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First published online February 20, 2008; 10.1104/pp.107.113217

Plant Physiology 146:1862-1877 (2008)
© 2008 American Society of Plant Biologists

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SYSTEMS BIOLOGY, MOLECULAR BIOLOGY, AND GENE REGULATION

DNA-Binding Study Identifies C-Box and Hybrid C/G-Box or C/A-Box Motifs as High-Affinity Binding Sites for STF1 and LONG HYPOCOTYL5 Proteins1,[C],[W],[OA]

Young Hun Song2, Cheol Min Yoo2,3, An Pio Hong, Seong Hee Kim, Hee Jeong Jeong, Su Young Shin, Hye Jin Kim, Dae-Jin Yun, Chae Oh Lim, Jeong Dong Bahk, Sang Yeol Lee, Ron T. Nagao, Joe L. Key and Jong Chan Hong*

Division of Applied Life Science (BK21 Program), Plant Molecular Biology and Biotechnology Research Center, Environmental Biotechnology Research Center, National Core Research Center, Gyeongsang National University, Jinju 660–701, Korea (Y.H.S., C.M.Y, A.P.H., S.H.K., H.J.J., S.Y.S., H.J.K., D.-J.Y., C.O.L., J.D.B., S.Y.L., J.C.H.); Division of Plant Sciences, University of Missouri, Columbia, Missouri 65211 (J.C.H.); and Department of Plant Biology, University of Georgia, Athens, Georgia 30602 (R.T.N., J.L.K.)

LONG HYPOCOTYL5 (HY5) is a bZIP (basic leucine zipper) transcription factor that activates photomorphogenesis and root development in Arabidopsis (Arabidopsis thaliana). Previously, STF1 (soybean [Glycine max] TGACG-motif binding factor 1), a homologous legume protein with a RING-finger motif and a bZIP domain, was reported in soybean. To investigate the role of STF1, the phenotypes of transgenic Arabidopsis plants overexpressing STF1 and HY5 were compared. In addition, the DNA-binding properties of STF1 and HY5 were extensively studied using random binding site selection and electrophoretic mobility shift assay. Overexpression of STF1 in the hy5 mutant of Arabidopsis restored wild-type photomorphogenic and root development phenotypes of short hypocotyl, accumulation of chlorophyll, and root gravitropism with partial restoration of anthocyanin accumulation. This supports that STF1 is a homolog of HY5 with a role in light and hormone signaling. The DNA-binding properties of STF1 and HY5 are shown to be similar to each other in recognizing many ACGT-containing elements with a consensus sequence motif of 5'-(G/A)(G/A) TGACGT(C/G/A)(A/T/G)-3'. The motif represents a characteristically strong preference for flanking sequence to TGACGT and a larger sequence than the sequences recognized by the G-box binding factor and TGA protein families. The finding of C-box, hybrid C/G-, and C/A-boxes as high-affinity binding sites over the G-box and parameters associated with HY5 recognition define the criteria of HY5/STF1 protein-DNA interaction in the promoter regions. This study helps to predict the precise in vivo binding sites of the HY5 protein from the vast number of putative HY5 genomic binding sites analyzed by chromatin immunoprecipitation on chip.


1 This work was supported by funds from the CFGC of the 21st Century Frontier Research Program (grant no. CG1313), the Basic Research Program (grant no. R01–2007–000–11232–0), and an Environmental Biotechnology National Core Research Center grant from KOSEF/MOST, Korea (grant no. R15–2003–012–01001–0). This work was also supported by a scholarship from the Division of Applied Life Science (BK21 Program), granted by the MEHRD, Korea (to Y.H.S., H.J.K., and S.Y.S.).

2 These authors contributed equally to the article.

3 Present address: Plant Biology Division, The Samuel Roberts Noble Foundation, Inc., Ardmore, OK 73401.

The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Jong Chan Hong (jchong{at}gnu.ac.kr).

[C] Some figures in this article are displayed in color online but in black and white in the print edition.

[W] The online version of this article contains Web-only data.

[OA] Open Access articles can be viewed online without a subscription.

www.plantphysiol.org/cgi/doi/10.1104/pp.107.113217

* Corresponding author; e-mail jchong{at}gnu.ac.kr.

Received November 16, 2007; accepted February 13, 2008; published February 20, 2008.




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