|Punshon, Tracy -|
|Hirschi, Kendal -|
|Yang, Jian -|
|Lanzirotti, Antonio -|
|Guerinot, Mary Lou -|
Submitted to: Plant Physiology
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: November 13, 2011
Publication Date: November 15, 2011
Citation: Punshon, T., Hirschi, K.D., Yang, J., Lanzirotti, A., Guerinot, M. 2011. The role of CAX1 and CAX3 in elemental distribution and abundance in Arabidopsis seed. Plant Physiology. 158(1):352-362. Interpretive Summary: The ability to alter nutrient partitioning within plant cells to improve nutritional quality is poorly understood. Here we investigate calcium distribution and abundance in plants using synchrotron x-ray fluorescence microscopy (SXRF). SXRF is a state-of-the-art technology that can be used to show the quantitative elemental characteristics of plant tissues, frequently without sample preparation. These high resolution pictures allow images showing tissue- or cell-level elementals, focusing on metals in particular parts of the cell. This work showcases this technology in plant biology and suggests we now have the means to analyze calcium distribution within many different agriculturally important crops. This could provide valuable information as we attempt to relate nutrient bioavailability with nutrient location within various types of plant cells.
Technical Abstract: The ability to alter nutrient partitioning within plant cells is poorly understood. In Arabidopsis (Arabidopsis thaliana), a family of endomembrane cation exchangers (CAXs) transports Ca(2+) and other cations. However, experiments have not focused on how the distribution and partitioning of calcium (Ca) and other elements within seeds are altered by perturbed CAX activity. Here, we investigate Ca distribution and abundance in Arabidopsis seed from cax1 and cax3 loss-of-function lines and lines expressing deregulated CAX1 using synchrotron x-ray fluorescence microscopy. We conducted 7- to 10-µm resolution in vivo x-ray microtomography on dry mature seed and 0.2-µm resolution x-ray microscopy on embryos from lines overexpressing deregulated CAX1 (35S-sCAX1) and cax1cax3 double mutants only. Tomograms showed an increased concentration of Ca in both the seed coat and the embryo in cax1, cax3, and cax1cax3 lines compared with the wild type. High-resolution elemental images of the mutants showed that perturbed CAX activity altered Ca partitioning within cells, reducing Ca partitioning into organelles and/or increasing Ca in the cytosol and abolishing tissue-level Ca gradients. In comparison with traditional volume-averaged metal analysis, which confirmed subtle changes in seed elemental composition, the collection of spatially resolved data at varying resolutions provides insight into the impact of altered CAX activity on seed metal distribution and indicates a cell type-specific function of CAX1 and CAX3 in partitioning Ca into organelles. This work highlights a powerful technology for inferring transport function and quantifying nutrient changes.