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Characterization of three male-sterile mutants of Arabidopsis thaliana exhibiting alterations in meiosis

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Abstract

Male-sterile mutants are being studied to deepen our understanding of the complex processes of microsporogenesis and microgametogenesis. Due to difficulties associated with isolating the mutated gene, there is currently very little molecular information on the defects responsible for male sterility. As a first step in utilizing male-sterile mutants to better understand the bio-chemical and molecular processes that control pollen development, we have characterized a number of Arabidopsis thaliana lines that were generated by seed transformation and exhibit male sterility. We report here the identification and characterization of three male-sterile A. thaliana lines, all of which are tagged with T-DNA and show aberrant meiosis. A detailed cytochemical study was conducted on these lines to better understand the timing and nature of each mutation and to investigate how these mutations affect subsequent steps of pollen development. All three mutants undergo apparently normal morphogenesis until the onset of meiosis. In one line (6492) the mutation is most notable at the tetrad stage when up to eight microspores can be seen in each callose-encased tetrad. The resulting mutant microspores are of variable sizes and contain different amounts of DNA. Two other mutants (7219 and 7593) possess many common features, including variable developmental pathways, failure to produce callose, production of vacuolate, coenocytic (multi-nucleate) cells that are surrounded by persistent microsporocyte walls, and asynchronous patterns of development. Unlike the situation in wild-type plants, where developmental stages are correlated with bud length, such correlations are almost impossible with these two mutants. The sporogenous tissue within all three of these mutant lines collapses prior to anthesis.

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References

  • Aarts MGM, Dirkse WG, Stiekema WJ, Pereira A (1993) Transposon tagging of a male sterility gene in Arabidopsis. Nature 363: 715–717

    Google Scholar 

  • Albertsen MC, Phillips RL (1981) Developmental cytology of 13 genetic male sterile loci in maize. Can J Genet Cytol 23: 195–208

    Google Scholar 

  • Bronner R (1975) Simultaneous demonstration of lipids and starch in plant tissues. Stain Technol 50: 1–4

    Google Scholar 

  • Brown RC, Lemmon BE (1991) Pollen development in orchids. I. Cytoskeleton and the control of division plane in irregular patterns of cytokinesis. Protoplasma 163: 9–18

    Google Scholar 

  • Chaudhury AM, Craig S, Bloemer KC, Farrell L, Dennis ES (1992) Genetic control of male fertility in higher plants. Aust J Plant Physiol 19: 419–426

    Google Scholar 

  • Chaudhury AM, Lavithis M, Taylor PE, Craig S, Singh MB, Signer ER, Knox RB, Dennis ES (1994) Genetic control of male fertility in Arabidopsis thaliana: structural analysis of premeiotic developmental mutants. Sex Plant Reprod 7: 17–28

    Google Scholar 

  • Clapham DH, Ostergren G (1984) Immunocytochemistry of tubulin at meiosis in Tradescantia by a protein-A gold method. Hereditas 101: 137–142

    Google Scholar 

  • Clark FJ (1940) Cytogenetic studies of divergent meiotic spindle formation in Zea mays. Am J Bot 27: 547–559

    Google Scholar 

  • Considine JA, Knox RB (1979) Development and histochemistry of the cells, cell walls, and cuticle of the dermal system of fruit of the grape, Vitis vinifera L. Protoplasma 99: 347–365

    Google Scholar 

  • Cresti M, Blackmore S, van Went JL (1992) Atlas of sexual reproduction in flowering plants. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Dawson J, Wilson ZA, Aarts MGM, Braithwaite AF, Briarty LG, Mulligan BJ (1993) Microspore and pollen development in six male-sterile mutants of Arabidopsis thaliana. Can J Bot 71: 629–638

    Google Scholar 

  • Delmer DP (1987) Cellulose biosynthesis. Annu Rev Plant Physiol 38: 259–290

    Google Scholar 

  • Dickinson HG (1987) The physiology and biochemistry of meiosis in the anther. Int Rev Cytol 107: 79–109

    Google Scholar 

  • Echlin P, Godwin H (1968) The ultrastructure and ontogeny of pollen in Helleborus foetidus L. I. The development of the tapetum and Ubisch bodies. J Cell Sci 3: 161–174

    Google Scholar 

  • Feldmann KA (1991) T-DNA insertion mutagenesis in Arabidopsis: mutational spectrum. Plant J 1: 71–82

    Google Scholar 

  • Feldmann KA, Marks MD (1987) Agrobacterium-mediated transformation of germinating seeds of Arabidopsis thaliana: a non-tissue culture approach. Mol Gen Genet 208: 1–9

    Google Scholar 

  • Fisher DB (1968) Protein staining of ribboned epon sections for light microscopy. Histochemie 16: 92–96

    Google Scholar 

  • Gahan PB (1984) Plant histochemistry and cytochemistry: an introduction. Academic Press, London, pp 116–117

    Google Scholar 

  • Gantotti BV, Woodske DVG (1991) Nuclear staining of Colletotrichum gloeosporiodes F. Sp. Malvae conidia with fluorescent and nonfluorescent stains. Biotech Histochem 1: 7–13

    Google Scholar 

  • Hayat MA (1989) Principles and techniques of electron microscopy. CRC, Boca Raton, Fla

    Google Scholar 

  • Heslop-Harrison J (1966) Cytoplasmic continuities during spore formation in flowering plants. Endeavour 25: 65–72

    Google Scholar 

  • Hoefert LL (1968) Polychromatic stains for thin sections of Beta embedded in epoxy resin. Stain Technol 43: 145–151

    Google Scholar 

  • Jensen WA (1962) Botanical histochemistry: principles and practice. Freeman, San Francisco, pp 198–199

    Google Scholar 

  • Kamalay JC, Goldberg RB (1984) Organ-specific nuclear RNAs in tobacco. Proc Natl Acad Sci USA 81: 2801–2805

    Google Scholar 

  • Kaul MLH (1988) Male sterility in higher plants. Springer, Berlin Heidelberg New York

    Google Scholar 

  • Kauss H (1987) Some aspects of calcium-dependent regulation in plant metabolism. Annu Rev Plant Physiol 38: 47–72

    Google Scholar 

  • Koltunow AM, Truettner J, Cox KH, Wallroth M, Goldberg RB (1990) Different temporal and spatial gene expression patterns occur during anther development. Plant Cell 2: 1201–1224

    CAS  PubMed  Google Scholar 

  • Larson A, Lewis CW (1962) Pollen wall development in Parkinsonia aculeata. Grana Palynol 3: 21–27

    Google Scholar 

  • Mascarenhas JP (1975) The biochemistry of angiosperm pollen development. Bot Rev 41: 259–314

    Google Scholar 

  • Mascarenhas JP (1992) Pollen gene expression: molecular evidence. Int Rev Cytol 107: 3–16

    Google Scholar 

  • McCormick S (1993) Male gametophyte development. Plant Cell 5: 1265–1275

    Article  PubMed  Google Scholar 

  • Moffatt B, Sommerville C (1988) Positive selection for male-sterile mutants of Arabidopsis lacking adenine phosphoribosyl transferase activity. Plant Physiol 86: 1150–1154

    Google Scholar 

  • Moffatt B, Pethe C, Laloue M (1991) Metabolism of benzyladenine is impaired in a mutant of Arabidopsis thaliana lacking adenine phosphoribosyltransferase activity. Plant Physiol 95: 900–908

    Google Scholar 

  • Muschietti J, Dircks L, Vancanneyt G, McCormick S (1994) LAT52 protein is essential for tomato pollen development: pollen expressing antisense LAT52 RNA hydrates and germinates abnormally and cannot achieve fertilization. Plant J 6: 321–338

    Google Scholar 

  • Owen HA, Makaroff CA (1995) Ultrastructure of microsporogenesis and microgametogenesis in Arabidopsis thaliana (L.) Heynh. ecotype Wassilewskija (Brassicaceae). Protoplasma 185: 7–21

    Google Scholar 

  • Preuss D, Lemieux B, Yen G, Davis RW (1993) A conditional sterile mutation eliminates surface components from Arabidopsis pollen and disrupts cell signaling during fertilization. Gene Develop 7: 974–985

    Google Scholar 

  • Preuss D, Rhee SY, Davis RW (1994) Tetrad analysis is possible in Arabidopsis with mutation of the QUARTET (QRT) genes. Science 264: 1458–1460

    Google Scholar 

  • Regan SM, Moffatt BA (1990) Cytochemical analysis of pollen development in wild-type Arabidopsis and a male-sterile mutant. Plant Cell 2: 877–889

    Google Scholar 

  • Sampson FB (1969) Cytokinesis in pollen mother cells of angiosperms, with emphasis on Laurelia novae-zelandiae (Monimiaceae). Cytologia 34: 627–634

    Google Scholar 

  • Sass JE (1958) Botanical microtechnique. Iowa State College Press, Ames, pp 12–77

    Google Scholar 

  • Schliwa M, vanBlerkom J (1981) Structural interaction of cytoskeletal components. J Cell Biol 90: 222–235

    Article  CAS  PubMed  Google Scholar 

  • Scott R (1993) Anther development: a molecular perspective. In: Jordan BR (ed) The molecular biology of flowering. CAB International, Wallingford, UK, pp 141–184

    Google Scholar 

  • Scott R, Hodge R, Paul W, Draper J (1991) The molecular biology of anther differentiation. Plant Sci 80: 167–191

    Article  CAS  Google Scholar 

  • Smith AG, Gasser CS, Budelier KA, Fraley RT (1990) Identification and characterization of stamen- and tapetum-specific genes from tomato. Mol Gen Genet 222: 9–16

    Google Scholar 

  • Smith MM, McCully ME (1978) A critical evaluation of the specificity of aniline blue induced florescence. Protoplasma 95: 229–254

    Google Scholar 

  • Staiger CJ, Cande WZ (1990) Microtubule distribution in dv, a maize meiotic mutant defective in the prophase to metaphase transition. Dev Biol 138: 231–242

    Google Scholar 

  • Staiger CJ, Cande WZ (1991) Microfilament distribution in maize meiotic mutants correlates with microtubule organization. Plant Cell 3: 637–644

    Google Scholar 

  • Staiger CJ, Cande WZ (1993) Cytoskeletal analysis of maize meiotic mutants. In: Ormrod JC Francis D (eds) Molecular and cell biology of the plant cell cycle. Kluwer, Dordrecht, Netherlands, pp 157–171

    Google Scholar 

  • Sutherland J, McCully ME (1976) A note on the structural changes in the walls of pericycle cells initiating lateral root meristems in Zea mays. Can J Bot 54: 2083–2087

    Google Scholar 

  • Worrall D, Hird DL, Hodge R, Paul W, Draper J, Scott R (1992) Premature dissolution of the microsporocyte callose wall causes male sterility in transgenic tobacco. Plant Cell 4: 759–771

    Article  CAS  PubMed  Google Scholar 

  • Xu H, Knox RB, Taylor PE, Singh MB (1995) Bcpl, a gene required for male fertility in Arabidopsis. Proc Natl Acad Sci USA 92: 2106–2110

    Google Scholar 

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Peirson, B.N., Owen, H.A., Feldmann, K.A. et al. Characterization of three male-sterile mutants of Arabidopsis thaliana exhibiting alterations in meiosis. Sexual Plant Reprod 9, 1–16 (1996). https://doi.org/10.1007/BF00230361

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  • DOI: https://doi.org/10.1007/BF00230361

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