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. 2021 Sep 8;53(9):1307–1318. doi: 10.1038/s12276-021-00655-2

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© The Author(s) 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. 1 — a Localization of uterine TAZ mRNA on days 2, 3, and 5–8 of pregnancy as determined by in situ hybridization. Scale bar, 60 μm. Asterisks indicate the embryo. b Western blotting analysis of TAZ protein in uteri during early pregnancy. TAZ, total TAZ protein; p-TAZ, phospho-TAZ protein. c Immunofluorescence analysis showed the marked nuclear localization of TAZ protein in decidual cells. d Localization of uterine TAZ mRNA under artificial decidualization. e Western blotting analysis of TAZ protein under artificial decidualization. Con, uninjected uterine horn, which served as the control; Oil, oil-induced decidualization. f Western blotting analysis of TAZ protein during in vitro decidualization. EP estrogen plus progesterone.