of the plant mitochondrial genome; model of a three-level selection process. Genetics 144, 369-382.
3. Backert, S., Meibner, K., and Borner, T. (1997). Unique features of the mitochondrial rolling circle-plasmid mp1 from the higher plant Chenopodium album (L.). Nucleic Acids Res. 25, 582-589.
4. Bendich, A.J. (1993). Reaching for the ring: The study of mitochondrial genome structure. Curr. Genet. 24, 279-290.
5. Bonhomme, S., Budar, F., Lancelin, D., Small, I., Defrance, M.C., and Pelletier, G. (1992). Sequence and transcript analysis of the NCO 2.5 Ogura-specific fragment are correlated with cytoplasmic male sterility in Brassica cybrids. Mol. Gen. Genet. 235, 340-348.
6. Chase, C.D. (1994). Expression of CMS unique and flanking mitochondrial DMA sequences in Phaseolus vulgaris L. Curr. Genet. 25, 245-251.
7. Chase, C.D., and Ortega, V.M. (1992). Organization of ATPA coding and 3′ flanking sequences associated with cytoplasmic male sterility in Phaseolus vulgaris L. Curr. Genet. 22, 147-153.
8. Dawson, A.J., Jones, V.P., and Leaver, C.J. (1984). The apocytochrome b gene in maize mitochondria does not contain introns and is preceded by a potential ribosome binding site. EMBO J. 3, 2107-2113.
9. Enriquez, J.A., Perez-Martos, A., Fernandez-Silva, P., Lopez-Perez, M.J., and Montoya, J. (1993). RNA synthesis in isolated mitochondria from brain cortex, cerebellum and stem: Evidence of different transcriptional rates. Int. J. Biochem. 25, 1951-1956.
10. Enriquez, J.A., Ramos, J., Perez-Martos, A., Lopez-Perez, M.J., and Montoya, J. (1994). Highly efficient DNA synthesis in isolated mitochondria from rat liver. Nucleic Acids Res, 22, 1861-1865.
11. Folkerts, O., and Hanson, M.R. (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.
12. Forde, B.G., Olivier, R.J.C., and Leaver, C.J. (1978). Variation in mitochondrial translation products associated with male-sterile cytoplasms in maize. Proc. Natl. Acad. Sci. USA 75, 3841-3845.
13. Grabau, E. (1985). Nucleotide sequence of the soybean mitochondrial 18S rRNA gene: Evidence for a slow rate of divergence in the plant mitochondrial genome. Plant Mol. Biol. 5, 119-124.
14. Gutierres, S., Lelandais, C., De Paepe, R., Vedel, F., and Chetrit, P. (1997). A mitochondrial sub-stoichiornetric orf87-nad3-nad1 exonA co-transcription unit present in Solanaceae was amplified in the genus Nicotiana. Curr. Genet. 31, 55-62.
15. Hanson, M.R. (1991). Plant mitochondrial mutations and male sterility. Annu. Rev. Genet. 25, 461-486.
16. He, S., Lyznik, A., and Mackenzie, S. (1995). Pollen fertility restoration by nuclear gene Fr in CMS bean: Nuclear-directed alteration of a mitochondrial population. Genetics 139, 955-962.
17. He, S., Abad, A.R., Gelvin, S.B., and Mackenzie, S.A. (1996). A cytoplasmic male sterility-associated mitochondrial protein causes pollen disruption in transgenic tobacco. Proc. Natl. Acad. Sci. USA 93, 11763-11768.
18. Janska, H., and Mackenzie, S.A. (1993). Unusual mitochondrial genome organization in cytoplasmic male sterile common bean and the nature of cytoplasmic reversion to fertility. Genetics 135, 869-879.
19. Johns, C., Lu, M., Lyznik, A., and Mackenzie, S. (1992). A mitochondrial DNA sequence is associated with abnormal pollen development in cytoplasmic male sterile bean plants. Plant Cell 4, 435-449.
20. Kanawawa, A., Tsutsumi, N., and Hirai, A. (1994). Reversible changes in the composition of the population of mtDNAs during dedifferentiation and regeneration in tobacco. Genetics 138, 865-870.
21. Laemmli, U.K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680-685.
22. Leaver, C.J., Isaac, P.G., Small, I.D., Bailey-Serres, J., Liddell, A.D., and Hawkesford, M.J. (1988). Mitochondrial genome diversity and cytoplasmic male sterility in higher plants. Philos. Trans. R. Soc. Lond. B 319, 165-176.
23. Lonsdale, D.M., Brears, T., Hodge, T.P., Melville, S.E., and Rottmann, W.H. (1988). The plant mitochondrial genome: Homologous recombination as a mechanism for generating heterogeneity. Philos. Trans. R. Soc. Lond. B 319, 149-163.
24. Mackenzie, S.A. (1991). Identification of a sterility-inducing cytoplasm in a fertile accession line of Phaseolus vulgaris L. Genetics 127, 411-416.
25. Mackenzie, S.A., and Chase, C.D. (1990). Fertility restoration is associated with loss of a portion of the mitochondrial genome in cytoplasmic male-sterile common bean. Plant Cell 2, 905-912.
26. Mackenzie, S.A., Pring, D.R., Bassett, M.J., and Chase, C.D. (1988). Mitochondrial DNA rearrangement associated with fertility restoration and cytoplasmic reversion to fertility in cytoplasmic male sterile Phaseolus vulgaris L. Proc. Natl. Acad. Sci. USA 85, 2714-2717.
27. Nei, M., and Li, W.-H. (1979). Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc. Natl. Acad. Sci. USA 76, 5269-5273.
28. Oldenburg, D.J., and Bendich, A.J. (1996). Size and structure of replicating mitochondrial DNA in cultured tobacco cells. Plant Cell 8, 447-461.
29. Pla, M., Mathieu, C., De Paepe, R., Chetrit, P., and Vedel, F. (1995). Deletion of the last two exons of the mitochondrial nad7 gene results in lack of the NAD7 polypeptide in a Nicotiana sylvestris CMS mutant. Mol. Gen. Genet. 248, 79-88.
30. Ragan, C.J., Wilson, M.T., Darley-Usmar, V.M., and Lowe, P.N. (1987). Subfractionation of mitochondria and isolation of proteins of oxidative phosphorylation. In Mitochondria: A Practical Approach, V.M. Darley-Usmar, D. Rickwood, and M.T. Wilson, eds (Washington DC: IRL Press), pp. 79-112.
31. Sakamoto, W., Kondo, H., Murata, M., and Motoyoshi, F. (1996). Altered mitochondrial gene expression in a maternal distorted leaf mutant of Arabidopsis induced by chloroplast mutator. Plant Cell 8, 1377-1390.
32. Sambrook, J., Fritsch, E.F., and Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual, 2nd ed. (Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press).
33. Sarria, R., Lyznik, A., Vallejos, E.C., and Mackenzie, S.A. (1998). A cytoplasmic male sterility-associated mitochondrial peptide in common bean is post-translationally regulated. Plant Cell 10, 1217-1228.
34. Small, I.D., Isaac, P.G., and Leaver, C.J. (1987). Stoichiometric differences in DNA molecules containing the atpA gene suggest mechanisms for the generation of mitochondrial diversity in maize. EMBO J. 6, 865-869.
35. Small, I.D., Suffolk, R., and Leaver, C.J. (1989). Evolution of plant mitochondrial genomes via sub-stoichiometric intermediates. Cell 58, 69-76.
36. Suzuki, T., Kawano, S., Sakai, A., Hirai, A., and Kuroiwa, T. (1996). Variability of mitochondrial subgenomic molecules in the meristematic cells of higher plants. Genes Genet. Syst. 71, 329-333.
37. Tohme, J., Gonzalez, D.O., Beebe, S., and Duque, M.C. (1996). AFLP analysis of gene pools of a wild bean core collection. Crop Sci. 36, 1375-1384.
38. Wolstenholme, D.R., and Fauron, C.M.-R. (1995). Mftochondrial genome organization. In The Molecular Biology of Plant Mitochondria, C.S. Levings III and I.K. Vasil, eds (Dordrecht, The Netherlands: Kluwer Academic Publishers), pp. 1-60.
39. Yamato, K., Ogura, Y., Kanegae, Y., Yamada, Y., and Ohyama, K. (1992). Mitochondrial genome structure of rice suspension culture from cytoplasmic male-sterile line (A-58 CMS): Reappraisal of the master circle. Theor. Appl. Genet. 83, 279-288.
40. Yesodi, V., Izhar, S., Gidoni, D., Tabib, Y., and Firon, N. (1995). Involvement of two different urf-s related mitochondrial sequences in the molecular evolution of the CMS-specific S-Pcf locus in petunia. Mol. Gen. Genet. 248, 540-546.