Loeffen J, Elpeleg O, Smeitink J, Smeets R, Stöckler-Ipsiroglu S, Mandel H, Sengers R, Trijbels F, van den Heuvel L
Nijmegen Center for Mitochondrial Disorders, Department of Pediatrics, The Netherlands.
Ann Neurol. 2001 Feb;49(2):195-201. doi: 10.1002/1531-8249(20010201)49:2<195::aid-ana39>3.0.co;2-m.
Human complex I is built up and regulated by genes encoded by the mitochondrial DNA (mtDNA) as well as the nuclear DNA (nDNA). In recent years, attention mainly focused on the relation between complex I deficiency and mtDNA mutations. However, a high percentage of consanguinity and an autosomal-recessive mode of inheritance observed within our patient group as well as the absence of common mtDNA mutations make a nuclear genetic cause likely. The NDUFS2 protein is part of complex I of many pro- and eukaryotes. The nuclear gene coding for this protein is therefore an important candidate for mutational detection studies in enzymatic complex I deficient patients. Screening of patient NDUFS2 cDNA by reverse transcriptase-polymerase chain reaction (RT-PCR) in combination with direct DNA sequencing revealed three missense mutations resulting in the substitution of conserved amino acids in three families.
人类复合体I由线粒体DNA(mtDNA)和核DNA(nDNA)编码的基因构建并调控。近年来,注意力主要集中在复合体I缺陷与mtDNA突变之间的关系上。然而,在我们的患者群体中观察到的高近亲结婚率和常染色体隐性遗传模式,以及常见mtDNA突变的缺失,使得核基因病因很有可能。NDUFS2蛋白是许多原核生物和真核生物复合体I的一部分。因此,编码该蛋白的核基因是酶复合体I缺陷患者突变检测研究的重要候选基因。通过逆转录聚合酶链反应(RT-PCR)结合直接DNA测序对患者的NDUFS2 cDNA进行筛查,在三个家族中发现了三个错义突变,导致保守氨基酸的替换。