The DrosDel Deletion Collection: A Drosophila Genomewide Chromosomal Deficiency Resource

Author:

Ryder Edward1,Ashburner Michael1,Bautista-Llacer Rosa1,Drummond Jenny1,Webster Jane1,Johnson Glynnis1,Morley Terri1,Chan Yuk Sang1,Blows Fiona1,Coulson Darin1,Reuter Gunter2,Baisch Heiko2,Apelt Christian2,Kauk Andreas2,Rudolph Thomas2,Kube Maria2,Klimm Melanie2,Nickel Claudia2,Szidonya Janos3,Maróy Peter3,Pal Margit4,Rasmuson-Lestander Åsa5,Ekström Karin5,Stocker Hugo6,Hugentobler Christoph6,Hafen Ernst6,Gubb David7,Pflugfelder Gert8,Dorner Christian8,Mechler Bernard9,Schenkel Heide9,Marhold Joachim9,Serras Florenci10,Corominas Montserrat10,Punset Adrià10,Roote John1,Russell Steven1

Affiliation:

1. Department of Genetics, University of Cambridge, Cambridge CB2 3EH, United Kingdom

2. Institute of Biology/Genetics, Martin Luther University, D-06120 Halle, Germany

3. Department of Genetics and Molecular Biology, University of Szeged, 6726 Szeged, Hungary

4. Institute of Biochemistry, Biological Research Center, Szeged H-6726, Hungary

5. Department of Molecular Biology, Umeå University, S-901 87 Umeå, Sweden

6. Zoologisches Institut der Universitat Zurich, 8057 Zurich, Switzerland

7. CIC Biogune, Parque Technologico de Bizkaia, Derio 48160, Spain

8. Institut für Genetik, Universität Mainz, 55128 Mainz, Germany

9. Department of Developmental Genetics, Deutsches Krebsforschungszentrum, D-69120 Heidelberg, Germany and

10. Departament de Genetica, Facultat de Biologia, Universitat de Barcelona, 08028 Barcelona, Spain

Abstract

Abstract We describe a second-generation deficiency kit for Drosophila melanogaster composed of molecularly mapped deletions on an isogenic background, covering ∼77% of the Release 5.1 genome. Using a previously reported collection of FRT-bearing P-element insertions, we have generated 655 new deletions and verified a set of 209 deletion-bearing fly stocks. In addition to deletions, we demonstrate how the P elements may also be used to generate a set of custom inversions and duplications, particularly useful for balancing difficult regions of the genome carrying haplo-insufficient loci. We describe a simple computational resource that facilitates selection of appropriate elements for generating custom deletions. Finally, we provide a computational resource that facilitates selection of other mapped FRT-bearing elements that, when combined with the DrosDel collection, can theoretically generate over half a million precisely mapped deletions.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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