Foundation for Applied Molecular Evolution (FfAME), Gainesville, Florida 32601, United States.
J Am Chem Soc. 2011 Sep 28;133(38):15105-12. doi: 10.1021/ja204910n. Epub 2011 Sep 6.
The next goals in the development of a synthetic biology that uses artificial genetic systems will require chemistry-biology combinations that allow the amplification of DNA containing any number of sequential and nonsequential nonstandard nucleotides. This amplification must ensure that the nonstandard nucleotides are not unidirectionally lost during PCR amplification (unidirectional loss would cause the artificial system to revert to an all-natural genetic system). Further, technology is needed to sequence artificial genetic DNA molecules. The work reported here meets all three of these goals for a six-letter artificially expanded genetic information system (AEGIS) that comprises four standard nucleotides (G, A, C, and T) and two additional nonstandard nucleotides (Z and P). We report polymerases and PCR conditions that amplify a wide range of GACTZP DNA sequences having multiple consecutive unnatural synthetic genetic components with low (0.2% per theoretical cycle) levels of mutation. We demonstrate that residual mutation processes both introduce and remove unnatural nucleotides, allowing the artificial genetic system to evolve as such, rather than revert to a wholly natural system. We then show that mechanisms for these residual mutation processes can be exploited in a strategy to sequence "six-letter" GACTZP DNA. These are all not yet reported for any other synthetic genetic system.
下一阶段的人工基因系统合成生物学的发展目标,将需要化学-生物学组合,从而实现对包含任意数量顺序和非顺序非标准核苷酸的 DNA 的扩增。这种扩增必须确保非标准核苷酸在 PCR 扩增过程中不会单向丢失(单向丢失会导致人工系统恢复为全天然遗传系统)。此外,还需要对人工遗传 DNA 分子进行测序的技术。本研究报告满足了三个目标,建立了一个包含四个标准核苷酸(G、A、C 和 T)和两个额外非标准核苷酸(Z 和 P)的六字母人工扩展遗传信息系统(AEGIS)。我们报告了聚合酶和 PCR 条件,可扩增具有多种连续非天然合成遗传成分的广泛 GACTZP DNA 序列,其突变率低(每理论循环 0.2%)。我们证明了残留的突变过程既能引入也能去除非天然核苷酸,从而使人工遗传系统能够进化,而不是恢复为全天然系统。然后,我们展示了可以利用这些残留突变过程的机制,来对“六字母”GACTZP DNA 进行测序。这些在任何其他合成遗传系统中都尚未报道过。