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. 2021 Sep 1;12:489. doi: 10.1186/s13287-021-02508-1

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© The Author(s) 2021

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. 3 — m⁶A peaks were significantly dysregulated during osteogenesis of hASCs. a Volcano plot displaying the DMGs (fold change ≥ 2 and p < 0.05). b Pie chart showing distribution of differentially methylated m⁶A peaks in different gene contexts. c Accumulation of differentially methylated m⁶A peaks along transcripts. d The m⁶A motifs significantly enriched across m⁶A peaks identified between uhASCs and dhASCs. DMGs, differentially methylated genes; hASCs, human adipose-derived stem cells; uhASCs, undifferentiated hASCs; dhASCs, osteogenically differentiated hASCs; FC, fold change