DOI QR코드

DOI QR Code

Overexpression of the Downward Leaf Curling (DLC) Gene from Melon Changes Leaf Morphology by Controlling Cell Size and Shape in Arabidopsis Leaves

  • Kee, Jae-Jun (Department of Biology, University of Incheon) ;
  • Jun, Sang Eun (Department of Molecular Biotechnology, Dong-A University) ;
  • Baek, Seung-A (Department of Biology, University of Incheon) ;
  • Lee, Tae-Soo (Department of Biology, University of Incheon) ;
  • Cho, Myung Rae (National Institute of Agricultural Biotechnology, Rural Development Administration) ;
  • Hwang, Hyun-Sik (Department of Genetic Engineering, Sungkyunkwan University) ;
  • Lee, Suk-Chan (Department of Genetic Engineering, Sungkyunkwan University) ;
  • Kim, Jongkee (Department of Applied Plant Science, Chung-Ang University) ;
  • Kim, Gyung-Tae (Department of Molecular Biotechnology, Dong-A University) ;
  • Im, Kyung-Hoan (Department of Biology, University of Incheon)
  • Received : 2009.04.30
  • Accepted : 2009.06.15
  • Published : 2009.08.31

Abstract

A plant-specific gene was cloned from melon fruit. This gene was named downward leaf curling (CmDLC) based on the phenotype of transgenic Arabidopsis plants overexpressing the gene. This expression level of this gene was especially upregulated during melon fruit enlargement. Overexpression of CmDLC in Arabidopsis resulted in dwarfism and narrow, epinastically curled leaves. These phenotypes were found to be caused by a reduction in cell number and cell size on the adaxial and abaxial sides of the epidermis, with a greater reduction on the abaxial side of the leaves. These phenotypic characteristics, combined with the more wavy morphology of epidermal cells in overexpression lines, indicate that CmDLC overexpression affects cell elongation and cell morphology. To investigate intracellular protein localization, a CmDLC-GFP fusion protein was made and expressed in onion epidermal cells. This protein was observed to be preferentially localized close to the cell membrane. Thus, we report here a new plant-specific gene that is localized to the cell membrane and that controls leaf cell number, size and morphology.

Keywords

Acknowledgement

Supported by : University of Incheon

References

  1. Barry, C.S., Fox, E.A., Yen, H.C., Lee, S., Ying, T.J., Grierson, D., and Giovannoni, J.J (2001). Analysis of the ethylene response in the epinastic [epi] mutant of tomato. Plant Physiol. 127, 58-66 https://doi.org/10.1104/pp.127.1.58
  2. Braun, N., Wyrzykowska, J., Muller, P., David, K., Couch, D., Perrot-Rechenmann, C., and Fleming, A.J. (2008). Conditional repression of AUXIN BINDING PROTEIN1 reveals that it coordinates cell division and cell expansion during postembryonic shoot development in Arabidopsis and tobacco. Plant Cell 20, 2746-2762 https://doi.org/10.1105/tpc.108.059048
  3. Cho, K.H., Jun, S.E., Lee, Y.K., Jeong, S.J., and Kim, K.T. (2007). Developmental process of leaf morphogenesis of Arabidopsis. J. Plant Biol. 50, 282-290 https://doi.org/10.1007/BF03030656
  4. Choi, J.W., Kim, G.B., Huh, Y., Kwon, M.R., Mok, I.G., Kim, J.W., Lee, T.S., Kim, S., and Im, K.H. (2004). Cloning of genes differentially expressed during the initial stage of fruit development in melon (Cucumis cv. Reticulatus). Mol. Cells 17, 237-241
  5. Clough, S.J., and Bent, A.F. (1998). Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 16, 735-743 https://doi.org/10.1046/j.1365-313x.1998.00343.x
  6. Cox, M., Benschop, J.J., Vreeburg, R.A., Wagemaker, C.A., Moritz, T., Peeters, A.J., and Voesenek, L.A. (2004). The roles of ethylene, auxin, abscisic acid, and gibberellin in the hyponastic growth of submerged Rumex palustris petioles. Plant Physiol. 136, 2948-2960 https://doi.org/10.1104/pp.104.049197
  7. Dale, J.E. (1988). The control of leaf expansion. Ann. Rev. Plant Physiol. Plant Mol. Biol. 39, 267-295 https://doi.org/10.1146/annurev.pp.39.060188.001411
  8. Horiguchi, G., Kim, G.-T., and Tsukaya, H. (2005). The transcription factor AtGRF5 and the transcription coactivator AN3 regulate cell proliferation in leaf primordia of Arabidopsis thaliana. Plant J. 43, 68-78 https://doi.org/10.1111/j.1365-313X.2005.02429.x
  9. Iwakawa, H., Iwasaki, M., Kojima, S., Ueno, Y., Soma, T., and Tanaka, H. (2007). Expression of the ASYMMETRIC LEAVES2 gene in the adaxial domain of Arabidopsis leaves represses cell proliferation in this domain and is critical for the development of properly expanded leaves. Plant J. 51, 173-184 https://doi.org/10.1111/j.1365-313X.2007.03132.x
  10. Kang, B.G. (1979). Epinasty. In Encyclopedia of Plant Physiology, New Series, Vol. 7., Physiology of Movements, W. Haupt, and M.E. Feinleib, eds. (Berlin, Germany: Springer-Verlag), pp. 647-667
  11. Keller, C.P., and Van Volkenburgh, E. (1997). Auxin-induced epinasty of tobacco leaf tissues. a nonethylene-mediated response. Plant Physiol. 113, 603-610 https://doi.org/10.1104/pp.113.2.603
  12. Kim, G.T., Tsukaya, H., and Uchimiya, H. (1998a). The RO-TUNDIFOLIA3 gone of Arabidopsis thaliana encodes a new member of the cytochrome P-450 family that is required for the regulated polar elongation of leaf cells. Genes Dev. 1, 2381-2391
  13. Kim, G.T., Tsukaya, H., and Uchimiya, H. (1998b). The CURLY LEAF gene controls both division and elongation of cells during the expansion of the leaf blade in Arabidopsis thaliana. Planta 206, 175-183 https://doi.org/10.1007/s004250050389
  14. Kim, G.T., Shoda, K., Tsuge, T., Cho, K.H., Uchimiya, H., Yokoyama, R., Nishitani, K., and Tsukaya, H. (2002). The ANGUSTIFOLIA gene of Arabidopsis, a plant CtBP gene, regulates leaf-cell expansion, the arrangement of cortical microtubules in leaf cells and expression of a gene involved in cell-wall formation. EMBO J. 21, 1267-1279 https://doi.org/10.1093/emboj/21.6.1267
  15. Lee, Y., Kim, G.T., Kim, I.J., Park, J., Kwak, S.S., Choi, G., and Chung, W.I. (2006). LONGIFOLIA1 and LONGIFOLIA2, two homologous genes, regulate longitudinal cell elongation in Arabidopsis. Development 133, 4305-4314 https://doi.org/10.1242/dev.02604
  16. Li, L.-C., Qin, G-J., Tsuge, T., Hou, X.-H., Ding, M.-Y., Aoyama, T., Oka, A., Chen, Z., Gu, H., Zhao, Y., et al. (2008). SPOROCYTELESS modulates YUCCA expression to regulate the development of lateral organs in Arabidopsis. New Phytol. 179, 751-764 https://doi.org/10.1111/j.1469-8137.2008.02514.x
  17. Murashige, T., and Skoog, F. (1962). A revised medium for rapid growth and bio-assays with tobacco tissue cultures. Physiol. Plant. 15, 473-497 https://doi.org/10.1111/j.1399-3054.1962.tb08052.x
  18. Nakai, K., and Horton, P. (1999). PSORT: a program for detecting sorting signals in proteins and predicting their subcellular localization. Trends Biochem. Sci. 24, 34-35 https://doi.org/10.1016/S0968-0004(98)01336-X
  19. Qin, G., Gu, H., Zhao, Y., Ma, Z., Shi, G., Yang, Y., Pichersky, E., Chen, H., Liu, M., Chen, Z., et al. (2005). An indole-3-acetic acid carboxyl methyltransferase regulates Arabidopsis leaf development. Plant Cell 17, 2693-2704 https://doi.org/10.1105/tpc.105.034959
  20. Schlagnhaufer, C.D., and Arteca, R.N. (1985). Brassinosteroidinduced epinasty in tomato plants. Plant Physiol. 78, 300-303 https://doi.org/10.1104/pp.78.2.300
  21. Schultz, J., Ponting, C.P., Hofmann, K., and Bork, P. (1997). SAM as a protein interaction domain involved in developmental regulation. Protein Sci. 6, 249-253 https://doi.org/10.1002/pro.5560060128
  22. Scott, A., Wyatt, S., Tsou, P.L., Robertson, D., and Stromgren, A.N. (1999). Model system for plant cell biology: GFP imaging in living onion epidermal cells. Biotechniques 26, 1125-1132
  23. Tsuge, T., Tsukaya, H., and Uchimiya, H. (1996). Two independent and polarized processes of cell elongation regulate leaf blade expansion in Arabidopsis thaliana (L.) Heynh. Development 122, 1589-1600
  24. Tsukaya, H. (1995). Developmental genetics of leaf morphogenesis in dicotyledonous plants. J. Plant Res. 111, 113-119 https://doi.org/10.1007/BF02507157
  25. Voesenek, L., Benschop, J.J., Bou, J., Cox, M., Groeeveld, H.W., Millenaar, F.F., Vreeburg, R.A., and Peeters, A.J. (2003). Interaction between plant hormones regulates submergenceinduced shoot elongation in the flooding-tolerant dicot Rumex palustris. Ann. Bot. 91, 205-211 https://doi.org/10.1093/aob/mcf116

Cited by

  1. Loss of a highly conserved sterile alpha motif domain gene (WEEP) results in pendulous branch growth in peach trees vol.115, pp.20, 2018, https://doi.org/10.1073/pnas.1704515115