Nuclear genes and mitochondrial translation: a new class of genetic disease

被引:95
作者
Jacobs, HT [1 ]
Turnbull, DM
机构
[1] Univ Tampere, Inst Med Technol, FI-33014 Tampere, Finland
[2] Tampere Univ Hosp, FI-33014 Tampere, Finland
[3] Univ Glasgow, Inst Biomed & Life Sci, Glasgow G12 8QQ, Lanark, Scotland
[4] Univ Newcastle Upon Tyne, Sch Med, Dept Neurol, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国惠康基金;
关键词
D O I
10.1016/j.tig.2005.04.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mitochondria contain a separate protein-synthesis machinery to produce the polypeptides encoded in mitochondrial DNA (mtDNA), and many mtDNA disease mutations affect this machinery. In humans, the mitochondrial rRNAs and tRNAs are encoded by mtDNA, whereas all proteins involved in mitochondrial translation are encoded by nuclear genes. Recently, several articles have discussed the identification of pathological mutations in nuclear genes encoding components of this protein-synthesis machinery, suggesting that these types of mutation are a frequent cause of human genetic diseases.
引用
收藏
页码:312 / 314
页数:3
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