| Autor: |
Zhang, Y., Kent, J.W., Olivier, M., Ali, O., Broeckel, U., Abdou, R.M., Dyer, T.D., Comuzzie, A., Curran, J.E., Carless, M.A., Rainwater, D.L., Göring, H.H.H., Blangero, J., Kissebah, A.H. |
| Předmět: |
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| Zdroj: |
Obesity (19307381); Oct2013, Vol. 21 Issue 10, p2099-2111, 13p |
| Abstrakt: |
Objective: Metabolic Syndrome (MetS) is a phenotype cluster predisposing to type 2 diabetes and cardiovascular disease. We conducted a study to elucidate the genetic basis underlying linkage signals for multiple representative traits of MetS that we had previously identified at two significant QTLs on chromosomes 3q27 and 17p12. Design and Methods: We performed QTL-specific genomic and transcriptomic analyses in 1,137 individuals from 85 extended families that contributed to the original linkage. We tested in SOLAR association of MetS phenotypes with QTL-specific haplotype-tagging SNPs as well as transcriptional profiles of peripheral blood mononuclear cells (PBMCs). Results: SNPs significantly associated with MetS phenotypes under the prior hypothesis of linkage mapped to seven genes at 3q27 and seven at 17p12. Prioritization based on biologic relevance, SNP association, and expression analyses identified two genes: insulin-like growth factor 2 mRNA-binding protein 2 ( IGF2BP2) at 3q27 and tumor necrosis factor receptor 13B ( TNFRSF13B) at 17p12. Prioritized genes could influence cell-cell adhesion and adipocyte differentiation, insulin/glucose responsiveness, cytokine effectiveness, plasma lipid levels, and lipoprotein densities. Conclusions: Using an approach combining genomic, transcriptomic, and bioinformatic data we identified novel candidate genes for MetS. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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