An international scholastic network to generate LexA enhancer-trap lines for Drosophila

Abstract
Conditional gene regulation in Drosophila through binary expression systems like the LexA-LexAop system provides a superb tool for investigating gene and tissue function. To increase the availability of defined LexA enhancer trap insertions, we present molecular, genetic and tissue expression studies of 301 novel Stan-X LexA enhancer traps derived from mobilization of the index SX4 line. This includes insertions into distinct loci on the X, II and III chromosomes that were not previously associated with enhancer traps or targeted LexA constructs, an insertion into ptc, and eleven insertions into natural transposons. A subset of enhancer traps was expressed in CNS neurons known to produce and secrete insulin, an essential regulator of growth, development and metabolism. Fly lines described here were generated and characterized through studies by students and teachers in an international network of genetics classes at public, independent high schools, and universities serving a diversity of students, including those underrepresented in science. Thus, a unique partnership between secondary schools and university-based programs has produced and characterized novel resources in Drosophila, establishing instructional paradigms devoted to unscripted experimental science.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Author's list was updated. The abstract was supplemented to reflect changes in results. The results have been expanded and include two new figures, Figure 3, showcasing the expression pattern of an enhancer trap in ptc, and Figure 6, displaying novel data of enhancer trapping natural transposable elements. The supplement is expanded by Suppl. Table 2, covering split read fragments used in Figure 6, and Suppl. Figure 3 analyzing snucRNAseq data for IPCs and CC cells. The methods are updated to cover all changes.
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