Arabidopsis Basic Leucine Zipper Transcription Factors Involved in an Abscisic Acid-Dependent Signal Transduction Pathway under Drought and High-Salinity Conditions

The induction of the dehydration-responsive Arabidopsis gene, rd29B, is mediated mainly by abscisic acid (ABA). Promoter analysis of rd29B indicated that two ABA-responsive elements (ABREs) are required for the dehydration-responsive expression of rd29B as cisacting elements. Three cDNAs encoding ba...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 97; no. 21; pp. 11632 - 11637
Main Authors Uno, Yuichi, Furihata, Takashi, Abe, Hiroshi, Yoshida, Riichiro, Shinozaki, Kazuo, Yamaguchi-Shinozaki, Kazuko
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences of the United States of America 10.10.2000
National Acad Sciences
National Academy of Sciences
The National Academy of Sciences
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Summary:The induction of the dehydration-responsive Arabidopsis gene, rd29B, is mediated mainly by abscisic acid (ABA). Promoter analysis of rd29B indicated that two ABA-responsive elements (ABREs) are required for the dehydration-responsive expression of rd29B as cisacting elements. Three cDNAs encoding basic leucine zipper (bZIP)-type ABRE-binding proteins were isolated by using the yeast one-hybrid system and were designated AREB1, AREB2, and AREB3 (ABA-responsive element binding protein). Transcription of the AREB1 and AREB2 genes is up-regulated by drought, NaCl, and ABA treatment in vegetative tissues. In a transient transactivation experiment using Arabidopsis leaf protoplasts, both the AREB1 and AREB2 proteins activated transcription of a reporter gene driven by ABRE. AREB1 and AREB2 required ABA for their activation, because their transactivation activities were repressed in aba2 and abi1 mutants and enhanced in an era1 mutant. Activation of AREBs by ABA was suppressed by protein kinase inhibitors. These results suggest that both AREB1 and AREB2 function as transcriptional activators in the ABA-inducible expression of rd29B, and further that ABA-dependent posttranscriptional activation of AREB1 and AREB2, probably by phosphorylation, is necessary for their maximum activation by ABA. Using cultured Arabidopsis cells, we demonstrated that a specific ABA-activated protein kinase of 42-kDa phosphorylated conserved N-terminal regions in the AREB proteins.
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Communicated by Maarten Koornneef, Wageningen Agricultural University, Wageningen, The Netherlands
To whom reprint requests should be addressed. E-mail: kazukoys@jircas.affrc.go.jp or sinozaki@rtc.riken.go.jp.
Present address: Faculty of Agriculture, Kobe University, 1–1, Rokko, Kobe 657, Japan.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.190309197