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Effect of jasmonic acid on developmental morphology during in vitro tuberization of Dioscorea alata (L.)

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Abstract

A developmental morphology study was performed during different stages of in vitro yam microtuber formation on both hormone-free medium (HF) and medium supplemented with 10 µM of jasmonic acid (JA). The axillary protuberance, considered as the first morphological evidence for microtuber formation, became visible after one-week of culture in JA-medium and after three weeks of culture in HF-medium. In addition, the formation of the axillary protuberance in JA-cultures preceded the stem elongation, whereas in HF-medium stem elongation was visible before the formation of the axillary protuberance. Tuberization improvement in medium supplemented with JA is likely to be the result of morphogenetic modifications occurring during the early stages of microtuber formation. At the molecular level, 2D-PAGE analysis of HF- and JA-cultures allowed the identification of four differentially expressed polypeptides, including two putative pathogenesis-related proteins and one putative glutathione S-transferase. For JA-cultures, three additional differentially expressed polypeptides were identified.

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References

  • Bazabakana R., Fauconnier M.L., Diallo B., Dupont J.P., Homès J. and Jaziri M. 1999. Control of Dioscorea alatamicrotuber dormancy and germination by jasmonic acid. Plant Growth Regul. 27: 113-117.

    Article  Google Scholar 

  • Bex F., Murphy K., Wattiez R., Burny A. and Gaynor R.B. 1999. Phosphorylation of the Human T-cell leukemia virus type 1 transactivator Tax on adjacent serine residues is critical for Tax activation. J. Virol. 73: 738-745.

    PubMed  Google Scholar 

  • Boyer C., Hilbert J.L. and Vasseur J. 1993. Embryogenesis-related protein synthesis and accumulation during early acquisition of somatic enbryogenesis competence in Chicorium. Plant Sci. 93: 41-53.

    Article  Google Scholar 

  • Espiand H. 1983. Conséquences de la culture in vitrosur la morphogenèse de boutures nodales de l’igname (Dioscorea alataL. cv. ≪Tahiti≫). Thèse de doctorat, Université de Paris XI, France.

    Google Scholar 

  • Hendriks T., Vreugdenhil D. and Stiekema W.J. 1991. Patatin and four serine proteinase inhibitor genes are differentially expressed during potato tuber development. Plant Mol. Biol. 17: 385-394.

    PubMed  Google Scholar 

  • Heukeshoven J. and Dernick R. 1988. Improved silver staining procedure for fast staining in phastsytem development unit. I. Staining of sodium dodecyl sulfate gels. Electrophoresis 9: 28-32.

    PubMed  Google Scholar 

  • Jackson S.D. 1999. Multiple signaling pathways control tuber induction in potato. Plant Physiol. 119: 1-8.

    Article  PubMed  Google Scholar 

  • Laemmli U.K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680-685.

    PubMed  Google Scholar 

  • Matsuki T., Tazaki H., Fujimori T. and Hogetsu T. 1992. The influences of jasmonic acid methyl ester on microtubules in potato cells and formation of potato tubers. Biosci. Biotechnol. Biochem. 56: 1329-1333.

    Google Scholar 

  • Matton D.P. and Brisson N. 1989. Cloning, expression, and sequence conservation of pathogenesis-related transcripts of potato. Mol. Plant Microbe Interact. 2: 325-331.

    PubMed  Google Scholar 

  • Mitsumori C., Yamagishi K., Fujino K. and Kikuta Y. 1994. Detection of immunologically related Kunitz and Bowman-Birk proteinase inhibitors expressed during potato tuber development. Plant Mol. Biol. 26: 961-969.

    PubMed  Google Scholar 

  • Murashige T. and Skoog F. 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15: 473-497.

    Google Scholar 

  • Prat S., Frommer W.B., Hofgen R., Keil M., Kossmann J., Koster-Topfer M. et al. 1990. Gene expression during tuber development in potato plants. FEBS Letter 268: 334-338.

    Article  Google Scholar 

  • Takahashi Y. and Nagata T. 1992. parB: an auxin-regulated gene encoding glutathione S-transferase. Proc. Natl. Acad. Sci. 89: 56-59.

    PubMed  Google Scholar 

  • Takahashi Y., Sakai T., Ishida S. and Nagata T. 1995. Identification of auxin-responsive elements of parBand their expression in apices of shoot and root. Proc Natl. Acad. Sci. 92: 6359-6363.

    PubMed  Google Scholar 

  • Viola R., Robert A., Haupt S., Gazzani S., Hancock R., Marmiroli N. et al. 2001. Tuberization in potato involves a switch from apoplastic to symplastic phloem unloading. Plant Cell 13: 385-398.

    Article  PubMed  Google Scholar 

  • Warner S.A., Scott R. and Draper J. 1992. Characterisation of a wound-induced transcript from the monocot Asparagusthat shares similarity with a class of intracellular pathogenesis-related (PR) proteins. Plant Mol. Biol. 19: 555-561.

    PubMed  Google Scholar 

  • Watanabe N., Kamei S., Ohkubo A., Yamanaka M., Ohsawa S., Makino K. et al. 1986. Urinary protein as measured with a pyrogallol red-molybdate complex, manually in a hitachi 726 automated analyzer. Clin. Chem. 32: 1551-1554.

    PubMed  Google Scholar 

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Bazabakana, R., Wattiez, R., Baucher, M. et al. Effect of jasmonic acid on developmental morphology during in vitro tuberization of Dioscorea alata (L.). Plant Growth Regulation 40, 229–237 (2003). https://doi.org/10.1023/A:1025087111148

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  • DOI: https://doi.org/10.1023/A:1025087111148

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