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. 2022 Oct 27;5:1137. doi: 10.1038/s42003-022-04066-5

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© The Author(s) 2022

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. 3 — a Contribution of different forebrain domains to LS populations. Double-labelling for CB, CR or PV and the fluorescent reporter protein GFP/YFP/TdT in the various transgenic lines at P30. White arrows and arrowheads indicate double and single labelled cells, respectively. b–d Histograms showing the percentage of neurons double labelled for GFP/YFP/TdT over the total population. Each transgenic mouse line is identified by a different colour as shown in a and as summarised in Fig. 2d, e. n = 3 brains per transgenic line per marker except the following where n = 2 for Dbx-Cre;YFP mice: CR R and C, PV R and C. Histograms show mean + SEM. Source data are provided in Supplementary Data 1. Scale bar: 25 μm.