Combinatorial interactions of multiple cis-elements regulating the induction of the Arabidopsis XERO2 dehydrin gene by abscisic acid and cold

被引:25
作者
Chung, Susanna [1 ]
Parish, Roger W. [1 ]
机构
[1] La Trobe Univ, Dept Bot, Bundoora, Vic 3086, Australia
关键词
cold; abscisic acid; promoter; cis-elements; dehydrins; XERO2;
D O I
10.1111/j.1365-313X.2007.03399.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Multiple combinations of mutations in the promoter of the XERO2 dehydrin gene were used to identify elements involved in ABA and cold induction. Mutating one of the three ACGT elements (ACGT1) increases expression in the absence of cold or ABA. An AT-rich element is a novel partner (coupling element) of ACGT-containing ABA-responsive cis-elements. A 12-bp palindrome also acts as a coupling element for ABA induction and includes one of the three dehydration-responsive element/C-repeat (DRE/CRT) elements and two overlapping motifs (TGTCG and TCGGC) previously shown to be statistically enriched in ABA-dependent and 'VP1 or ABA'-dependent activated genes (Plant Physiol. 2005; 139:437). At least two of the DRE/CRT elements are required for significant cold induction. During cold induction the AT-rich element also functions as a coupling element and ACGT1 is involved in repressing this induction. Two of the ACGT and DRE/CRT elements overlap, and mutating a single base in the ACGT of either of the two GCCGACGT sequences while retaining a DRE element reduced both ABA and cold induction. Changing the spatial relationships between the elements by deletion, inversion or insertion of DNA sequences reduced both cold and ABA induction. Overexpression of CBF1, -2 or -3 induced XERO2 expression in untreated plants. The ABI5 transcription factor may have a role in ABA-induced XERO2 expression, whereas ABI3 and ABI4 do not. The GCA2 gene was essential for both cold and ABA induction. A combination of the same overlapping and shared elements is used in the regulation of transcription by ABA and cold.
引用
收藏
页码:15 / 29
页数:15
相关论文
共 76 条
[31]   ACGT-containing abscisic acid response element (ABRE) and coupling element 3 (CE3) are functionally equivalent [J].
Hobo, T ;
Asada, M ;
Kowyama, Y ;
Hattori, T .
PLANT JOURNAL, 1999, 19 (06) :679-689
[32]   A bZIP factor, TRAB1, interacts with VP1 and mediates abscisic acid-induced transcription [J].
Hobo, T ;
Kowyama, Y ;
Hattori, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15348-15353
[33]  
Jefferson RA., 1987, PLANT MOL BIOL REP, V5, P387, DOI DOI 10.1007/BF02667740
[34]   Requirement of a CCGAC cis-acting element for cold induction of the BN115 gene from winter Brassica napus [J].
Jiang, C ;
Iu, B ;
Singh, J .
PLANT MOLECULAR BIOLOGY, 1996, 30 (03) :679-684
[35]   Isolation of a novel class of bZIP transcription factors that interact with ABA-responsive and embryo-specification elements in the Dc3 promoter using a modified yeast one-hybrid system [J].
Kim, SY ;
Chung, HJ ;
Thomas, TL .
PLANT JOURNAL, 1997, 11 (06) :1237-1251
[36]   Arabidopsis ABI5 subfamily members have distinct DNA-binding and transcriptional activities [J].
Kim, SY ;
Ma, JZ ;
Perret, P ;
Li, ZS ;
Thomas, TL .
PLANT PHYSIOLOGY, 2002, 130 (02) :688-697
[37]   Maize DRE-binding proteins DBF1 and DBF2 are involved in rab17 regulation through the drought-responsive element in an ABA-dependent pathway [J].
Kizis, D ;
Pagès, M .
PLANT JOURNAL, 2002, 30 (06) :679-689
[38]   The sfr6 mutation in arabidopsis suppresses low-temperature induction of genes dependent on the CRT DRE sequence motif [J].
Knight, H ;
Veale, EL ;
Warren, GJ ;
Knight, MR .
PLANT CELL, 1999, 11 (05) :875-886
[39]   Abscisic acid induces CBF gene transcription and subsequent induction of cold-regulated genes via the CRT promoter element [J].
Knight, H ;
Zarka, DG ;
Okamoto, H ;
Thomashow, ME ;
Knight, MR .
PLANT PHYSIOLOGY, 2004, 135 (03) :1710-1717
[40]   Microarray expression analyses of Arabidopsis guard cells and isolation of a recessive abscisic acid hypersensitive protein phosphatase 2C mutant [J].
Leonhardt, N ;
Kwak, JM ;
Robert, N ;
Waner, D ;
Leonhardt, G ;
Schroeder, JI .
PLANT CELL, 2004, 16 (03) :596-615