Seo Young Jun, Matsuda Shigeo, Romesberg Floyd E
Department of Chemistry, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
J Am Chem Soc. 2009 Apr 15;131(14):5046-7. doi: 10.1021/ja9006996.
Expansion of the genetic alphabet with a third base pair would have immediate biotechnology applications and also lay the foundation for a semisynthetic organism with an expanded genetic code. A variety of unnatural base pairs have been shown to be formed efficiently and selectively during DNA replication, and the pairs formed between the unnatural nucleotide d5SICS and either dMMO2 or dNaM are particularly interesting because they have been shown to be replicated with efficiencies and fidelities that are beginning to approach those of a natural base pair. Not only are these unnatural base pairs promising for different applications, but they also demonstrate that nucleobase shape and hydrophobicity are sufficient to control replication. While a variety of unnatural base pairs have been shown to be substrates for transcription, none are transcribed in both possible strand contexts, and the transcription of a fully hydrophobic base pair has not been demonstrated. We show here that both of the unnatural base pairs d5SICS:dMMO2 and d5SICS:dNaM are selectively transcribed by T7 RNA polymerase and that the efficiency of d5SICS:dNaM transcription in both possible strand contexts is only marginally reduced relative to that of a natural base pair. Thus, as with replication, we find that hydrogen-bonding is not essential for transcription and may be replaced with packing and hydrophobic forces. The results also demonstrate that d5SICS:dNaM is both replicated and transcribed with efficiencies and fidelities that should be sufficient for use as part of an in vitro expanded genetic alphabet.
用第三碱基对扩展遗传字母表将立即在生物技术中得到应用,也为具有扩展遗传密码的半合成生物体奠定基础。已证明多种非天然碱基对在DNA复制过程中能高效且选择性地形成,非天然核苷酸d5SICS与dMMO2或dNaM之间形成的碱基对尤其令人感兴趣,因为已证明它们在复制效率和保真度上开始接近天然碱基对。这些非天然碱基对不仅在不同应用中很有前景,还表明核碱基形状和疏水性足以控制复制。虽然已证明多种非天然碱基对是转录的底物,但没有一个能在两种可能的链环境中都被转录,且尚未证明完全疏水的碱基对能被转录。我们在此表明,非天然碱基对d5SICS:dMMO2和d5SICS:dNaM都能被T7 RNA聚合酶选择性转录,并且d5SICS:dNaM在两种可能的链环境中的转录效率相对于天然碱基对仅略有降低。因此,与复制一样,我们发现氢键对于转录并非必不可少,可能会被堆积和疏水作用力所取代。结果还表明,d5SICS:dNaM在复制和转录方面的效率和保真度足以用作体外扩展遗传字母表的一部分。