Fig. 7
- ID
- ZDB-IMAGE-251017-11
- Genes
- Antibodies
- Publication
- Xian et al., 2025 - ATP5F1A deficiency causes developmental delay and motor dysfunction in humans and zebrafish
- All Figures
- Figures for Xian et al., 2025
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Fig. 7 RNA-seq analysis of zebrafish model reveals the molecular regulatory network of atp5fa1 knockdown. A Transcriptome correlation analysis between samples (Pearson correlation coefficient heat map based on FPKM value). B Volcano plot of differentially expressed genes between control-MO group and atp5fa1-MO group. C Gene Ontology (GO) enrichment analysis of differentially expressed genes. D Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis of differentially expressed genes between the control-MO group and the atp5fa1-MO group. E qPCR validation of neurotransmission-related genes (gabra1, grin1a, gad1b, gria3a, grm1a, hcn1, syngr1a, syt16) (mean ± SD, n = 15 embryos/group; **P < 0.01, *** P < 0.001, ****P < 0.0001, Student t-test). F qPCR validation of Apelin-autophagy relative genes apln, becn1, and map1lc3b (mean ± SD, n = 15 embryos/group; **P < 0.01, ***P < 0.001, ****P < 0.0001, Student t-test). G) Western blot analysis of autophagy-related proteins P62, Lc3b-I, and Lc3b-II in control-MO and atp5fa1-MO zebrafish larvae at 72hpf. H Quantitative analysis of Lc3b-II protein expression normalized to Gapdh (mean ± SD, n = 3; **P < 0.01, Student t-test). I Quantitative analysis of P62 protein expression normalized to Gapdh (mean ± SED, n = 3; ***P < 0.001, Student t-test)