Identification of Salt-responsive Biosynthesis Genes in Rice via Microarray Analysis

Chang-Kug Kim; Hyeon-So Ji; Hak-Bum Kim; Doh-Won Yun; Gang-Seob Lee; Ung-Han Yoon; Tae-Ho Kim; Dong-Suk Park; Young-Joo Seol; Yong-Jae Won

doi:10.4172/2375-4338.1000102

ISSN: 2375-4338

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Identification of Salt-responsive Biosynthesis Genes in Rice via Microarray Analysis

Chang-Kug Kim ^1#,Hyeon-So Ji ^1#,Hak-Bum Kim¹,Doh-Won Yun ²,Gang-Seob Lee¹,Ung-Han Yoon¹,Tae-Ho Kim¹,Dong-Suk Park¹,Young-Joo Seol¹and Yong-Jae Won^3*
¹Genomics Division, National Academy of Agricultural Science (NAAS), Rural Development Administration (RDA), Suwon 441-707, Korea
²Planning & Coordination Division, National Academy of Agricultural Science, Suwon 441-707, Republic of Korea
³Rice Research Division, National Institute of Crop Science, Suwon 441-857, Korea
^#These authors contributed equally to this work
Corresponding Author :	Yong-Jae Won Rice Research Division National Institute of Crop Science Suwon 441-857, Korea Tel: 82-31-290-6710 Fax: 82-31-290-6730 E-mail: yjwon@korea.kr
Received June 11, 2013; Accepted July 24, 2013; Published July 26, 2013
Citation: Chang-Kug K, Hyeon-So J, Hak-Bum K, Doh-Won Y, Gang-Seob L, et al. (2013) Identification of Salt-responsive Biosynthesis Genes in Rice via Microarray Analysis. J Rice Res 1:102. doi: 10.4172/jrr.1000102
Copyright: © 2013 Chang-Kug K, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Abstract

We used a multiple screening process to identify genes involved in salt tolerance–specific biosynthesis and metabolism in rice (Oryza sativa L.). We selected 8,275 salt tolerance–related candidate genes using expression profiles generated across four stages on a microarray containing 135,000 probes (135 K microarray) in Oryza sativa. Using our method, we screened 342 ortholog genes, and 74 pathway genes associated with salt –response–related biosynthesis. Finally, we identified six genes by comparison of pathway-network genes and orthologous genes. The six genes were anchored to the chromosomes of rice to characterize their genetic-map positions and were used to construct the phylogenetic tree. The results were verified by reverse transcription–polymerase chain reaction.

Keywords
Microarray analysis; Salinity; Salt-responsive genes
Introduction
In rice, abiotic stresses are responsible for most of the reduction that differentiates yield potential from harvestable yield. Salinity is a major abiotic stress that plants encounter in irrigated agricultural land, and salt stress may induce alterations in biochemical pathways and physiological responses [1]. Salt stress can lead to changes in development, growth, and productivity. Indeed, soil salinity causes severe losses in crop productivity worldwide mainly because it inhibits biomass yield [2-4]. To minimize the deleterious effects of salt stress, plants need to coordinate the activation and effects of several molecular mechanisms [5]. In many important plants, salt stress negatively affects germination, root development, and biomass production, resulting in the significant yield loss [6]. Using stress-resistance mutants, many studies have discovered the mechanisms by which plants mediate and attenuate salt stress. In transgenic overexpression of specific genes, homologous genes responsible for mediating salt tolerance have been identified [7], and pathways involved in detoxification and growth regulation have been found [8]. Thus, components of salt-stress signaling [9] stimulate the activation of specific signaling pathways in the cell [10]. High salt-tolerant mutant rice has been generated by transgenic modulation of salt-response gene expression [11]. However, although these studies have provided specific information about the underpinnings of salt tolerance, salt tolerance is a complex trait controlled by many quantitative trait loci. Thus, it is very difficult to define the genes whose products comprise a salinity-resistance signaling pathway [12]. Thus, it is necessary to apply high-throughput technologies to identify genes related to salt-responsive biosynthesis [13,14].
Rice (Oryza sativa L.), the most consumed grain in Asia, is a significant staple for feeding much of the world’s population, and its productivity is greatly affected by high salinity. This study, modification of rice strains to tolerate and thrive in high salt concentrations will allow inhabitants in these high-saline areas to also thrive. Thus, the further elucidation of the genes and proteins involved in promoting high-salt tolerance is vitally important. Recently, microarray analyses of the salt-stress response of many plant species have been performed that examined cell cultures, whole plants, or specific plant organs. Several microarray-based platforms are available for abiotic stress-related transcriptome studies of plants [15,16]. In this study, we examined the effects of high salt concentrations on gene expression responses in rice to better understand the genetic regulation of growth and metabolism in a high salinity environment. We identified candidate genes for the regulation of the salt stress expression network pathway using a microarray containing 135,000 probes (135 K microarrays), Clusters of Orthologous Groups (COGs), pathway, gene mapping, and phylogenetic tree analyses.
Materials and Methods
Rice
For this study, we selected two Ds mutant lines, Salt10 and Salt23, which showed increased salt tolerance as compared with their original variety, Dongjin. The high salt-tolerance mutants were generated with the Ac/Ds insertional gene trap system using Dongjin cultivar [17]. These mutant lines showed salt stress tolerance degree of 5~6 in two independent seedling salt stress tests using Yoshida nutritional solution [18] including 0.6% NaCl, while Dongjin’s degree was 9 in nine grade evaluation method which regards most resistant reference line as 1 and most susceptible line as 9. We expected both mutant cultivars to be useful in the analysis of gene expression specific to salt-responsive biosynthesis because these mutants have a similar genetic background and exhibit greater salt tolerance than the control Dongjin.
Experimental design
We assessed gene expression between inbred control and mutants of high salt-tolerant rice during four different salt treatment stages. We grew seedlings of these two mutant lines and Dongjin on water for the first week after germination and on Yoshida nutrient solution for the next two weeks in a growth chamber with 15 hour day-length and 30°C/20°C (day/night) temperature. Subsequently, salt treatment was conducted by transferring rice seedlings to Yoshida nutrient solution including 0.6% NaCl. The plants were subjected to salt stress conditions for the indicated time periods [12], upper parts of rice seedlings were taken at 0, 1, 3, and 6 hours after salt treatment for RNA extraction. After salt treatment, we cut the leaves on each plant at four different stages. We froze the harvested samples in liquid nitrogen and extracted the total RNA from the leaf tissues by using RNeasy^® plant mini-kits (Qiagen Inc., Valencia, CA, USA) with DNase (Qiagen Inc.) to remove residual DNA, and quantified RNA by using a Nanodrop ND-1000 spectrophotometer (Thermo Fisher Scientific Inc., Wilmington, NC, USA). For transcriptome analysis, we used 135K Oryza sativa microarrays [19] to perform a total of 36 experiments during four salt stress-treatment stages with two replicates.
Ortholog and pathway analysis
In order to identify ortholog, we classified the genes identified in our microarray experiments by comparing them to those in the eukaryotic NCBI/COGs database (http://www.ncbi.nlm.nih.gov/COG/). To identify interaction networks, our microarray experiment data represented potential interactions between expressed genes and the salt-responsive pathway. We performed an enriched-pathways analysis and calculated p-values with Fisher’s exact test to determine the most significant signaling network responses using Pathway Studio^® software 8.0 (Ariadne Inc., Rockville, MD, USA).
Phylogenetic with gene mapping analysis
In the phylogenetic analysis, amino-acid sequences of the salt tolerance-related genes were aligned using Clustal Omega (EMBL European Bioinformatics Institute, http://www.ebi.ac.uk/Tools/msa/clustalo/) Multiple Sequence Alignment program using the default options. In addition, we mapped all of the selected salt tolerancerelated genes onto the 12 chromosomes of rice. To find the best mapping position, we used the BLASTN program with cutoff value ≤ 2.0×10^-10 using the FSTVAL (G.G. BioTech Inc., Yongin, Korea, http://www.ebi.ac.uk/Tools/msa/clustalo/). The phylogenetic trees were constructed using the maximum likelihood algorithm in Molecular Evolutionary Genetics Analysis version 5 program (MEGA5, http://www.megasoftware.net/).
Reverse-transcription-polymerase chain reaction analysis (RT-PCR)
We used 5 μg RNA from each sample to synthesize complementary DNA, employing the EcoDry Premix Oligo dT kit (TaKaRaBio, Otsu, Shiga, Japan). To validate our RT-PCR results, we performed each experiment three times. We performed PCR with 10 pmol of each primer under the following conditions: 94°C for 5 min; 24 cycles of 94°C for 30 sec; 58°C for 30 sec; 72°C for 1 min; and a 10 min extension at 72°C. To measure the different expression of each target gene, we used Ubiquitin as a loading control for the primer sequences (Table 1).
Results and Discussion
Candidate genes associated with salt-responsive biosynthesis genes
We performed a total of 36 microarray experiments, analyzing three cultivars at four stages with three replications. Using the signalintensity values from the microarrays, we screened 8,275 genes to identify those with at least a 3-fold difference in expression between the two groups. We assumed that the observed differences in expression were related to the transcriptional regulation of salt-responsive genes because we based them on three separate signal-intensity ratios, two high salt-tolerance cultivars compared with the one weak salt-tolerance cultivar, and all of the cultivars experienced the same controlled experimental conditions. To identify conserved orthologous genes, we performed COGs analyses using the 8,275 candidate genes. In the COGs analyses, we placed 1,795 genes into functional categories on which we performed BLAST searches for each of the four stages. We screened a total of 342 orthologous genes using the COGs analyses, which use ortholog similarities to categorize conserved genes.
Pathway associated with salt-responsive genes
To identify genes involved in specific salt-responsive related pathways among the 8,275 differentially expressed genes, we performed an enriched-pathways analysis. We acquired a total of 729 microarray candidate genes for which evidence was found for involvement of salt tolerance in rice. Using a Fisher’s exact test to determine the most significant responses genes, we found 74 interconnected genes linked to specific salt-responsive pathways. Finally, we used these genes to construct an interconnected network to contain the salinity response, including Na⁺/H⁺ antiporter, and K⁺ channel pathways (Figure 1). These results illustrate the functional diversity of proteins that may be activated during increasing salt tolerance.
Anchored genes involved in salt-responsive biosynthesis
To screen the final candidate genes, we compared the 74 pathway genes and the 342 ortholog genes. We found six genes that were differentially expressed between the high- and weak-tolerance cultivars continuously during the four different stages. The putative proteins encoded by the three up-regulated genes (AK107809, J065130P18 and J065183J16) are a hypothetical protein, a wound-induced protein, and a conserved hypothetical protein, respectively. The three down-regulated genes (AK069955, AK110629 and AK067929) are nod factor-binding lectin-nucleotide phosphohydrolase, a conserved hypothetical protein, and a hypothetical protein, respectively. However, these genes identified by our method did not include any of the well-known genes in the salt-responsive biosynthesis pathway which in response to salt stress, salt-related genes are up- or down-regulated. We assume that this lack of identification might have resulted because many of the previously identified genes are not expressed continuously during the four salt treatment stages or might only be strongly expressed during a few of the four salt-treatment stages. To reveal the chromosome position relationship between the previously known genes and those identified by our analysis, we mapped the 74 pathway genes and anchored six genes onto the 12 chromosomes of the genome sequence of rice (Figure 2). The six genes were observed on five chromosomes (A03, A04, A07, A11 and A12). The mapping results of the six genes on the rice genome are presented with related mapping information in Table 2.
A phylogenetic analysis was performed to identify relationships between anchored genes and the others salt responsive-related genes based on the maximum likelihood method. Using the six anchored genes and 68 pathway genes, phylogenetic analysis was performed. All salt tolerance-related genes were clustered into three groups (Groups I to III). Intriguingly, Group I contain only down-regulated genes and up-regulated genes were found in Groups II and III (Figure 3). Thus, the six anchored genes identified included one wound-stress gene, four hypothetical protein genes, and one nod factor-binding function gene. These results suggest that the six genes of rice do not share the same genetic background with the previously known salt responsive-related pathway genes.
RT-PCR analysis of selected genes
To verify the six hypothetical genes identified by COGs and pathway analyses, we performed RT-PCR using the same RNA samples used in the microarray experiments. Three of six genes were up-regulated (AK107809, J065130P18, and J065183J16) and three genes were down-regulated (AK069955, AK110629, and AK067929) during all of the treatment stages tested (Figure 4). Among the six genes expressed at higher levels in the Dongjin cultivar, AK107809, J065130P18, and J065183J16 were expressed during all of the examined developmental stages. Therefore, these genes may play a role in salt tolerance or are related to salt stress-resistance increasing which are encoded a hypothetical protein, a wound-induced protein, and a conserved hypothetical protein, respectively. The three down-regulated genes were expressed at lower levels in the Dongjin cultivar that lacked salt tolerance or salt stress-resistance. Therefore, these genes may have additional functions other than salt stress biosynthesis. It is likely that the three up-regulated genes either play regulatory roles in increasing salt tolerance or are related to salt stress-resistance signaling during metabolite biosynthesis, whereas the down-regulated genes likely inhibit salt tolerance-resistance biosynthesis.
Conclusions
We identified six putative genes with different functions that appear to be related to the regulation of salt-responsive biosynthesis and/or metabolism in rice, using 135K microarrays. Using a screening method to combine ortholog, pathway, gene mapping, and phylogenetic analyses, we performed a multi-processes analysis to screen salt tolerance-related biosynthesis genes during four salttreatment stages in rice. After this analysis, we identified six genes that are most likely involved in regulation of either salt tolerance biosynthesis or metabolism. Our results suggest that these six genes participate in the production or control of salt tolerance during all of the treatment stages. Although there is no direct evidence, we suggest our methodology aided the identification of candidate genes after microarray experiment in the rice. While these genes will require further study to support the findings of our microarray analyses, our screening method does demonstrate a new and robust approach with which to identify genes involved in salt tolerance in rice.
Acknowledgement
This study was conducted with support from the Research Program for Agricultural Science & Technology Development (Project No. PJ006651) of the National Academy of Agricultural Science, and the Next-Generation BioGreen 21 Program (SSAC, grant number PJ009614), Rural Development Administration, Republic of Korea.
References
Walia H, Wilson C, Condamine P, Liu X, Ismail AM, et al. (2005) Comparative transcriptional profiling of two contrasting rice genotypes under salinity stress during the vegetative growth stage. Plant Physiol 139: 822-835. Munns R, Tester M (2008) Mechanisms of salinity tolerance. Annu Rev Plant Biol 59: 651-681. Wankhade SD, Bahaji A, Mateu-Andres I, Cornejo MJ (2010) Phenotypic indicators of NaCl tolerance levels in rice seedlings: variations in development and leaf anatomy. Acta Physiologiae Plantarum 32: 1161-1169 Pardo JM (2010) Biotechnology of water and salinity stress tolerance. Curr Opin Biotechnol 21:185–196. Zhang L, Tian LH, Zhao JF, Song Y, Zhang CJ, et al. (2009) Identification of an apoplastic protein involved in the initial phase of salt stress response in rice root by two-dimensional electrophoresis.. Plant Physiol 149: 916-928. Kawasaki S, Borchert C, Deyholos M, Wang H, Brazille S, et al. (2001) Gene expression profiles during the initial phase of salt stress in rice. Plant Cell 13: 889-905. Xu D, Duan X, Wang B, Hong B, Ho THD, et al. (1996) Expression of a Late Embryogenesis Abundant Protein Gene, HVA1, from Barley Confers Tolerance to Water Deficit and Salt Stress in Transgenic Rice. Plant Physiol 110: 249-257. Dubouzet JG, Sakuma Y, Ito Y, Kasuga M, Dubouzet EG, et al. (2003) OsDREB genes in rice, Oryza sativa L., encode transcription activators that function in drought-, high-salt- and cold-responsive gene expression. Plant J 33: 751-763. Kasuga M, Liu Q, Miura S, Yamaguchi-Shinozaki K, Shinozaki K (1999) Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor. Nat Biotechnol 17: 287-291. Guo Y, Song Y (2009) Differential proteomic analysis of apoplastic proteins during initial phase of salt stress in rice. Plant Signal Behav 4: 121-122. Lin HX, Zhu MZ, Yano M, Gao JP, Liang ZW, et al. (2004) QTLs for Na+ and K+ uptake of the shoots and roots controlling rice salt tolerance. Theor Appl Genet 108: 253-260. Kawasaki S, Borchert C, Deyholos M, Wang H, Brazille S, et al. (2001) Gene expression profiles during the initial phase of salt stress in rice. Plant Cell 13: 889-906. Seki M, Narusaka M, Ishida J, Nanjo T, Fujita M, et al. (2002) Monitoring the expression profiles of 7000 Arabidopsis genes under drought, cold and high-salinity stresses using a full-length cDNA microarray. Plant J 31: 279-292. Zhu JK (2001) Plant salt tolerance. Trends Plant Sci 6: 66-71. Takahashi S, Seki M, Ishida J, Satou M, Sakurai T, et al. (2004) Monitoring the expression profiles of genes induced by hyperosmotic, high salinity, and oxidative stress and abscisic acid treatment in Arabidopsis cell culture using a full-length cDNA microarray. Plant Mol Biol 56: 29-55. Kim CK, Lee YH, Hong JK, Park DS, Kim MK, et al. (2012) Identification and characterization of flowering repressor-related genes in Chinese cabbage. BioChip J 6: 120-127. Kim CK, Kikuchi S, Kim YK, Park SH, Yoon UH, et al. (2010) Computational identification of seed-specific transcription factors involved in anthocyanin production in black rice. BioChip J 4: 247-255. Yoshida S, Forno DA, Cock JH, Gomez KA (1976) Laboratory manual for physiological studies of rice. (3rdedn), IRRI, Manila. Kim CK, Cho MA, Choi YH, Kim JA, Kim YH, et al. (2011) Identification and characterization of seed-specific transcription factors regulating anthocyanin biosynthesis in black rice. J Appl Genet 52: 161-169.