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pmid:28831411
Whole transcriptome data of zebrafish exposed to chronic dose of depleted uranium.
Olivier Armant · Kewin Gombeau · Christelle Adam Guillermin
Data in brief · 2017 doi:10.1016/j.dib.2017.07.071
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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The effects of chronic exposure to DU at concentration close to the environmental standards (0.3-30 µg DU/L) are scarcely characterised. Genomic alterations caused by low doses of pollutants can potentially propagate over generations, but how these effects may affect the health of the progeny remain uncertain for the vast majority of toxicants. The present dataset describes the transcriptomic effects of a chronic exposure to 20 µg DU/L during 10 days on adult zebrafish (Danio rerio) organs, the brain, the testis and the ovaries. The potential multigenerational effects of DU were assessed on the progeny of the adult exposed fish at the two-cells stage and after four days of development. We describe in this article the summary statistics of the differential gene expression analysis and focus on key molecular pathways affected by an exposure to a low concentration of DU. The data presented in this study supports the observation made in Armant et al. 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The number of genes is indicated for each category.", "rows": [["DU/Ctrl", "Up-regulated", "Down-regulated", "Total"], ["Two-cells", "2482", "4106", "6588"], ["96 hpf", "573", "62", "635"], ["Brain", "46", "1026", "1072"], ["Testis", "132", "295", "427"], ["Ovaries", "302", "169", "471"]], "row_count": 6, "column_count": 4, "numeric_cells": 16, "header_rows": 1, "locator": "section[5]/table-wrap[3]#t0015"}}, {"id": "asset:table:pmid:28831411:4", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:907bb7fb61421165a0a33fe18bbec88c850a80b14bcb5089356244d9a911cf0a", "bytes": 3023, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[5]/table-wrap[4]#t0020", "version": null, "note": "Gene ontology analysis. The list provides the top 5 biological pathways impacted by DU in each dataset based on smallest p-values.", "structure": {"pmcid": "PMC5554979", "section_index": 5, "section_title": "Data", "row_count": 60, "column_count": 3}, "table": {"label": "Table 4", "caption": "Gene ontology analysis. The list provides the top 5 biological pathways impacted by DU in each dataset based on smallest p-values.", "rows": [["Set of genes", "Gene ontology term", "p-value"], ["Down in DU exposed brain", "Visual perception", "2.7E−08"], ["", "Sensory perception of light stimulus", "2.7E−08"], ["", "Cell adhesion", "6.3E−07"], ["", "Biological adhesion", "6.3E−07"], ["", "Response to light stimulus", "5.1E−06"], ["", "", ""], ["Up in DU exposed brain", "Response to lipid", "2.4E−03"], ["", "Response to lipopolysaccharide", "2.7E−03"], ["", "Ovulation", "3.1E−03"], ["", "Response to molecule of bacterial origin", "3.1E−03"], ["", "Response to organic substance", "3.5E−03"], ["", "", ""], ["Down in DU exposed testis", "Cell adhesion", "1.0E−04"], ["", "Biological adhesion", "1.0E−04"], ["", "Fin regeneration", "3.4E−04"], ["", "cGMP biosynthetic process", "4.9E−04"], ["", "cGMP metabolic process", "4.9E−04"], ["", "", ""], ["Up in DU exposed testis", "Centromere complex assembly", "8.2E−04"], ["", "Regulation of synapse structure or activation", "3.4E−03"], ["", "Peptidoglycan biosynthetic process", "4.4E−03"], ["", "Peptidoglycan-based cell wall biogenesis", "4.4E−03"], ["", "Protein side chain deglutamylation", "4.4E−03"], ["", "", ""], ["Down in DU exposed ovaries", "Aspartate family amino acid metabolic pr.", "4.1E−04"], ["", "Endomembrane system organization", "4.7E−03"], ["", "Androgen biosynthetic process", "5.9E−03"], ["", "Mitochondrial protein catabolic process", "5.9E−03"], ["", "Mitophagy by induced vacuole formation", "5.9E−03"], ["", "", ""], ["Up in DU exposed ovaries", "Neural tube development", "7.8E−07"], ["", "Embryonic appendage morphogenesis", "2.6E−06"], ["", "Pectoral fin development", "4.7E−06"], ["", "Fin morphogenesis", "5.2E−06"], ["", "Appendage morphogenesis", "8.2E−06"], ["", "", ""], ["Down in 2 cells stage", "ncRNA metabolic process", "1.6E−14"], ["", "Nucleic acid metabolic process", "3.6E−14"], ["", "Cellular macromolecule metabolic process", "3.7E−12"], ["", "Organelle organization", "2.6E−11"], ["", "Heterocycle metabolic process", "3.2E−11"], ["", "", ""], ["Up in 2 cells stage", "Cytoplasmic transport", "3.8E−06"], ["", "Organelle organization", "7.2E−06"], ["", "ER to Golgi vesicle-mediated transport", "1.1E−05"], ["", "Double-strand break repair", "1.3E−05"], ["", "mRNA processing", "1.5E−05"], ["", "", ""], ["Down in 96hpf larva", "Thyroid hormone generation", "2.1E−03"], ["", "Thyroid hormone metabolic process", "2.1E−03"], ["", "Hydrogen peroxide biosynthetic process", "2.1E−03"], ["", "Circadian rhythm", "3.0E−03"], ["", "Homophilic cell adhesion via plasma memb.", "3.4E−03"], ["", "", ""], ["Up in 96hpf larva", "Oxidation-reduction process", "6.6E−22"], ["", "Single-organism metabolic process", "1.4E−20"], ["", "Small molecule metabolic process", "1.4E−16"], ["", "Organic acid metabolic process", "9.9E−15"], ["", "Lipid metabolic process", "1.3E−14"]], "row_count": 60, "column_count": 3, "numeric_cells": 54, "header_rows": 1, "locator": "section[5]/table-wrap[4]#t0020"}}], "gaps": []}, "analysis": {"state": "complete", "methods": [{"id": "method-1", "family": "differential_expression", "specific": "deseq2", "label": "Differential expression analysis", "dsl_operations": ["normalise_counts", "differential_expression_fit", "fdr_bh"], "missing_operations": [], "expressible": true, "parameters": {}, "data_shapes": ["count_matrix_with_condition"], "evidence": {"score": 1.0, "band": "verbatim", "quote": "Quantification and normalization of the mapped reads at the level of gene model were performed with DESeq. 2 [4]. 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