Dolce V, Fiermonte G, Runswick M J, Palmieri F, Walker J E
Department of Pharmaco-Biology, Laboratory of Biochemistry and Molecular Biology, University of Bari, Via E. Orabona 4, 70125 Bari, Italy.
Proc Natl Acad Sci U S A. 2001 Feb 27;98(5):2284-8. doi: 10.1073/pnas.031430998. Epub 2001 Feb 20.
The synthesis of DNA in mitochondria requires the uptake of deoxynucleotides into the matrix of the organelle. We have characterized a human cDNA encoding a member of the family of mitochondrial carriers. The protein has been overexpressed in bacteria and reconstituted into phospholipid vesicles where it catalyzed the transport of all four deoxy (d) NDPs, and, less efficiently, the corresponding dNTPs, in exchange for dNDPs, ADP, or ATP. It did not transport dNMPs, NMPs, deoxynucleosides, nucleosides, purines, or pyrimidines. The physiological role of this deoxynucleotide carrier is probably to supply deoxynucleotides to the mitochondrial matrix for conversion to triphosphates and incorporation into mitochondrial DNA. The protein is expressed in all human tissues that were examined except for placenta, in accord with such a central role. The deoxynucleotide carrier also transports dideoxynucleotides efficiently. It is likely to be medically important by providing the means of uptake into mitochondria of nucleoside analogs, leading to the mitochondrial impairment that underlies the toxic side effects of such drugs in the treatment of viral illnesses, including AIDS, and in cancer therapy.
线粒体中DNA的合成需要脱氧核苷酸进入细胞器的基质。我们已鉴定出一个编码线粒体载体家族成员的人类cDNA。该蛋白已在细菌中过表达,并重组到磷脂囊泡中,在那里它催化所有四种脱氧(d)NDP的转运,以及效率较低的相应dNTP的转运,以交换dNDP、ADP或ATP。它不转运dNMP、NMP、脱氧核苷、核苷、嘌呤或嘧啶。这种脱氧核苷酸载体的生理作用可能是为线粒体基质提供脱氧核苷酸,以便转化为三磷酸形式并掺入线粒体DNA。除胎盘外,在所检测的所有人类组织中均表达该蛋白,这与它的核心作用相符。脱氧核苷酸载体也能有效转运双脱氧核苷酸。通过提供核苷类似物进入线粒体的途径,它可能在医学上具有重要意义,导致线粒体损伤,而这正是此类药物在治疗包括艾滋病在内的病毒性疾病以及癌症治疗中产生毒副作用的基础。