| Multi-tissue gene-expression analysis in a mouse model of thyroid hormone resistance (2004) | |||||||||||
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| Abstract Background Resistance to thyroid hormone (RTH) is caused by mutations of the thyroid hormone receptor β (TRβ) gene. To understand the transcriptional program underlying TRβ mutant-induced phenotypic expression of RTH, cDNA microarrays were used to profile the expression of 11,500 genes in a mouse model of human RTH. Results We analyzed transcript levels in cerebellum, heart and white adipose tissue from a knock-in mouse (TRβ PV/PV mouse) that harbors a human mutation (referred to as PV) and faithfully reproduces human RTH. Because TRβ PV/PV mice have elevated thyroid hormone (T3), to define T3-responsive genes in the context of normal TRβ, we also analyzed T3 effects in hyperthyroid wild-type gender-matched littermates. Microarray analysis revealed 163 genes responsive to T3 treatment and 187 genes differentially expressed between TRβ PV/PV mice and wild-type littermates. Both the magnitude and gene make-up of the transcriptional response varied widely across tissues and conditions. We identified genes modulated in T3-dependent PV-independent, T3- and PV-dependent, and T3-independent PV-dependent pathways that illuminated the biological consequences of PV action in vivo . Most T3-responsive genes that were dysregulated in the heart and white adipose tissue of TRβ PV/PV mice were repressed in T3-treated wild-type mice and upregulated in TRβ PV/PV mice, suggesting the inappropriate activation of T3-suppressed genes in RTH. Conclusions Comprehensive multi-tissue gene-expression analysis uncovered complex multiple signaling pathways that mediate the molecular actions of TRβ mutants in vivo . In particular, the T3-independent mutant-dependent genomic response unveiled the contribution of a novel 'change-of-function' of TRβ mutants to the pathogenesis of RTH. Thus, the molecular actions of TRβ mutants are more complex than previously envisioned. | |||||||||||
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