首页> 美国卫生研究院文献>Journal of Lipid Research >Single nucleotide polymorphisms in the FADS gene cluster are associated with delta-5 and delta-6 desaturase activities estimated by serum fatty acid ratios
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Single nucleotide polymorphisms in the FADS gene cluster are associated with delta-5 and delta-6 desaturase activities estimated by serum fatty acid ratios

机译:FADS基因簇中的单核苷酸多态性与通过血清脂肪酸比率估算的delta-5和delta-6去饱和酶活性有关

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摘要

Genetic variability in the FADS1-FADS2 gene cluster [encoding delta-5 (D5D) and delta-6 (D6D) desaturases] has been associated with plasma long-chain PUFA (LCPUFA) and lipid levels in adults. To better understand these relationships, we further characterized the association between FADS1-FADS2 genetic variability and D5D and D6D activities in adolescents. Thirteen single nucleotide polymorphisms (SNPs) were genotyped in 1,144 European adolescents (mean ± SD age: 14.7 ± 1.4 y). Serum phospholipid fatty acid levels were analyzed using gas chromatography. D5D and D6D activities were estimated from the C20:4n-6/C20:3n-6 and C20:3n-6/C18:2n-6 ratios, respectively. Minor alleles of nine SNPs were associated with higher 18:2n-6 levels (1.9E-18 ≤ P ≤ 6.1E-5), lower C20:4n-6 levels (7.1E-69 ≤ P ≤ 1.2E-12), and lower D5D activity (7.2E-44 ≤ P ≤ 4.4E-5). All haplotypes carrying the rs174546 minor allele were associated with lower D5D activity, suggesting that this SNP is in linkage disequilibrium with a functional SNP within FADS1. In contrast, only the rs968567 minor allele was associated with higher D6D activity (P = 1.5E-6). This finding agrees with an earlier in vitro study showing that the minor allele of rs968567 is associated with a higher FADS2 promoter activity. These results suggest that rare alleles of several SNPs in the FADS gene cluster are associated with higher D6D activity and lower D5D activity in European adolescents.
机译:FADS1-FADS2基因簇中的遗传变异性[编码delta-5(D5D)和delta-6(D6D)去饱和酶]与成年人血浆长链PUFA(LCPUFA)和脂质水平相关。为了更好地理解这些关系,我们进一步表征了FADS1-FADS2遗传变异与青少年D5D和D6D活动之间的关联。在1,144个欧洲青少年中对13个单核苷酸多态性(SNP)进行了基因分型(平均±SD年龄:14.7±1.4 y)。使用气相色谱法分析血清磷脂脂肪酸水平。 D5D和D6D活性分别根据C20:4n-6 / C20:3n-6和C20:3n-6 / C18:2n-6比率估算。 9个SNP的次要等位基因与较高的18:2n-6水平(1.9E-18≤P≤6.1E-5),较低的C20:4n-6水平(7.1E-69≤P≤1.2E-12)相关,和较低的D5D活性(7.2E-44≤P≤4.4E-5)。所有携带rs174546次要等位基因的单倍型均与较低的D5D活性相关,这表明该SNP与FADS1中的功能性SNP处于连锁不平衡状态。相反,只有rs968567次要等位基因与更高的D6D活性相关(P = 1.5E-6)。这一发现与早期的体外研究一致,后者表明rs968567的次要等位基因与较高的FADS2启动子活性有关。这些结果表明,FADS基因簇中几个SNP的稀有等位基因与欧洲青少年中较高的D6D活性和较低的D5D活性相关。

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