TY - JOUR
T1 - Fatty acid desaturase 2 promoter mutation is not responsible for Δ6-desaturase deficiency
AU - Gregory, Melissa
AU - Lester, Sue
AU - Cook-Johnson, Rebecca
AU - Gibson, Robert
AU - Proudman, S
AU - Cleland, Leslie
AU - James, Michael
PY - 2011/11
Y1 - 2011/11
N2 - 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.
AB - 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.
KW - Δ6-desaturase
KW - FADS2 promoter
KW - polymorphism
KW - polyunsaturated fatty acids
UR - http://www.scopus.com/inward/record.url?scp=80054794425&partnerID=8YFLogxK
U2 - 10.1038/ejhg.2011.104
DO - 10.1038/ejhg.2011.104
M3 - Article
SN - 1018-4813
VL - 19
SP - 1202
EP - 1204
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
IS - 11
ER -