Cell competition, the conditional loss of viable genotypes only when surrounded by other cells, is a phenomenon observed in certain genetic mosaic conditions. We conducted a chemical mutagenesis and screen to recover new mutations that affect cell competition between wild-type and RpS3 heterozygous cells. Mutations were identified by whole-genome sequencing, making use of software tools that greatly facilitate the distinction between newly induced mutations and other sources of apparent sequence polymorphism, thereby reducing false-positive and false-negative identification rates. In addition, we utilized iPLEX MassARRAY for genotyping recombinant chromosomes. These approaches permitted the mapping of a new mutation affecting cell competition when only a single allele existed, with a phenotype assessed only in genetic mosaics, without the benefit of complementation with existing mutations, deletions, or duplications. These techniques expand the utility of chemical mutagenesis and whole-genome sequencing for mutant identification. We discuss mutations in the Atm and Xrpl genes identified in this screen.
CITATION STYLE
Lee, C. H., Rimesso, G., Reynolds, D. M., Cai, J., & Baker, N. E. (2016). Whole-genome sequencing and iPLEX MassARRAY genotyping map an ems-induced mutation affecting cell competition in drosophila melanogaster. G3: Genes, Genomes, Genetics, 6(10), 3207–3217. https://doi.org/10.1534/g3.116.029421
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