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
Departments of Neurology, The Medical School, University of Newcastle upon Tyne, Newcastle upon Tyne, United Kingdom NE2 4HH.
Am J Hum Genet. 1999 May;64(5):1330-9. doi: 10.1086/302361.
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.
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。