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采用激光诱导荧光检测的毛细管电泳法分析聚合酶链反应产物及其在中链酰基辅酶A脱氢酶缺乏症诊断中的应用。

Analysis of polymerase chain reaction-product by capillary electrophoresis with laser-induced fluorescence detection and its application to the diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency.

作者信息

Arakawa H, Uetanaka K, Maeda M, Tsuji A, Matsubara Y, Narisawa K

机构信息

School of Pharmaceutical Sciences, Showa University, Tokyo, Japan.

出版信息

J Chromatogr A. 1994 Oct 7;680(2):517-23. doi: 10.1016/0021-9673(94)85151-4.

Abstract

Capillary gel electrophoresis with laser-induced fluorescence (CGE-LIF) has been developed to detect polymerase chain reaction (PCR) amplified samples. LIF detection was performed using Thiazole Orange as the fluorescent intercalating dye. This method was ca. 100x as sensitive as that with UV detection. The highly sensitive CGE-LIF was applied to the detection of the most prevalent mutation (lysine329-to-glutamic acid substitution) in medium-chain acyl-coenzyme A dehydrogenase (MCAD) deficiency. The disorder, which shows an autosomal recessive inheritance, is known to be highly prevalent among Caucasian population and often mimics as Reye-like syndrome or sudden infant death. A DNA fragment containing the mutation site was PCR-amplified with two sets of allele specific oligonucleotide primers, followed by CGE-LIF. The mutant allele produced a 175-base pairs DNA fragment, which the normal allele generated a 202-base pairs DNA fragment. CGE-LIF clearly distinguished these PCR products, facilitating rapid diagnosis of MCAD deficiency.

摘要

已开发出具有激光诱导荧光的毛细管凝胶电泳(CGE-LIF)用于检测聚合酶链反应(PCR)扩增的样本。使用噻唑橙作为荧光嵌入染料进行LIF检测。该方法的灵敏度约为紫外检测的100倍。高灵敏度的CGE-LIF被应用于检测中链酰基辅酶A脱氢酶(MCAD)缺乏症中最常见的突变(赖氨酸329突变为谷氨酸)。这种呈常染色体隐性遗传的疾病在白种人群中高度流行,常被误诊为瑞氏样综合征或婴儿猝死。用两组等位基因特异性寡核苷酸引物对包含突变位点的DNA片段进行PCR扩增,然后进行CGE-LIF分析。突变等位基因产生一个175个碱基对的DNA片段,而正常等位基因产生一个202个碱基对的DNA片段。CGE-LIF能清晰地区分这些PCR产物,有助于快速诊断MCAD缺乏症。

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