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. 2021 Aug 9;12(8):780. doi: 10.1038/s41419-021-04034-7

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© The Author(s) 2021, corrected publication 2021

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. 6 — a Wild type and Fanci^−/− spermatocytes were immunolabeled with SYCP1 and SYCP3 in leptotene (Lep), zygotene (Zyg), pachytene (Pac), and diplotene (Dip) spermatocytes. Meiotic stages were determined on the basis of SYCP3 signals. b Percentage of each stage of meiotic prophase as determined by SYCP3 immunostaining. In each group, six mice were analyzed. Data are presented as mean ± SD. Ns no statistical significant difference. Chi-square test (Fisher’s exact test). c Wild type and Fanci^−/− spermatocytes were immunolabeled with γ-H2AX and SYCP3 at leptotene (Lep), zygotene (Zyg), pachytene (Pac), and diplotene (Dip) spermatocytes. d Spermatocytes immunolabeled for RNA Polymerase II (RNA Pol II) and SYCP3 at diplotene spermatocytes. Arrows represent the sex chromosomes. Scale bars, 5 μm.