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. 2019 Jan 31;20:23. doi: 10.1186/s13059-019-1633-3

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 4 — Characterization of the incorporation of TP1 and H2A.L.2 into spermatid chromatin in the absence of H2A.B.3. a Elongating/condensing spermatids immunostained with anti-TP1 antibodies (turquoise) and counterstained with DAPI (blue). The outlines of the spermatids nuclei are shown as a white trace in TP1 panels. b The quantification of the number of wild type and H2A.B.3^−/y step 10–12 spermatids with a delayed wave of TP1 release. c HA.L.2 localization in condensing wild type and H2A.B.3^−/y spermatid. White arrows point to pericentric heterochromatin. d The quantification of the number of wild type and H2A.B.3^−/y condensing spermatids with H2A.L.2 enriched in pericentric heterochromatin (HC)