Versatile gene-specific sequence tags for Arabidopsis functional genomics:: Trancript profiling and reverse genetics applications

被引:245
作者
Hilson, P [1 ]
Allemeersch, J
Altmann, T
Aubourg, S
Avon, A
Beynon, J
Bhalerao, RP
Bitton, F
Caboche, M
Cannoot, B
Chardakov, V
Cognet-Holliger, C
Colot, V
Crowe, M
Darimont, C
Durinck, S
Eickhoff, H
de Longevialle, AF
Farmer, EE
Grant, M
Kuiper, MTR
Lehrach, H
Léon, C
Leyva, A
Lundeberg, J
Lurin, C
Moreau, Y
Nietfeld, W
Paz-Ares, J
Reymond, P
Rouzé, P
Sandberg, G
Segura, MD
Serizet, C
Tabrett, A
Taconnat, L
Thareau, V
Van Hummelen, P
Vercruysse, S
Vuylsteke, M
Weingartner, M
Weisbeek, PJ
Wirta, V
Wittink, FRA
Zabeau, M
Small, I
机构
[1] Univ Ghent VIB, Dept Plant Syst Biol, B-9052 Ghent, Belgium
[2] UEVE, CNRS, INRA, Unite Rech Genom Vegetale, F-91057 Evry, France
[3] Katholieke Univ Leuven, Fac Engn, Dept Elect Engn, ESAT, B-3001 Heverlee, Belgium
[4] Univ Potsdam, Inst Biochem & Biol Genet, Max Planck Inst Mol Pflanzenphysiol, D-14476 Golm, Germany
[5] Hort Res Int, Warwick CV35 9EF, England
[6] Swedish Univ Agr Sci, Dept Forest Genet & Plant Physiol, S-90183 Umea, Sweden
[7] Univ London Imperial Coll Sci Technol & Med, Dept Agr Sci, Ashford TN25 5AH, Kent, England
[8] INRA, Genet & Ameliorat Plantes Stn, F-78026 Versailles, France
[9] John Innes Ctr, CH-1015 Lausanne, Switzerland
[10] Univ Lausanne, Dept Plant Mol Biol, Gene Express Lab, CH-1015 Lausanne, Switzerland
[11] Max Planck Inst Mol Genet, Dept Vertebrate Genom, D-14195 Berlin, Germany
[12] CSIC, Ctr Nacl Biotecnol, Dept Plant Mol Genet, E-28049 Madrid, Spain
[13] AlbaNova Univ Ctr, Royal Inst Technol, KTH, Dept Biotechnol, S-10691 Stockholm, Sweden
[14] Univ Louvain VIB, UZ Gasthuisberg, MicroArray Facil, B-3000 Louvain, Belgium
[15] Univ Utrecht, Dept Mol Genet, NL-3584 CH Utrecht, Netherlands
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1101/gr.2544504
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
Microarray transcript profiling and RNA interference are two new technologies crucial for large-scale gene function studies in multicellular eukaryotes. Both rely on sequence-specific hybridization between complementary nucleic acid strands, inciting us to create a collection of gene-specific sequence tags (GSTs) representing at least 21,500 Arabidopsis genes and which are compatible with both approaches. The GSTs were carefully selected to ensure that each of them shared no significant similarity with any other region in the Arabidopsis genome. They were synthesized by PCR amplification from genomic DNA. Spotted microarrays fabricated from the GSTs show good dynamic range, specificity, and sensitivity in transcript profiling experiments. The GSTs have also been transferred to bacterial plasmid vectors via recombinational cloning protocols. These cloned GSTs constitute the ideal starting point for a variety of functional approaches, including reverse genetics. We have subcloned GSTs on a large scale into vectors designed for gene silencing in plant cells. We show that in planta expression of GST hairpin RNA results in the expected phenotypes in silenced Arabidopsis lines. These versatile GST resources provide novel and powerful tools for functional genomics.
引用
收藏
页码:2176 / 2189
页数:14
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