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Acta Physiologiae Plantarum

, Volume 36, Issue 6, pp 1585–1592 | Cite as

Dynamic analysis of Arabidopsis seed shape reveals differences in cellulose mutants

  • José Javier Martín
  • Ángel Tocino
  • Ramón Ardanuy
  • Juana G. de Diego
  • Emilio CervantesEmail author
Original Paper

Abstract

In a previous work, the shape of Arabidopsis seed was described as a cardioid modified by a factor of Phi. In addition, J index was defined as the similarity of the seed (in an orthogonal, bi-dimensional image) to a cardioid, thus allowing the quantitative comparison of seed shape in seeds of varieties and mutants at different stages of development. Here, J index is used for modeling changes in seed morphology during the dynamic process of seed imbibition before germination. The analysis was carried out by means of a general linear model with two fixed factors (genotype and time) applied to two Arabidopsis varieties: Columbia and Wassilewskija and two mutants in cellulose synthesis: prc1-1 (CESA6 in Columbia) and kor1-1 (in Wassilewskija). Equations representing the changes in seed form during imbibition are given. The analysis of changes in seed shape by this procedure provides (1) a quantitative method to record changes in seed shape and to compare between genotypes or treatments showing the time points with maximum differences, and (2) the observation of remarkable differences between wild-type seeds and mutants in cellulose biosynthesis, indicating new phenotypic characteristics previously unknown in the latter. While wild-type seeds increase their J index values during imbibition, in the cellulose mutants J index values decrease. In addition, shape comparisons were done with other mutants. Seeds of ga1-1 mutants behave like cellulose mutants, whereas different ethylene mutants present varied responses. Quantitative analysis of seed morphology is a new basis for the record of differences between wild-type and mutants as well as for phenotypic characterization.

Keywords

Arabidopsis Cardioid Cellulose mutants Imbibition Seed Shape 

Notes

Acknowledgments

We thank Samantha Vernhettes for kindly providing us with seeds of wild type Arabidopsis varieties and mutants.

Conflict of interest

The authors declare that they have no conflict of interest.

Supplementary material

Supplementary material 1 (MPG 8737 kb)

Supplementary material 2 (MPG 10464 kb)

References

  1. Cervantes E, Martín JJ, Ardanuy R, de Diego JG, Tocino A (2010) Modeling the Arabidopsis seed shape by a cardioid: efficacy of the adjustment with a scale change with factor equal to the Golden Ratio and analysis of seed shape in ethylene mutants. J Plant Physiol 167:408–410PubMedCrossRefGoogle Scholar
  2. Cervantes E, Martín JJ, de Diego JG, Chan PK, Gresshoff P, Tocino A (2012) Seed shape in model legumes: approximation by a cardioid reveals differences between Lotus and Medicago. J Plant Physiol 169(14):1359–1365PubMedCrossRefGoogle Scholar
  3. Chang C, Kwok SF, Bleecker AB, Meyerowitz EM (1993) Arabidopsis ethylene-response gene ETR1: similarity of product to two component regulators. Science 262:539–541PubMedCrossRefGoogle Scholar
  4. Christensen R (2011) Plane answers to complex questions: the theory of linear models, 4th edn. Springer-Verlag, NYGoogle Scholar
  5. Desprez T, Vernhettes S, Fagard M, Refrégier G, Desnos T, Aletti E, Py N, Pelletier S, Höfte H (2002) Resistance against herbicide isoxaben and cellulose deficiency caused by distinct mutations in same cellulose synthase isoform CESA6. Plant Physiol 128(2):482–490PubMedCentralPubMedCrossRefGoogle Scholar
  6. Desprez T, Juraniec M, Crowell EF, Jouy H, Pochylova Z, Parcy F, Höfte H, Gonneau M, Vernhettes S (2007) Organization of cellulose synthase complexes involved in primary cell wall synthesis in Arabidopsis thaliana. PNAS 104(39):15572–15577PubMedCentralPubMedCrossRefGoogle Scholar
  7. Fagard M, Desnos T, Desprez T, Goubet F, Refrégier G, Mouille G, McCann M, Rayon C, Vernhettes S, Höfte H (2000) Procuste-1 encodes a cellulose synthase required for the normal cell elongation specifically in roots and dark-grown hypocotyls of Arabidopsis. Plant Cell 12:2409–2423PubMedCentralPubMedCrossRefGoogle Scholar
  8. Hermans C, Porco S, Vandenbussche F, Gille S, De Pessemier J, Van Der Straeten D, Verbruggen N, Bush DR (2011) Dissecting the role of CHITINASE-LIKE1 in nitrate-dependent changes in root architecture. Plant Physiol 157:1313–1326. doi: 10.1104/pp.111.181461 PubMedCentralPubMedCrossRefGoogle Scholar
  9. Kieber JJ, Rothenberg M, Roman G, Feldmann KA, Ecker JR (1993) CTR1, a negative regulator of the ethylene response pathway in Arabidopsis, encodes a member of the raf family of protein kinases. Cell 72(3):427–441PubMedCrossRefGoogle Scholar
  10. Ko J-H, Kim JH, Jayanty SS, Howe GA, Han K-H (2006) Loss of function of COBRA, a determinant of oriented cell expansion, invokes cellular defence responses in Arabidopsis thaliana. J Exp Bot 57(12):2923–2936PubMedCrossRefGoogle Scholar
  11. Koornneef M, van Eden J, Hanhart CJ, de Jongh AMM (1983) Genetic fine-structure of the GA-7 locus in the higher plant Arabidopsis thaliana (L.). Heynh Genet Res Camb 41:57–68CrossRefGoogle Scholar
  12. McCullagh Peter, Nelder John (1989) Generalized linear models, 2nd edn. Chapman and Hall/CRC, Boca RatonCrossRefGoogle Scholar
  13. Nicol F, His I, Jauneau A, Vernhettes S, Canut H, Hofte H (1998) A plasma membrane–bound putative endo-1,4-β-d-glucanase is required for normal wall assembly and cell elongation in Arabidopsis. EMBO J 17:5563–5576PubMedCentralPubMedCrossRefGoogle Scholar
  14. Robert C, Noriega A, Tocino A, Cervantes E (2008) Morphological analysis of seed shape in Arabidopsis thaliana reveals altered polarity in mutants of the ethylene signalling pathway. J Plant Physiol 2008(165):911–919CrossRefGoogle Scholar
  15. Schwartz H (1980) Two-dimensional feature-shape indices. Mikroskopie (Wien) 37(Suppl.):64–67Google Scholar
  16. Zuo J, Niu Q-W, Nishizawa N, Wu Y, Kost B, Chua N-H (2000) KORRIGAN, an Arabidopsis endo-1,4-β-glucanase, localizes to the cell plate by polarized targeting and is essential for cytokinesis. Plant Cell 12:1137–1152PubMedCentralPubMedGoogle Scholar

Copyright information

© Franciszek Górski Institute of Plant Physiology, Polish Academy of Sciences, Kraków 2014

Authors and Affiliations

  • José Javier Martín
    • 1
  • Ángel Tocino
    • 2
  • Ramón Ardanuy
    • 3
  • Juana G. de Diego
    • 4
  • Emilio Cervantes
    • 1
    Email author
  1. 1.IRNASA-CSICSalamancaSpain
  2. 2.Department of MathematicsUniversity of SalamancaSalamancaSpain
  3. 3.Department of StatisticsUniversity of SalamancaSalamancaSpain
  4. 4.Department of Biochemistry and Molecular BiologyUniversity of SalamancaSalamancaSpain

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