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Error correction of microchip synthesized genes using Surveyor nuclease
Author(s) -
Ishtiaq Saaem,
Siying Ma,
Jiayuan Quan,
Jingdong Tian
Publication year - 2011
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkr887
Subject(s) - biology , exonuclease , polymerase chain reaction , endonuclease , nuclease , gene , computational biology , exonuclease iii , dna , genetics , microbiology and biotechnology , polymerase , escherichia coli
The development of economical and high-throughput gene synthesis technology has been hampered by the high occurrence of errors in the synthesized products, which requires expensive labor and time to correct. Here, we describe an error correction reaction (ECR), which employs Surveyor, a mismatch-specific DNA endonuclease, to remove errors from synthetic genes. In ECR reactions, errors are revealed as mismatches by re-annealing of the synthetic gene products. Mismatches are recognized and excised by a combination of mismatch-specific endonuclease and 3'→5' exonuclease activities in the reaction mixture. Finally, overlap extension polymerase chain reaction (OE-PCR) re-assembles the resulting fragments into intact genes. The process can be iterated for increased fidelity. With two iterations, we were able to reduce errors in synthetic genes by >16-fold, yielding a final error rate of ∼1 in 8700  bp.

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