Molecular breeding of polymerases for amplification of ancient DNA

被引:95
作者
d'Abbadie, Marc
Hofreiter, Michael
Vaisman, Alexandra
Loakes, David
Gasparutto, Didier
Cadet, Jean
Woodgate, Roger
Paeaebo, Svante
Holliger, Philipp
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[2] Max Planck Inst Mol Anthropol, Dept Evolutionary Genet, D-04103 Leipzig, Germany
[3] NICHHD, NIH, Sect DNA Replicat Repair & Mutagenesis, Bethesda, MD 20892 USA
[4] CEA Grenoble, Commiss Energia Atom, Dept Rech Fondamentale Mat Condensee, Lab Lesions Acides Nucl,SCIB UMR 3,CEA UJF, F-38054 Grenoble 9, France
基金
英国医学研究理事会;
关键词
D O I
10.1038/nbt1321
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In the absence of repair, lesions accumulate in DNA. Thus, DNA persisting in specimens of paleontological, archaeological or forensic interest is inevitably damaged(1). We describe a strategy for the recovery of genetic information from damaged DNA. By molecular breeding(2) of polymerase genes from the genus Thermus ( Taq ( Thermus aquaticus), Tth ( Thermus thermophilus) and Tfl ( Thermus flavus)) and compartmentalized self-replication(3,4) selection, we have evolved polymerases that can extend single, double and even quadruple mismatches, process non-canonical primer-template duplexes and bypass lesions found in ancient DNA, such as hydantoins and abasic sites. Applied to the PCR amplification of 47,000-60,000-year-old cave bear DNA, these outperformed Taq DNA polymerase by up to 150% and yielded amplification products at sample dilutions at which Taq did not. Our results demonstrate that engineered polymerases can expand the recovery of genetic information from Pleistocene specimens and may benefit genetic analysis in paleontology, archeology and forensic medicine.
引用
收藏
页码:939 / 943
页数:5
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