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. 2021 Oct 20;9:747969. doi: 10.3389/fcell.2021.747969

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Copyright © 2021 Parihar, Bendelac-Kapon, Gur, Abbou, Belorkar, Achanta, Kinberg, Vadigepalli and Fainsod.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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RA responsiveness and differential expression dynamics of select RA network genes and targets in different clutches. (A–F) Embryos were treated at midblastula (st.8.5) with increasing concentrations of RA (1–1,000 nM) or DEAB 1–50 μM) to generate a gradient of RA responses. At mid gastrula (st. 11) the changes in RA network genes was determined by qPCR. (A) hoxa1.L, hoxa1.S; (B) dhrs3.L, dhrs3.S; (C) cyp26a1.L, cyp26a1.S; (D) rdh10.L, rdh10.S; (E) aldh1a2.L, aldh1a2.S; (F) aldh1a3.L, aldh1a3.S. (G) Dynamic expression patterns of multiple RA network genes across the different clutches. The data was combined from RNAseq (clutches A-F) and HT-qPCR (clutches G-L). The clutches are ordered left to right based on the earliest time at which hoxa1 expression returned to the baseline levels.