An unnatural hydrophobic base pair system: site-specific incorporation of nucleotide analogs into DNA and RNA

被引:186
|
作者
Hirao, Ichiro
Kimoto, Michiko
Mitsui, Tsuneo
Fujiwara, Tsuyoshi
Kawai, Rie
Sato, Akira
Harada, Yoko
Yokoyama, Shigeyuki
机构
[1] RIKEN, Genom Sci Ctr, Prot Res Grp, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
[3] Univ Tokyo, Grad Sch Sci, Dept Biophys & Biochem, Bunkyo Ku, Tokyo 1130033, Japan
[4] RIKEN Harima Inst Spring 8, Sayo, Hyogo 6795148, Japan
关键词
D O I
10.1038/nmeth915
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Methods for the site-specific incorporation of extra components into nucleic acids can be powerful tools for creating DNA and RNA molecules with increased functionality. We present an unnatural base pair system in which DNA containing an unnatural base pair can be amplified and function as a template for the site-specific incorporation of base analog substrates into RNA via transcription. The unnatural base pair is formed by specific hydrophobic shape complementation between the bases, but lacks hydrogen bonding interactions. In replication, this unnatural base pair exhibits high selectivity in combination with the usual triphosphates and modified triphosphates, gamma-amidotriphosphates, as substrates of 3' to 5' exonuclease-proficient DNA polymerases, allowing PCR amplification. In transcription, the unnatural base pair complementarity mediates the incorporation of these base substrates and their analogs, such as a biotinylated substrate, into RNA by T7 RNA polymerase (RNAP). With this system, functional components can be site-specifically incorporated into a large RNA molecule.
引用
收藏
页码:729 / 735
页数:7
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