Owen F, Poulter M, Collinge J, Leach M, Shah T, Lofthouse R, Chen Y F, Crow T J, Harding A E, Hardy J
Division of Psychiatry, Clinical Research Centre, Harrow, Middlesex, United Kingdom.
Exp Neurol. 1991 May;112(2):240-2. doi: 10.1016/0014-4886(91)90075-n.
A number of mutations have been demonstrated in the open reading frame (ORF) of the prion protein (PrP) gene in patients with familial Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. On the basis of detecting an insertion in the ORF of the PrP gene in a patient originally suspected to be suffering from familial Alzheimer-type dementia, we screened 101 individuals with atypical dementias for the known PrP gene mutations. Insertions were found in five individuals, whereas none of the other reported mutations in the PrP gene was detected in the present study. One of the five insertions was larger than that described previously, suggesting that the individuals with these mutations are unlikely to be all lineally related and that insertions in the PrP gene may not be uncommon in prion diseases.
在患有家族性克雅氏病或格斯特曼-施特劳斯勒综合征的患者中,已在朊病毒蛋白(PrP)基因的开放阅读框(ORF)中证实了一些突变。基于在一名最初怀疑患有家族性阿尔茨海默病型痴呆的患者的PrP基因ORF中检测到一个插入片段,我们对101名非典型痴呆患者进行了已知PrP基因突变的筛查。在5名个体中发现了插入片段,而在本研究中未检测到PrP基因中其他已报道的突变。这5个插入片段中的一个比先前描述的更大,这表明具有这些突变的个体不太可能都有直系亲缘关系,并且PrP基因中的插入片段在朊病毒疾病中可能并不罕见。