移码突变
外显子
突变
遗传学
基因
终止密码子
表型
生物
分子生物学
作者
Delphine Borgel,Sophie Gandrille,M Gouault-Heilmann,M Aïach
出处
期刊:PubMed
日期:1994-08-01
卷期号:5 (4): 593-600
被引量:11
摘要
The authors used a strategy combining the amplification-refractory mutations system (ARMS) and denaturing gradient gel electrophoresis (DGGE) to screen the active protein S (PS) gene in a family with PS deficiency, and found a frameshift mutation in exon V. The protein, if expressed, would have an aberrant amino acid sequence from positions 82 to 90 and a premature stop codon in position 91. The mutation co-segregated with the deficient phenotype and was not found in 120 normal chromosomes. It is proposed that the deletion of a T in the codon corresponding to Pro 82 described here is responsible for the deficient phenotype.
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