Wellcome Trust Centre for Mitochondrial Research, Institute of Neuroscience (S.A.H., E.L.B., A.I.P., M.C.R., S.A., G.F., Y.S.N., D.M.T., G.S.G., R.W.T.), The Medical School, Institute of Genetic Medicine (R.H.), Newcastle University; Nuffield Department of Obstetrics and Gynaecology (J.P.), University of Oxford; Department of Neurology (M.R.R.), King's College Hospital NHS Foundation Trust, London; Departments of Neurology and Neuropathology (O.O., N.B.), Cork University Hospital, Ireland; and The Walton Centre for Neurology and Neurosurgery (C.F.D.), Liverpool, UK.
Neurol Genet. 2016 Jun 23;2(4):e82. doi: 10.1212/NXG.0000000000000082. eCollection 2016 Aug.
Pathogenic mitochondrial tRNA (mt-tRNA) gene mutations represent a prominent cause of primary mitochondrial DNA (mtDNA)-related disease despite accounting for only 5%-10% of the mitochondrial genome.(1,2) Although some common mt-tRNA mutations, such as the m.3243A>G mutation, exist, the majority are rare and have been reported in only a small number of cases.(3) The MT-TP gene, encoding mt-tRNA(Pro), is one of the less polymorphic mt-tRNA genes, and only 5 MT-TP mutations have been reported as a cause of mitochondrial muscle disease to date (table e-1 at Neurology.org/ng, P6-10). We report 5 patients with myopathic phenotypes, each harboring different pathogenic mutations in the MT-TP gene, highlighting the importance of MT-TP mutations as a cause of mitochondrial muscle disease and the requirement to study clinically relevant tissue.
致病性线粒体 tRNA(mt-tRNA)基因突变是原发性线粒体 DNA(mtDNA)相关疾病的一个主要原因,尽管它们仅占线粒体基因组的 5%-10%。(1,2)尽管存在一些常见的 mt-tRNA 突变,如 m.3243A>G 突变,但大多数是罕见的,仅在少数病例中报道过。(3)MT-TP 基因编码 mt-tRNA(Pro),是较少多态性的 mt-tRNA 基因之一,迄今为止,只有 5 种 MT-TP 突变被报道为线粒体肌肉疾病的病因(Neurology.org/ng 上的表 e-1,P6-10)。我们报告了 5 名具有肌病表型的患者,他们每个人的 MT-TP 基因中都存在不同的致病性突变,这突出了 MT-TP 突变作为线粒体肌肉疾病病因的重要性,以及研究临床相关组织的必要性。