Document Type : Original Article

Authors

1 Former PhD student, Plant Breeding and Biotechnology Department, Faculty of Plant Production, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran

2 Associate Professor of Plant Breeding and Biotechnology Department, Faculty of Plant Production, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran

3 Assistant Professor of Plant Breeding and Biotechnology Department, Faculty of Plant Production, Gorgan University of Agricultural Sciences and Natural Resources, Gorgan, Iran

4 Assistant Professor, Rice Research Institute of Iran, Mazandaran Branch, Agricultural Research, Education and Extension Organization (AREEO), Amol, Iran

5 Professor of Plant Biochemistry Department, Heinrich Heine University (HHU), Düsseldorf, Germany

6 Assistant Professor of Plant Biochemistry Department, Heinrich Heine University (HHU), Düsseldorf, Germany

Abstract

Introduction
Salinity as one of the major abiotic stresses influences plant growth and development. Among the cereal, rice is the most sensitive to salinity stress, with 30 mmol NaCl already strongly reducing the growth and yield of rice plants. Over the past few decades, significant efforts have been made worldwide to understand mechanisms of salinity tolerance and to breed salt-tolerant varieties in rice. Plants respond to salt stress through perceiving and transducing the osmotic and ion signals to cell interiors, followed by modification of cellular characteristics.
So far, no specific sensor or receptor for Na+ has been identified in plants. However, the salt overly sensitive (SOS) signaling pathway and calcineurin B-like (CBL)/CBL-interacting kinase (CIPK) pathway has been well characterized in Arabidopsis. Salt-induced elevation in cytosolic Ca2+ activates the SOS2-SOS3 protein kinase complex, which phosphorylates and stimulates the activity of SOS1, a plasma membrane Na+/H+ antiporter. In rice, the OsSOS1, OsSOS2/OsCIPK24 and OsSOS3/OsCBL4 genes have been isolated and the function and relationship between them investigated. Among them, OsCIPK24 and OsCBL4 act in concert to activate OsSOS1. In this research, we used RNA-seq approach to dissect signaling pathway in response to salinity stress using salt-tolerant and sensitive rice cultivars.
Materials and methods
The seeds of two rice (Oryza sativa L. ssp. Indica) genotypes with different salinity tolerance were obtained from International Rice Research Institute (IRRI) in Philippines. The plants were grown hydroponically in the greenhouse of Heinrich-Heine-University (HHU), Düsseldorf, Germany. The two-week old seedlings were exposed to 150 mM (15 dSm-1) NaCl salinity. The root and shoot samples were harvested at 6h and 54h post-treatment in three biological replications. 48 samples were sequenced by Illumina platform and the raw filtered reads were mapped on rice reference genome. Tuxedo instruction was applied to identifying the differentially expressed genes (DEGs). MapMan software was used to identify the genes involved in signaling pathway
Results and discussion
In RNA-Seq analysis, 48 samples were sequenced by Illumina platform and 15483 differentially expressed genes (DEGs) were identified. Out of the DEGs (from the comparison between the cultivars), 525 and 1472 genes were salt-specific in 6 and 54h time points in roots respectively. Out of the salt-specific DEGs in shoots, 635 and 606 genes were in 6 and 54h respectively. MapMan pathway analysis detected 91 genes in signaling pathway. Out of the genes, 27 genes showed high expression. Out of the genes, 21 genes showed more expression in tolerant cultivar CSR28 compared to sensitive cultivar IR28. The most difference between the cultivars was observed in roots after 54h of salt treatment suggesting the critical role of roots in salt tolerance induction. Receptor like kinase (RLK) proteins played the most important role among the identified signaling genes. Several important genes involved in major signaling processes such as OsSIK1, OsSAPK4, OsCIPK05, OsCIPK14, OsCBL4 and OsPP2C1 were identified in this research.
Conclusion
Salt-tolerant cultivars use better signaling pathways to sensing of stress and having the stronger osmotic and ionic reactions to cope with salinity stress. In the present research, huge number of differentially expressed genes generated using rice tolerant cultivar CSR28 and sensitive cultivar IR28 at 6 and 54h sampling times by RNA-Seq method. The comparison of the cultivars at specific salt stress showed that 91 genes (including 27 high expressed genes) were involved in signaling pathway. Kinase proteins played the most important role among the signaling pathway genes. The important genes identified in this research can be applied in the selecting and developing of salt-tolerant rice cultivars.
Acknowledgements
We appreciate the International Rice Research Institute (IRRI) for providing the seeds. We also acknowledge the excellent technical assistance of Gorgan University of Agricultural Sciences and Natural Resources (GAU), Gorgan, Iran and Heinrich-Heine-University (HHU), Düsseldorf, Germany.

Keywords

Main Subjects

Akbarzadeh Lelekami, M., Pahlevani, M. H., Zaynali Nezhad, K., Mahdavi Mashaki, K., PM Weber, A., Brilhaus, D., 2020. Response of some of primary metabolites in rice (Oryza sativa L.) root to salinity stress. Journal of Crop Breeding. 12, 210-217. [In Persian with English summary].
Andrews, S., 2010. FastQC: a quality control tool for high throughput sequence data. Available online at: http://www.bioinformatics.babraham.ac.uk/projects/fastqc
Asano, T., Hayashi, N., Kobayashi, M., Aoki, N., Miyao, A., Mitsuhara, I., Kikuchi, S., 2012. A rice calcium‐dependent protein kinase OsCPK12 oppositely modulates salt‐stress tolerance and blast disease resistance. The Plant Journal. 69, 26-36.
Bolger, A. M., Lohse, M., Usadel, B., 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 30, 2114-2120.
Chen, X. F., Gu, Z. M., Feng, L., Zhang, H. S., 2011. Molecular analysis of rice CIPKs involved in both biotic and abiotic stress responses. Rice Science. 18, 1-9.
Chinnusamy, V., Jagendorf, A., Zhu, J. K., 2005. Understanding and improving salt tolerance in plants. Crop Science. 45, 437-448.
Cotsaftis, O., Plett, D., Johnson, A. A., Walia, H., Wilson, C., Ismail, A. M., Close, T. J., Tester, M., Baumann, U., 2011. Root-specific transcript profiling of contrasting rice genotypes in response to salinity stress. Molecular Plant. 4, 25-41.
Howe, E. A., Sinha, R., Schlauch, D., Quackenbush, J., 2011. RNA-Seq analysis in MeV. Bioinformatics. 27, 3209-3210.
Hunter, M. C., Smith, R. G., Schipanski, M. E., Atwood, L. W., Mortensen, D. A., 2017. Agriculture in 2050: Recalibrating targets for sustainable intensification. Bioscience. 67, 386-391.
Jung, S.E., Bang, S.W., Kim, S.H., Seo, J.S., Yoon, H.-B., Kim, Y.S., Kim, J.K., 2021. Overexpression of OsERF83, a vascular tissue-specific transcription factor gene, confers drought tolerance in rice. International Journal of Molecular Sciences. 22, 7656.
Kobayashi, Y., Yamamoto, S., Minami, H., Kagaya, Y., Hattori, T., 2004. Differential activation of the rice sucrose nonfermenting1–related protein kinase2 family by hyperosmotic stress and abscisic acid. The Plant Cell. 16, 1163-1177.
Lim, C.W., Yang, S.H., Shin, K.H., Lee, S.C., Kim, S.H., 2015. The AtLRK10L1.2, Arabidopsis ortholog of wheat LRK10, is involved in ABA-mediated signaling and drought resistance. Plant Cell Reports. 34, 447-455.
Luan, S., 2003. Protein phosphatases in plants. Annual Review of Plant Biology. 54, 63-92.
Luan, S., 2009. The CBL–CIPK network in plant calcium signaling. Trends in Plant Science. 14, 37-42.
Mansuri, R.M., Shobbar, Z.S., Jelodar, N.B., Ghaffari, M.R., Nematzadeh, G.A., Asari, S., 2019. Dissecting molecular mechanisms underlying salt tolerance in rice: a comparative transcriptional profiling of the contrasting genotypes. Rice. 12, 13.
Mantri, N., Patade, V., Penna, S., Ford, R., & Pang, E., 2012. Abiotic stress responses in plants: present and future. Springer. 1-19.
Martínez-Atienza, J., Jiang, X., Garciadeblas, B., Mendoza, I., Zhu, J.-K., Pardo, J.M., Quintero, F.J., 2007. Conservation of the salt overly sensitive pathway in rice. Plant Physiology. 143, 1001-1012.
Miyakawa, T., Hatano, K.I., Miyauchi, Y., Suwa, Y.I., Sawano, Y., Tanokura, M., 2014. A secreted protein with plant-specific cysteine-rich motif functions as a mannose-binding lectin that exhibits antifungal activity. Plant Physiology. 166, 766-778.
Nagy, E.D., Lee, T.C., Ramakrishna, W., Xu, Z., Klein, P.E., SanMiguel, P., Schertz, K., 2007. Fine mapping of the Pc locus of Sorghum bicolor, a gene controlling the reaction to a fungal pathogen and its host-selective toxin. Theoretical and Applied Genetics. 114, 961-970.
Naithani, S., Dikeman, D., Garg, P., Al-Bader, N., Jaiswal, P., 2021. Beyond gene ontology (GO): using biocuration approach to improve the gene nomenclature and functional annotation of rice S-domain kinase subfamily. PeerJ. 9, e11052.
Nongpiur, R.C., Singla-Pareek, S.L., Pareek, A., 2020. The quest for osmosensors in plants. Journal of Experimental Botany. 71, 595-607.
Ouyang, S.Q., Liu, Y.F., Liu, P., Lei, G., He, S.J., Ma, B., Zhang, W.K., Zhang, J.S., Chen, S.Y., 2010. Receptor‐like kinase OsSIK1 improves drought and salt stress tolerance in rice (Oryza sativa) plants. The Plant Journal. 62, 316-329.
Qiu, Q.S., Guo, Y., Dietrich, M.A., Schumaker, K.S., Zhu, J.K., 2002. Regulation of SOS1, a plasma membrane Na+/H+ exchanger in Arabidopsis thaliana, by SOS2 and SOS3. Proceedings of the National Academy of Sciences. 99, 8436-8441.
Reddy, A. S., 2001. Calcium: silver bullet in signaling. Plant Science. 160, 381-404.
Saijo, Y., Hata, S., Kyozuka, J., Shimamoto, K., Izui, K., 2000. Over‐expression of a single Ca2+‐dependent protein kinase confers both cold and salt/drought tolerance on rice plants. The Plant Journal. 23, 319-327.
Schweighofer, A., Hirt, H., Meskiene, I., 2004. Plant PP2C phosphatases: emerging functions in stress signaling. Trends in Plant Science. 9, 236-243.
Shiu, S.H., Karlowski, W.M., Pan, R., Tzeng, Y. H., Mayer, K.F., Li, W. H., 2004. Comparative analysis of the receptor-like kinase family in Arabidopsis and rice. The Plant Cell. 16, 1220-1234.
Singh, A., Giri, J., Kapoor, S., Tyagi, A.K., Pandey, G.K., 2010. Protein phosphatase complement in rice: genome-wide identification and transcriptional analysis under abiotic stress conditions and reproductive development. BMC Genomics. 11, 1-18.
Thimm, O., Bläsing, O., Gibon, Y., Nagel, A., Meyer, S., Krüger, P., Selbig, J., Müller, L.A., Rhee, S.Y., Stitt, M., 2004. MAPMAN: a user‐driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes. The Plant Journal. 37, 914-939.
Todaka, D., Nakashima, K., Shinozaki, K., Yamaguchi-Shinozaki, K., 2012. Toward understanding transcriptional regulatory networks in abiotic stress responses and tolerance in rice. Rice. 5, 6.
Trapnell, C., Pachter, L., Salzberg, S.L., 2009. TopHat: discovering splice junctions with RNA-Seq. Bioinformatics. 25, 1105-1111.
Trapnell, C., Williams, B.A., Pertea, G., Mortazavi, A., Kwan, G., Van Baren, M.J., Salzberg, S.L., Wold, B.J., Pachter, L., 2010. Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nature Biotechnology. 28, 511-515.
Trapnell, C., Roberts, A., Goff, L., Pertea, G., Kim, D., Kelley, D.R., Pimentel, H., Salzberg, S.L., Rinn, J.L., Pachter, L., 2012. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nature Protocols. 7, 562-578.
Trapnell, C., Hendrickson, D. G., Sauvageau, M., Goff, L., Rinn, J.L., Pachter, L., 2013. Differential analysis of gene regulation at transcript resolution with RNA-seq. Nature Biotechnology. 31, 46-53.
Vij, S., Giri, J., Dansana, P.K., Kapoor, S., Tyagi, A.K., 2008. The receptor-like cytoplasmic kinase (OsRLCK) gene family in rice: organization, phylogenetic relationship, and expression during development and stress. Molecular Plant. 1, 732-750.
Walia, H., Wilson, C., Zeng, L., Ismail, A.M., Condamine, P., Close, T. J., 2007. Genome-wide transcriptional analysis of salinity stressed japonica and indica rice genotypes during panicle initiation stage. Plant Molecular Biology. 63, 609-623.
Wang, C., Li, D., Wang, P., Chen, D., Chen, X., 2020. Genome-wide analysis of HAESA/HAESA-like kinase family in rice. American Journal of Plant Sciences. 11, 1254.
Xiang, Y., Huang, Y., Xiong, L., 2007. Characterization of stress-responsive CIPK genes in rice for stress tolerance improvement. Plant Physiology. 144, 1416-1428.
Yoshida, S., Forno, D.A., Cock, J. H., 1971. Laboratory manual for physiological studies of rice. Laboratory Manual for Physiological Studies of Rice. IRRI. 83p.
You, J., Zong, W., Hu, H., Li, X., Xiao, J., Xiong, L., 2014. A stress-responsive NAC1-regulated protein phosphatase gene rice protein phosphatase18 modulates drought and oxidative stress tolerance through abscisic acid-independent reactive oxygen species scavenging in rice. Plant Physiology. 166(4), 2100-2114.