| Literature DB >> 20980269 |
Nobutaka Mitsuda1, Miho Ikeda, Shinobu Takada, Yuko Takiguchi, Youichi Kondou, Takeshi Yoshizumi, Miki Fujita, Kazuo Shinozaki, Minami Matsui, Masaru Ohme-Takagi.
Abstract
Yeast one-hybrid screening is widely used for the identification of transcription factors (TFs) that interact with specific DNA sequences. However, screening a whole cDNA library is not efficient for the identification of TFs because TF genes represent only a small percentage of clones in a cDNA library. Here, we present the development of an efficient yeast one-hybrid screening system using a prey library composed only of approximately 1,500 TF cDNAs of Arabidopsis thaliana. This library enabled us to isolate a TF that binds to a specific promoter sequence with high efficiency, even when the promoter region of the gene of interest was directly employed as bait. Furthermore, this library was also successfully applied as a yeast two-hybrid library to find TFs that interact with specific proteins. This efficient system will contribute to the elucidation of gene regulatory networks in plants.Entities:
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Year: 2010 PMID: 20980269 DOI: 10.1093/pcp/pcq161
Source DB: PubMed Journal: Plant Cell Physiol ISSN: 0032-0781 Impact factor: 4.927