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采用RNA-SSCP分析对遗传缺陷进行分子筛查:苯丙酮尿症和胱氨酸尿症模型

Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria model.

作者信息

Giannattasio S, Bisceglia L, Lattanzio P, Grifa A, Dianzani I, Gasparini P, Marra E

机构信息

CNR, Centro di Studio sui Mitocondri e Metabolismo Energetico, Bari, Italy.

出版信息

Mol Cell Probes. 1995 Jun;9(3):201-5. doi: 10.1006/mcpr.1995.0032.

Abstract

RNA single-strand conformation polymorphism (rSSCP) is a recently developed method for detecting genetic defects. This technique requires DNA amplification with a polymerase chain reaction making use of one T7 promoter-containing primer. Amplification products are subsequently transcribed in vitro and the labelled transcripts are analysed for single-strand conformation changes. rSSCP has been applied to mutation screening of the phenylalanine hydroxylase gene and rBAT cDNA, from PKU and cystinuric patients, respectively. Experimental evidence shows that 83% and 86% of screened PKU and cystinuric mutations, respectively, give rise to detectable rSSCP signals. Thus, results obtained show that RNA single-strand conformation polymorphism analysis is generally applicable and is a suitable technique for detecting genetic disease causing mutations, both in basic research and in clinical practice.

摘要

RNA单链构象多态性(rSSCP)是一种最近开发的用于检测基因缺陷的方法。该技术需要利用一个含T7启动子的引物通过聚合酶链反应进行DNA扩增。随后对扩增产物进行体外转录,并分析标记的转录本的单链构象变化。rSSCP已分别应用于苯丙酮尿症(PKU)患者的苯丙氨酸羟化酶基因和胱氨酸尿症患者的rBAT cDNA的突变筛查。实验证据表明,分别有83%和86%的筛查出的PKU和胱氨酸尿症突变会产生可检测到的rSSCP信号。因此,所获得的结果表明,RNA单链构象多态性分析普遍适用,并且是一种在基础研究和临床实践中检测导致基因突变的遗传疾病的合适技术。

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