Published October 2010 | Version Accepted Version
Journal Article Open

Engineering the genomes of wild insect populations: Challenges, and opportunities provided by synthetic Medea selfish genetic elements

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon National Health Research Institutes
  • 3. ROR icon University of California, Los Angeles

Abstract

Advances in insect transgenesis and our knowledge of insect physiology and genomics are making it possible to create transgenic populations of beneficial or pest insects that express novel traits. There are contexts in which we may want the transgenes responsible for these traits to spread so that all individuals within a wild population carry them, a process known as population replacement. Transgenes of interest are unlikely to confer an overall fitness benefit on those who carry them. Therefore, an essential component of any population replacement strategy is the presence of a drive mechanism that will ensure the spread of linked transgenes. We discuss contexts in which population replacement might be desirable and the requirements a drive system must satisfy to be both effective and safe. We then describe the creation of synthetic Medea elements, the first selfish genetic elements synthesized de novo, with the capability of driving population replacement, in this case in Drosophila. The strategy used to create Drosophila Medea is applicable to a number of other insect species and the Medea system satisfies key requirements for scientific and social acceptance. Finally, we highlight several challenges to implementing population replacement in the wild.

Additional Information

© 2010 Elsevier Ltd. Received 17 February 2010; revised 26 May 2010; accepted 27 May 2010. Available online 9 June 2010. This work was supported by grants to BAH (DP1 OD003878) and MG (5K02AG031915-02; 5RO1AG033410-02; 5RO1NS048396-05) from the NIH, and to C-H. Chen from the Caltech Moore Foundation Center for Biological Circuit Design. We appreciate comments from several anonymous reviewers.

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Accepted Version - nihms-218145.pdf

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Additional details

Identifiers

PMCID
PMC3601555
Eprint ID
19632
DOI
10.1016/j.jinsphys.2010.05.022
Resolver ID
CaltechAUTHORS:20100824-112026353

Funding

NIH
DP1 OD003878
NIH
5K02AG031915-02
NIH
5RO1AG033410-02
NIH
5RO1NS048396-05
Gordon and Betty Moore Foundation

Dates

Created
2010-08-26
Created from EPrint's datestamp field
Updated
2021-11-08
Created from EPrint's last_modified field