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Differential accumulation of Aux/IAA mRNA during seedling development and gravity response in cucumber (Cucumis sativus L.)

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Abstract

The plant hormone auxin transcriptionally activates Aux/IAA genes. We have isolated three Aux/IAA cDNA from cucumber, two cDNAs (CS-IAA1 and CS-IAA2) containing the complete open reading frame (ORF), and one partial cDNA (CS-IAA3). Northern blotting analysis showed that Aux/IAA mRNAs were induced during the emergence of radicles from seed coats. After radicle emergence, their mRNAs accumulated in the basal part of the hypocotyl much more than in the apical part, and later in elongating region of hypocotyls. CS-IAA1 and CS-IAA3 mRNA significantly accumulated in response to auxin, although the increment of the former mRNA accumulation by auxin application was much greater than that of the latter. CS-IAA2 did not show an apparent change by auxin treatment in our experiment. In horizontally germinating seedlings, the transition zone between hypocotyl and root curves was due to downward gravitropic growth. On the other hand, vertically germinating seedlings of cucumber do not curve in the early stage of seedling development. The CS-IAA1 mRNA accumulation in horizontally germinating seedlings was more than that in vertically germinating ones during radicle emergence. Furthermore, asymmetric distribution of CS-IAA1 mRNA was detected in the transition zone in in situ hybridization analysis. These results suggest that the CS-IAA1 gene product may be involved in the gravity response during early development of seedlings.

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References

  • Abel, S. and Theologis, A. 1995. A polymorphic bipartite motif signals nuclear targeting of early auxin-inducible proteins related to PS-IAA4 from pea (Pisum sativum). Plant J. 8: 87–96.

    Google Scholar 

  • Abel, S. and Theologis, A. 1996. Early gene and auxin action. Plant Physiol. 111: 9–17.

    Google Scholar 

  • Abel, S., Oeller, P.W. and Theologis, A. 1994. Early auxin-induced genes encode short-lived nuclear proteins. Proc. Natl. Acad. Sci. USA 91: 326–330.

    Google Scholar 

  • Abel, S., Nguyen, M.D. and Theologis, A. 1995. The PS-IAA4/5-like family of early auxin-inducible mRNAs in Arabidopsis thaliana. J. Mol. Biol. 251: 533–549.

    Google Scholar 

  • Ainley, W.M., Walker, J.C., Nagao, R.T. and Key, J.L. 1988. Sequence and characterization of two auxin-regulated genes from soybean. J. Biol. Chem. 263: 10658–10666.

    Google Scholar 

  • Barlow, P.W. and Rathfelder, E.L. 1985. Distribution and redistribution of extension growth along vertical and horizontal gravireacting maize roots. Planta 165: 134–141.

    Google Scholar 

  • Chomczynski, P. and Mackey, K. 1995. Modification of the TRI reagentTM procedure for isolation of RNA from polysaccharideand proteoglycan-rich sources. BioTechiques 19: 942–945.

    Google Scholar 

  • Cosgrove, D.J. 1990. Rapid, bilateral changes in growth rate and curvature during gravitropism of cucumber hypocotyls: implications for mechanism of growth control. Plant Cell Environ. 13: 227–234.

    Google Scholar 

  • Demura, T. and Fukuda, H. 1996. In situ hybridization to cellular RNA using 35S-labeled cRNA probes. Plant Tissue Cult. Lett. 13: 343–349.

    Google Scholar 

  • Gee, M.A., Hagen, G., and Guilfoyle, T.J. 1991. Tissue-specific and organ-specific expression of soybean auxin-responsive transcripts GH3 and SAURs. Plant Cell 3: 419–430.

    Google Scholar 

  • Guilfoyle, T., Hagen, G., Ulmasov, T. and Murfett, J. 1998. How does auxin turn on genes? Plant Physiol. 118: 341–347.

    Google Scholar 

  • Kim, J., Harter, K. and Theologis, A. 1997. Protein-protein interactions among the Aux/IAA proteins. Proc. Natl. Acad. Sci. USA 94: 11786–11791.

    Google Scholar 

  • Kobayashi, S., Saito, H. and Okada, M. 1994. A simplified and efficient method for in situ hybridization to whole Drosophila embryos, using electrophoresis for removing non-hybridized probes. Dev. Growth Differ. 36: 629–632.

    Google Scholar 

  • Luschnig, C., Gaxiola, R.A., Grisafi, P. and Fink, G.R. 1998. EIR1, a root-specific protein involved in auxin transport, is required for gravitropism in Arabidopsis thaliana. Genes Dev. 12: 2175–2187.

    Google Scholar 

  • MacDonald, I.R., Gordon, D.C., Hart, J.W. and Maher, E.P. 1983. The positive hook: the role of gravity in the formation and opening of the apical hook. Planta 158: 76–81.

    Google Scholar 

  • Mito, N. and Bennett, A.B. 1995. The diageotropica mutation and synthetic auxins differentially affect the expression of auxinregulated genes in tomato. Plant Physiol. 109: 293–297.

    Google Scholar 

  • Murray, M.G. and Thompson, W.F. 1980. Rapid isolation of high molecular weight plant DNA. Nucl. Acids Res. 8: 4321–4325.

    Google Scholar 

  • Rouse, D., Mackay, P., Stirnberg, P., Estelle, M. and Leyser, O. 1998. Changes in auxin response from mutations in an AUX/IAA gene. Science 279: 1371–1373.

    Google Scholar 

  • Sandberg, G., Ernstsen, A. and Hamnede, M. 1987. Dynamics of indole-3-acetic acid and indole-3-ethanol during development and germination of Pinus sylvestris seeds. Physiol. Plant. 71: 411–418.

    Google Scholar 

  • Takahashi, H. and Scott, T.K. 1994. Gravity-regulated formation of the peg in developing cucumber seedlings. Planta 193: 580-584.

    Google Scholar 

  • Takahashi, H. and Suge, H. 1988. Involvement of ethylene in gravity-regulated peg development in cucumber seedling. Plant Cell Physiol. 29: 313–320.

    Google Scholar 

  • Theologis, A., Huynh, T.V. and Davis, R.W. 1985. Rapid induction of specific mRNAs by auxin in pea epicotyl tissue. J. Mol. Biol. 183: 53–68.

    Google Scholar 

  • Tillberg, E. 1977. Indoleacetic acid levels in Phaseolus, Zea, and Pincus during seed germination. Plant Physiol. 60: 317–319.

    Google Scholar 

  • Walker, J.C. and Key, J.L. 1982. Isolation of cloned cDNAs to auxin-responsive poly(A)C RNAs of elongating soybean hypocotyl. Proc. Natl. Acad. Sci. USA 79: 7185–7189.

    Google Scholar 

  • Witztum, A. and Gersani, M. 1975. The role of polar movement of IAA in the development of the peg in Cucumis sativus L. Bot. Gaz. 136: 5–16.

    Google Scholar 

  • Wong, L.M., Abel, S., Shen, N., de la Foata, M., Mall, Y. and Theologis, A. 1996. Differential activation of the primary auxin response genes, PS-IAA4/5 and PS-IAA6, during early plant development. Plant J. 9: 587–599.

    Google Scholar 

  • Wyatt, R.E., Ainley, W.M., Nagao, R.T., Conner, T.W. and Key, J.L. 1993. Expression of the Arabidopsis AtAux2-11 auxinresponsive gene in transgenic plants. Plant Mol. Biol. 22: 731–749.

    Google Scholar 

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Fujii, N., Kamada, M., Yamasaki, S. et al. Differential accumulation of Aux/IAA mRNA during seedling development and gravity response in cucumber (Cucumis sativus L.). Plant Mol Biol 42, 731–740 (2000). https://doi.org/10.1023/A:1006379804678

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