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. 2022 Mar 1;5:180. doi: 10.1038/s42003-022-03127-z

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — a H1-AF488 injected in C. cinerea accumulated in the cell nuclei (orange arrows). Two representative injections are shown. The white arrow shows the injection sites. b Following injection of a hyphal tip, time-lapse monitoring showed the growth of the injected cell, similar to the surrounding hyphae. The injected H1-AF488 remained at its location along the whole time-course. The fluorescence images in (a), and the brightfield and fluorescence images at 0, 24, and 48 h in (b) are summed slices of Z-stacks. Scale bar: 20 µm.