Abstract
BackgroundThe wide distribution of Aedes aegypti, the main vector of dengue and yellow fever viruses, currently puts three billion people in the world at risk of infection with these viruses. Continuous transmission of these and other viruses despite aggressive efforts to prevent this emphasizes the need to develop new control strategies. Proposals to control disease transmission based on vector engineering, including both population suppression and population replacement, rely on the development of transgenes under the control of regulatory elements able to drive molecules in a specific tissue, time and strength.MethodsHere we report the characterization of a promoter active in both the female germline and early zygote, derived from the transcription factor bZip1 in the mosquito Ae. aegypti, using transposon-based methods and RT-qPCR.ResultsWe generated seven transgenic lines carrying AabZip1-reporter constructs and observed expression in both the ovary and early embryo. RT-qPCR analysis was performed to evaluate transcript expression patterns for each line, confirming that transgenic expression from the AabZip1 promoter largely recapitulated the endogenous expression pattern, albeit the strength of maternal expression appeared to be strongly influenced by chromosomal position.ConclusionsThis study provides a new regulatory sequence that can be useful for generating transgenic lines that can become a tool in vector control strategies.
Highlights
The wide distribution of Aedes aegypti, the main vector of dengue and yellow fever viruses, currently puts three billion people in the world at risk of infection with these viruses
Promoter sequences driving maternal or zygotic expression are essential for the development of gene drive approaches based on maternal-effect dominant embryonic arrest (Medea) or homing-based drive, which are an essential part of the population replacement strategy [10,11,12]
In contrast to the kinesin light chain gene (KLC2.2) which was bZip1 promoter yields expression similar to the endogenous bZip1 gene We sought to evaluate if a genomic fragment (4587 bp) upstream of the open reading frame (ORF) of the AabZip1 gene was able to drive the expression of a heterologous gene in a manner that recapitulated the endogenous expression of this gene
Summary
The wide distribution of Aedes aegypti, the main vector of dengue and yellow fever viruses, currently puts three billion people in the world at risk of infection with these viruses. Promoter sequences driving maternal or zygotic expression are essential for the development of gene drive approaches based on maternal-effect dominant embryonic arrest (Medea) or homing-based drive, which are an essential part of the population replacement strategy [10,11,12]. Such promoters may be useful for manipulating sex ratios as sex determination occurs early during development which can be used for suppression strategies
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