Suppr超能文献

DrosDel文库:一组用于在黑腹果蝇中产生定制染色体畸变的P因子插入序列。

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

作者信息

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

机构信息

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

出版信息

Genetics. 2004 Jun;167(2):797-813. doi: 10.1534/genetics.104.026658.

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.

摘要

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。

相似文献

2
The DrosDel deletion collection: a Drosophila genomewide chromosomal deficiency resource.
Genetics. 2007 Sep;177(1):615-29. doi: 10.1534/genetics.107.076216. Epub 2007 Aug 24.
3
Systematic gene targeting on the X chromosome of Drosophila melanogaster.
Chromosoma. 2004 Dec;113(6):271-5. doi: 10.1007/s00412-004-0313-5. Epub 2004 Oct 12.
4
Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome.
Nat Genet. 2004 Mar;36(3):288-92. doi: 10.1038/ng1312. Epub 2004 Feb 22.
5
Phenotypes Associated with Second Chromosome P Element Insertions in Drosophila melanogaster.
G3 (Bethesda). 2016 Aug 9;6(8):2665-70. doi: 10.1534/g3.116.030940.
6
Transposable elements as tools for genomics and genetics in Drosophila.
Brief Funct Genomic Proteomic. 2003 Apr;2(1):57-71. doi: 10.1093/bfgp/2.1.57.
8
A complementary transposon tool kit for Drosophila melanogaster using P and piggyBac.
Nat Genet. 2004 Mar;36(3):283-7. doi: 10.1038/ng1314. Epub 2004 Feb 22.
10
Minos as a genetic and genomic tool in Drosophila melanogaster.
Genetics. 2005 Oct;171(2):571-81. doi: 10.1534/genetics.105.041848. Epub 2005 Jun 21.

引用本文的文献

1
ETS transcription factor pointed controls germline survival in Drosophila.
PLoS Genet. 2025 Aug 25;21(8):e1011809. doi: 10.1371/journal.pgen.1011809. eCollection 2025 Aug.
2
Depletion of aneuploid cells is shaped by cell-to-cell interactions.
Cell Genom. 2025 Aug 13;5(8):100894. doi: 10.1016/j.xgen.2025.100894. Epub 2025 Jun 3.
3
The Cul3 ubiquitin ligase engages Insomniac as an adaptor to impact sleep and synaptic homeostasis.
PLoS Genet. 2025 Jan 22;21(1):e1011574. doi: 10.1371/journal.pgen.1011574. eCollection 2025 Jan.
6
Shared Transcriptomic Signatures of Inflammaging Among Diverse Strains of Drosophila melanogaster.
Res Sq. 2024 Apr 3:rs.3.rs-4146509. doi: 10.21203/rs.3.rs-4146509/v1.
7
Tob Regulates the Timing of Sleep Onset at Night in .
J Neurosci. 2024 May 1;44(18):e0389232024. doi: 10.1523/JNEUROSCI.0389-23.2024.
8
Pre-Pulse Inhibition of an escape response in adult fruit fly, .
Res Sq. 2024 Jan 23:rs.3.rs-3853873. doi: 10.21203/rs.3.rs-3853873/v1.
9
Role of BicDR in bristle shaft construction and support of BicD functions.
J Cell Sci. 2024 Jan 15;137(2). doi: 10.1242/jcs.261408. Epub 2024 Jan 31.

本文引用的文献

1
The Minute Reaction in the Development of DROSOPHILA MELANOGASTER.
Genetics. 1929 Jul;14(4):366-419. doi: 10.1093/genetics/14.4.366.
2
Non-Disjunction as Proof of the Chromosome Theory of Heredity.
Genetics. 1916 Jan;1(1):1-52. doi: 10.1093/genetics/1.1.1.
3
Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome.
Nat Genet. 2004 Mar;36(3):288-92. doi: 10.1038/ng1312. Epub 2004 Feb 22.
4
Rapid evolution of male-biased gene expression in Drosophila.
Proc Natl Acad Sci U S A. 2003 Aug 19;100(17):9894-9. doi: 10.1073/pnas.1630690100. Epub 2003 Aug 7.
5
Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence.
Genome Biol. 2002;3(12):RESEARCH0079. doi: 10.1186/gb-2002-3-12-research0079. Epub 2002 Dec 23.
6
The FlyBase database of the Drosophila genome projects and community literature.
Nucleic Acids Res. 2003 Jan 1;31(1):172-5. doi: 10.1093/nar/gkg094.
8
A deletion-generator compound element allows deletion saturation analysis for genomewide phenotypic annotation.
Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):9948-53. doi: 10.1073/pnas.142310099. Epub 2002 Jul 2.
9
The art and design of genetic screens: Drosophila melanogaster.
Nat Rev Genet. 2002 Mar;3(3):176-88. doi: 10.1038/nrg751.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验