Biomedicum Helsinki, Research Programme of Molecular Neurology, University of Helsinki, Finland.
Methods. 2010 Aug;51(4):405-10. doi: 10.1016/j.ymeth.2010.03.009. Epub 2010 Apr 10.
Defective mitochondrial DNA (mtDNA) replication is a common cause of human disease in children and adults. mtDNA replication relies on a large set of nuclear-encoded proteins that either belong to the replication machinery itself, or participate in the nucleotide pool regulation. Identification of patient mutations in the corresponding genes has revealed that dysfunctional mtDNA replication can cause highly variable disease phenotypes. We describe here the strategies that have been undertaken to generate mouse models for mtDNA replication diseases. Such models are essential tools for understanding the consequences of mtDNA replication defects on different tissues and on the metabolism of the whole organism.
线粒体 DNA(mtDNA)复制缺陷是儿童和成人多种疾病的常见原因。mtDNA 复制依赖于一整套核编码蛋白,这些蛋白要么属于复制机制本身,要么参与核苷酸池的调节。在相应基因中鉴定出患者突变表明,mtDNA 复制功能障碍可导致高度可变的疾病表型。本文描述了用于 mtDNA 复制疾病的小鼠模型的生成策略。这些模型是理解 mtDNA 复制缺陷对不同组织和整个生物体代谢影响的重要工具。