Malfroy L, Viratelle C, Coppin H, Borot N, Roth M P
Institut Fédératif de Recherche INSERM/CNRS/UPS, CHU Purpan, Toulouse, France.
Hum Genet. 1995 Dec;96(6):737-8. doi: 10.1007/BF00210310.
Polymorphic (CTC)n and (TAAA)n sequences were identified in exons 1 and 8 of the myelin oligodendrocyte glycoprotein (MOG) gene. The different alleles were detected by a method combining fluorescence labeling of polymerase chain reaction (PCR) products and use of an automated DNA sequencer. Although only two alleles differing by the number of leucine residues encoded by the (CTC)n array were detected at the first locus, seven alleles were identified at the second. The high degree of polymorphism (75%) of the tetranucleotide repeat makes this marker informative for association or linkage studies with diseases such as hemochromatosis or multiple sclerosis.
在髓鞘少突胶质细胞糖蛋白(MOG)基因的外显子1和8中鉴定出多态性(CTC)n和(TAAA)n序列。通过一种将聚合酶链反应(PCR)产物的荧光标记与自动DNA测序仪的使用相结合的方法检测到不同的等位基因。尽管在第一个位点仅检测到由(CTC)n阵列编码的亮氨酸残基数量不同的两个等位基因,但在第二个位点鉴定出了七个等位基因。四核苷酸重复序列的高度多态性(75%)使得该标记对于与血色素沉着症或多发性硬化症等疾病的关联或连锁研究具有信息价值。