@article{b5b7d07a4ae64c24bc0273f3e322e45f,
title = "Whole-genome sequencing and iPLEX MassARRAY genotyping map an ems-induced mutation affecting cell competition in drosophila melanogaster",
abstract = "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.",
keywords = "Cell competition, Drosophila melanogaster, Flybook, Whole-genome sequencing, Xrp1, iPLEX MassARRAY",
author = "Lee, {Chang Hyun} and Gerard Rimesso and Reynolds, {David M.} and Jinlu Cai and Baker, {Nicholas E.}",
note = "Funding Information: We thank A. Jenny, M. Kiparaki, and J. Secombe for comments on the manuscript, and H. Bellen and I. Hariharan for advice. Confocal Imaging was performed at the Analytical Imaging Facility, Albert Einstein College of Medicine, supported by National Cancer Institute cancer center support grant (P30CA013330). Whole-genome sequencing, subsequent analysis for variant calling, and iPLEX MassARRAY were carried out by the Epigenomics Core, Computational Genomics Core, and the Genomics Core of Albert Einstein College of Medicine, respectively. Stocks obtained from the Bloomington Drosophila Stock Center [National Institutes of Health (NIH) P40OD018537] were used in this study. Stocks obtained from the Bloomington Drosophila Stock Center (NIH P40OD018537) were used in this study. Research supported by grants from the NIH (EY018910 and GM104213) and Research to Prevent Blindness (2013 Senior Investigator Award to N.E.B. and unrestricted grant to the Department of Ophthalmology and Visual Sciences). Some data in this paper are from a thesis submitted in partial fulfillment of the requirements for the Degree of Doctor of Philosophy in the Graduate Division of Medical Sciences, Albert Einstein College of Medicine, Yeshiva University to C.H.L. Publisher Copyright: {\textcopyright} 2016 Lee et al.",
year = "2016",
doi = "10.1534/g3.116.029421",
language = "English (US)",
volume = "6",
pages = "3207--3217",
journal = "G3: Genes, Genomes, Genetics",
issn = "2160-1836",
publisher = "Genetics Society of America",
number = "10",
}