A network approach to micronutrient genetics: interactions with lipid metabolism

被引:12
|
作者
Lietz, Georg [2 ,3 ]
Hesketh, John [1 ,3 ]
机构
[1] Univ Newcastle, Inst Cell & Mol Biosci, Sch Med, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Newcastle, Sch Agr Food & Rural Dev, Newcastle Upon Tyne, Tyne & Wear, England
[3] Univ Newcastle, Human Nutr Res Ctr, Sch Med, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国生物技术与生命科学研究理事会;
关键词
carotenoids; folate; lipoprotein; selenium; single-nucleotide polymorphism; zinc; SINGLE-NUCLEOTIDE POLYMORPHISM; GPX1 PRO198LEU POLYMORPHISM; BREAST-CANCER RISK; B TYPE-I; BETA-CAROTENE; SELENOPROTEIN-P; CACO-2; CELLS; 3'-UNTRANSLATED REGION; ALCOHOL-CONSUMPTION; ENDOTHELIAL-CELLS;
D O I
10.1097/MOL.0b013e3283295ecf
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose of review Although interactions between fat soluble micronutrients and lipid metabolism in relation to absorption, status and body composition have been well described, there is new evidence to suggest that key genes have profound effects on how micronutrients and lipids are handled in a range of cells and organs. This review highlights the importance of genetic variation in folate, selenium, zinc and carotenoid metabolism and the recent findings of micro-macro nutrient interactions. Recent findings Although the methylenetetrahydrofolate reductase gene has been linked to CVD for some time, recent findings indicate that single-nucleotide polymorphisms (SNPs) in this gene are also linked to diabetes and may influence the pathogenesis of this disease through elevated alanine amino transferase concentrations. A recent selenium supplementation trial showed that SNPs can affect responses of GPx4, GPx1 and GPx3 protein expression or activity in response to Se supplementation or withdrawal. There is convincing evidence to Suggest that the high variability of plasma carotenoids seen in human populations is at least partly caused by multiple genetic variations in genes involved in lipoprotein metabolism and lipid transfer. The most striking evidence of an interaction between carotenoid and lipid metabolism, however, comes from the observation that BCMO1 ' mice develop liver steatosis independent of the vitamin A content of the diet, and the discovery of common SNPs in this gene indicates that this interaction might be of clinical significance. Summary Knowledge of genetic variants that affect micronutrient metabolism and responses to micronutrient supplementation were until recently largely limited to methylenetetrahydrofolate reductase. However, identification of novel functional SNPs in BCMO1, the critical enzyme of beta-carotene metabolism, and in several key selenoproteins indicates the potential importance of micronutrient-gene interactions.
引用
收藏
页码:112 / 120
页数:9
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