The NemaGENETAG initiative: large scale transposon insertion gene-tagging in Caenorhabditis elegans

被引:29
作者
Bazopoulou, Daphne [1 ]
Tavernarakis, Nektarios [1 ]
机构
[1] Fdn Res & Technol Hellas, Inst Mol Biol & Biotechnol, Iraklion 70013, Crete, Greece
关键词
Caenorhabditis elegans; Mariner; Mos1; Gene tagging; Tc1; Transposon; GERM-LINE TRANSFORMATION; MOSQUITO ANOPHELES-STEPHENSI; BEETLE TRIBOLIUM-CASTANEUM; MEDIATED ENHANCER TRAP; PIGGYBAC TRANSPOSON; DROSOPHILA-MELANOGASTER; ELEMENT MINOS; IN-VIVO; TC1/MARINER SUPERFAMILY; ACETYLCHOLINE-RECEPTOR;
D O I
10.1007/s10709-009-9361-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The nematode Caenorhabditis elegans is a widely appreciated, powerful platform in which to study important biological mechanisms related to human health. More than 65% of human disease genes have homologues in the C. elegans genome, and essential aspects of mammalian cell biology, neurobiology and development are faithfully recapitulated in this organism. The EU-funded NemaGENETAG project was initiated with the aim to develop cutting-edge tools and resources that will facilitate modelling of human pathologies in C. elegans, and advance our understanding of animal development and physiology. The main objective of the project involves the generation and evaluation of a large collection of transposon-tagged mutants. In the process of achieving this objective the NemaGENETAG consortium also endeavours to optimize and automate existing transposon-mediated mutagenesis methodologies based on the Mos1 transposable element, in addition to developing alternatives using other transposon systems. The final product of this initiative-a comprehensive collection of transposon-tagged alleles-together with the acquisition of efficient transposon-based tools for mutagenesis and transgenesis in C. elegans, should yield a wealth of information on gene function, immediately relevant to key biological processes and to pharmaceutical research and development.
引用
收藏
页码:39 / 46
页数:8
相关论文
共 60 条
[1]   The versatile worm:: genetic and genomic resources for Caenorhabditis elegans research [J].
Antoshechkin, Igor ;
Sternberg, Paul W. .
NATURE REVIEWS GENETICS, 2007, 8 (07) :518-532
[2]   Genetic dissection of neural circuits by Tol2 transposon-mediated Gal4 gene and enhancer trapping in zebrafish [J].
Asakawa, Kazuhide ;
Suster, Maximiliano L. ;
Mizusawa, Kanta ;
Nagayoshi, Saori ;
Kotani, Tomoya ;
Urasaki, Akihiro ;
Kishimoto, Yasuyuki ;
Hibi, Masahiko ;
Kawakami, Koichi .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (04) :1255-1260
[3]   High-throughput enhancer trap by remobilization of transposon Minos in Ciona intestinalis [J].
Awazu, Satoko ;
Matsuoka, Terumi ;
Inaba, Kazuo ;
Satoh, Nori ;
Sasakura, Yasunori .
GENESIS, 2007, 45 (05) :307-317
[4]   Enhancer trapping in zebrafish using the Sleeping Beauty transposon -: art. no. 62 [J].
Balciunas, D ;
Davidson, AE ;
Sivasubbu, S ;
Hermanson, SB ;
Welle, Z ;
Ekker, SC .
BMC GENOMICS, 2004, 5 (1)
[5]  
Bessereau Jean-Louis, 2006, V351, P59
[6]   Mobilization of a Drosophila transposon in the Caenorhabditis elegans germ line [J].
Bessereau, JL ;
Wright, A ;
Williams, DC ;
Schuske, K ;
Davis, MW ;
Jorgensen, EM .
NATURE, 2001, 413 (6851) :70-74
[7]   A piggyBac transposon gene trap for the analysis of gene expression and function in drosophila [J].
Bonin, CP ;
Mann, RS .
GENETICS, 2004, 167 (04) :1801-1811
[8]   Eight genes are required for functional reconstitution of the Caenorhabditis elegans levamisole-sensitive acetylcholine receptor [J].
Boulin, Thomas ;
Gielen, Marc ;
Richmond, Janet E. ;
Williams, Daniel C. ;
Paoletti, Pierre ;
Bessereau, Jean-Louis .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (47) :18590-18595
[9]   Mos1-mediated insertional mutagenesis in Caenorhabditis elegans [J].
Boulin, Thomas ;
Bessereau, Jean-Louis .
NATURE PROTOCOLS, 2007, 2 (05) :1276-1287
[10]  
BRENNER S, 1974, GENETICS, V77, P71