Functional interactions between a glutamine synthetase promoter and MYB proteins

Authors

  • Josefa Gómez-Maldonado,

    1. Biología Molecular y Bioquímica, Instituto Andaluz de Biotencología, Unidad Asociada UMA-CSIC, Universidad de Málaga, Campus Universitairo de Teatinos, E-29071 Málaga, Spain
    Search for more papers by this author
  • Concepción Avila,

    1. Biología Molecular y Bioquímica, Instituto Andaluz de Biotencología, Unidad Asociada UMA-CSIC, Universidad de Málaga, Campus Universitairo de Teatinos, E-29071 Málaga, Spain
    Search for more papers by this author
  • Fernando de la Torre,

    1. Biología Molecular y Bioquímica, Instituto Andaluz de Biotencología, Unidad Asociada UMA-CSIC, Universidad de Málaga, Campus Universitairo de Teatinos, E-29071 Málaga, Spain
    Search for more papers by this author
  • Rafael Cañas,

    1. Biología Molecular y Bioquímica, Instituto Andaluz de Biotencología, Unidad Asociada UMA-CSIC, Universidad de Málaga, Campus Universitairo de Teatinos, E-29071 Málaga, Spain
    Search for more papers by this author
  • Francisco M. Cánovas,

    1. Biología Molecular y Bioquímica, Instituto Andaluz de Biotencología, Unidad Asociada UMA-CSIC, Universidad de Málaga, Campus Universitairo de Teatinos, E-29071 Málaga, Spain
    Search for more papers by this author
  • Malcolm M. Campbell

    Corresponding author
    1. Department of Plant Sciences, University of Oxford, South Parks Road, Oxford OX1 3RB, UK
    Search for more papers by this author

(fax +44 1865 274074; e-mail malcolm.campbell@plants.ox.ac.uk).

Summary

In Scots pine (Pinus sylvestris), ammonium assimilation is catalysed by glutamine synthetase (GS) [EC 6.3.1.2], which is encoded by two genes, PsGS1a and PsGS1b. PsGS1b is expressed in the vascular tissue throughout the plant body, where it is believed to play a role in recycling ammonium released by various facets of metabolism. The mechanisms that may underpin the transcriptional regulation of PsGS1b were explored. The PsGS1b promoter contains a region that is enriched in previously characterized cis-acting elements, known as AC elements. Pine nuclear proteins bound these AC element-rich regions in a tissue-specific manner. As previous experiments had shown that R2R3-MYB transcription factors could interact with AC elements, the capacity of the AC elements in the PsGS1b promoter to interact with MYB proteins was examined. Two MYB proteins from loblolly pine (Pinus taeda), PtMYB1 and PtMYB4, bound to the PsGS1b promoter were able to activate transcription from this promoter in yeast, arabidopsis and pine cells. Immunolocalization experiments revealed that the two MYB proteins were most abundant in cells previously shown to accumulate PsGS1b transcripts. Immunoprecipitation analysis and supershift electrophoretic mobility shift assays implicated these same two proteins in the formation of complexes between pine nuclear extracts and the PsGS1b promoter. Given that these MYB proteins were previously shown to have the capacity to activate gene expression related to lignin biosynthesis, we hypothesize that they may function to co-regulate lignification, a process that places significant demands on nitrogen recycling, and GS, the major enzyme involved in the nitrogen recycling pathway.

Ancillary