转座因子
生物
插入突变
遗传学
基因
基因组
黑腹果蝇
P元素
基因靶向
突变
计算生物学
突变
作者
Hugo J. Bellen,Robert Levis,Guochun Liao,Yuchun He,Joseph W. Carlson,Garson Tsang,Martha Evans-Holm,P. Robin Hiesinger,Karen L. Schulze,Gerald M. Rubin,Roger A. Hoskins,Allan C. Spradling
出处
期刊:Genetics
[Oxford University Press]
日期:2004-06-01
卷期号:167 (2): 761-781
被引量:853
标识
DOI:10.1534/genetics.104.026427
摘要
Abstract The Berkeley Drosophila Genome Project (BDGP) strives to disrupt each Drosophila gene by the insertion of a single transposable element. As part of this effort, transposons in >30,000 fly strains were localized and analyzed relative to predicted Drosophila gene structures. Approximately 6300 lines that maximize genomic coverage were selected to be sent to the Bloomington Stock Center for public distribution, bringing the size of the BDGP gene disruption collection to 7140 lines. It now includes individual lines predicted to disrupt 5362 of the 13,666 currently annotated Drosophila genes (39%). Other lines contain an insertion at least 2 kb from others in the collection and likely mutate additional incompletely annotated or uncharacterized genes and chromosomal regulatory elements. The remaining strains contain insertions likely to disrupt alternative gene promoters or to allow gene misexpression. The expanded BDGP gene disruption collection provides a public resource that will facilitate the application of Drosophila genetics to diverse biological problems. Finally, the project reveals new insight into how transposons interact with a eukaryotic genome and helps define optimal strategies for using insertional mutagenesis as a genomic tool.
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