Genetics, Vol. 167, 797-813, June 2004, Copyright © 2004
doi:10.1534/genetics.104.026658

The DrosDel Collection

A Set of P-Element Insertions for Generating Custom Chromosomal Aberrations in Drosophila melanogaster

* Department of Genetics, University of Cambridge, Cambridge CB2 3EH, United Kingdom
{dagger} Institute of Genetics, Martin Luther University, D-06120 Halle, Germany
§ Department of Molecular Biology, Umeå University, S-901 87 Umeå, Sweden
{ddagger} Department of Genetics and Molecular Biology, University of Szeged, 6726 Szeged, Hungary
** Institute of Molecular Biotechnology, Austrian Academy of Sciences, A-1030 Vienna, Austria
{dagger}{dagger} Zoologisches Institut der Universitat Zurich, 8057 Zurich, Switzerland
{ddagger}{ddagger} Biologie du Developpement, CNRS, Institute Jacques Monod, FR-75251 Paris, France
§§ Institut für Genetik, Universität Mainz, 55128 Mainz, Germany
*** Lehrstuhl für Genetik, Universität Würzburg, Am Hubland, 97074 Würzburg, Germany
{dagger}{dagger}{dagger} Department of Developmental Genetics, A040, Deutsches Krebsforschungszentrum, D-69120 Heidelberg, Germany
{ddagger}{ddagger}{ddagger} Departament de Genetica, Facultat de Biologia, Universitat de Barcelona, 08028 Barcelona, Spain
§§§ Institute of Zoology, University of Regensburg, D-93040 Regensburg, Germany
**** Développement, Evolution, Plasticité du Système Nerveux, CNRS, 91190 Gif-sur-Yvette, France

1 Corresponding author: Department of Genetics, University of Cambridge, Downing St., Cambridge CB2 3EH, United Kingdom.
E-mail: s.russell{at}gen.cam.ac.uk

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.




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