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. 2024 Sep 18;634(8035):979–985. doi: 10.1038/s41586-024-07963-3

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© The Author(s) 2024

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 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/.

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Extended Data Fig. 1 — a, MIWI2 (green), HA (red) and DAPI (blue) staining of E16.5 foetal testis sections from Spocd1^HA/+ mice treated with PBS or RNase A prior to fixation. b, HA (red) and DAPI (blue) staining of E16.5 foetal testis sections from E16.5 Miwi2^−/−;Spocd1^HA/+ and Miwi2^+/−;Spocd1^HA/+ mice. c, d, SPIN1 (green) and DAPI (blue) staining of E16.5 Miwi2^+/− and Miwi2^−/− E16.5 foetal testis sections. (c) shows a zoom-in of the cell highlighted with a dashed rectangle in (d). Images of (a-d) are representative of n = 3 biological replicates. Scale bars are 5 μm (a), 10 μm (b, d) and 2 µm (c).