Literature DB >> 14617098

Sequence database of 1172 T-DNA insertion sites in Arabidopsis activation-tagging lines that showed phenotypes in T1 generation.

Takanari Ichikawa1, Miki Nakazawa, Mika Kawashima, Shu Muto, Kazushi Gohda, Kumiko Suzuki, Akie Ishikawa, Hiroko Kobayashi, Takeshi Yoshizumi, Yuko Tsumoto, Yumi Tsuhara, Haruko Iizumi, Yukiko Goto, Minami Matsui.   

Abstract

Plant genomic resources harbouring gain-of-function mutations remain rare, even though this type of mutation is believed to be one of the most useful for elucidating the function of unknown genes that have redundant partners in the genome. An activation-tagging T-DNA was introduced into the genome of Arabidopsis creating 55,431 independent transformed lines. Of these T1 lines, 1,262 showed phenotypes different from those of wild-type plants. We called these lines 'AT1Ps' (activation T1 putants). The phenotypes observed include abnormalities in morphology, growth rate, plant colour, flowering time and fertility. Similar phenotypes re-appeared either in dominant or semi-dominant fashion in 17% of 177 AT2P plants tested. Plasmid rescue or an adaptor-PCR method was used to identify 1172 independent genomic loci of T-DNA integration sites in the AT1P plants. Mapping of the integration sites revealed that the chromosomal distribution of these sites is similar to that observed in conventional T-DNA knock-out lines, except that the intragenic type of integration is slightly lower (27%) in the AT1P plants compared to that observed in other random knock-out populations (30-35%). Ten AT2P lines that showed dominant phenotypes were chosen to monitor expression levels of genes adjacent to the T-DNA integration sites by RT-PCR. Activation was observed in 7 out of 17 of the adjacent genes detected. Genes located up to 8.2 kb away from the enhancer sequence were activated. One of the seven activated genes was located close to the left-border sequence of the T-DNA, having an estimated distance of 5.7 kb from the enhancer. Surprisingly, one gene, the first ATG of which is located 12 kb away from the enhancer, showed reduced mRNA accumulation in the tagged line. Application of the database generated to Arabidopsis functional genomics research is discussed. The sequence database of the 1172 loci from the AT1P plants is available (http://pfgweb.gsc.riken.go.jp/index.html).

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Year:  2003        PMID: 14617098     DOI: 10.1046/j.1365-313x.2003.01876.x

Source DB:  PubMed          Journal:  Plant J        ISSN: 0960-7412            Impact factor:   6.417


  29 in total

1.  A rice gene activation/knockout mutant resource for high throughput functional genomics.

Authors:  Yue-Ie Hsing; Chyr-Guan Chern; Ming-Jen Fan; Po-Chang Lu; Ku-Ting Chen; Shuen-Fang Lo; Peng-Kai Sun; Shin-Lon Ho; Kuo-Wei Lee; Yi-Chieh Wang; Wen-Lii Huang; Swee-Suak Ko; Shu Chen; Jyh-Long Chen; Chun-I Chung; Yao-Cheng Lin; Ai-Ling Hour; Yet-Walt Wang; Ya-Chi Chang; Min-Wei Tsai; Yi-Show Lin; Yin-Chin Chen; Hsing-Mu Yen; Charng-Pei Li; Chiu-Kai Wey; Ching-Shan Tseng; Ming-Hsing Lai; Sheng-Chung Huang; Liang-Jwu Chen; Su-May Yu
Journal:  Plant Mol Biol       Date:  2006-11-21       Impact factor: 4.076

2.  Activation tagging, an efficient tool for functional analysis of the rice genome.

Authors:  Shuyan Wan; Jinxia Wu; Zhiguo Zhang; Xuehui Sun; Yaci Lv; Ci Gao; Yingda Ning; Jun Ma; Yupeng Guo; Qian Zhang; Xia Zheng; Caiying Zhang; Zhiying Ma; Tiegang Lu
Journal:  Plant Mol Biol       Date:  2008-10-02       Impact factor: 4.076

3.  RETARDED GROWTH OF EMBRYO1, a new basic helix-loop-helix protein, expresses in endosperm to control embryo growth.

Authors:  Youichi Kondou; Miki Nakazawa; Mika Kawashima; Takanari Ichikawa; Takeshi Yoshizumi; Kumiko Suzuki; Akie Ishikawa; Tomoko Koshi; Ryo Matsui; Shu Muto; Minami Matsui
Journal:  Plant Physiol       Date:  2008-06-20       Impact factor: 8.340

4.  Increased level of polyploidy1, a conserved repressor of CYCLINA2 transcription, controls endoreduplication in Arabidopsis.

Authors:  Takeshi Yoshizumi; Yuko Tsumoto; Tomoko Takiguchi; Noriko Nagata; Yoshiharu Y Yamamoto; Mika Kawashima; Takanari Ichikawa; Miki Nakazawa; Naoki Yamamoto; Minami Matsui
Journal:  Plant Cell       Date:  2006-09-29       Impact factor: 11.277

5.  High-throughput generation of an activation-tagged mutant library for functional genomic analyses in tobacco.

Authors:  Feng Liu; Daping Gong; Qian Zhang; Dawei Wang; Mengmeng Cui; Zhiguo Zhang; Guanshan Liu; Jinxia Wu; Yuanying Wang
Journal:  Planta       Date:  2014-11-19       Impact factor: 4.116

6.  Hairy root-activation tagging: a high-throughput system for activation tagging in transformed hairy roots.

Authors:  Hikaru Seki; Tomoko Nishizawa; Nobukazu Tanaka; Yasuo Niwa; Shigeo Yoshida; Toshiya Muranaka
Journal:  Plant Mol Biol       Date:  2005-11       Impact factor: 4.076

7.  Activation tagging approach in a model legume, Lotus japonicus.

Authors:  Ryujiro Imaizumi; Shusei Sato; Nanako Kameya; Ikuo Nakamura; Yasukazu Nakamura; Satoshi Tabata; Shin-Ichi Ayabe; Toshio Aoki
Journal:  J Plant Res       Date:  2005-11-05       Impact factor: 2.629

Review 8.  Unintended consequences of plant transformation: a molecular insight.

Authors:  Marcin Filipecki; Stefan Malepszy
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

9.  Functional identification of Arabidopsis stress regulatory genes using the controlled cDNA overexpression system.

Authors:  Csaba Papdi; Edit Abrahám; Mary Prathiba Joseph; Cristina Popescu; Csaba Koncz; László Szabados
Journal:  Plant Physiol       Date:  2008-04-25       Impact factor: 8.340

Review 10.  Phenome analysis in plant species using loss-of-function and gain-of-function mutants.

Authors:  Takashi Kuromori; Shinya Takahashi; Youichi Kondou; Kazuo Shinozaki; Minami Matsui
Journal:  Plant Cell Physiol       Date:  2009-06-05       Impact factor: 4.927

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