Fatty acid desaturase 2 promoter mutation is not responsible for Δ6-desaturase deficiency

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作者
Melissa K Gregory
Susan E Lester
Rebecca J Cook-Johnson
Robert A Gibson
Susanna M Proudman
Leslie G Cleland
Michael J James
机构
[1] Rheumatology Unit,
[2] Royal Adelaide Hospital,undefined
[3] Basil Hetzel Institute for Medical Research,undefined
[4] Queen Elizabeth Hospital,undefined
[5] Food Science,undefined
[6] School of Agriculture,undefined
[7] Food and Wine,undefined
[8] University of Adelaide,undefined
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FADS2 promoter; polymorphism; polyunsaturated fatty acids; Δ6-desaturase;
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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.
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页码:1202 / 1204
页数:2
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