采用非同位素单链构象多态性分析法在遗传性多神经病病例中检测到新的突变基因(转甲状腺素蛋白精氨酸58)

New mutant gene (transthyretin Arg 58) in cases with hereditary polyneuropathy detected by non-isotope method of single-strand conformation polymorphism analysis.

作者信息

Saeki Y, Ueno S, Yorifuji S, Sugiyama Y, Ide Y, Matsuzawa Y

机构信息

Second Department of Internal Medicine, Osaka University Medical School, Japan.

出版信息

Biochem Biophys Res Commun. 1991 Oct 15;180(1):380-5. doi: 10.1016/s0006-291x(05)81304-x.

Abstract

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.

摘要

对患有腕管综合征的母子的转甲状腺素蛋白(TTR)基因进行单链构象多态性(SSCP)分析以检测突变。通过聚合酶链反应扩增包含TTR编码序列的DNA片段,热变性后在中性聚丙烯酰胺凝胶上进行电泳。凝胶中的单链DNA片段转移至尼龙膜,与生物素化的TTR cDNA探针杂交,随后进行化学发光DNA检测。在患者DNA的外显子3片段中发现了迁移率改变。外显子3的测序分析证实了T----G碱基变化,导致Leu 58----Arg替换。TTR Arg 58是通过SSCP分析检测到的首个突变TTR基因。通过本方法,今后在非放射性实验设施中能够快速灵敏地检测TTR基因不同位点的新突变。

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