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Genome-wide epigenomic screening reveals role of genes, cellular factors in thyroid disease

Date:
September 20, 2012
Source:
American Thyroid Association
Summary:
Genome-wide epigenomic screening can pinpoint disease-associated variants and identify novel genetic–epigenetic interactions in autoimmune thyroid diseases, according to new data.
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Genome-wide epigenomic screening can pinpoint disease-associated variants and identify novel genetic-epigenetic interactions in autoimmune thyroid diseases, according to new data presented at the 82nd Annual Meeting of the American Thyroid Association (ATA) in Québec City, Québec, Canada.

Since cytokines are key mediators of tissue inflammation and infiltration, a team of researchers from Mount Sinai School of Medicine in New York City tested the hypothesis that inflammatory cytokines, specifically interferon-alpha, a prime cytokine in the etiology of autoimmune thyroid disease, promote thyroid cell dysfunction through epigenetic modifications of autoimmune thyroid diseases genes. Interferon-alpha (IFNa) has also been shown to precipitate autoimmune thyroid diseases when used as therapeutic agent. The researchers had previously shown that IFNa increases mRNA expression of major AITD susceptibility genes in both cell lines and a mouse model of IFNa thyroid expression.

Researchers mapped modifications of histone patterns [histone H3 mono- and trimethylated at Lys-4 (H3K4me1 and H3K4me3)] induced by IFNa at these loci using ChIP-seq in human thyroid cells. ChIP-seq data were integrated with RNA-seq and bioinformatic analyses. Integration of ChIP-seq and RNA-seq data showed that significantly upregulated pathways included genes characterized by H3K4me3 enrichment in the 5'-regions, demonstrating a correlation between H3K4me3 and pathway activation by IFNa. Most upregulated genes/pathways participate in innate immunity and host defense response. IFNa induced enrichment of H3K4me1 mostly in noncoding gene regions.

Researchers next used the potential of H3K4me1 to mark regulatory regions to identify functional AITD-associated single-nucleotide polymorphisms (SNPs). An AITD-associated SNPs, in thyroglobulin (TG) gene was marked by enrichment of H3K4me1. This same SNP was previously shown by us through bioinformatic analyses followed by ChIP, luciferase reporter, and siRNA assays to bind interferon regulatory factor-1 (IRF1) and to modulate TG promoter activity in an allele-dependent manner.

"It is well-established that autoimmune thyroid diseases result from interactions between genetic and environmental factors. However, until now, the complex interplay between genes and intra- and extra-cellular factors to trigger pathological autoimmune responses has remained undefined," said Douglas Forrest, PhD, of the National Institute of Diabetes and Digestive and Kidney Diseases.


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The above story is based on materials provided by American Thyroid Association. Note: Materials may be edited for content and length.


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American Thyroid Association. "Genome-wide epigenomic screening reveals role of genes, cellular factors in thyroid disease." ScienceDaily. ScienceDaily, 20 September 2012. <www.sciencedaily.com/releases/2012/09/120920115632.htm>.
American Thyroid Association. (2012, September 20). Genome-wide epigenomic screening reveals role of genes, cellular factors in thyroid disease. ScienceDaily. Retrieved May 30, 2015 from www.sciencedaily.com/releases/2012/09/120920115632.htm
American Thyroid Association. "Genome-wide epigenomic screening reveals role of genes, cellular factors in thyroid disease." ScienceDaily. www.sciencedaily.com/releases/2012/09/120920115632.htm (accessed May 30, 2015).

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