A genome-wide gain-of-function analysis of rice genes using the FOX-hunting system

Hidemitsu Nakamura(Institute of Agrobiological Sciences), Makoto Hakata(Institute of Agrobiological Sciences), Kou Amano(Institute of Agrobiological Sciences), Akio Miyao(Institute of Agrobiological Sciences), Naoko Toki(Keio University), Mariko Kajikawa(Institute of Agrobiological Sciences), Jinhuan Pang(Institute of Agrobiological Sciences), Naokuni Higashi(Institute of Agrobiological Sciences), Shigeko Ando(Institute of Agrobiological Sciences), Seiichi Toki(Institute of Agrobiological Sciences), Miki Fujita(RIKEN BioResource Research Center), Akiko Enju(RIKEN Center for Sustainable Resource Science), Motoaki Seki(RIKEN Center for Sustainable Resource Science), Miki Nakazawa(RIKEN Center for Sustainable Resource Science), Takanari Ichikawa(RIKEN Center for Sustainable Resource Science), Kazuo Shinozaki(RIKEN BioResource Research Center), Minami Matsui(RIKEN Center for Sustainable Resource Science), Yoshiaki Nagamura(Institute of Agrobiological Sciences), Hirohiko Hirochika(Institute of Agrobiological Sciences), Hiroaki Ichikawa(Institute of Agrobiological Sciences)
Plant Molecular Biology
October 9, 2007
Cited by 102Open Access
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Abstract

The latest report has estimated the number of rice genes to be approximately 32,000. To elucidate the functions of a large population of rice genes and to search efficiently for agriculturally useful genes, we have been taking advantage of the Full-length cDNA Over-eXpresser (FOX) gene-hunting system. This system is very useful for analyzing various gain-of-function phenotypes from large populations of transgenic plants overexpressing cDNAs of interest and others with unknown or important functions. We collected the plasmid DNAs of 13,980 independent full-length cDNA (FL-cDNA) clones to produce a FOX library by placing individual cDNAs under the control of the maize Ubiquitin-1 promoter. The FOX library was transformed into rice by Agrobacterium-mediated high-speed transformation. So far, we have generated approximately 12,000 FOX-rice lines. Genomic PCR analysis indicated that the average number of FL-cDNAs introduced into individual lines was 1.04. Sequencing analysis of the PCR fragments carrying FL-cDNAs from 8615 FOX-rice lines identified FL-cDNAs in 8225 lines, and a database search classified the cDNAs into 5462 independent ones. Approximately 16.6% of FOX-rice lines examined showed altered growth or morphological characteristics. Three super-dwarf mutants overexpressed a novel gibberellin 2-oxidase gene,confirming the importance of this system. We also show here the other morphological alterations caused by individual FL-cDNA expression. These dominant phenotypes should be valuable indicators for gene discovery and functional analysis.


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