Literature DB >> 21842904

Amplification, mutation, and sequencing of a six-letter synthetic genetic system.

Zunyi Yang1, Fei Chen, J Brian Alvarado, Steven A Benner.   

Abstract

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.

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Year:  2011        PMID: 21842904      PMCID: PMC3427765          DOI: 10.1021/ja204910n

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  26 in total

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8.  PCR with an expanded genetic alphabet.

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9.  PCR amplification of DNA containing non-standard base pairs by variants of reverse transcriptase from Human Immunodeficiency Virus-1.

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  68 in total

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Review 4.  In vitro selection using modified or unnatural nucleotides.

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6.  Synthetic biology: Six pack and stack.

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7.  Heat flux across an open pore enables the continuous replication and selection of oligonucleotides towards increasing length.

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Review 8.  Reprogramming the genetic code.

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9.  Structural insights into DNA replication without hydrogen bonds.

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Review 10.  Engineering reduced evolutionary potential for synthetic biology.

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