Transposons are used as robust, precise genetic tools in a range of model and nonmodelorganisms in which, through techniques such as gene tagging and trapping andenhancer trapping, they have enabled the identification of genes based on their function.This technology has complimented whole genome projects and accelerated genediscovery. In many organisms, transposons have a clear applied function in enablinggenetic transformation to occur and high frequency transformation is now standard in them. In medicine, transposons are now sought as human gene therapy vectors. In mosquitoes however, complete transposon-based genetic technology is yet to be fully established. Transposons from three separate families are used to generate transformants at low frequencies, however none can be remobilized at any reasonablefrequency in the germ-line and the widely used piggyBac transposon becomes dormant even in the soma. As a result the gene discovery technologies that abound in otherorganisms still lag far behind in mosquitoes, despite the availability of whole genomeprojects for these pests. This proposal seeks to develop transposons as truly robust genetic tools in Aedes aegypti through the understanding and circumvention of recentlydiscovered small RNA pathways (piRNA) that in other animals, regulate transpositionin both the germ-line and the soma. We present data demonstrating the presence ofthese pathways in wild-type and transgenic lines of Ae. aegypti. We describe experiments that will enable the comprehensive characterization of these pathways in Ae. aegypti. We will experimentally address their ability to silence newly introducedtransposons with respect to the timing of this immune response and to whetherendogenous mosquito transposon small RNAs with sequence homologies to these newtransposons can also trigger this response. We outline three strategies that we believe can circumvent the piRNA response of Ae. aegypti. The ability to use transposons aseffective genetic tools in mosquitoes will accelerate the pace of gene discovery and sodirectly increase the ability to identify and use mosquito genes in a wide range ofgenetic and chemical control strategies designed to reduce the spread of pathogens by these insect vectors.

Public Health Relevance

Mosquitoes transmit pathogens that exact a terrible disease burden throughout the world. Identifying and understanding the function of mosquito genes that are responsible for the pestiferous nature of mosquitoes has been the aim of mosquito genome projects however our inability to harness transposons as effective genetic tools in mosquitoes has limited our ability to identify genes based on function. We seek to develop transposons as robust and complete genetic tools in mosquitoes by understanding their regulation by the piRNA pathways and then by circumventing this system. The outcome will be a set of generic genetic tools that will enable the identification of the function of mosquito genes and so accelerate the generation of sustainable solutions for mosquito-borne disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56AI088852-01A1
Application #
8084387
Study Section
Special Emphasis Panel (ZRG1-IDM-A (02))
Program Officer
Costero, Adriana
Project Start
2010-07-19
Project End
2012-06-30
Budget Start
2010-07-19
Budget End
2012-06-30
Support Year
1
Fiscal Year
2010
Total Cost
$600,696
Indirect Cost
Name
University of California Riverside
Department
Zoology
Type
Schools of Earth Sciences/Natur
DUNS #
627797426
City
Riverside
State
CA
Country
United States
Zip Code
92521