The DrosDel collection:: A set of P-element insertions for generating custom chromosomal aberrations in Drosophila melanogaster

被引:273
作者
Ryder, E
Blows, F
Ashburner, M
Bautista-Llacer, R
Coulson, D
Drummond, J
Webster, J
Gubb, D
Gunton, N
Johnson, G
O'Kane, CJ
Huen, D
Sharma, P
Asztalos, Z
Baisch, H
Schulze, J
Kube, M
Kittlaus, K
Reuter, G
Maroy, P
Szidonya, J
Rasmuson-Lestander, A
Ekström, K
Dickson, B
Hugentobler, C
Stocker, H
Hafen, E
Lepesant, JA
Pflugfelder, G
Heisenberg, M
Mechler, B
Serras, F
Corominas, M
Schneuwly, S
Preat, T
Roote, J
Russell, S
机构
[1] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
[2] Univ Halle Wittenberg, Inst Genet, D-06120 Halle An Der Saale, Germany
[3] Umea Univ, Dept Biol Mol, S-90187 Umea, Sweden
[4] Univ Szeged, Dept Genet & Mol Biol, H-6726 Szeged, Hungary
[5] Austrian Acad Sci, Inst Mol Biotechnol, A-1030 Vienna, Austria
[6] Univ Zurich, Inst Zool, CH-8057 Zurich, Switzerland
[7] Inst Jacques Monod, CNRS, FR-75251 Paris, France
[8] Johannes Gutenberg Univ Mainz, Inst Genet, D-55128 Mainz, Germany
[9] Univ Wurzburg, Lehrstuhl Genet, D-97074 Wurzburg, Germany
[10] Deutsch Krebsforschungszentrum, Dept Dev Genet, D-69120 Heidelberg, Germany
[11] Univ Barcelona, Fac Biol, Dept Genet, Barcelona 08028, Spain
[12] Univ Regensburg, Inst Zool, D-93040 Regensburg, Germany
[13] CNRS, F-91190 Gif Sur Yvette, France
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1534/genetics.104.026658
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 rising the collection to generate a second-generation deficiency kit that is precisely mapped to the genome sequence.
引用
收藏
页码:797 / 813
页数:17
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