: The long-term goal of this project is to understand the behavior of introduced transposable elements in transgenic mosquitoes that are vectors of human disease. It is the central proposition of the research described herein that the ability of a transposable element to be used both as an efficient genetic tool in the laboratory in mosquitoes, as well as an effective """"""""gene driving mechanism"""""""" of beneficial effector genes in the field is determined by both how the transposable element functions, and how it interacts with the new host mosquito genome. This proposition will be examined using the Hermes transposable element, which is a member of the hAT family of transposable elements, and which is an effective transformation vector of the mosquito, Aedes aegypti.
The Specific Aims of this proposal are thus: 1/ to purify and characterize the Hermes transposase, 2) to understand the structure: function relationships of the Hermes element, 3) to examine interactions of the Hermes transposase, and 4) to isolate hyperactive mutants of Hermes transposase and to test them for hyperactivity in mosquitoes. Purified biologically active Hermes transposase will be used to determine the optimal physical and biological parameters for Hermes element excision and transposition and for the role that host factors may play in Hermes element transposition in mosquitoes. Regions of the both the transposase and the element, such as the inverted terminal repeats and adjacent conserved motifs, that are required for transposition will be identified and, using mutagenesis, their precise roles in this process determined. The role of circular forms of the Hermes element, which we have identified to be present in transgenic insects containing autonomous forms of Hermes element will be investigated. Finally, both eukaryotic and prokaryotic based expression systems, both of which produce active Hermes transposase, will be used to identify hyperactive forms of the Hermes element system that will then be tested for elevated levels of activity in Ae. aegypti. To date we know little about how the transposable elements used to genetically transform mosquitoes either work or behave in mosquito genomes. This now constitutes the most significant bottleneck to the extension of transposable element-based technologies into medically important mosquito species. This technology will complement existing approaches to the control of mosquito-borne disease control and will provide new avenues with which to approach urgent problems arising from the increase in the geographical distribution of these devastating diseases which impact both human health and national economies. This new technology will enable mosquito genes required for pathogen transmission to be identified and isolated, will improve the efficiency with which transgenic mosquito strains can be identified, and will also provide important data concerning the likelihood that genes that prevent pathogen transmission can be spread through mosquito populations by transposable elements.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI045741-06
Application #
6844705
Study Section
Special Emphasis Panel (ZRG1-TMP (99))
Program Officer
Costero, Adriana
Project Start
1999-09-30
Project End
2008-12-31
Budget Start
2005-01-01
Budget End
2005-12-31
Support Year
6
Fiscal Year
2005
Total Cost
$428,749
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
Wright, Jennifer A; Smith, Ryan C; Li, Xianghong et al. (2013) IPB7 transposase behavior in Drosophila melanogaster and Aedes aegypti. Insect Biochem Mol Biol 43:899-906
Li, Xianghong; Ewis, Hosam; Hice, Robert H et al. (2013) A resurrected mammalian hAT transposable element and a closely related insect element are highly active in human cell culture. Proc Natl Acad Sci U S A 110:E478-87
Woodard, Lauren E; Li, Xianghong; Malani, Nirav et al. (2012) Comparative analysis of the recently discovered hAT transposon TcBuster in human cells. PLoS One 7:e42666
Arensburger, Peter; Hice, Robert H; Zhou, Liqin et al. (2011) Phylogenetic and functional characterization of the hAT transposon superfamily. Genetics 188:45-57
Smith, Ryan C; Atkinson, Peter W (2011) Mobility properties of the Hermes transposable element in transgenic lines of Aedes aegypti. Genetica 139:7-22
O'Brochta, David A; Stosic, Christina D; Pilitt, Kristina et al. (2009) Transpositionally active episomal hAT elements. BMC Mol Biol 10:108
Smith, R C; Walter, M F; Hice, R H et al. (2007) Testis-specific expression of the beta2 tubulin promoter of Aedes aegypti and its application as a genetic sex-separation marker. Insect Mol Biol 16:61-71
O'Brochta, David A; Subramanian, Ramanand A; Orsetti, Jamison et al. (2006) hAT element population genetics in Anopheles gambiae s.l. in Mozambique. Genetica 127:185-98
Arensburger, Peter; Kim, Yu-Jung; Orsetti, Jamison et al. (2005) An active transposable element, Herves, from the African malaria mosquito Anopheles gambiae. Genetics 169:697-708
Irvin, Nic; Hoddle, Mark S; O'Brochta, David A et al. (2004) Assessing fitness costs for transgenic Aedes aegypti expressing the GFP marker and transposase genes. Proc Natl Acad Sci U S A 101:891-6

Showing the most recent 10 out of 16 publications