journal article Jul 01, 2003

Integration of Wounding and Osmotic Stress Signals Determines the Expression of the AtMYB102 Transcription Factor Gene

View at Publisher Save 10.1104/pp.102.019273
Abstract
Abstract
Transcript levels of the Arabidopsis R2R3-AtMYB102 transcription factor gene, previously named AtM4, are rapidly induced by osmotic stress or abscisic acid (ABA) treatment. Reporter gene expression studies revealed that in addition, wounding is required for full induction of the gene. Histochemical analysis showed a local β-glucuronidase induction around the wounding site, especially in veins. In ABA-treated plants, wounding-induced β-glucuronidase activity could be mimicked by the wound signaling compound methyl jasmonate. In silico studies of the AtMYB102 promoter sequence and its close homolog AtMYB74 demonstrated several conserved putative stress regulatory elements such as an ABA-responsive element, its coupling element 1 (CE1), and a W box. Interestingly, further studies showed that the 5′-untranslated region is essential for the osmotic stress and wounding induced expression of the AtMYB102 gene. This 5′-untranslated region contains putative conserved regulatory elements such as a second W box and an overlapping MYB-binding element. These studies suggest that AtMYB102 expression depends on and integrates signals derived from both wounding and osmotic stress.
Topics

No keywords indexed for this article. Browse by subject →

References
35
[1]
Birkenmeier GF, Ryan CA (1998) Wound signaling in tomato plants. Evidence that aba is not a primary signal for defense gene activation. Plant Physiol  117  :  687–693 10.1104/pp.117.2.687
[2]
Carles C, Bies-Etheve N, Aspart L, Leon-Kloosterziel KM, Koornneef M,  Echeverria M, Delseny M (2002) Regulation of Arabidopsis thaliana Em genes: role of ABI5. Plant J  30  :  373–383 10.1046/j.1365-313x.2002.01295.x
[3]
Carrera E, Prat S (1998) Expression of the Arabidopsis abi1-1 mutant allele inhibits proteinase inhibitor wound-induction in tomato. Plant J  15  :  765–771 10.1046/j.1365-313x.1998.00261.x
[4]
Clough SJ, Bent AF (1998) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J  16  :  735–743 10.1046/j.1365-313x.1998.00343.x
[5]
Eulgem T, Rushton PJ, Schmelzer E, Hahlbrock K, Somssich IE (1999) Early nuclear events in plant defence signalling: rapid gene activation by WRKY transcription factors. EMBO J  18  :  4689–4699 10.1093/emboj/18.17.4689
[6]
Gosti F, Bertauche N, Vartanian N, Giraudat J (1995) Abscisic acid-dependent and -independent regulation of gene expression by progressive drought in Arabidopsis thaliana. Mol Gen Genet  246  :  10–18 10.1007/bf00290128
[7]
Hara K, Yagi M, Kusano T, Sano H (2000) Rapid systemic accumulation of transcripts encoding a tobacco WRKY transcription factor upon wounding. Mol Gen Genet  263  :  30–37 10.1007/pl00008673
[8]
General roles of abscisic and jasmonic acids in gene activation as a result of mechanical wounding.

T Hildmann, M Ebneth, H Peña-Cortés et al.

The Plant Cell 10.1105/tpc.4.9.1157
[9]
Hong SW, Jon JH, Kwak JM, Nam HG (1997) Identification of a receptor-like protein kinase gene rapidly induced by abscisic acid, dehydration, high salt, and cold treatments in Arabidopsis thaliana. Plant Physiol  113  :  1203–1212 10.1104/pp.113.4.1203
[10]
Iuchi S, Kobayashi M, Taji T, Naramoto M, Seki M, Kato T, Tabata S,  Kakubari Y, Yamaguchi-Shinozaki K, Shinozaki K (2001) Regulation of drought tolerance by gene manipulation of 9-cis-epoxycarotenoid dioxygenase, a key enzyme in abscisic acid biosynthesis in Arabidopsis. Plant J  27  :  325–333 10.1046/j.1365-313x.2001.01096.x
[11]
Kiyosue T, Yamaguchi-Shinozaki K, Shinozaki K (1994) Cloning of cDNAs for genes that are early-responsive to dehydration stress (ERDs) in Arabidopsis thaliana L.: identification of three ERDs as HSP cognate genes. Plant Mol Biol  25  :  791–798 10.1007/bf00028874
[12]
Knight MR, Read ND, Campbell AK, Trewavas AJ (1993) Imaging calcium dynamics in living plants using semisynthetic recombinant aequorins. J Cell Biol  121  :  83–90 10.1083/jcb.121.1.83
[13]
Koornneef M, Alonso-Blanco C, Stam P (1998) Genetic analysis. Methods Mol Biol  82  :  105–117 10.1385/0-89603-391-0:105
[14]
Kranz HD, Denekamp M, Greco R, Jin H, Leyva A, Meissner RC, Petroni  K, Urzainqui A, Bevan M, Martin C et al. (1998) Towards functional characterisation of the members of the R2R3-MYB gene family from Arabidopsis thaliana. Plant J  16  :  263–276 10.1046/j.1365-313x.1998.00278.x
[15]
Leon J, Rojo E, Sanchez-Serrano JJ (2001) Wound signalling in plants. J Exp Bot  52  :  1–9 10.1093/jexbot/52.354.1
[16]
Maeo K, Hayashi S, Kojima-Suzuki H, Morikami A, Nakamura K (2001) Role of conserved residues of the WRKY domain in the DNA-binding of tobacco WRKY family proteins. Biosci Biotechnol Biochem  65  :  2428–2436 10.1271/bbb.65.2428
[17]
Niu X, Helentjaris T, Bate NJ (2002) Maize ABI4 binds Coupling Element1 in abscisic acid and sugar response genes. Plant Cell  14  :  2565–2575 10.1105/tpc.003400
[18]
Orozco-Cardenas M, Ryan CA (1999) Hydrogen peroxide is generated systemically in plant leaves by wounding and systemin via the octadecanoid pathway. Proc Natl Acad Sci USA  96  :  6553–6557 10.1073/pnas.96.11.6553
[19]
Peña-Cortés H, Fisahn J, Willmitzer L (1995) Signals involved in wound-induced proteinase inhibitor II gene expression in tomato and potato plants. Proc Natl Acad Sci USA  92  :  4106–4113 10.1073/pnas.92.10.4106
[20]
Quaedvlieg N, Dockx J, Keultjes G, Kock P, Wilmering J, Weisbeek P,  Smeekens S (1996) Identification of a light-regulated MYB gene from an Arabidopsis transcription factor gene collection. Plant Mol Biol  32  :  987–993 10.1007/bf00020495
[21]
Reymond P, Weber H, Damond M, Farmer EE (2000) Differential gene expression in response to mechanical wounding and insect feeding in Arabidopsis. Plant Cell  12  :  707–720 10.2307/3870996
[22]
Robatzek S, Somssich IE (2002) Targets of AtWRKY6 regulation during plant senescence and pathogen defense. Genes Dev  16  :  1139–1149 10.1101/gad.222702
[23]
Rojo E, Leon J, Sanchez-Serrano JJ (1999) Cross-talk between wound signalling pathways determines local versus systemic gene expression in Arabidopsis thaliana. Plant J  20  :  135–142 10.1046/j.1365-313x.1999.00570.x
[24]
Ryan CA (2000) The systemin signaling pathway: differential activation of plant defensive genes. Biochim Biophys Acta  1477  :  112–121 10.1016/s0167-4838(99)00269-1
[25]
Ryu SB, Wang X (1998) Increase in free linolenic and linoleic acids associated with phospholipase D-mediated hydrolysis of phospholipids in wounded castor bean leaves. Biochim Biophys Acta  1393  :  193–202 10.1016/s0005-2760(98)00048-4
[26]
Sakuma Y, Liu Q, Dubouzet JG, Abe H, Shinozaki K, Yamaguchi-  Shinozaki K (2002) DNA-binding specificity of the ERF/AP2 domain of Arabidopsis DREBs, transcription factors involved in dehydration. Biochem Biophys Res Commun  290  :  998–1009 10.1006/bbrc.2001.6299
[27]
Shav-Tal Y, Zipori D (2002) PSF and p54(nrb)/NonO: multi-functional nuclear proteins. FEBS Lett  531  :  109–114 10.1016/s0014-5793(02)03447-6
[28]
Sickinger S, Schweizer M (1999) A high affinity binding site for the polypyrimidine tract binding protein (PTB) is located in the 5′-untranslated region of the rat proteinase alpha1-inhibitor 3 variant I gene. Biol Chem  380  :  1217–1223 10.1515/bc.1999.154
[29]
Tan BC, Schwartz SH, Zeevaart JA, McCarty DR (1997) Genetic control of abscisic acid biosynthesis in maize. Proc Natl Acad Sci USA  94  :  12235–12240 10.1073/pnas.94.22.12235
[30]
Titarenko E, Rojo E, Leon J, Sanchez-Serrano JJ (1997) Jasmonic acid-dependent and -independent signaling pathways control wound-induced gene activation in Arabidopsis thaliana. Plant Physiol  115  :  817–826 10.1104/pp.115.2.817
[32]
Agrobacterium tumefaciens -mediated transformation of Arabidopsis thaliana root explants by using kanamycin selection

Dirk Valvekens, Marc Van Montagu, Mieke Van Lijsebettens

Proceedings of the National Academy of Sciences 10.1073/pnas.85.15.5536
[33]
Yamaguchi-Shinozaki K, Shinozaki K (1993) Characterization of the expression of a desiccation-responsive rd29 gene of Arabidopsis thaliana and analysis of its promoter in transgenic plants. Mol Gen Genet  236  :  331–340 10.1007/bf00277130
[34]
Yamaguchi-Shinozaki K, Shinozaki K (1994) A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress. Plant Cell  6  :  251–264 10.1105/tpc.6.2.251
[35]
Molecular Aspects of Osmotic Stress in Plants

Jian-Kang Zhu, Paul M. Hasegawa, Ray A. Bressan et al.

Critical Reviews in Plant Sciences 10.1080/07352689709701950
Metrics
186
Citations
35
References
Details
Published
Jul 01, 2003
Vol/Issue
132(3)
Pages
1415-1423
License
View
Cite This Article
Marten Denekamp, Sjef C. Smeekens (2003). Integration of Wounding and Osmotic Stress Signals Determines the Expression of the AtMYB102 Transcription Factor Gene. Plant Physiology, 132(3), 1415-1423. https://doi.org/10.1104/pp.102.019273
Related

You May Also Like

Superoxide Dismutases

Constantine N. Giannopolitis, Stanley K. Ries · 1977

5,382 citations

Non-Photochemical Quenching. A Response to Excess Light Energy

Patricia Müller, Xiao-Ping Li · 2001

2,354 citations