• Peter J Castaldi, Feng Guo, Dandi Qiao, Fei Du, NaingZun Zar ChiZZC1 Channing Division of Network Medicine and., Yan Li, Betty Pham, Tarjei S Mikkelsen, Michael H Cho, Edwin K Silverman, and Xiaobo Zhou.
• 1 Channing Division of Network Medicine and.
• Am. J. Respir. Crit. Care Med. 2019 Jan 1; 199 (1): 526152-61.

RationaleThe identification of causal variants responsible for disease associations from genome-wide association studies (GWASs) facilitates functional understanding of the biological mechanisms by which those genetic variants influence disease susceptibility.ObjectiveWe aim to identify causal variants in or near the FAM13A (family with sequence similarity member 13A) GWAS locus associated with chronic obstructive pulmonary disease (COPD).MethodsWe used an integrated approach featuring conditional genetic analysis, massively parallel reporter assays (MPRAs), traditional reporter assays, chromatin conformation capture assays, and clustered regularly interspaced short palindromic repeats (CRISPR)-based gene editing to characterize COPD-associated regulatory variants in the FAM13A region in human bronchial epithelial cell lines.Measurements And Main ResultsConditional genetic association suggests the presence of two independent COPD association signals in FAM13A. MPRAs identified 45 regulatory variants within FAM13A, among which six variants were prioritized for further investigation. Three COPD-associated variants demonstrated significant allele-specific activity in reporter assays. One of three variants, rs2013701, was tested in the endogenous genomic context by CRISPR-based genome editing that confirmed its allele-specific effects on FAM13A expression and on cell proliferation, providing functional characterization for this COPD-associated variant.ConclusionsThe human GWAS association near FAM13A may contain independent association signals. MPRAs identified multiple functional variants in this region, including rs2013701, a putative COPD-causing variant with allele-specific regulatory activity.

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