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Home › Dataset Library › Transcription profiling of mouse liver to TCDD

Dataset: Transcription profiling of mouse liver to TCDD

Background; Mouse and rat models are mainstays in pharmacology, toxicology and drug development – but differences between strains and...

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Background; Mouse and rat models are mainstays in pharmacology, toxicology and drug development – but differences between strains and between species complicate data interpretation and application to human health. Dioxin-like polyhalogenated aromatic hydrocarbons represent a major class of environmentally and economically relevant toxicants. In mammals dioxin exposure leads to a broad spectrum of adverse affects, including hepatotoxicity of varying severity. Several studies have shown that dioxins extensively alter hepatic mRNA levels. Surprisingly, though, analysis of a limited portion of the transcriptome revealed that rat and mouse responses diverge greatly (Boverhof et al. Toxicol Sci 94:398–416, 2006). Results; We employed oligonucleotide arrays to compare the response of 8,125 rat and mouse orthologs. We confirmed that there is limited inter-species overlap in dioxin-responsive genes. Rat-specific and mouse-specific genes are enriched for specific functional groups which differ between species, conceivably accounting for species-specificities in liver histopathology. While no evidence for the involvement of copy-number variation was found, extensive inter-species variation in the transcriptional-regulatory network was identified; Nr2f1 and Fos emerged as candidates to explain species-specific and species-independent responses, respectively. Conclusion; Our results suggest that a small core of genes is responsible for mediating the similar features of dioxin hepatotoxicity in rats and mice but non-overlapping pathways are simultaneously at play to result in distinctive histopathological outcomes. The extreme divergence between mouse and rat transcriptomic responses appears to reflect divergent transcriptional-regulatory networks. Taken together, these data suggest that both rat and mouse models should be used to screen the acute hepatotoxic effects of drugs and toxic compounds. Experiment Overall Design: Wild-type C57BL/6 mice were treated with 1000 ug/kg TCDD (n=6) or with cornoil vehicle as control (n=5) for 19 hours. Their livers were then excised, RNA extracted, and the resulting samples hybridized to Affymetrix MOE430-2 arrays to survey changes in the transcriptome profile.

Species:
mouse

Samples:
11

Source:
E-GEOD-10769

PubMed:
18796159

Updated:
Dec.12, 2014

Registered:
Nov.10, 2014


Factors: (via ArrayExpress)
Sample
GSE10769GSM273062
GSE10769GSM273063
GSE10769GSM273066
GSE10769GSM273067
GSE10769GSM273069
GSE10769GSM273070
GSE10769GSM273061
GSE10769GSM273064
GSE10769GSM273065
GSE10769GSM273068
GSE10769GSM273071

Tags

  • class
  • liver

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