Laboratory of Medicinal Chemistry, Rega, Institute for Medical Research, KU Leuven, Minderbroedersstraat 10, 3000, Leuven, Belgium.
ISSB, Génopole, Genavenir 6, Equipe Xénome, 5 rue Henri Desbruères, 91030, Evry Cedex, France.
Angew Chem Int Ed Engl. 2016 Jun 20;55(26):7515-9. doi: 10.1002/anie.201601529. Epub 2016 May 9.
The ability of alternative nucleic acids, in which all four nucleobases are substituted, to replicate in vitro and to serve as genetic templates in vivo was evaluated. A nucleotide triphosphate set of 5-chloro-2'-deoxyuridine, 7-deaza-2'-deoxyadenosine, 5-fluoro-2'-deoxycytidine, and 7-deaza-2'deoxyguanosine successfully underwent polymerase chain reaction (PCR) amplification using templates of different lengths (57 or 525mer) and Taq or Vent (exo-) DNA polymerases as catalysts. Furthermore, a fully morphed gene encoding a dihydrofolate reductase was generated by PCR using these fully substituted nucleotides and was shown to transform and confer trimethoprim resistance to E. coli. These results demonstrated that fully modified templates were accurately read by the bacterial replication machinery and provide the first example of a long fully modified DNA molecule being functional in vivo.
我们评估了替代核酸(其中所有四个核碱基均被取代)在体外复制和在体内作为遗传模板的能力。使用 5-氯-2'-脱氧尿苷、7-脱氮-2'-脱氧腺苷、5-氟-2'-脱氧胞苷和 7-脱氮-2'-脱氧鸟苷的核苷酸三磷酸集成功地进行了聚合酶链反应(PCR)扩增,使用不同长度的模板(57 或 525mer)和 Taq 或 Vent(外切)DNA 聚合酶作为催化剂。此外,使用这些完全取代的核苷酸通过 PCR 生成了完全变形的编码二氢叶酸还原酶的基因,并显示出转化和赋予大肠杆菌对甲氧苄啶的抗性。这些结果表明,完全修饰的模板被细菌复制机制准确读取,并提供了第一个在体内具有功能的长完全修饰 DNA 分子的例子。