NEW MUTANT-GENE (TRANSTHYRETIN ARG-58) IN CASES WITH HEREDITARY POLYNEUROPATHY DETECTED BY NONISOTOPE METHOD OF SINGLE-STRAND CONFORMATION POLYMORPHISM ANALYSIS

被引:46
作者
SAEKI, Y
UENO, S
YORIFUJI, S
SUGIYAMA, Y
IDE, Y
MATSUZAWA, Y
机构
[1] OSAKA UNIV,SCH MED,DEPT NEUROL,FUKUSHIMA KU,OSAKA 553,JAPAN
[2] KANAZAWA CITY HOSP,KANAZAWA 921,JAPAN
[3] KANAZAWA UNIV,SCH MED,DEPT NEUROL,KANAZAWA,ISHIKAWA 920,JAPAN
关键词
D O I
10.1016/S0006-291X(05)81304-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Single-strand conformation polymorphism (SSCP) was analyzed to detect a mutation in the transthyretin (TTR) gene from the mother and son showing polyneuropathy with carpal tunnel syndrome. DNA segments containing TTR coding sequence were amplified by polymerase chain reaction, heat denatured and electrophoresed on a neutral polyacrylamide gel. The single-stranded DNA fragments in the gel were transferred to a nylon membrane and hybridized with biotinylated TTR cDNA probe, followed with chemiluminescent DNA detection. The mobility shift was found in the fragments of exon 3 from the patients' DNA. Sequencing analyses of the exon 3 confirmed a T → G base change, resulting in a Leu 58 → Arg substitution. TTR Arg 58 is the first mutant TTR gene that has been detected by SSCP analysis. The rapid and sensitive detection of new mutations at various sites on the TTR gene is hereafter possible by the present method in the facilities for non-radioactive experiments. © 1991 Academic Press, Inc.
引用
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页码:380 / 385
页数:6
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