Dresden University of Technology, Department of Child and Adolescent Psychiatry, Translational Developmental Neuroscience Section, Dresden, Germany.
Can J Psychiatry. 2012 Mar;57(3):168-76. doi: 10.1177/070674371205700306.
Our pilot study evaluates the impact of environmental factors, such as nutrition and smoking status, on epigenetic patterns in a disease-associated gene.
We measured the effects of malnutrition and cigarette smoking on proopiomelanocortin (POMC) promoter-specific DNA methylation in female patients with and without anorexia nervosa (AN). POMC and its derived peptides (alpha melanocyte stimulating hormone and adrenocorticotropic hormone) are implicated in stress and feeding response. Promoter-specific DNA methylation of the POMC gene was determined in peripheral blood mononuclear cells of 54 healthy female control subjects, 40 underweight patients with AN, and 21 weight-restored patients with AN using bisulfite sequencing. Malnutrition was characterized by plasma leptin.
POMC promoter-specific DNA methylation was not affected by diagnosis or nutritional status but significantly negatively associated with cigarette smoking.
Although malnutrition may be expected to reduce DNA methylation through its effects on one-carbon metabolism, our negative results are in line with several in vitro and clinical studies that did not show a direct relation between gene-specific DNA methylation and folate levels. In contrast, smoking has been repeatedly reported to alter DNA methylation of specific genes and should be controlled for in future epigenetic studies.
我们的初步研究评估了营养和吸烟状况等环境因素对疾病相关基因中表观遗传模式的影响。
我们测量了营养不良和吸烟对厌食症(AN)女性患者和非 AN 女性患者的 POMC 启动子特异性 DNA 甲基化的影响。POMC 及其衍生肽(α-黑色素细胞刺激素和促肾上腺皮质激素)参与应激和摄食反应。采用亚硫酸氢盐测序法,在 54 名健康女性对照者、40 名消瘦型 AN 患者和 21 名体重恢复型 AN 患者的外周血单核细胞中测定 POMC 基因启动子特异性 DNA 甲基化。营养不良的特征是血浆瘦素。
POMC 启动子特异性 DNA 甲基化不受诊断或营养状况的影响,但与吸烟显著负相关。
尽管营养不良可能通过其对一碳代谢的影响降低 DNA 甲基化,但我们的阴性结果与几项体外和临床研究一致,这些研究并未显示基因特异性 DNA 甲基化与叶酸水平之间存在直接关系。相比之下,吸烟已被反复报道会改变特定基因的 DNA 甲基化,在未来的表观遗传学研究中应加以控制。