Skip to main content
Log in

Auxin distribution in Lotus japonicus during root nodule development

  • Published:
Plant Molecular Biology Aims and scope Submit manuscript

Abstract

For this work, Lotus japonicus transgenic plants were constructed expressing a fusion reporter gene consisting of the genes β-glucuronidase (gus) and green fluorescent protein (gfp) under control of the soybean auxin-responsive promoter GH3. These plants expressed GUS and GFP in the vascular bundle of shoots, roots and leafs. Root sections showed that in mature parts of the roots GUS is mainly expressed in phloem and vascular parenchyma of the vascular cylinder. By detecting GUS activity, we describe the auxin distribution pattern in the root of the determinate nodulating legume L. japonicus during the development of nodulation and also after inoculation with purified Nod factors, N-naphthylphthalamic acid (NPA) and indoleacetic acid (IAA). Differently than white clover, which forms indeterminate nodules, L. japonicus presented a strong GUS activity at the dividing outer cortical cells during the first nodule cell divisions. This suggests different auxin distribution pattern between the determinate and indeterminate nodulating legumes that may be responsible of the differences in nodule development between these groups. By measuring of the GFP fluorescence expressed 21 days after treatment with Nod factors or bacteria we were able to quantify the differences in GH3 expression levels in single living roots. In order to correlate these data with auxin transport capacity we measured the auxin transport levels by a previously described radioactive method. At 48 h after inoculation with Nod factors, auxin transport showed to be increased in the middle root segment. The results obtained indicate that L. japonicus transformed lines expressing the GFP and GUS reporters under the control of the GH3 promoter are suitable for the study of auxin distribution in this legume.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Boot, K.J.M., van Brussel, A.A.N., Tak, T., Spaink, H.P. and Kijne, J.W. 1999. Lipochitin oligosaccharides from Rhizobium leguminosarum bv. viciae reduce auxin transport capacity in Vicia sativa subsp. nigra roots. Mol. Plant-Microbe Interact. 12: 839–844.

    Google Scholar 

  • Brown, D.E., Rashotte, A.M., Murphy, A.S., Normanly, J., Tague, B.W., Peer,W.A., Taiz, L., and Guday, G.K. 2001. Flavonoids act as negative regulators of auxin transport in vivo in Arabidopsis. Plant Physiol. 126: 524–535.

    Google Scholar 

  • Casimiro, I., Marchant, A., Bhalerao, R.P., Beeckman, T., Dhooge, S., Swarup, R., Graham, N., Inzé, D., Sandberg, G., Casero, P.J. and Bennett, M. 2001. Auxin transport promotes Arabidopsis lateral root initiation. Plant Cell 13: 843–852.

    Google Scholar 

  • de Billy, F., Grosjean, C., May, S., Bennett, M. and Cullimore, J.V. 2001. Expression studies on AUX1-like genes in Medicago truncatula suggest that auxin is required at two steps in early nodule development. Mol. Plant-Microbe Interact. 14: 267–277.

    Google Scholar 

  • DeLong, A., Mockaitis, K. and Christensen, S. 2002. Protein phosphorylation in the delivery of and response to auxin signals. Plant Mol. Biol. 49: 285–303.

    Google Scholar 

  • Dénarié, J., Debellé, F. and Promé, J.-C. 1996. Rhizobium lipochitooligosaccharide nodulation factors: signaling molecules mediating recognition and morphogenesis. Annu. Rev. Biochem. 65: 503–535.

    Google Scholar 

  • Ditta, G., Stanfield, S., Corbin, D. and Helinski, D.R. 1980. Broad host range DNA cloning system for gram-negative bacteria: construction of a gene bank of Rhizobium meliloti. Proc. Natl. Acad. Sci. USA 77: 7347–7351.

    Google Scholar 

  • Geldner, N., Friml, J., Stierhof, Y. D., Jurgens, G. and Palme, K. 2001. Auxin transport inhibitors block PIN1 cycling and vesicle trafficking. Nature 413: 425–428.

    Google Scholar 

  • Hagen, G., Martin, G., Li, Y. and Guilfoyle, T. 1991. Auxin-induced expression on the soybean GH3 promoter in transgenic tobacco plants. Plant Mol. Biol. 17: 567–579.

    Google Scholar 

  • Hajdukiewicz, P., Svab, Z. and Maliga, P. 1994. The small, versatile pPZP family of Agrobacterium binary vectors for plant transformation. Plant Mol. Biol. 25: 989–994.

    Google Scholar 

  • Handberg, K. and Stougaard, J. 1992. Lotus japonicus, an autogamous, diploid legume species for classical and molecular genetics. Plant J. 2: 487–496.

    Google Scholar 

  • Hoekema, A., Hooykaas, P. and Schilperoort, R. 1984. Transfer of octopine T-DNA segment to plant cells mediated by different types of Agrobacterium tumors of root inducing plasmids: generality of virulence systems. J. Bact. 158: 383–385.

    Google Scholar 

  • Jacobs, M. and Rubery, P.H. 1988. Naturally occurring auxin transport regulators. Science 241: 346–349.

    Google Scholar 

  • Jiang, Q.Z. and Gresshoff, P.M. 1997. Classical and molecular genetics of the model legume Lotus japonicus. Mol. Plant-Microbe Interact. 10: 59–68.

    Google Scholar 

  • Jones, A.M. 1998. Auxin transport: down and out and up again. Science 282: 2201–2203.

    Google Scholar 

  • Kijne, J.W. 1992, The Rhizobium infection process. In:G. Stacey, R.H. Burris and H.J. Evans (Eds.) Biological Nitrogen Fixation, Chapman & Hall, New York, pp. 349–398.

    Google Scholar 

  • Larkin, P.J., Gibson, J.M., Mathesius, U., Weinman, J., Gartner, E., Hall, E., Tanner, G.J., Rolfe, B.G. and Djordjevic, M.A. 1996. Transgenic white clover. Studies with the auxin-responsive promoter, GH3, in root gravitropism and lateral root development. Transgen. Res. 5: 325–335.

    Google Scholar 

  • Laskowski, M.J., Williams, M.E., Nusbaum, H.C. and Sussex, M. 1995. Formation of lateral root meristems is a two-stage process. Development. 121: 3303–3310.

    Google Scholar 

  • Li, Y., Wu, Y.H., Hagen, G. and Guilfoyle, T. 1999. Expression of the auxin-inducible GH3 promoter/GUS fusion gene as a useful molecular marker for auxin physology. Plant Cell Physiol. 40: 675–682.

    Google Scholar 

  • Lomax, T.L., Muday, G.K. and Rubery, P. 1995. Auxin transport. In: P.J. Davies (Ed.) Plant Hormones: Physiology, Biochemistry and Molecular Biology, Kluwer Academic Publishers, Dordrecht, Netherlands, pp. 509–530.

    Google Scholar 

  • López-Lara, I.M., van den Berg, J.D.J., Thomas-Oates, J.E., Glushka, J., Lugtenberg, B.J.J. and Spaink, H.P. 1995. Structural identification of the lipo-chitin oligosaccharide nodulation signals of Rhizobium loti. Mol. Microbiol. 15: 627–638.

    Google Scholar 

  • Mathesius, U. 2001. Flavonoids induced in cells undergoing nodule organogenesis in white clover are regulators of auxin breakdown by peroxidase. J. Exp. Bot. 52 (Suppl): 419–426.

    Google Scholar 

  • Mathesius, U., Schlaman, H.R.M., Spaink, H.P., Sautter, C., Rolfe, B.G. and Djordjevic, M.A. 1998. Auxin transport inhibition precedes root nodule formation in white clover roots and is regulated by flavonoids and derivatives of chitin oligosaccharides. Plant J. 14: 23–34.

    Google Scholar 

  • Pacios-Bras, C., van der Burgt, Y.E.M., Deelder, A.M., Vinuesa, P., Werner, D. and Spaink, H.P. 2002. Novel lipochitin oligosaccharide structures produced by Rhizobium etli KIM5s. Carbohydrate Res. 337: 1193–1202.

    Google Scholar 

  • Pacios Bras, C., Alberich Jordá, M., Wijfjes, A.H.M., Harteveld, M., Stuurman, N., Thomas-Oates, J.E. and Spaink, H.P. 2000. A Lotus japonicus nodulation system based on heterologous expression of the fucosyl transferase NodZ and the acetyl transferase NolL in Rhizobium leguminosarum. Mol. Plant-Microbe Interact. 13: 475–479.

    Google Scholar 

  • Quaedvlieg, N.E.M., Schlaman, H.R.M., Admiraal, P.C., Wijting, S.E., Stougaard, J. and Spaink, H.P. 1998. Fusions between green fluorescent protein and β-glucuronidase as sensitive and vital bifunctional reporters in plants. Plant Mol. Biol. 37: 715–727.

    Google Scholar 

  • Rashotte, A., DeLong, A. and Muday, G.K. 2001. Genetic and chemical reductions in protein phosphatase activity alter auxin transport, gravity respponse and lateral root growth. Plant Cell 13: 1683–1697.

    Google Scholar 

  • Rinhardt, D., Mandel, T. and Kuhlemeier, C. 2000. Auxin regulates the initiation and radial position of plant lateral organs. Plant Cell 12: 507–518.

    Google Scholar 

  • Sabatini, S., Beis, D., Wolkenfelt, H., Murfett, J., Guilfoyle, T., Malamy, J., Benfey, P., Leyser, O., Bechtold, N., Weisbeek, P. and Scheres, B. 1999. An auxin-dependent distal organizer of pattern and polarity in the Arabidopsis root. Cell 99: 463–472.

    Google Scholar 

  • Sambrook, J., Fritsch, E.F. and Maniatis, T. 1989. Molecular Cloning: A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory Press, Plainview, NY.

    Google Scholar 

  • Schlaman, W.R.M., Phillips, D.A. and Kondorosi, E. 1998, Genetic organization and transcriptional regulation of rhizobial nodulation genes. In: H.P. Spaink, A. Kondorosi and P.J.J. Hooykaas (Eds.) The Rhizobiaceae, Kluwer Academic Publishers, Dordrecht/Boston/London, pp. 361–386.

    Google Scholar 

  • Spaink, H.P. 2000. Root nodulation and infection factors produced by rhizobial bacteria. Annu. Rev. Microbiol. 54: 257–288.

    Google Scholar 

  • Sullivan, J.T., Patrick, H.N., Lowther, W.L., Scott, D.B. and Ronson, C.W. 1995. Nodulating strains of Rhizobium loti arise through chromosomal symbiotic gene transfer in the environment. Proc. Natl. Acad. Sci. USA 92: 8985–8989.

    Google Scholar 

  • Swarup, R., Friml, J., Marchant, A., Ljung, K., Sandberg, G., Palme, K. and Bennett, M. 2001. Localization of the auxin permease AUX1 suggests two functionally distinct hormone transport pathways operate in the Arabidopsis root apex. Genes Dev. 15: 2648–2653.

    Google Scholar 

  • Szczyglowski, K., Shaw, R.S., Wopereis, J., Copeland, S., Hamburger, D., Kasiborski, B., Dazzo, F.B. and Bruijn, F.J. 1998. Nodule organogenesis and symbiotic mutants of the model legume Lotus japonicus. Mol. Plant-Microbe Interact. 11: 684–697.

    Google Scholar 

  • van Brussel, A.A.N., Zaat, S.A.J., Canter Cremers, H.C.J., Wijffelman, C.A., Pees, E., Tak, T. and Lugtenberg, B.J.J. 1986. Role of plant root exudate and sym plasmid-localized nodulation genes in the synthesis by Rhizobium leguminosarum of Tsr factor which causes thick and short roots on common vetch. J. Bact. 165: 517–522.

    Google Scholar 

  • Wang, H., Qi M. and Cutle, A.J. 1993. A simple method of preparing plant samples for PCR. Nucl. Acids Res. 21: 4153–4154.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Herman P. Spaink.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pacios-Bras, C., Schlaman, H.R., Boot, K. et al. Auxin distribution in Lotus japonicus during root nodule development. Plant Mol Biol 52, 1169–1180 (2003). https://doi.org/10.1023/B:PLAN.0000004308.78057.f5

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/B:PLAN.0000004308.78057.f5

Navigation