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Journal Article

Functional analysis of the coronary heart disease risk locus on chromosome 21q22

Authors

Publication date

2017

Summary

Background: The coronary heart disease (CHD) risk locus on 21q22 (lead SNP rs9982601) lies within a β€œgene desert.” The aim of this study was to assess if this locus is associated with CHD risk factors and to identify the functional variant(s) and gene(s) involved. Methods: A phenome scan was performed with UCLEB Consortium data. Allele-specific protein binding was studied using electrophoretic mobility shift assays. Dual-reporter luciferase assays were used to assess the impact of genetic variation on expression. Expression quantitative trait analysis was performed with Advanced Study of Aortic Pathology (ASAP) and Genotype-Tissue Expression (GTEx) consortium data. Results: A suggestive association between QT interval and the locus was observed (rs9982601 𝑝 = 0.04). One variant at the locus, rs28451064, showed allele-specific protein binding and its minor allele showed 12% higher luciferase expression (𝑝 = 4.82 Γ— 10βˆ’3) compared to the common allele. The minor allele of rs9982601 was associated with higher expression of the closest upstream genes (SLC5A3 1.30-fold increase 𝑝 = 3.98 Γ— 10βˆ’5; MRPS6 1.15-fold increase 𝑝 = 9.60 Γ— 10βˆ’4) in aortic intima media in ASAP. Both rs9982601 and rs28451064 showed a suggestive association with MRPS6 expression in relevant tissues in the GTEx data. Conclusions: A candidate functional variant, rs28451064, was identified. Future work should focus on identifying the pathway(s) involved.

Published in

Disease Markers

Volume and page numbers

2017 , 1 -10

DOI

http://dx.doi.org/10.1155/2017/1096916

ISSN

16

Subjects

Medicine, Science And Technology, Health, and Biology

Notes

Open Access; Copyright Β© 2017 Katherine E. Beaney et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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