Tsukuda K, Suzuki Y, Kameoka K, Osawa N, Goto Y, Katagiri H, Asano T, Yazaki Y, Oka Y
Third Department of Internal Medicine, Faculty of Medicine, University of Tokyo, Japan.
Diabet Med. 1997 Dec;14(12):1032-7. doi: 10.1002/(SICI)1096-9136(199712)14:12<1032::AID-DIA504>3.0.CO;2-Y.
To investigate the prevalence and clinical characteristics of diabetes mellitus caused by mitochondrial gene mutations in the tRNA[Leu(UUR)] region, a known 'hot spot' for pathogenic mutations, we screened 440 diabetic patients with diabetic mothers for 11 mitochondrial gene mutations reported in mitochondrial neuromuscular disorders; nucleotide pairs (np) 3250, 3251, 3252, 3254, 3256, 3260, 3271, 3291, 3302 and 3303 in addition to an A to G transition at np 3243. The dot-blot hybridization method using 32P-labelled sequence-specific oligonucleotides as probes was used. One subject carrying a T to C transition at np 3271 and seven carrying the A to G transition at np 3243 were identified, while none of the other diabetic patients screened had these mutations in the tRNA[Leu(UUR)] region. The patient with the 3271 mutation, a 39-year-old male, had excellent glycaemic control with diet alone and had neither hearing impairment nor symptoms suggesting mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). Thus, among patients with maternally transmitted diabetes, the prevalence of the 3271 mutation was approximately one-seventh that of the 3243 mutation, and other mutations are even more rare in the mitochondrial tRNA[Leu(UUR)] region.
为了研究线粒体基因tRNA[Leu(UUR)]区域(已知的致病突变“热点”)突变导致的糖尿病的患病率和临床特征,我们对440名母亲患有糖尿病的糖尿病患者进行了筛查,检测线粒体神经肌肉疾病中报道的11种线粒体基因突变;除了第3243位核苷酸对(np)发生A到G的转变外,还检测了np3250、3251、3252、3254、3256、3260、3271、3291、3302和3303。使用以32P标记的序列特异性寡核苷酸为探针的斑点杂交法。我们鉴定出1名携带np3271处T到C转变的患者和7名携带np3243处A到G转变的患者,而其他接受筛查的糖尿病患者在tRNA[Leu(UUR)]区域均无这些突变。携带3271突变的患者为一名39岁男性,仅通过饮食就能很好地控制血糖,既没有听力障碍,也没有提示线粒体肌病、脑病、乳酸酸中毒和卒中样发作(MELAS)的症状。因此,在母系遗传的糖尿病患者中,3271突变的患病率约为3243突变患病率的七分之一,而其他突变在线粒体tRNA[Leu(UUR)]区域更为罕见。