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. 2018 Dec 1;5:59. doi: 10.1038/s41438-018-0068-4

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© The Author(s) 2018

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 A wild-type callus was treated with DMSO or 40 mmol NAA. Callus extracts were treated with the MdIAA121-His fusion protein and then incubated for the indicated periods. Actin was used as a loading control. b MG132 inhibited the degradation of MdIAA121. A wild-type apple callus extract was treated with DMSO or 100 mM MG132 for 0.5 h and then incubated with MdIAA121-His for the indicated periods