Ryder Edward, Blows Fiona, Ashburner Michael, Bautista-Llacer Rosa, Coulson Darin, Drummond Jenny, Webster Jane, Gubb David, Gunton Nicola, Johnson Glynnis, O'Kane Cahir J, Huen David, Sharma Punita, Asztalos Zoltan, Baisch Heiko, Schulze Janet, Kube Maria, Kittlaus Kathrin, Reuter Gunter, Maroy Peter, Szidonya Janos, Rasmuson-Lestander Asa, Ekström Karin, Dickson Barry, Hugentobler Christoph, Stocker Hugo, Hafen Ernst, Lepesant Jean Antoine, Pflugfelder Gert, Heisenberg Martin, Mechler Bernard, Serras Florenci, Corominas Montserrat, Schneuwly Stephan, Preat Thomas, Roote John, Russell Steven
Department of Genetics, University of Cambridge, Cambridge CB2 3EH, United Kingdom.
Genetics. 2004 Jun;167(2):797-813. doi: 10.1534/genetics.104.026658.
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.
我们描述了一组P因子插入,它们在生成黑腹果蝇的定制染色体畸变方面具有相当大的用途。我们动员了一对工程化的P因子p[RS3]和p[RS5],以收集3243个明确映射到果蝇基因组序列的品系。该集合平均每35 kb包含一个元件。我们展示了该集合在生成定制染色体缺失方面的用途,这些缺失的端点以碱基对分辨率映射到基因组序列。该集合是在一个同基因品系中产生的,因此为对遗传背景敏感的筛选提供了一个统一的背景。整个集合,连同用于设计和生成定制缺失的计算和遗传工具箱,都是公开可用的。使用该集合,理论上通过简单的眼色选择可以产生超过12,000个大小在1 bp到1 Mb之间的缺失。此外,还可以产生另外37,000个可通过分子筛选选择的缺失。我们现在正在使用该集合来生成一个精确映射到基因组序列的第二代缺失试剂盒。