Foury F
Laboratoire d'Enzymologie, Université de Louvain, Belgium.
J Biol Chem. 1989 Dec 5;264(34):20552-60.
The nuclear gene MIP1 is strictly required for mitochondrial DNA replication and mitochondrial DNA polymerase activity (Genga, A., Bianchi, L., and Foury, F. (1986) J. Biol. Chem. 261, 9328-9332). The MIP1 gene was cloned by genetic complementation of the mip1-1 allele after cell transformation with a yeast genomic library and was mapped to the right arm of chromosome XV about 20 centimorgans distal to the cpa1 gene by Southern blot hybridization and tetrad analysis. The mapping of the 5' ends of the MIP1 transcript and the nucleotide sequence analysis of a 4.7-kilobase DNA fragment complementing the mip1-1 allele allowed the determination of an open reading frame of 3762 nucleotides encoding a basic protein of 143.5 kDa. The following data show that the MIP1 gene encodes the catalytic subunit of the replicative mitochondrial DNA polymerase. 1) The mutant ts71 exhibits both a thermosensitive mitochondrial DNA replication in vivo and a thermosensitive mitochondrial DNA polymerase activity is observed, when compared to that of the wild type strain. 3) Chromosomal disruption of the MIP1 gene by an 80% deletion of the gene and its replacement by URA3 gene is not lethal to the cell but elicits total loss of mitochondrial DNA and mitochondrial DNA polymerase activity. 4) The MIP1 protein exhibits sequence similarities with both eukaryotic nuclear DNA polymerases and reverse transcriptases. There is no significant resemblance with prokaryotic DNA polymerases.
核基因MIP1对于线粒体DNA复制和线粒体DNA聚合酶活性是严格必需的(根加,A.,比安基,L.,和富里,F.(1986年)《生物化学杂志》261,9328 - 9332)。在用酵母基因组文库对细胞进行转化后,通过mip1 - 1等位基因的遗传互补克隆了MIP1基因,并通过Southern印迹杂交和四分体分析将其定位到第十五号染色体右臂上,位于cpa1基因远端约20厘摩处。对MIP1转录本5′端的定位以及对与mip1 - 1等位基因互补的4.7千碱基DNA片段的核苷酸序列分析,使得能够确定一个3762个核苷酸的开放阅读框,其编码一个143.5 kDa的碱性蛋白。以下数据表明MIP1基因编码复制性线粒体DNA聚合酶的催化亚基。1)与野生型菌株相比,突变体ts71在体内表现出温度敏感的线粒体DNA复制,并且观察到温度敏感的线粒体DNA聚合酶活性。3)通过对MIP1基因进行80%的缺失并将其替换为URA3基因来对该基因进行染色体破坏,对细胞并非致死,但会导致线粒体DNA和线粒体DNA聚合酶活性完全丧失。4)MIP1蛋白与真核细胞核DNA聚合酶和逆转录酶都表现出序列相似性。与原核DNA聚合酶没有显著相似性。