Abstract
In Zea mays L. plants carrying the S-type of sterility-inducing cytoplasm, male fertility is determined by a gametophytic, nuclear restoration-of-fertility gene. Haploid pollen carrying the fertility-restoring allele (historically designated Rf3) is starch-filled and functional, whereas pollen carrying the nonrestoring allele (historically designated rf3) is shrunken and nonfunctional. Because restoration of fertility occurs in haploid tissue, the dominance relationship of restoring and nonrestoring alleles is unknown. We have tested the dominance relationship of the restoring and nonrestoring alleles at the rf3 locus in diploid pollen. The meiotic mutant elongate was used to generate tetraploid plants carrying both Rf3 and rf3 alleles in the S cytoplasm. These plants shed predominantly starch-filled pollen, consistent with dominance of the restoring allele. Restriction fragment length polymorphisms linked to the rf3 locus demonstrated cotransmission of rf3 and Rf3 alleles through heterozygous diploid pollen, providing conclusive genetic evidence that the restoring allele is the dominant or functional form of this restoration-of-fertility gene. We suggest that other S-cytoplasm restorers result from loss-of-function mutations and propose analysis of unreduced gametes as a test of this model.
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Selected References
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- Abad A. R., Mehrtens B. J., Mackenzie S. A. Specific expression in reproductive tissues and fate of a mitochondrial sterility-associated protein in cytoplasmic male-sterile bean. Plant Cell. 1995 Mar;7(3):271–285. doi: 10.1105/tpc.7.3.271. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barkan A., Miles D., Taylor W. C. Chloroplast gene expression in nuclear, photosynthetic mutants of maize. EMBO J. 1986 Jul;5(7):1421–1427. doi: 10.1002/j.1460-2075.1986.tb04378.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Barkan A. Nuclear Mutants of Maize with Defects in Chloroplast Polysome Assembly Have Altered Chloroplast RNA Metabolism. Plant Cell. 1993 Apr;5(4):389–402. doi: 10.1105/tpc.5.4.389. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Church G. M., Gilbert W. Genomic sequencing. Proc Natl Acad Sci U S A. 1984 Apr;81(7):1991–1995. doi: 10.1073/pnas.81.7.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Conley C. A., Hanson M. R. Tissue-Specific Protein Expression in Plant Mitochondria. Plant Cell. 1994 Jan;6(1):85–91. doi: 10.1105/tpc.6.1.85. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dewey R. E., Levings C. S., 3rd, Timothy D. H. Novel recombinations in the maize mitochondrial genome produce a unique transcriptional unit in the Texas male-sterile cytoplasm. Cell. 1986 Feb 14;44(3):439–449. doi: 10.1016/0092-8674(86)90465-4. [DOI] [PubMed] [Google Scholar]
- Feinberg A. P., Vogelstein B. "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum. Anal Biochem. 1984 Feb;137(1):266–267. doi: 10.1016/0003-2697(84)90381-6. [DOI] [PubMed] [Google Scholar]
- Grelon M., Budar F., Bonhomme S., Pelletier G. Ogura cytoplasmic male-sterility (CMS)-associated orf138 is translated into a mitochondrial membrane polypeptide in male-sterile Brassica cybrids. Mol Gen Genet. 1994 Jun 3;243(5):540–547. doi: 10.1007/BF00284202. [DOI] [PubMed] [Google Scholar]
- Hanson M. R. Plant mitochondrial mutations and male sterility. Annu Rev Genet. 1991;25:461–486. doi: 10.1146/annurev.ge.25.120191.002333. [DOI] [PubMed] [Google Scholar]
- Heery D. M., Gannon F., Powell R. A simple method for subcloning DNA fragments from gel slices. Trends Genet. 1990 Jun;6(6):173–173. doi: 10.1016/0168-9525(90)90158-3. [DOI] [PubMed] [Google Scholar]
- Huang J., Struck F., Matzinger D. F., Levings C. S., 3rd Flower-enhanced expression of a nuclear-encoded mitochondrial respiratory protein is associated with changes in mitochondrion number. Plant Cell. 1994 Mar;6(3):439–448. doi: 10.1105/tpc.6.3.439. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krishnasamy S., Makaroff C. A. Organ-specific reduction in the abundance of a mitochondrial protein accompanies fertility restoration in cytoplasmic male-sterile radish. Plant Mol Biol. 1994 Nov;26(3):935–946. doi: 10.1007/BF00028860. [DOI] [PubMed] [Google Scholar]
- Monéger F., Smart C. J., Leaver C. J. Nuclear restoration of cytoplasmic male sterility in sunflower is associated with the tissue-specific regulation of a novel mitochondrial gene. EMBO J. 1994 Jan 1;13(1):8–17. doi: 10.1002/j.1460-2075.1994.tb06230.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Singh M., Brown G. G. Characterization of expression of a mitochondrial gene region associated with the Brassica "Polima" CMS: developmental influences. Curr Genet. 1993 Oct;24(4):316–322. doi: 10.1007/BF00336783. [DOI] [PubMed] [Google Scholar]
- Tzagoloff A., Dieckmann C. L. PET genes of Saccharomyces cerevisiae. Microbiol Rev. 1990 Sep;54(3):211–225. doi: 10.1128/mr.54.3.211-225.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Xu H., Knox R. B., Taylor P. E., Singh M. B. Bcp1, a gene required for male fertility in Arabidopsis. Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):2106–2110. doi: 10.1073/pnas.92.6.2106. [DOI] [PMC free article] [PubMed] [Google Scholar]