Development of a new flippase-dependent mouse model for red fluorescence-based isolation of KrasG12Doncogene-expressing tumor cells

Author:

Hrckulak DusanORCID,Krausova Michaela,Onhajzer JakubORCID,Stastna Monika,Kriz Vitezslav,Janeckova LucieORCID,Korinek VladimirORCID

Abstract

AbstractProto-oncogene KRAS, GTPase (KRAS) is one of the most intensively studied oncogenes in cancer research. Although several mouse models allow for regulated expression of mutant Kras, selective isolation and analysis of transforming or tumor cells that produce the Kras oncogene remains a challenge. In our study, we present a knock-in model of oncogenic variant KrasG12Dthat enables the “activation” of KrasG12Dexpression together with production of red fluorescent protein tdTomato. Both proteins are expressed from the endogenousKraslocus after recombination of a transcriptional stop box in the genomic DNA by the enzyme flippase (Flp). We have demonstrated the functionality of the allele termedRedRas(abbreviatedKrasRR) underin vitroconditions with mouse embryonic fibroblasts and organoids andin vivoin the lung and colon epithelium. After recombination with adenoviral vectors carrying theFlpgene, theKrasRRallele itself triggers formation of lung adenomas. In the colon epithelium, it causes the progression of adenomas that are triggered by the loss of tumor suppressor adenomatous polyposis coli (Apc). Importantly, cells in which recombination has successfully occurred can be visualized and isolated using the fluorescence emitted by tdTomato. Furthermore, we show that KrasG12Dproduction enables intestinal organoid growth independent of epidermal growth factor (EGF) signaling and that the KrasG12Dfunction is effectively suppressed by specific inhibitor MRTX1133.

Publisher

Cold Spring Harbor Laboratory

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