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Fig. 1

ID
ZDB-FIG-230707-47
Publication
Zhang et al., 2023 - Wdr5-mediated H3K4me3 coordinately regulates cell differentiation, proliferation termination, and survival in digestive organogenesis
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Fig. 1

The differentiation of intestine, liver, and exocrine-pancreas is impaired in wdr5/− mutant embryos

a Whole-mount in situ hybridization (WISH) of wild type (WT) and wdr5/− mutant embryos at 3 dpf to show the expression of differentiation genes for different digestive organs including: the fabp10a and gc for liver, prss1and ela2l for exocrine pancreas, fabp2 and chia.1 for intestine as indicated. b Hematoxylin-Eosin (H&E) staining of cryosections to show liver (L), intestine (I) and exocrine pancreas (P) in WT and wdr5−/− mutant embryos at 3 dpf. Scale bar: 40 μm. c WISH of wdr5 in WT at one cell stage, 1, 2 and 3 dpf. d Heatmap of genes related to endodermal organ differentiation in WT and wdr5−/− mutant embryos at 3 dpf. e Volcano plot to show differential expressed regulators of endodermal organ development between WT and wdr5/− mutant embryos at 3 dpf (wdr5−/− mutant vs WT, |log2FoldChange | ≥ 1, Padj < 0.05). f WISH of WT and wdr5−/− mutant embryos at different time points with different digestive organ development regulators including: pan-endodermal marker foxa3, hepatic marker prox1a and intestine marker cdx1b as indicated. n indicates the number of zebrafish embryos in each group.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
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