The DrosDel Collection

Author:

Ryder Edward1,Blows Fiona1,Ashburner Michael1,Bautista-Llacer Rosa1,Coulson Darin1,Drummond Jenny1,Webster Jane1,Gubb David1,Gunton Nicola1,Johnson Glynnis1,O'Kane Cahir J1,Huen David1,Sharma Punita1,Asztalos Zoltan1,Baisch Heiko2,Schulze Janet2,Kube Maria2,Kittlaus Kathrin2,Reuter Gunter2,Maroy Peter3,Szidonya Janos3,Rasmuson-Lestander Åsa4,Ekström Karin4,Dickson Barry5,Hugentobler Christoph6,Stocker Hugo6,Hafen Ernst6,Lepesant Jean Antoine7,Pflugfelder Gert8,Heisenberg Martin9,Mechler Bernard10,Serras Florenci11,Corominas Montserrat11,Schneuwly Stephan12,Preat Thomas13,Roote John1,Russell Steven1

Affiliation:

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

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

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

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

5. Institute of Molecular Biotechnology, Austrian Academy of Sciences, A-1030 Vienna, Austria

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

7. Biologie du Developpement, CNRS, Institute Jacques Monod, FR-75251 Paris, France

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

9. Lehrstuhl für Genetik, Universität Würzburg, Am Hubland, 97074 Würzburg, Germany

10. Department of Developmental Genetics, A040, Deutsches Krebsforschungszentrum, D-69120 Heidelberg, Germany

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

12. Institute of Zoology, University of Regensburg, D-93040 Regensburg, Germany

13. Développement, Evolution, Plasticité du Système Nerveux, CNRS, 91190 Gif-sur-Yvette, France

Abstract

Abstract We describe a collection of P-element insertions that have considerable utility for generating custom chromosomal aberrations in Drosophila melanogaster. We have mobilized a pair of engineered P elements, p{RS3} and p{RS5}, to collect 3243 lines unambiguously mapped to the Drosophila genome sequence. The collection contains, on average, an element every 35 kb. We demonstrate the utility of the collection for generating custom chromosomal deletions that have their end points mapped, with base-pair resolution, to the genome sequence. The collection was generated in an isogenic strain, thus affording a uniform background for screens where sensitivity to genetic background is high. The entire collection, along with a computational and genetic toolbox for designing and generating custom deletions, is publicly available. Using the collection it is theoretically possible to generate >12,000 deletions between 1 bp and 1 Mb in size by simple eye color selection. In addition, a further 37,000 deletions, selectable by molecular screening, may be generated. We are now using the collection to generate a second-generation deficiency kit that is precisely mapped to the genome sequence.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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