Related Experiment Video
Updated: May 27, 2026

10:36
Rare Event Detection Using Error-corrected DNA and RNA Sequencing
Published on: August 3, 2018
Error correction of microchip synthesized genes using Surveyor nuclease
Ishtiaq Saaem1, Siying Ma, Jiayuan Quan
1Department of Biomedical Engineering, Duke University, Durham, NC27708, USA.
Nucleic Acids Research
|December 1, 2011
Summary
This study introduces an error correction reaction (ECR) to improve synthetic gene accuracy. The ECR method significantly reduces errors in synthesized genes, making gene synthesis more reliable and cost-effective.
Area of Science:
- Molecular Biology
- Synthetic Biology
- Biotechnology
Background:
- High-throughput gene synthesis is crucial for biotechnology but limited by errors.
- Current error correction methods are costly and time-consuming.
Purpose of the Study:
- To develop an efficient and economical method for correcting errors in synthetic genes.
- To enhance the fidelity of gene synthesis technologies.
Main Methods:
- An error correction reaction (ECR) utilizing Surveyor endonuclease was developed.
- ECR involves re-annealing synthetic genes to reveal mismatches, followed by enzymatic excision of errors.
- Overlap extension polymerase chain reaction (OE-PCR) was used to reassemble corrected gene fragments.
Main Results:
- The ECR method effectively removes errors from synthetic genes.
- Iterating the ECR process increased gene synthesis fidelity.
- Two iterations of ECR reduced errors by over 16-fold, achieving an error rate of approximately 1 in 8700 base pairs.
Conclusions:
- ECR is a highly effective strategy for improving the accuracy of synthetic genes.
- This method offers a cost-effective and high-throughput solution for gene synthesis error correction.
- ECR has the potential to significantly advance synthetic biology applications.
Related Concept Videos
Mismatch Repair
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
Mismatch Repair
Overview
Gene Conversion
Other than maintaining genome stability via DNA repair, homologous recombination plays an important role in diversifying the genome. In fact, the recombination of sequences forms the molecular basis of genomic evolution. Random and non-random permutations of genomic sequences create a library of new amalgamated sequences. These newly formed genomes can determine the fitness and survival of cells. In bacteria, homologous and non-homologous types of recombination lead to the evolution of new...
Genome Copying Errors
DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their survival. Therefore, the copying errors are checked and repaired at three levels.
Base Excision Repair
One of the common DNA damages is the chemical alteration of single bases by alkylation, oxidation, or deamination. The altered bases cause mispairing and strand breakage during replication. This type of damage causes minimal change to the DNA double helix structure and can be repaired by the base excision repair (BER) pathways. BER corrects damaged DNA sequences by removing the damaged base and restoring the original base sequence using the complementary strand as a template.
The first step of...
The first step of...
Nucleotide Excision Repair
Overview

