Silver Matt J, Corbin Karen D, Hellenthal Garrett, da Costa Kerry-Ann, Dominguez-Salas Paula, Moore Sophie E, Owen Jennifer, Prentice Andrew M, Hennig Branwen J, Zeisel Steven H
*Medical Research Council International Nutrition Group, London School of Hygiene and Tropical Medicine, London, United Kingdom; Medical Research Council Unit, Banjul, The Gambia; Nutrition Research Institute, North Carolina Research Campus, Kannapolis, North Carolina, USA; Department of Nutrition, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA; University College London Genetics Institute, University College London, United Kingdom; Toxicology Services, Incorporated, Chapel Hill, North Carolina, USA; and Maternal and Child Nutrition Group, Medical Research Council Human Nutrition Research, Cambridge, United Kingdom.
*Medical Research Council International Nutrition Group, London School of Hygiene and Tropical Medicine, London, United Kingdom; Medical Research Council Unit, Banjul, The Gambia; Nutrition Research Institute, North Carolina Research Campus, Kannapolis, North Carolina, USA; Department of Nutrition, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA; University College London Genetics Institute, University College London, United Kingdom; Toxicology Services, Incorporated, Chapel Hill, North Carolina, USA; and Maternal and Child Nutrition Group, Medical Research Council Human Nutrition Research, Cambridge, United Kingdom
FASEB J. 2015 Aug;29(8):3426-35. doi: 10.1096/fj.15-271056. Epub 2015 Apr 28.
Choline is an essential nutrient, and the amount needed in the diet is modulated by several factors. Given geographical differences in dietary choline intake and disparate frequencies of single-nucleotide polymorphisms (SNPs) in choline metabolism genes between ethnic groups, we tested the hypothesis that 3 SNPs that increase dependence on dietary choline would be under negative selection pressure in settings where choline intake is low: choline dehydrogenase (CHDH) rs12676, methylenetetrahydrofolate reductase 1 (MTHFD1) rs2236225, and phosphatidylethanolamine-N-methyltransferase (PEMT) rs12325817. Evidence of negative selection was assessed in 2 populations: one in The Gambia, West Africa, where there is historic evidence of a choline-poor diet, and the other in the United States, with a comparatively choline-rich diet. We used 2 independent methods, and confirmation of our hypothesis was sought via a comparison with SNP data from the Maasai, an East African population with a genetic background similar to that of Gambians but with a traditional diet that is higher in choline. Our results show that frequencies of SNPs known to increase dependence on dietary choline are significantly reduced in the low-choline setting of The Gambia. Our findings suggest that adequate intake levels of choline may have to be reevaluated in different ethnic groups and highlight a possible approach for identifying novel functional SNPs under the influence of dietary selective pressure.
胆碱是一种必需营养素,饮食中所需的胆碱量受多种因素调节。鉴于不同地区饮食中胆碱摄入量存在差异,且不同种族之间胆碱代谢基因的单核苷酸多态性(SNP)频率也各不相同,我们检验了以下假设:在胆碱摄入量较低的环境中,3种会增加对膳食胆碱依赖性的SNP将受到负选择压力,这3种SNP分别是胆碱脱氢酶(CHDH)rs12676、亚甲基四氢叶酸还原酶1(MTHFD1)rs2236225和磷脂酰乙醇胺-N-甲基转移酶(PEMT)rs12325817。我们在两个人群中评估了负选择的证据:一个是西非冈比亚的人群,有历史证据表明该地区饮食中胆碱含量较低;另一个是美国人群,其饮食中胆碱含量相对较高。我们使用了两种独立的方法,并通过与来自马赛人的SNP数据进行比较来验证我们的假设,马赛人是东非人群,其遗传背景与冈比亚人相似,但传统饮食中的胆碱含量较高。我们的结果表明,在冈比亚胆碱摄入量较低的环境中,已知会增加对膳食胆碱依赖性的SNP频率显著降低。我们的研究结果表明,可能需要重新评估不同种族人群中胆碱的适当摄入量,并突出了一种在饮食选择压力影响下识别新型功能性SNP的可能方法。