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. 2023 Jun 22;42(4):591–596. doi: 10.1038/s41587-023-01831-7

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© The Author(s) 2023

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. 2 — a, Genome browser snapshots showing three examples of transcripts with dynamic m⁶A enrichment during mouse oocyte and embryo development (transcript IDs: ENSMUST00000186548.6 for Tet3, ENSMUST00000005279.7 for Klf5 and ENSMUST00000112693.9 for Rif1). b, Number of m⁶A peaks and m⁶A-marked gene transcripts. c, PCA of m⁶A signal. d, Metagene profiles showing the enrichment of m⁶A peaks along protein-coding gene transcripts. e, Consensus motifs identified within m⁶A peaks identified in biological replicate 1.