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Gohl, D.M., Silies, M.A., Gao, X.J., Bhalerao, S., Luongo, F.J., Lin, C.C., Potter, C.J., Clandinin, T.R. (2011). A versatile in vivo system for directed dissection of gene expression patterns.  Nat. Methods 8(3): 231--237.
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Research paper

Tissue-specific gene expression using the upstream activating sequence (UAS)–GAL4 binary system has facilitated genetic dissection of many biological processes in Drosophila melanogaster. Refining GAL4 expression patterns or independently manipulating multiple cell populations using additional binary systems are common experimental goals. To simplify these processes, we developed a convertible genetic platform, the integrase swappable in vivo targeting element (InSITE) system. This approach allows GAL4 to be replaced with any other sequence, placing different genetic effectors under the control of the same regulatory elements. Using InSITE, GAL4 can be replaced with LexA or QF, allowing an expression pattern to be repurposed. GAL4 can also be replaced with GAL80 or split-GAL4 hemi-drivers, allowing intersectional approaches to refine expression patterns. The exchanges occur through efficient in vivo manipulations, making it possible to generate many swaps in parallel. This system is modular, allowing future genetic tools to be easily incorporated into the existing framework.

PubMed ID
PubMed Central ID
PMC3079545 (PMC) (EuropePMC)
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Personal communication to FlyBase

InSITE insertions.
Gohl, 2011.3.3, InSITE insertions. [FBrf0213434]

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    Parent Publication
    Publication Type
    Nat. Methods
    Nature Methods
    Publication Year
    1548-7091 1548-7105
    Data From Reference
    Alleles (18)
    Genes (8)
    Natural transposons (2)
    Insertions (26)
    Experimental Tools (11)
    Transgenic Constructs (23)