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Variations in endopolyploidy level during the short period of the early growing stage in the roots and leaves of maize (Zea mays) seedlings

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Abstract

We used a flow cytometer to investigate the variations in endopolyploidy (the frequencies of nuclei with DNA contents equivalent to 4C through 16C) during the short period of the early growing stage in vigorously growing young tissues of maize seedlings. We examined different portions of the root and leaves that had been growing for 7 (day 7) and 13 (day 13) days after germination. Endoreplication showed two opposing phenomena without aging. In one case, the endopolyploidy of the first leaf was higher on day 13 than on day 7. In the latter case, endopolyploidy decreased, as clearly revealed by a comparison of the endopolyploidy of the second leaves and the 160–170 mm portion of the seminal root on days 7 and 13. Endopolyploidy was also lower in the top of the leaf. In roots, endopolyploidy was increased by the exogenous application of abscisic acid for only 1 day. The levels of endopolyploidy increased without an increase in cell size in the roots. These results showed that endoreplication occurs in actively growing and young tissue and that the variation can be induced in the short period examined.

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References

  • Barlow EWR (1986) Water relations of expanding leaves. Aust J Plant Physiol 13:45–58

    Article  Google Scholar 

  • Barrow M, Meister A (2003) Endopolyploidy in seed plants is differently correlated to systematics, organ, life strategy and genome size. Plant Cell Environ 26:571–584

    Article  Google Scholar 

  • Bertin N (2005) Analysis of the tomato fruit growth response to temperature and plant fruit load in relation to cell division, cell expansion and DNA endoreduplication. Ann Bot 95:439–447

    Article  CAS  PubMed  Google Scholar 

  • Bertin N, Borel C, Brunel B, Cheniclet C, Causse M (2003) Do genetic make-up and growth manipulation affect tomato fruit size by cell number, or cell size and DNA endoreduplication? Ann Bot 92:415–424

    Article  CAS  PubMed  Google Scholar 

  • Bertin N, Lecomte A, Brunel B, Fishman S, Génard M (2007) A model describing cell polyploidization in tissues of growing fruit as related to cessation of cell proliferation. J Exp Bot 58:1903–1913

    Article  CAS  PubMed  Google Scholar 

  • Bino RJ, Lanteri S, Verhoeven HA, Kraak HL (1993) Flow-cytometric determination of nuclear replication stages in seed tissues. Ann Bot 72:181–187

    Article  Google Scholar 

  • Borisjuk L, Weber H, Panitz R, Manteuffed R, Wobus W (1995) Embryogenesis of Vicia faba L.: histodifferentiation in relation to starch and storage protein synthesis. J Plant Physiol 147:203–218

    CAS  Google Scholar 

  • DeRocher EJ, Harkins KR, Galbraith DW, Bohnet HJ (1990) Developmentally regulated systemic endopolyploidy in succulents with small genomes. Science 250:99–101

    Article  CAS  Google Scholar 

  • Fountain MD, Valdes O, Fettig S, Beck E (2003) Expression of cell cycle control factors in non-dividing and ageing photoautotrophic plant cells. Physiol Plant 119:30–39

    Article  CAS  Google Scholar 

  • Gahan PB, Hurst PR (1976) Effects of ageing on the cell cycle in Zea mays. Ann Bot 40:887–890

    Google Scholar 

  • Galbraith DW, Harkins KR, Knapp S (1991) Systemic endopolyploidy in Arabidopsis thaliana. Plant Physiol 96:985–989

    Article  CAS  PubMed  Google Scholar 

  • Gilissen LJW, van Staveren MJ, Creemers-Molenaar J, Verhoeven HA (1993) Development of polysomaty in seedlings and plants of Cucumis sativus L. Plant Sci 91:171–179

    Article  CAS  Google Scholar 

  • Grafi G (1998) Cell cycle regulation of DNA replication: the endoreduplication perspective. Exp Cell Res 244:372–378

    Article  CAS  PubMed  Google Scholar 

  • Jones H, Leigh RA, Tomos AD, Jones RGW (1987) The effect of abscisic acid on cell turgor pressures, solute content and growth of wheat roots. Planta 170:257–262

    Article  CAS  Google Scholar 

  • Kowles RV, Srienc F, Phillips RL (1990) Endoreduplication of nuclear DNA in the developing maize endosperm. Dev Gene 11:125–132

    Article  CAS  Google Scholar 

  • Kowles RV, Yerk GL, Haas KM, Phillips RL (1997) Maternal effects influencing DNA endoreduplication in developing endosperm of Zea mays. Genome 40:798–805

    Article  CAS  PubMed  Google Scholar 

  • Kudo N, Kimura Y (2001) Pattern of endopolyploidy during seedling development in cabbage (Brassica oleracea L.). Ann Bot 87:275–281

    Article  Google Scholar 

  • Kudo N, Kimura Y (2002) Flow-cytometric analysis for systemic endopolyploidy in development of radish (Raphanus sativus L.). Plant Biotechnol 19:45–52

    CAS  Google Scholar 

  • Kudo N, Ikeda K, Kimura Y, Mii M (2003) The occurrence of endopolyploid cells during seedling development of Allium fistulosum L. Plant Biotechnol 20:311–315

    CAS  Google Scholar 

  • Lagunes-Espinoza LDC, Huyghe C, Bousseau D, Barre P (2000) Endoreduplication occurs during pod wall development in template grain legumes. Ann Bot 86:185–190

    Article  Google Scholar 

  • Larkins BA, Dilkes BP, Dante RA, Coelho CM, Woo Y, Liu Y (2001) Investigating the hows and whys of DNA endoreduplication. J Exp Bot 52:183–192

    Article  CAS  PubMed  Google Scholar 

  • Lim WL, Loh CS (2003) Endopolyploidy in Vanda Miss Joaquim (Orchidaceae). New Phytol 159:279–287

    Article  CAS  Google Scholar 

  • Lur HS, Setter T (1993) Role of auxin in maize endosperm development. Plant Physiol 103:273–280

    CAS  PubMed  Google Scholar 

  • Mambelli S, Seter TL (1998) Inhibition of maize endosperm cell division and endoreplication by exogenously applied abscisic acid. Physiol Plant 104:266–272

    Article  CAS  Google Scholar 

  • Melaragno JE, Mehrotra B, Coleman AW (1993) Relationship between endopolyploidy and cell size in epidermal tissue of Arabidopsis. Plant Cell 5:1661–1668

    Article  PubMed  Google Scholar 

  • Milborrow BV (1974) The chemistry and physiology of abscisic acid. Ann Rev Plant Physiol 25:259–307

    Article  CAS  Google Scholar 

  • Mishiba K, Okamoto T, Mii M (2001) Increasing ploidy level in cell suspension cultures of Doritaenopsis by exogenous application of 2,4-dichlorophenoxyacetic acid. Physiol Plant 112:142–148

    Article  CAS  PubMed  Google Scholar 

  • Nagl W (1978) Endopolyploidy and polyteny in differentiation and evolution. Elsevier, Amsterdam

    Google Scholar 

  • Ogawa A, Yamauchi A (2006) Root osmotic adjustment under osmotic stress in maize seedlings. 1. Transient change of growth and water relations in roots in response to osmotic stress. Plant Prod Sci 9:27–38

    Article  Google Scholar 

  • Ogawa A, Kawashima C, Yamauchi A (2005) Sugar accumulation along the seminal root axis, as affected by osmotic stress in maize: a possible physiological basis for plastic lateral root development. Plant Prod Sci 8:173–180

    Article  Google Scholar 

  • Ogawa A, Ando F, Toyofuku K, Kawashima C (2009) Sucrose metabolism for the development of seminal root in maize seedlings. Plant Prod Sci 12:9–16

    Article  CAS  Google Scholar 

  • Rayburn AL, Auger JA, Benzinger EA, Hepburn AG (1989) Detection of intraspecific DNA content variation in Zea mays L. by flow cytometry. J Exp Bot 40:1179–1183

    Article  CAS  Google Scholar 

  • Smulders MJM, Rus-Kortekaas W, Gilissen LJW (1994) Development of polysomaty during differentiation in diploid and tetraploid tomato (Lycopersicon esculentum) plants. Plant Sci 97:53–60

    Article  Google Scholar 

  • Wilhelm E, Biradar DP, Bullock DG, Rayburn AL (1995) Endopolyploidization of mesocotyls in Nebraska maize populations selected for cold tolerance. Crop Sci 35:958–961

    Article  Google Scholar 

  • Yang M, Loh SC (2004) Systemic endopolyploidy in Spathoglottis plicata (Orchidaceae) development. BMC Cell Biol 5:33

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Atsushi Ogawa.

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Ogawa, A., Taguchi, N. & Miyoshi, K. Variations in endopolyploidy level during the short period of the early growing stage in the roots and leaves of maize (Zea mays) seedlings. Plant Biotechnol Rep 4, 117–123 (2010). https://doi.org/10.1007/s11816-010-0127-2

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  • DOI: https://doi.org/10.1007/s11816-010-0127-2

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