Abiotic stress-responsive expression of wali1 and wali5 genes from ...

Short Communication Plant Signaling & Behavior 7:11, 1–4; November 2012; © 2012 Landes Bioscience

Abiotic stress-responsive expression of wali1 and wali5 genes from wheat Bharti Garg,1 Swati Puranik,2 Narendra Tuteja1 and Manoj Prasad2,* International Centre for Genetic Engineering and Biotechnology; Aruna Asaf Ali Marg; New Delhi, India; 2National Institute of Plant Genome Research; Aruna Asaf Ali Marg; New Delhi, India

Keywords: Triticum aestivum, wheat, wali1, wali5, Aluminium responsive, abiotic stress

Two cDNA clones, encoding Aluminum-responsive wali1 and wali5, were identified in dehydration stress-specific cDNA library from wheat. Their sequence variations and structural dissimilarities indicated them to be non-homologous genes. Expression of both genes was induced by various abiotic stresses as well as in response to plant hormones and oxidative molecules. Further, they were expressed differentially in shoot and root tissues of wheat seedlings, their transcripts being specifically abundant in roots. Previously characterized as being only Aluminum treatment induced, this report proposes them as novel candidates for stress-responsive studies.

Introduction Environmental stresses such as dehydration, salinity, low temperature and metal stress lead to various biochemical, physiological and molecular adjustments in plants.1 These responses are thought to be a result of stimulus perception and signal transduction in plant cell, often involving interplay of phytohormones. The stress signaling pathways are generally mediated via hormones like absissic acid (ABA), ethephone, jasmonic and salicyclic acid.2 Stress responses involve cell-to-cell signaling and expression of many novel stress-responsive genes, exact role of many being still unclear.3-5 Two such cDNA clones (GenBank Accession number JK546491 and JK546492), isolated from a dehydration stress subtractive cDNA library in wheat (Garg et al., unpublished), showed homology to wali1 and wali5 genes, that have been previously reported as being specifically responsive to Aluminum stress.6 BLAST analysis against the non-redundant protein sequences revealed that wali1 (GenBank Accession number L11879) was highly similar to metallothionin-like proteins (E-value: 2.00e-77) 6 whereas wali5 (GenBank Accession number L11882) showed homology to a Bowmans birk protease inhibitorlike protein (E-value: 5.00e-72).6 Initially reported to be induced in response to Aluminum-stress in wheat, their expression behavior in other stress conditions, like dehydration and salinity, remain unexplored to date. We therefore aimed to characterize these genes, with respect to their diverse three dimensional (3D) structure alongwith spatial and temporal regulation of their transcript expression under different stresses and hormonal treatments. All plant materials were grown under same environmental conditions, wheat seeds were germinated in composite soil (peat

compost to vermiculite, 3:1) and grown under optimal growth conditions.1 Ten days old seedlings were treated with 20% polyethylene glycol-6000 (dehydration), 200mM NaCl (salinity), 100mM ABA, 4°C (cold), 10mM hydrogen peroxide (H2O2) and 100μM ethephone as described elsewhere.7 Total RNA was isolated during 1, 6, 12 and 24 h after stress treatments by using TRIzol Reagent (Life technologies, Rockville, MD, USA) as described earlier.8 For, northern blot analysis about 20μg of total RNA from each sample was electrophoresed on 1.2% denaturing gel. Three biological replicates were taken for each sample (n = 3). Motif Scan analysis (http://myhits.isb-sib.ch/cgi-bin/motif_ scan/)9 of wali1 protein by using default parameters revealed the presence of several domains such as the Casein kinase domain, ATP/GTP binding site, site with protein kinase activity, N-glycosylation site alongwith a DNA-binding domain. The protein was predicted to be localized in nucleus according to Plantmploc (http://www.csbio.sjtu.edu.cn/bioinf/plant-multi/)10 and putative nucleus localization signals (NLSs) were found at C-terminal end of the protein (www.sbc.su.se/~maccallr/ nucpred/). Absence of transmembrane helices indicates that this protein was highly unlikely to be associated with nuclear membrane. On the other hand, Wali5 was found to contain a transmembrane helix as well as a NLS, and was predicted to be present in cell membrane and nucleus as a glycosylphosphatidylinositolanchored protein (www.csbio.sjtu.edu.cn/bioinf/MemType/).11 Secondary structure prediction for wali1 and wali5 proteins was performed using SOPMA (http://npsa-pbil.ibcp.fr/cgi-bin/ npsa_automat.pl?page=/NPSA/npsa_sopma.html).12 Wali1 consisted of 19 α helices, 7 β turns joined by 7 extended sheets and 42 random coils (Fig. 1A), whereas wali5 had 21 α helices and 6 β turns joined by 8 extended sheets and 54 random coils (Fig.

*Correspondence to: Manoj Prasad; Email: [email protected] Submitted: 07/14/12; Revised: 08/17/12; Accepted: 08/19/12 http://dx.doi.org/10.4161/psb.21885 www.landesbioscience.com

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1B). As three-dimensional (3D) structure of a protein could facilitate understanding its molecular function, ab initio modeling of wali1 and wali5 was performed by I-TASSER server due to unavailability of any significant homologous template in the protein database for modeling the complete sequence (Fig. 1C and D). The modeled structure was validated with PROSA (https://prosa.services.came.sbg.ac.at/prosa.php/)13 which gave a calculated z-score of -4.9 for wali1 and -4.11 for wali5. This value was in the range of native conformations of other experimentally determined protein structures having similar size. Temporal and tissue specific expression of wali1 and wali5 under different abiotic stresses was determined by northern blotting and signal intensities were quantified by densitometry analysis of three independent technical replicates. wali1 and wali5 were induced in roots and shoots of ten days old wheat seedlings under various abiotic stresses, hormonal response and in presence of a ROS mediator (H2O2). Transcripts of wali1 accumulated in roots in response to all the stresses but in shoots, elevated expression was observed due to cold and ABA treatment (Fig. 2A-F). Our observations are consistent with several previous studies on other Metallothionin-like genes which reportedly show comparable stress- and tissue-specific expressions.14-17 Studies have also shown that transcription of metallothionin can be induced by plant hormones like ABA and etheylene.18 Ethephone enhanced the production of reactive oxygen species, leading to the expression of

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metallothionin II in rice.19 Further, various oxidants such as H2O2, SNP and Paraquat have also been reported to be involved in the regulation of metallothionin expression by formation of disulphide bonds between cysteine residues of metallothionins.20,21 Interestingly, wali5 was highly induced (~7-folds) by dehydration till 6h in roots, while in shoots, its expression was observed in during later time period of dehydration stress (Fig. 3A). Other stresses like salinity, cold, ABA and H2O2 rapidly upregulated wali5 upto 3-folds in roots (Fig. 3B-F). Protease inhibitors are known to be induced when plants are subjected to abiotic stress or exogenous supply of phytohormones for appropriate regulation of protein turn-over during environmental constraints.22 The expression of protease inhibitors in response to drought or salinity stress has been extensively studied. Salt stress has been shown to result in the accumulation of bowman birk protease inhibitor transcripts in wheat.22 Cystatin (a cysteine protease inhibitor) in chestnut and barley, and rice OCPI1 (Oryza sativa chymotrypsin inhibitor-like 1) can both be induced by drought, salinity, exogenous abscisic acid and cold stress.23-25 Conclusions The wali1 and wali5 genes both encode for nuclear proteins, with wali5 being membrane-anchored. Structurally, these non-homologous proteins show presence of various motifs. They both appear


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Figure 1. (A-D) Structural features of wali1 and wali5. Comparison of secondary structure of (A) wali1 and (B) wali5 by SOPMA program. The helix, sheet, turn and coil are indicated by vertical lines shown in different color as blue, red, green and purple, respectively. Three dimensional structure of (C) wali1 and (D) wali 5 proteins by I-TASSER server.

to be expressed higher in roots than shoots and are also rapidly induced by various kinds of stresses including dehydration, salinity, cold, H2O2 and plant hormones (ABA and ethephone). Among all abiotic stresses, they showed maximum expression in response to dehydration and salt treatments. These genes have been previously reported as Aluminum-stress responsive genes. Based on our results, it may be suggested that apart from Aluminum stress, wali1 and wali5 have a generalized response for abiotic stresses. Therefore, it may be hypothesized that wali1 and wali5 augment common metal as well as abiotic stress-responsive machinery, induction of which eventually leads to higher vigor in plants. Further exploration of biological roles of these two interesting candidates through genetic engineering will endow us with understanding novel pathways governing stress adaptation in plants. Disclosure of Potential Conflicts of Interest

No potential conflicts of interest were disclosed. Acknowledgments

Grateful thanks are due to the Directors, International Centre for Genetic Engineering and Biotechnology and National Institute of Plant Genome Research, New Delhi, India for providing facilities.

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Figure 2. (A-F) Temporal and tissue-specific expression of wali1 transcripts under various abiotic stresses in root and shoot tissues of wheat. The relative mRNA expression for each transcript was calculated in dehydration, salt, abscissic acid, cold, hydrogen peroxide and ethephone relative to its expression in control plants. Bars indicate the standard error (± SE) calculated from three independent northern blotting experiments.

Figure 3. (A-F) Temporal and tissue-specific expression of wali5 gene in root and shoot under various abiotic stresses. The relative mRNA expression for each transcript was calculated in dehydration, salt, ABA, cold, H2O2 and ethephone relative to its expression in control plants. Bars indicate the standard error (± SE) calculated from three independent northern blotting experiments.

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