This repository contains raw data associated with the publication: 'A comparative meta-proteomic pipeline for the identification of plasmodesmata proteins and regulatory conditions in diverse plant species' -by Philip Kirk; Sam Amsbury; Liam German; Rocio Gaudioso-Pedraza; YOSELIN BENITEZ-ALFONSO. BMC. Biology (2022) Data is compressed into '.zip' files named according to which figure in the paper the data relates to. For more details on how the data was obtained please consult the Methods section in the publication. Note: Raw data used for Figure 1-4 is provided within the supplementary files Additional File 1 and Additional File 2 published with the manuscript. ---------------------------------------------------------------------------------- Figure 5: GFP diffusion in the root meristem of Arabidopsis thaliana is restricted in 3% PEG and 75 mM sodium chloride. The data for this figure was collected from plants that were germinated directly on the treatment and grown for 4 days (subfolder 4dpg) or plants grown in control and transferred to the treatment 24 hours before data collection (subfolder 4dpg1dpt). The folder structure within these subfolders is identical. Raw confocal images of root tips are in the 'images' folder. These images are in'.czi' format that can be opened with Fiji imaging software. These images were used to generate fluorescence profiles across transects of the root (see publication for details). The transects generated for the publication are stored in a '.csv' format within 'lateral analysis' or 'tz to tip analysis'. The column in the 'csv' named 'Value' is the mean fluorescence value (arbitrary units, AU) at a given point along the transect. How this data is used is described in the methods section. ---------------------------------------------------------------------------------- Figure 6: SHR-GFP expression is reduced in the root meristem of Arabidopsis thaliana grown in 75 mM sodium chloride. Data for this figure are derived from confocal images in a '.czi' format that can be opened with Fiji imaging software. This data is used to generate lateral fluorescent profiles (as described in Methods) as depicted in Figure 6a. The fluorescent profiles are stored in the folder '30 um from qc lateral analysis'. In a separate analysis, fluorescence was measured for the endodermis, stele and QC using Fiji/ImageJ. The fluorescence readings are recorded in 'endo vasc' (which related to Figure 6 d,f) and qc vasc (which relates to Figure 6 e,g) ---------------------------------------------------------------------------------- Figure 7: The Medicago truncatula protein Medtr1g073320 is regulated in response to rhizobia and co-localizes with callose at plasmodesmata. This figure shows representative cropped confocal images. The raw confocal images are in a '.czi' format and can be opened with Fiji imaging software. ---------------------------------------------------------------------------------- Figure 8: Ectopic Medtr1g073320 expression affects rhizobia infection and callose regulation in nitrate replete conditions. Figure S9. Medtr1g073320 regulates rhizobia infection and nodulation in full-nitrate conditions. These figures share the same dataset containing root phenotyping data presented here in Excel. Column legend: Nitrate = nitrate treatment, cm = length of root in cm, IT = infection thread count, IT density = IT per cm of root, IP = infection pockets, IP density = IP per cm of root, Nodules = nodules count, nodules density = nodules per cm of root. ---------------------------------------------------------------------------------- Figure S4. Aniline blue staining reveals callose deposits in Arabidopsis root exposed to PEG and NaCl. This figure uses representative confocal images. The raw confocal images are in a '.czi' format and can be opened with Fiji imaging software. ---------------------------------------------------------------------------------- Figure S5. Ectopic expression of the callose regulatory protein PDLP1 restricts root growth and response to 3% PEG. This folder contains scans of plates containing WT (wt) or PDLP1OE (LP1OE) seedlings grown on either control (con), 0 mM nitrate (lowN), 0 mM K+ (lowK), 3% PEG (peg) or 75 mM NaCl (nacl) in '.tif' format. Rootnav was used to measure root morphology In these images. The spreadsheet 'formatted perplant .csv' contains the exported data and is clearly annotated. ---------------------------------------------------------------------------------- Figure S6. Medtr1g073320 is a PDLP- family member upregulated upon rhizobia inoculation in Medicago truncatula roots. Spreadsheet with qPCR data obtained for the housekeeping gene actin and Medtr1g073320 (pdlp) in a variety of treatments. CT values and data analysis to extract differential expression is shown. ---------------------------------------------------------------------------------- Figure S7. Medtr1g073320 localizes with callose at plasmodesmata. This figure shows representative confocal images. The raw confocal images are in a '.czi' format and can be opened with Fiji imaging software. ---------------------------------------------------------------------------------- Figure S8. Medtr1g073320 overexpression improves root and shoot weight. Spreadsheet recording the root and shoot biomass (grams) of Medicago plants transformed with an empty vector (control) or with a construct that lead to overexpression of Medtr1g073320. ----------------------------------------------------------------------------------