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Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361.
2
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本文引用的文献

1
RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS.肌肉组织的快速检查。一种用于新鲜冷冻活检切片的改良三色染色法。
Neurology. 1963 Nov;13:919-23. doi: 10.1212/wnl.13.11.919.
2
Clinical features, investigation, and management of patients with defects of mitochondrial DNA.线粒体DNA缺陷患者的临床特征、检查及管理
J Neurol Neurosurg Psychiatry. 1997 Nov;63(5):559-63. doi: 10.1136/jnnp.63.5.559.
3
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome.一种与成人起病的 Leigh 综合征相关的线粒体 DNA 苏氨酸转运 RNA(Val)点突变。
Neurology. 1997 Aug;49(2):589-92. doi: 10.1212/wnl.49.2.589.
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Mitochondrial DNA mutations and pathogenesis.线粒体DNA突变与发病机制。
J Bioenerg Biomembr. 1997 Apr;29(2):131-49. doi: 10.1023/a:1022685929755.
5
Reversal of a mitochondrial DNA defect in human skeletal muscle.
Nat Genet. 1997 Jul;16(3):222-4. doi: 10.1038/ng0797-222.
6
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.单倍型和系统发育分析表明,一种欧洲特有的线粒体DNA背景通过增加原发性突变11778和14484的外显率,在Leber遗传性视神经病变的表达中发挥作用。
Am J Hum Genet. 1997 May;60(5):1107-21.
7
In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells.野生型及携带线粒体DNA突变的人类细胞中细胞色素c氧化酶对呼吸作用的体内调控
Proc Natl Acad Sci U S A. 1997 Feb 18;94(4):1166-71. doi: 10.1073/pnas.94.4.1166.
8
A new mtDNA mutation showing accumulation with time and restriction to skeletal muscle.一种新的线粒体DNA突变,其表现为随时间积累且局限于骨骼肌。
Am J Hum Genet. 1997 Feb;60(2):373-80.
9
Classification of European mtDNAs from an analysis of three European populations.通过对三个欧洲人群的分析对欧洲线粒体DNA进行分类。
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In vivo labeling and analysis of human mitochondrial translation products.人线粒体翻译产物的体内标记与分析
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细胞色素C氧化酶亚基II基因起始密码子中的线粒体DNA突变导致该蛋白水平降低,并引发线粒体脑肌病。

An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.

作者信息

Clark K M, Taylor R W, Johnson M A, Chinnery P F, Chrzanowska-Lightowlers Z M, Andrews R M, Nelson I P, Wood N W, Lamont P J, Hanna M G, Lightowlers R N, Turnbull D M

机构信息

Departments of Neurology, The Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne, United Kingdom NE2 4HH.

出版信息

Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361.

DOI:10.1086/302361
PMID:10205264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1377869/
Abstract

A novel heteroplasmic 7587T-->C mutation in the mitochondrial genome which changes the initiation codon of the gene encoding cytochrome c oxidase subunit II (COX II), was found in a family with mitochondrial disease. This T-->C transition is predicted to change the initiating methionine to threonine. The mutation load was present at 67% in muscle from the index case and at 91% in muscle from the patient's clinically affected son. Muscle biopsy samples revealed isolated COX deficiency and mitochondrial proliferation. Single-muscle-fiber analysis revealed that the 7587C copy was at much higher load in COX-negative fibers than in COX-positive fibers. After microphotometric enzyme analysis, the mutation was shown to cause a decrease in COX activity when the mutant load was >55%-65%. In fibroblasts from one family member, which contained >95% mutated mtDNA, there was no detectable synthesis or any steady-state level of COX II. This new mutation constitutes a new mechanism by which mtDNA mutations can cause disease-defective initiation of translation.

摘要

在一个患有线粒体疾病的家族中,发现线粒体基因组中存在一种新的异质性7587T→C突变,该突变改变了编码细胞色素c氧化酶亚基II(COX II)的基因的起始密码子。这种T→C转换预计会将起始甲硫氨酸变为苏氨酸。先证者肌肉中的突变负荷为67%,其临床受累儿子肌肉中的突变负荷为91%。肌肉活检样本显示孤立性COX缺乏和线粒体增殖。单肌纤维分析显示,7587C拷贝在COX阴性纤维中的负荷远高于COX阳性纤维。经过显微光度酶分析,当突变负荷>55%-65%时,该突变显示会导致COX活性降低。在一名家庭成员的成纤维细胞中,其突变型mtDNA含量>95%,未检测到COX II的合成或任何稳态水平。这种新突变构成了mtDNA突变导致疾病——翻译起始缺陷的一种新机制。