Zinc Finger Recombinases with Adaptable DNA Sequence Specificity
2011

Zinc Finger Recombinases with Adaptable DNA Sequence Specificity

publication Evidence: moderate

Author Information

Author(s): Chris Proudfoot, Arlene L. McPherson, Andreas F. Kolb, W. Marshall Stark

Primary Institution: College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom

Hypothesis

Can engineered zinc finger recombinases (ZFRs) be designed to promote site-specific recombination at various natural DNA sequences?

Conclusion

Engineered ZFRs can efficiently mediate site-specific recombination at multiple sequences within a genomic locus of biotechnological interest.

Supporting Evidence

  • ZFRs can be designed to target many new sequences.
  • Pairs of evolved ZFRs with different DNA-binding specificities can cooperate to recombine asymmetric Z-sites.
  • ZFRs have the potential to be used for genomic surgery.

Takeaway

Scientists created special proteins that can cut and paste DNA at specific spots, which could help in genetic engineering and treating diseases.

Methodology

The study involved creating and testing engineered zinc finger recombinases for their ability to recombine specific DNA sequences in E. coli.

Limitations

The specificity of the recombinases may not be completely abolished, leading to potential off-target effects.

Digital Object Identifier (DOI)

10.1371/journal.pone.0019537

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