Roses Allen D
Department of Neurobiology and Neurology and the Deane Drug Discovery Institute, Duke University, Durham, North Carolina 27708, USA.
Arch Neurol. 2010 May;67(5):536-41. doi: 10.1001/archneurol.2010.88.
I coauthored a recently published research article describing a variable length, poly-T polymorphism in the TOMM40 gene, adjacent to apolipoprotein E (APOE) on chromosome 19, that accounts for the age at onset distribution for a complex disease, late-onset Alzheimer disease. These new data explain the mean age at disease onset for patients with the APOE4/4 genotype and differentiate 2 forms of TOMM40 poly-T polymorphisms linked to APOE, with each form associated with a different age at disease onset distribution. When linked to APOE3 (encoding the epsilon3 isoform of APOE), the longer TOMM40 poly-T repeats (19-39 nucleotides) at the rs10524523 (hereafter, 523) locus are associated with earlier age at onset and the shorter TOMM40 523 alleles (11-16 nucleotides) are associated with later age at onset. The data suggest that the poly-T alleles are codominant, with the age at onset phenotype determined by the 2 inherited 523 alleles, but with variable expressivity. Additional data will further refine the relationship between the length of the poly-T alleles and age at disease onset and determine if the relationship is linear.
我与人共同撰写了一篇最近发表的研究文章,描述了位于19号染色体上载脂蛋白E(APOE)附近的TOMM40基因中的可变长度多聚T多态性,该多态性解释了一种复杂疾病——晚发性阿尔茨海默病的发病年龄分布情况。这些新数据解释了携带APOE4/4基因型患者的疾病平均发病年龄,并区分了与APOE相关的两种形式的TOMM40多聚T多态性,每种形式都与不同的疾病发病年龄分布相关。当与APOE3(编码APOE的ε3亚型)连锁时,rs10524523(以下简称523)位点处较长的TOMM40多聚T重复序列(19 - 39个核苷酸)与较早的发病年龄相关,而较短的TOMM40 523等位基因(11 - 16个核苷酸)与较晚的发病年龄相关。数据表明多聚T等位基因是共显性的,发病年龄表型由两个遗传的523等位基因决定,但具有可变的表达性。更多数据将进一步完善多聚T等位基因长度与疾病发病年龄之间的关系,并确定这种关系是否呈线性。