A first version of the Caenorhabditis elegans promoterome

被引:118
作者
Dupuy, D
Li, QR
Deplancke, B
Boxem, M
Hao, T
Lamesch, P
Sequerra, R
Bosak, S
Doucette-Stamm, L
Hope, IA
Hill, DE
Walhout, AJM
Vidal, M [1 ]
机构
[1] Harvard Univ, Sch Med, Ctr Canc Syst Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Canc Biol, Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Univ Massachusetts, Sch Med, Worcester, MA 01605 USA
[5] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA 01605 USA
[6] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[7] Univ Leeds, Sch Biol, Leeds LS2 9JT, W Yorkshire, England
[8] Agencourt Biosci Corp, Beverly, MA 01915 USA
关键词
D O I
10.1101/gr.2497604
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An important aspect of the development of systems biology approaches in metazoans is the characterization of expression patterns of nearly all genes predicted from genome sequences. Such "localizome" maps should provide information on where (in what cells or tissues) and when (at what stage of development or under what conditions) genes are expressed. They should also indicate in what cellular compartments the corresponding proteins are localized. Caenorhabditis elegans is particularly suited for the development of a localizome neap since all its 959 adults: somatic cells can be visualized by microscopy, and its cell lineage has been completely described. Here we address one of the challenges of C. elegans localizome mapping projects: that of obtaining a genome-wide resource of C, elegans promoters needed to generate transgenic animals expressing localization markers such as the green fluorescent protein (GFP). To ensure high flexibility for future uses, we utilized the newly developed Multisite Gateway system. We generated and validated "version 1.1" of the Promoterome: a resource of similar to6000 C elegans promoters. These promoters can be transferred easily into various Gateway Destination vectors to drive expression of markers such as GFP, alone (promoter::GFP constructs), or in fusion with protein-encoding open reading frames available in ORFeome resources (promoter:: ORF::GFP).
引用
收藏
页码:2169 / 2175
页数:7
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