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. 2020 Jun 11;9:8. doi: 10.1186/s13619-020-00049-1

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© The Author(s) 2020

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 7 — Up-regulation of proteins related to 26S proteasome and cell cycle arrest in capn3b^Δ19Δ14 at 3dpH. a Venn diagram showing the number of ‘Sham unique’, ‘PH unique’ and ‘Shared’ proteins up-regulated in capn3b^Δ19Δ14 (cutoff value: MU/WT > 1.45). b Top 10 categories obtained from GO analysis of biological process for the 325 uniquely up-regulated proteins in capn3b^Δ19Δ14 at 3dpH. c-e Comparison of the change (in log10 value of the ratio of MU/WT) of 32 26S proteasome subunits (c), 12 cell cycle negative regulators (d) and 29 DNA-repair related proteins (e) between the PH-group and sham-group at 3dpH