Visualization of Sex-Dimorphic Changes in the Intestinal Transcriptome of Fabp2 Gene-Ablated Mice

• Published in: Journal of nutrigenetics and nutrigenomics Vol. 5; no. 1; pp. 45 - 55
• Main Authors: Sugiyama, Michael G., Hobson, Luc, Agellon, Al B., Agellon, Luis B.
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland 01.01.2012
• Subjects: Animals; Down-Regulation; Fatty Acid-Binding Proteins - genetics; Female; Intestines - metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Original Paper; Sex Characteristics; Transcriptome; Up-Regulation; Transcriptome analysis; Fatty acid binding proteins; Sex differences; Lipid metabolism; Method; Small intestine; KEGG pathways
• ISSN: 2504-3161; 2504-3188; 1661-6758
• DOI: 10.1159/000337193

Background/Aims: Sex differences in gene expression program have not been effectively explored at the transcriptome level. We aimed to develop a method for the analysis of transcriptome data to identify sex differences and sex-dimorphic responses to experimental conditions in mice. Methods: Profiling of the small intestine transcriptome of chow-fed C57BL/6J (wild-type, WT) and Fabp2 –/– mice was carried out by microarray analysis. Sex-specific and androgynous effects of Fabp2 gene ablation were examined using FlexArray V1.6 by comparing WT to Fabp2 –/– mice. The data generated were exported into a single spreadsheet, collated and transformed to identify the differentially expressed genes for pathway analysis. Results: The method revealed enrichment of 17 sex-dimorphic pathways in the small intestine of WT mice compared to only 4 in Fabp2 –/– mice. Comparison of the effects of Fabp2 loss in individual sexes revealed a male-specific upregulation of 5 pathways involved in the production of unsaturated fatty acids, and a female-specific downregulation of pathways involved in xenobiotic metabolism. Conclusions: Our approach detected the common as well as sex-differential pathways that are modified due to the loss of Fabp2. These findings suggest that the pathways involved in nutrient and xenobiotic metabolism in the intestine are regulated by sex-specific mechanisms.