Dikshit M, Agarwal R
Division of Biochemistry, Department of Chemistry, University of Pune, Pune 411 007, India.
J Genet. 2001 Aug;80(2):111-6. doi: 10.1007/BF02728336.
More than 100 mutations have been reported till date in the rhodopsin gene in patients with retinitis pigmentosa. The present study was undertaken to detect the reported rhodopsin gene point mutations in Indian retinitis pigmentosa patients. We looked for presence or absence of codon 345 and 347 mutations in exon 5 of the gene using the technique of allele-specific polymerase chain reaction by designing primers for each mutation. We have examined 100 patients from 76 families irrespective of genetic categories. Surprisingly, in our sample the very widely reported highly frequent mutations of codon 347 (P --> S/A/R/Q/L/T) were absent while the codon 345 mutation V --> M was seen in three cases in one family (autosomal dominant form) and in one sporadic case (total two families). This is the first report on codon 345 and 347 mutation in Indian retinitis pigmentosa subjects.
迄今为止,已报道超过100种视紫红质基因突变与色素性视网膜炎患者有关。本研究旨在检测印度色素性视网膜炎患者中已报道的视紫红质基因点突变。我们通过为每个突变设计引物,利用等位基因特异性聚合酶链反应技术,检测该基因第5外显子中密码子345和347突变的有无。我们检查了来自76个家庭的100名患者,不论其遗传类型。令人惊讶的是,在我们的样本中,广为报道的高频密码子347突变(P→S/A/R/Q/L/T)并不存在,而密码子345突变V→M在一个家庭(常染色体显性遗传型)的3例患者以及1例散发病例(共两个家庭)中被发现。这是关于印度色素性视网膜炎患者密码子345和347突变的首次报道。