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Published March 27, 2023 | Published + Supplemental Material
Journal Article Open

Cell-specific occupancy dynamics between the pioneer-like factor Opa/ZIC and Ocelliless/OTX regulate early head development in embryos

Abstract

During development, embryonic patterning systems direct a set of initially uncommitted pluripotent cells to differentiate into a variety of cell types and tissues. A core network of transcription factors, such as Zelda/POU5F1, Odd-paired (Opa)/ZIC3 and Ocelliless (Oc)/OTX2, are conserved across animals. While Opa is essential for a second wave of zygotic activation after Zelda, it is unclear whether Opa drives head cell specification, in the Drosophila embryo. Our hypothesis is that Opa and Oc are interacting with distinct cis-regulatory regions for shaping cell fates in the embryonic head. Super-resolution microscopy and meta-analysis of single-cell RNAseq datasets show that opa's and oc's overlapping expression domains are dynamic in the head region, with both factors being simultaneously transcribed at the blastula stage. Additionally, analysis of single-embryo RNAseq data reveals a subgroup of Opa-bound genes to be Opa-independent in the cellularized embryo. Interrogation of these genes against Oc ChIPseq combined with in situ data, suggests that Opa is competing with Oc for the regulation of a subgroup of genes later in gastrulation. Specifically, we find that Oc binds to late, head-specific enhancers independently and activates them in a head-specific wave of zygotic transcription, suggesting distinct roles for Oc in the blastula and gastrula stages.

Additional Information

© 2023 Fenelon, Gao, Borad, Abbasi, Pachter and Koromila. 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. We are grateful to Rhea Datta and Angela Stathopoulos for generously providing us with fly lines, antibodies, and ChIPseq data. We would further like to thank Anupama Chandrasekhar for her help with the StarkLab database; Hinduja Sathishkumar and Saubia Zareen, students in the Koromila Lab, for their assistance with administrative tasks and fly husbandry; and Mounia Lagha for helpful discussions. This work was made possible by funding from the UTA STARS program and the Bioinformatics Resource Center at the Beckman Institute of Caltech. This work was made possible by funding from the UTA STARS program. Author contributions. TK conceived and directed the project. TK and KF planned the experimental approaches and oversaw the computational approach. KF performed in situ hybridizations and designed the image analysis pipeline. KF and PB performed the imaging and image analyses. FG wrote the bioinformatic scripts and carried out the bioinformatic analyses. LP gave input for writing the manuscript. KF, SA, and TK compiled embryo. images from the Stark database, made ChIP peak alignments and designed figures. TK and KF analyzed the data and wrote the manuscript. Data availability statement. The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Published - fcell-11-1126507.pdf

Supplemental Material - Data_Sheet_1.pdf

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Additional details

Created:
August 22, 2023
Modified:
December 22, 2023