Robinson P A, Leek J P, Thompson J, Carr I M, Bailey A, Moynihan T P, Coletta P L, Lench N J, Markham A F
Molecular Medicine Unit, St. James's University Hospital, University of Leeds, UK.
Mamm Genome. 1995 Oct;6(10):725-31. doi: 10.1007/BF00354295.
We have identified a novel ubiquitin conjugating enzyme gene, L-UBC, which maps to human Chromosome (Chr) 14q24.3. This is also the location of the major early onset familial Alzheimer's disease gene (FAD3). L-UBC encodes a protein that demonstrates homology to the yeast ubiquitin conjugating enzyme, UBC-4, and human UbcH5. Their functions are to ubiquitinate specific proteins targeted for degradation. The protein also exhibits very strong homology to a rabbit protein, E2-F1, which mediates p53 degradation driven by papilloma virus E6 protein in vitro. The accumulation of specific proteins that have undergone aberrant processing in neurofibrillary tangles and amyloid plaques is the classic pathological feature in brains of Alzheimer's disease patients. Abnormal ubiquitination has previously been suggested to play a role in the etiology of Alzheimer's disease. This gene therefore represents a plausible candidate gene for FAD3.
我们已经鉴定出一个新的泛素结合酶基因L-UBC,它定位于人类染色体(Chr)14q24.3。这也是主要的早发性家族性阿尔茨海默病基因(FAD3)的所在位置。L-UBC编码一种与酵母泛素结合酶UBC-4以及人类UbcH5具有同源性的蛋白质。它们的功能是将特定的蛋白质泛素化以便进行降解。该蛋白质还与一种兔蛋白E2-F1具有很强的同源性,E2-F1在体外介导乳头瘤病毒E6蛋白驱动的p53降解。在神经原纤维缠结和淀粉样斑块中经历异常加工的特定蛋白质的积累是阿尔茨海默病患者大脑中的经典病理特征。先前有人提出异常泛素化在阿尔茨海默病的病因学中起作用。因此,该基因是FAD3一个合理的候选基因。