SCD rs41290540 single‐nucleotide polymorphism modifies miR‐498 binding and is associated with a decreased risk of coronary artery disease

• Main Authors: Zhou Liu, Xiaojian Yin, Hui Mai, Guangning Li, Zhijun Lin, Wanxin Jie, Kanglan Li, Haihong Zhou, Shouchao Wei, Li Hu, Wanjuan Peng, Jiajing Lin, Feng Yao, Hua Tao, Xing‐dong Xiong, Keshen Li
• Format: Article
• Language: English
• Published: Wiley 2020-03-01
• Series: Molecular Genetics & Genomic Medicine
• Subjects: 3′‐untranslated region; coronary artery disease; microRNA; single‐nucleotide polymorphism; stearoyl‐CoA desaturase
• Online Access: https://doi.org/10.1002/mgg3.1136

Abstract Background Atherosclerosis is the primary cause of coronary artery disease (CAD), and stearoyl‐CoA desaturase (SCD) is associated with atherosclerosis. However, the associations between variants of SCD and CAD have not yet been decided. Methods This study analyzed SCD rs41290540 single‐nucleotide polymorphism (SNP) in the 3′‐untranslated region for an association with a risk of CAD among the Chinese Han population. CAD patients and controls were genotyped for SNP rs41290540 in SCD by SNaPshot. The binding affinity of miR‐498 to rs41290540 was determined by a luciferase assay, and SCD expression was assessed using Western blot. Results A total of 969 CAD patients and 1,095 control subjects were involved in this study. The SCD rs41290540CC genotype is associated with a decreased risk of CAD compared with the AA genotype. Furthermore, the CC genotype is associated with lower serum total cholesterol (TC). Western blot analysis demonstrated that miR‐498 suppressed the expression of SCD. A luciferase assay confirmed that rs41290540 A>C variation in the SCD 3′UTR inhibits miR‐498 binding. Conclusion This study demonstrates that the SCD rs41290540 may be associated with a decreased risk of CAD, lower serum TC, and decreased miR‐498 binding.