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Dynamic cortical behavior of plant protoplasts reveals unexpected similarities between plant and animal cells

<p>The raw data presented in this folder corresponds to the publication<br># Dynamic cortical behavior of plant protoplasts reveals unexpected similarities between plant and animal cells</p> <p>Johanna E. M. Dickmann 1,2, Marjolaine Martin 1,&sect;, Claire Lionnet 1,&sect;, Zoe Nemec-Venza 1, Olivier Hamant 1,2</p> <p>1 Laboratoire Reproduction et D&eacute;veloppement des Plantes, ENS de Lyon, INRAE, CNRS, UCBL1 &nbsp;<br>2 Correspondence: olivier.hamant@ens-lyon.fr, johanna.dickmann@ens-lyon.fr &nbsp;<br>&sect; Equal contribution &nbsp;</p> <p>ORCIDs:<br>* Johanna Dickmann: 0000-0002-0861-4440<br>* Zoe Nemec-Venza: 0000-0002-2346-2596<br>* Olivier Hamant: 0000-0001-6906-6620</p> <p>Submitted to bioRxiv in November 2024 &nbsp;</p> <p>This work was funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) &ndash; project number 521501033 to J.D. and the European Research Council (ERC-2021-AdG-101019515 &ldquo;Musix&rdquo; to O.H.).</p> <p>## Data organization</p> <p>The data are organized according to the figure panels in the publication. For large experiments, the folders may contain subfolders for each experimental repeat and/or condition. For explanations on the data and the methods, please refer to the publication.</p> <p>All data presented here are the original raw data output of the microscopes in the CZI format, a proprietary format developed by Zeiss, encapsulating both 4D image data and metadata, i.e. acquisition settings. This format is supported by open-source software such as Fiji and Open Microscopy Environment.</p> <p>Refer to the README files in the subfolders for information on which exact file was used to display in the figure.</p> <p>## Explanation of the file names</p> <p>### Arabidopsis experiments</p> <p>The filenames contain the following information, separated by underscores:<br>* an experiment identifier (e.g.&rdquo;PLA001&rdquo;, &ldquo;PRO077&rdquo;)</p> <p>* the line of the imaged plant material (e.g. &ldquo;pUBQ10-LTi6B-TdTomato&rdquo;)</p> <p>* sometimes information on the ecotype of the line (e.g. &ldquo;Col-0&rdquo;)</p> <p>* the age of the plants (e.g. &ldquo;7d&rdquo; = 7 day old plants)</p> <p>* sometimes information on a stain added (e.g. &ldquo;FM4-64_0_5ugPml&rdquo; = FM4-64 dye at a final concentration of 5 ug/ml)</p> <p>* sometimes information on a treatment (e.g. &ldquo;beforeFDA&rdquo; = image taken before FDA was added; &ldquo;FDA2.5ugPml&rdquo; = after adding FDA at a final concentration of 2.5 ug/ml, sometimes with additional information on the time between adding the FDA and imaging, e.g. &ldquo;25min&rdquo;)</p> <p>* sometimes information on the centrifugation speed (e.g. &ldquo;100g&rdquo;)</p> <p>* sometimes information on the imaging support (e.g. &ldquo;bucket&rdquo; = NOA73 container, &ldquo;wells&rdquo; = NOA73 microwells, &ldquo;coverslip&rdquo;)</p> <p>* sometimes information on the imaging mode (&ldquo;z-stack&rdquo;, &ldquo;t-series&rdquo; = time series/timelapse, &ldquo;6x&rdquo; = zoom of 6 in Zen software)</p> <p>* the solution the sample was imaged in (&ldquo;Solution A&rdquo; or &ldquo;A&rdquo; = hyperosmotic buffer with D-mannitol, &ldquo;AS&rdquo; = hyperosmotic buffer with D-sorbitol)</p> <p>* sometimes information on experimental setup (&ldquo;ON&rdquo; = overnight timelapse imaging)</p> <p>* increasing numbers at the end of the file name indicate subsequent fields of view or positions imaged with the same settings</p> <p>* for Fig. 1A: information about the length of the plasmolysis (&ldquo;50 min&rdquo;)</p> <p>* for Fig. 4c,d: information on which solution the protoplasts are and have been imaged in: &ldquo;A&rdquo; = hyperosmotic buffer solution with 600 mM D-mannitol. &ldquo;B&rdquo; = &nbsp;hyperosmotic buffer solution with 280 mM D-mannitol. Times indicate time between addition of new buffer and onset of imaging of the position list.</p> <p>* for Fig. 4e-f: the concentration of the hyperosmotic buffer solution is indicated. For the control, the number of additions of hyperosmotic buffer solution with 600 mM D-mannitol is indicated.</p> <p>### Physcomitrium patens experiments</p> <p>The filenames contain the following information, separated by underscores:<br>* an experiment identifier (e.g. "PyP001") &nbsp;</p> <p>* &ldquo;Physco_wt&rdquo; referring to Physcomitrium patens wild type</p> <p>* the age of the moss tissue used for protoplasting (e.g. &ldquo;6d&rdquo; = 6 days)</p> <p>* information on the stain added (e.g. &ldquo; Fm4-64_2ugPml&rdquo; = FM4-64 dye at a final concentration of 2 ug/ml)</p> <p>* information on the imaging support (e.g. &ldquo;bucket&rdquo; = NOA73 container, &ldquo;coverslip&rdquo;)</p> <p>### Maize experiments</p> <p>The filenames contain the following information, separated by underscores:<br>* the date on which the experiment was performed (yyyymmdd)</p> <p>* the plant species (&ldquo;Maize&rdquo;)</p> <p>* sometimes information in the solution used for digestion ("A+E" = hyperosmotic buffer solution with D-mannitol)</p> <p>### Bead experiments</p> <p>The filenames contain the following information, separated by underscores:<br>* an experiment identifier (e.g. &ldquo;beads008&rdquo;)</p> <p>* a description of the beads (&ldquo;fluoresbrite1micron&rdquo; = Fluoresbrite beads of a diameter of 1 um)</p> <p>* sometimes a short description of the protocol (e.g. &ldquo;SolAwashed-2-3mLsolA&rdquo; = NOA73 microwells were washed in hyperosmotic buffer with 600 mM D-mannitol 2x prior to imaging, beads were imaged in 3 ml hyperosmotic buffer solution with 600 mM D-mannitol.)</p> <p>* an information on the size of the field of view (e.g. &ldquo;small FOV&rdquo; = small field of view, i.e. one microwell with beads)</p> <p>* information at which approx. height of the microwell the image was taken (&ldquo;TopOfWells&rdquo; = close to the opening of the wells on the top)</p> <p>* sometimes information on the zoom of the Zen software (e.g. &ldquo;7x&rdquo;)</p>

ShareScore

36/100

Overall dataset sharing score

Score breakdown

These five areas show where the dataset supports — or may limit — practical reuse.

Stewardship
8
Harmonization
4
Access
12
Reuse readiness
8
Engagement
4

Topics

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