A mechanistic view of human mitochondrial DNA polymerase γ: Providing insight into drug toxicity and mitochondrial disease

被引:17
作者
Bailey, Christopher M. [1 ]
Anderson, Karen S. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06520 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2010年 / 1804卷 / 05期
关键词
DNA polymerase gamma; Mitochondrial genome; Nucleoside analog toxicity; Progressive external ophthalmoplegia; Pre-steady-state kinetics; DEOXYRIBONUCLEIC-ACID POLYMERASE; TRANSFER-RNA SYNTHETASES; CHRONIC HEPATITIS-B; ACCESSORY SUBUNIT; REVERSE-TRANSCRIPTASE; MULTIPLE DELETIONS; NUCLEOSIDE ANALOG; ANTIRETROVIRAL THERAPY; CATALYTIC SUBUNIT; CRYSTAL-STRUCTURE;
D O I
10.1016/j.bbapap.2010.01.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial DNA polymerase gamma (Pol gamma) is the sole polymerase responsible for replication of the mitochondrial genome. The study of human Pol gamma is of key importance to clinically relevant issues such as nucleoside analog toxicity and mitochondrial disorders such as progressive external ophthalmoplegia. The development of a recombinant form of the human Pol gamma holoenzyme provided an essential tool in understanding the mechanism of these clinically relevant phenomena using kinetic methodologies. This review will provide a brief history on the discovery and characterization of human mitochondrial DNA polymerase gamma, focusing on kinetic analyses of the polymerase and mechanistic data illustrating structure-function relationships to explain drug toxicity and mitochondrial disease. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1213 / 1222
页数:10
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