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Fatty acid desaturase 2 promoter mutation is not responsible for Delta6-desaturase deficiency

机译:脂肪酸去饱和酶2启动子突变不是Delta6-去饱和酶缺乏的原因

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摘要

Dietary essential polyunsaturated fatty acids (PUFAs) require fatty acid desaturases (FADS) for conversion to long-chain PUFAs (LCPUFAs), which are critical for many aspects of human health. A Δ6-desaturase deficiency in a single patient was attributed to an insertion mutation in the FADS2 promoter. Later population studies have shown this thymidine nucleotide (T) insertion to be a common polymorphism (rs3834458). We examined correlations between rs3834458 variants and fatty acid evidence of FADS2 activity in a cohort of rheumatoid arthritis patients selected for low or nil consumption of n-3 LCPUFA as fish or fish oil. The presence of the T allele was associated with higher FADS2 activity, as indicated by higher conversion of plasma n-3 PUFA to LCPUFA. However, the T-insertion/deletion polymorphism did not affect FADS2 promoter activity in luciferase reporter assays in HepG2 or NIH/3T3 cells. Our results indicate that the polymorphism rs3834458 does not appear to directly affect FADS2 promoter activity and is not responsible for a previously reported Δ6-desaturase deficiency.
机译:饮食中必需的多不饱和脂肪酸(PUFA)需要脂肪酸去饱和酶(FADS)才能转化为长链PUFA(LCPUFAs),这对人体健康至关重要。单个患者中的Δ6-去饱和酶缺乏症归因于FADS2启动子的插入突变。后来的人群研究表明,这种胸苷核苷酸(T)插入是常见的多态性(rs3834458)。我们检查了rs3834458变异体与FADS2活性的脂肪酸证据之间的相关性,该队列研究针对以低或无n-3 LCPUFA食用鱼或鱼油的类风湿性关节炎患者。 T等位基因的存在与较高的FADS2活性相关,如血浆n-3 PUFA向LCPUFA的较高转化率所表明。然而,在HepG2或NIH / 3T3细胞中的荧光素酶报告基因分析中,T插入/缺失多态性并不影响FADS2启动子活性。我们的结果表明,多态性rs3834458似乎并不直接影响FADS2启动子活性,并且对先前报道的Δ6-去饱和酶缺乏症不负责任。

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