Lawless Matthew W, Mankan Arun K, Norris Suzanne
Hepatology Research Division, Department of Clinical Medicine, Institute of Molecular Medicine, Trinity College Dublin, St James Hospital, Dublin 8, Ireland.
Med Hypotheses. 2008;70(4):783-4. doi: 10.1016/j.mehy.2007.07.041. Epub 2007 Sep 29.
Hereditary hemochromatosis (HH) is a genetic disease associated with iron overload, in which individuals homozygous for the mutant C282Y HFE associated allele are at risk of developing liver disease, diabetes and arthritis. Conformational diseases are a class of disorders associated with the expression of misfolded protein and examples include conditions such as Alzheimer's, Parkinson's, Z alpha 1-antitrypsin deficiency and Huntington's diseases. HFE C282Y is a mutant protein that does not fold correctly forming aggregates and is retained in the Endoplasmic Reticulum (ER). Consequently, we propose that HH associated with the C282Y HFE mutation should be considered a conformational disorder.
遗传性血色素沉着症(HH)是一种与铁过载相关的遗传疾病,其中,与突变的C282Y HFE相关等位基因纯合的个体有患肝病、糖尿病和关节炎的风险。构象病是一类与错误折叠蛋白表达相关的疾病,例如阿尔茨海默病、帕金森病、Zα1抗胰蛋白酶缺乏症和亨廷顿病等病症。HFE C282Y是一种不能正确折叠而形成聚集体并滞留在内质网(ER)中的突变蛋白。因此,我们认为与C282Y HFE突变相关的HH应被视为一种构象病。