Document Type : Original Article

Authors

1 Department of Genetic Engineering and Biology, Genetics and Agricultural Biotechnology Institute of Tabarestan (GABIT), Sari Agricultural Sciences and Natural Resources University (SANRU), Iran

2 Assistant Professor, Crop and Horticultural Science Research Department, Mazandaran Agricultural and Natural Resources Research and Education Center, AREEO, Sari, Iran

Abstract

Introduction
Abiotic stress has always affected the plants growth and development through morphological and physiological, biochemical and anatomical alterations, leading to reduce yield and limit the crop area. Development is a completed process that depends on a cell to cell communication to regulate growth and differentiation. In the past, phytohormones were considered the important players of cell signaling. High-throughput techniques have led to finding many new plant peptides over the last years. DEVILS are small peptides that play an important role in plant growth and development and are effective in controlling plant responses to environmental changes caused by stress. These small peptides act in the growth process of plants similar to phytohormones and are called peptide hormones that play a role in plants as molecular messengers. Aeluropus littoralis, belongs to Poaceae that can tolerate NaCl up to 600 mM and grows in marshes, salty and drought lands. Because of C4 photosynthesis system and proper physiological properties, A. littoralis as a halophyte plant could be known as a great source of genes related to salt tolerance.

Materials and methods
In this research, the changes of expression of four genes namaly AlDVL1, AlDVL2, AlDVL3, and AlDVL6 were investigated under salinity stress (600 mM) in Aeluropus littoralis as a halophyte plant at five time-points of 0, 3, 6, 48 and 168 hours post stress (hps). Leaves and roots were sampled and grounded in liquid nitrogen, and total RNA was extracted using Threezol reagent (Riragene). First strand cDNA synthesis and RT-qPCR were performed according to kit instructions. PCR amplification was performed in C1000™ Thermal Cycler (Bio-Rad, USA) according to the company’s suggestions. The 2-ΔΔct method was applied for the relative expression analysis.

Results and discussion
The results showed that the expression pattern of AlDVL genes was affected by salinity stress and had a significant change in root and leaf tissues. In all of genes except AlDVL6, expression changes in the leaf were higher than the root. The highest value of expression in the leaf and root tissue was observed at 48 hps (12.12) and 168 hps (14.83) for AlDVL2, respectively. Expression pattern of AlDVL genes was tissue-specific, and different pattern was observed in root and leaf tissues, while in each tissue, all genes had similar pattern. For example, in all of the studied genes in leaf tissue, the amount of expression of genes was first reduced in the initial time-point, and then the expression increased to 48 hours after the stress and eventually decreased over 168 hps. This trend of change was observed among different genes with a slight difference in leaf tissue. In the root tissue, the trend of gene expression was similar except for the AlDVL3 gene. From the first hours to 48 hps, gene expression value was declined, but was peaked at 168 hps. According to the results, it can be stated that the genes act specifically in each tissue. The results of correlation analysis in different tissues showed that AlDVL6 and AlDVL3 expression correlation in both leaf and root tissues had a negative and significant relation (-0.6) with inverse effects.

Conclusions
Halophyte plants by regulating their gene expression can respond to different various abiotic stresses. Expression pattern of phytohormones -related genes in leaf and root tissue can be taken as an indication of their functional relevance at different time-points of salt stress.

Keywords

 
Agarwal, M., Shrivastava, N., Padh, H., 2008. Advances in molecular marker techniques and their applications in plant sciences. Plant Cell Reports. 27, 617-631.
Aglawe, S., Fakrudin, B., Patole, C., Bhairappanavar, S., Koti, R., Krishnaraj, P., 2012. Quantitative RT-PCR analysis of 20 transcription factor genes of MADS, ARF, HAP2, MBF and HB families in moisture stressed shoot and root tissues of sorghum. Physiology and Molecular Biology of Plants. 18, 287-300.
Andrews, S.J., Rothnagel, J.A., 2014. Emerging evidence for functional peptides encoded by short open reading frames. Nature Reviews Genetics. 15, 193.
Azri, W., Barhoumi, Z., Chibani, F., Borji, M., Bessrour, M., Mliki, A., 2016. Proteomic responses in shoots of the facultative halophyte Aeluropus littoralis (Poaceae) under NaCl salt stress. Functional Plant Biology. 43, 1028-1047.
Barhoumi, Z., 2019. Physiological response of the facultative halophyte, Aeluropus littoralis, to different salt types and levels. Plant Biosystems. 153, 298-305.
Barhoumi, Z., Djebali, W., Chaïbi, W., Abdelly, C., Smaoui, A., 2007. Salt impact on photosynthesis and leaf ultrastructure of Aeluropus littoralis. Journal of Plant Research. 120, 529-537.
Barzegargolchini, B., Movafeghi, A., Dehestani, A., Mehrabanjoubani, P., 2017. Increased cell wall thickness of endodermis and protoxylem in Aeluropus littoralis roots under salinity: the role of LAC4 and PER64 genes. Journal of Plant Physiology. 218, 127-134.
Chien, P.S., Nam, H.G., Chen, Y.R., 2015. A salt-regulated peptide derived from the CAP superfamily protein negatively regulates salt-stress tolerance in Arabidopsis. Journal of Experimental Botany. 66, 5301-5313.
Cui, Y., Li, M., Yin, X., Song, S., Xu, G., Wang, M., Li, C., Peng, C., Xia, X., 2018. OsDSSR1, a novel small peptide, enhances drought tolerance in transgenic rice. Plant Science. 270, 85-96.
Czyzewicz, N., Yue, K., Beeckman, T., De Smet, I., 2013. Message in a bottle: small signalling peptide outputs during growth and development. Journal of Experimental Botany. 64, 5281-5296.
De Coninck, B., De Smet, I., 2016. Plant peptides – taking them to the next level. Journal of Experimental Botany. 67, 4791-4795.
Delay, C., Imin, N., Djordjevic, M.A., 2013. CEP genes regulate root and shoot development in response to environmental cues and are specific to seed plants. Journal of Experimental Botany. 64, 5383-5394.
Faraji, S., Najafi-Zarrini, H., Hashemi-Petroudi, S., Ranjbar, G., 2017. AlGLY I gene implicated in salt stress response from halophyte Aeluropus littoralis. Russian Journal of Plant Physiology. 64, 850-860.
Fatemi, F., Hashemipetroudi, S.H., Nematzadeh, G.A., Askari, H., Abdollahi, M.R., 2019. Exploiting differential gene expression to discover ionic and osmotic-associated transcripts in the halophyte grass Aeluropus littoralis. Biological Procedures Online. 21, 14.
Ghorbani, H.R., Samizadeh Lahiji, H., Nematzadeh, G.A., 2017. Expression pattern analysis of transcription factors from Aeluropus littoralis in response to salt stress and recovery condition. Journal of Plant Molecular Breeding. 5, 19-30.
Gulzar, S., Khan, M.A., Ungar, I.A., 2003. Effects of salinity on growth, ionic content, and plant–water status of Aeluropus lagopoides. Communications in Soil Science and Plant Analysis. 34, 1657-1668.
Guo, P., Yoshimura, A., Ishikawa, N., Yamaguchi, T., Guo, Y., Tsukaya, H., 2015. Comparative analysis of the RTFL peptide family on the control of plant organogenesis. Journal of Plant Research. 128, 497-510.
Hashemipetroudi, S.H., Nematzadeh, G.A., Ahmadian, G.R., Yamchi, A., Kuhlmann, M., 2016a. Expression analysis of salt stress related expressed sequence tags (ESTs) from Aeluropus littoralis by quantitative real-time PCR. Bioscience Biotechnology Research Communications. 9, 445-456.
Hashemipetroudi, S.H., Nematzadeh, G.A., Ahmadian, G.R., Yamchi, A., Kuhlmann, M., 2016b. Identification and validation of Aeluropus littoralis reference genes for Quantitative Real-Time PCR Normalization. Journal of Biological Research-Thessaloniki. 23, 18.
Hashemipetroudi, S.H., Nematzadeh, G.A., Askari, H., Ghahary, S., 2014. Involvement of Cytosine DNA methylation in different developmental stages of Aeluropus littoralis. Journal of Plant Molecular Breeding. 2, 56-67.
Hashemipetroudi, S.H., Nematzadeh, G.A., Askari, H., Ghasemi, Y., 2012. Pattern of DNA cytosine methylation in Aeluropus littoralis during temperature stress. Journal of Plant Molecular Breeding. 1, 16-24.
Hashemipetroudi, S.H., Nematzadeh, G.A., Kuhlmann, M., 2019. Identification and analysis of a DEVIL paralog gene cluster in Aeluropus littoralis by comparative genomic approach. Crop Bitechnology. 9, 79-92.
Jain, M., Nijhawan, A., Tyagi, A.K., Khurana, J.P., 2006. Validation of housekeeping genes as internal control for studying gene expression in rice by quantitative real-time PCR. Biochemical and Biophysical Research Communications. 345, 646-651.
Jam, M., Alemzadeh, A., Tale, A.M., Esmaeili-Tazangi, S., 2014. Heavy metal regulation of plasma membrane H+-ATPase gene expression in halophyte Aeluropus littoralis. Molecular Biology Research Communications. 3, 129.
Li, X., Han, H., Chen, M., Yang, W., Liu, L., Li, N., Ding, X., Chu, Z., 2017. Overexpression of OsDT11, which encodes a novel cysteine-rich peptide, enhances drought tolerance and increases ABA concentration in rice. Plant Molecular Biology. 93, 21-34.
Marshall, E., Costa, L.M., Gutierrez-Marcos, J., 2011. Cysteine-rich peptides (CRPs) mediate diverse aspects of cell–cell communication in plant reproduction and development. Journal of Experimental Botany. 62, 1677-1686.
Matsubayashi, Y., 2014. Posttranslationally modified small-peptide signals in plants. Annual Review of Plant Biology. 65, 385-413.
Modarresi, M., Nematzadeh, G., Moradian, F., Alavi, S., 2012. Identification and cloning of the Cu/Zn superoxide dismutase gene from halophyte plant Aeluropus littoralis. Russian Journal of Genetics. 48, 118-122.
Nakaminami, K., Okamoto, M., Higuchi-Takeuchi, M., Yoshizumi, T., Yamaguchi, Y., Fukao, Y., Shimizu, M., Ohashi, C., Tanaka, M., Matsui, M., 2018. AtPep3 is a hormone-like peptide that plays a role in the salinity stress tolerance of plants. Proceedings of the National Academy of Sciences. 115, 5810-5815.
Narita, N.N., Moore, S., Horiguchi, G., Kubo, M., Demura, T., Fukuda, H., Goodrich, J., Tsukaya, H., 2004. Overexpression of a novel small peptide ROTUNDIFOLIA4 decreases cell proliferation and alters leaf shape in Arabidopsis thaliana. The Plant Journal. 38, 699-713.
Pearce, G., Strydom, D., Johnson, S., Ryan, C.A., 1991. A polypeptide from tomato leaves induces wound-inducible proteinase inhibitor proteins. Science. 253, 895-897.
Qi, J., Yu, S., Zhang, F., Shen, X., Zhao, X., Yu, Y., Zhang, D., 2010. Reference gene selection for real-time quantitative polymerase chain reaction of mRNA transcript levels in Chinese cabbage (Brassica rapa L. ssp. pekinensis). Plant Molecular Biology Reporter. 28, 597-604.
Rabbani, M.A., Maruyama, K., Abe, H., Khan, M.A., Katsura, K., Ito, Y., Yoshiwara, K., Seki, M., Shinozaki, K., Yamaguchi-Shinozaki, K., 2003. Monitoring expression profiles of rice genes under cold, drought, and high-salinity stresses and abscisic acid application using cDNA microarray and RNA gel-blot analyses. Plant Physiology. 133, 1755-1767.
Saad, R.B., Halima, N.B., Ghorbel, M., Zouari, N., Romdhane, W.B., Guiderdoni, E., Al-Doss, A., Hassairi, A., 2018. AlSRG1, a novel gene encoding an RRM-type RNA-binding protein (RBP) from Aeluropus littoralis, confers salt and drought tolerance in transgenic tobacco. Environmental and Experimental Botany. 150, 25-36.
Silverstein, K.A., Moskal Jr, W.A., Wu, H.C., Underwood, B.A., Graham, M.A., Town, C.D., Vandenbosch, K.A., 2007. Small cysteine‐rich peptides resembling antimicrobial peptides have been under‐predicted in plants. The Plant Journal. 51, 262-280.
Valdivia, E.R., Hertweck, K.L., Cho, S.K., C. Walker, J., 2013. DVL/RTFL. In: Kastin, A. (ed.), Handbook of Biologically Active Peptides. Academic Press, San Diego, CA, USA, pp. 15-19.
Vanstraelen, M., Benková, E., 2012. Hormonal interactions in the regulation of plant development. Annual Review of Cell and Developmental Biology. 28, 463-487.
Wang, G., Zhang, G., Wu, M., 2016. CLE peptide signaling and crosstalk with phytohormones and environmental stimuli. Frontiers in Plant Science. 6, 1211.
Wen, J., Lease, K.A., Walker, J.C., 2004. DVL, a novel class of small polypeptides: overexpression alters Arabidopsis development. The Plant Journal. 37, 668-677.
Wen, J., Walker, J., 2006. DVL peptides are involved in plant development. In: Kastin, A. (ed.), Handbook of Biologically Active Peptides. Academic Press, San Diego, CA, USA, pp. 17-22.
Zouari, N., Saad, R.B., Legavre, T., Azaza, J., Sabau, X., Jaoua, M., Masmoudi, K., Hassairi, A., 2007. Identification and sequencing of ESTs from the halophyte grass Aeluropus littoralis. Gene. 404, 61-69.