Conditional male fertility in maize
- 68 Downloads
- 12 Citations
Abstract
This study compares conditional male fertility (CMF) in maize and petunia. CMF is a reversible defect in pollen germination or tube growth; pollen is nonfunctional in self-crosses but fully functional in outcrosses or when supplied with specific flavonol aglycones at pollination. CMF occurs in maize and petunia mutants that lack chalcone synthase (CHS) activity and therefore do not synthesize flavonols. In maize CMF seedlings and developing male florets, CHS transcripts accumulate to high levels, yet western blot analysis using an anti-CHS antiserum does not detect any CHS protein. This is in contrast to CMF petunia, where no CHS RNA is detected (Vogt et al. 1994). While CMF petunia pollen requires flavonols to germinate, CMF maize pollen germinates and grows both in vivo and in vitro without the addition of flavonols. However, pollen tubes abort after 12 h of growth which explains the lack of seed set in self crosses (Mo et al. 1992). Pollen tubes of CMF maize have an unusual morphology in vivo, with heavy callose deposits throughout the tube and tips that burst within the silk. Normal tube morphology and seed set are restored by adding flavonols to the silks at pollination. As previously shown with petunia, fecundity (seed set) may be enhanced in maize by adding quercetin and kaempferol at pollination.
Key words
Conditional male fertility Flavonols Maize PetuniaPreview
Unable to display preview. Download preview PDF.
References
- Ceska O, Styles ED (1984) Flavonoids from Zea mays pollen. Phytochemistry 23: 1822–1823Google Scholar
- Coe EH Jr, McCormick SM, Modena SA (1981) White pollen in maize. J Hered 72: 318–320Google Scholar
- Coe EH Jr, Neuffer MG, Hoisington DA (1988) The genetics of corn. In: Sprague GF, Dudley JW (eds) Corn and corn improvement. American Society of Agronomy, Madison, Wis pp 81–258Google Scholar
- Deboo GB, Albertsen MC, Taylor LP (1994) Flavanone 3-hydroxylase and flavorol accumulation are temporally coordinate in maize anthers. Plant J 7: 101–111Google Scholar
- Feinberg AP, Vogelstein B (1983) A technique for radiolabelling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 132: 6–13PubMedGoogle Scholar
- Franken P, Niesbach-Klösgen U, Weydemann U, Marérchal-Drouard L, Saedler H, Wienand U (1991) The duplicated chalcone synthase genes C 2 and Whp (white pollen) of Zea mays are independently regulated: evidence for translational control of Whp expression by the anthocyanin intensifying gene. EMBO J 10:2605–2612Google Scholar
- Herdt E, Sütfeld R, Wiermann R (1978) The occurrence of enzymes involved in phenylpropanoid metabolism in the tapetum fraction of anthers Cytobiologie 17: 433–441Google Scholar
- Hoekstra FA (1979) Mitochondrial development and activity of binucleate and trinucleate pollen during germination in vitro. Planta 145: 25–36Google Scholar
- Hoekstra FA, Bruinsma J (1979) Protein synthesis of binucleate and trinucleate pollen and its relationship to tube emergence and growth. Planta 146: 559–566Google Scholar
- Kho YO, Baer J (1968) Observing pollen tubes by means of fluorescence. Euphytica 17: 289–302Google Scholar
- Koes RE, van Blokland R, Quattrocchio F, van Tunen AJ, Mol JNM (1990) Chalcone synthase promoters in petunia are active in pigmented and unpigmented cell types. Plant Cell 2: 379–392Google Scholar
- Lawton MA, Lamb CJ (1987) Transcriptional activation of plant defense genes by fungal elicitor, wounding and infection. Mol Cell Biol 7: 335–341Google Scholar
- Long SR (1989) Rhizobium-legume nodulation: life together in the underground. Cell 56: 203–214Google Scholar
- Maes M, Messens E (1992) Phenol as grinding material in RNA reparations. Nucleic Acids Res 20: 4374Google Scholar
- Mo Y, Nagel C, Taylor LP (1992) Biochemical complementation of chalcone synthase mutants defines a role for flavonols in functional pollen. Proc Natl Acad Sci USA 89: 7213–7217PubMedGoogle Scholar
- Mogensen HL (1992) The male germ unit: concept, composition, and significance. Int Rev Cytol 140: 129–147Google Scholar
- Mulcahy GB, Mulcahy DL (1982) The two phases of growth of Petunia hybrida (Hort. Vilm-Andz) pollen tubes through compatible styles. J Palynology 18: 61–64Google Scholar
- Napoli C, Lemieux C, Jorgensen R (1990) Introduction of a chimeric chalcone synthase gene into petunia results in reversible co-suppression of homologous genes in trans. Plant Cell 2: 279–289Google Scholar
- Pfahler PL (1967) In vitro germination and pollen tube growth of maize (Zea mays L.) pollen. I. Calcium and boron effects. Can J Bot 45: 839–845Google Scholar
- Pollak PE, Vogt T, Mo Y, Taylor LP (1993) Chalcone synthase and flavonol accumulation in stigmas and anthers of Petunia hybrida. Plant Physiol 102: 925–932Google Scholar
- Rommeswinkel M, Karwatzki B, Beerhues L, Wiermann R (1992) Immunofluorescence localization of chalcone synthase in roots of Pisum sativum L. and Phaseolus vulgaris L. and comparable immunochemical analysis of chalcone synthase from pea leaves. Protoplasma 166: 115–121Google Scholar
- Rosen WG, Gawlik SR (1966a) Relation of lily pollen tube fine structure to pistil compatibility and mode of nutrition. Electron Microscopy 2: 313–314Google Scholar
- Rosen WG, Gawlik SR (1966b) Fine structure of lily pollen following various fixations and staining procedures. Protoplasma 61:181–191Google Scholar
- Sütfeld R, Kehrel B, Wiermann R (1978) Characterization, development and localization of “flavanone synthase” in tulip anthers. Z Naturforsch C33: 841–846Google Scholar
- Taylor LP, Briggs WR (1990) Genetic regulation and photocontrol of anthocyanin accumulation in maize seedlings. Plant Cell 2:115–127Google Scholar
- Taylor LP, Jorgensen R (1992) Conditional male fertility in chalcone synthase-deficient petunia. J Hered 83: 11–17Google Scholar
- Vogt T, Pollak P, Tarlyn N, Taylor LP (1994) Pollination- or wound-induced kaempferol accumulation in petunia stigmas enhances seed production. Plant Cell 6: 11–23Google Scholar
- Weiss D, van Tunen AJ, Halevy AH, Mol JNM, Gerats AGM (1990) Stamens and gibberellic acid in the regulation of flavonoid gene expression in the corolla of Petunia hybrida. Plant Physiol 94: 511–515Google Scholar
- Wiermann R, Vieth K (1983) Outer pollen wall, an important accumulation site for flavonoids. Protoplasma 118: 230–233Google Scholar
- Ylstra B, Touraev A, Benito Moreno RM, van Tunen AJ, Vicente O, Mol JNM, Heberle-Bors E (1992) Flavonols stimulate development, germination, and tube growth of tobacco pollen. Plant Physiol 100: 902–907Google Scholar
- Zerhack R, Dressler K, Hess D (1989) Flavonoid compounds from pollen and stigma of Petunia hybrida: Inducers of the vir region of the Agrobacterium tumefaciens Ti plasmid. Plant Sci 62: 83–91CrossRefGoogle Scholar