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The Zuker Collection: A Resource for the Analysis of Autosomal Gene Function in Drosophila melanogaster
Edmund J. Koundakjiana, David M. Cowana, Robert W. Hardya, and Ann H. Beckeraa Howard Hughes Medical Institute and Departments of Biology and Neurosciences, University of California, San Diego, California 92093
Corresponding author: Robert W. Hardy, 9500 Gilman Dr., CMM W 355, University of California, San Diego, CA 92093., bob{at}flyeye.ucsd.edu (E-mail)
Communicating editor: T. C. KAUFMAN
72,000 F3 cultures segregating for autosomes heavily treated with ethyl methanesulfonate (EMS),
12,000 lines in which the treated second or third chromosome survived in homozygous condition were selected. The dose of EMS induced an estimated rate of 1.21.5 x 103 mutations/gene and predicts five to six nonessential gene mutations per chromosome and seven to nine alleles per locus in the samples of 6000 second chromosomes and 6000 third chromosomes. Due to mosaic mutations induced in the initial exposure to the mutagen, many of the lines are segregating or are now fixed for lethal mutations on the mutagenized chromosome. The features of this collection, known as the Zuker collection, make it a valuable resource for forward and reverse genetic screens for mutations affecting a wide array of biological functions.
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