Abstract
Salinity stress is a critical challenge in crop production and requires innovative strategies to enhance the salt tolerance of plants. Insights from mangrove species, which are renowned for their adaptability to high-salinity environments, provides valuable genetic targets and resources for improving crops. A significant hurdle in salinity stress is the excessive uptake of sodium ions (Na+) by plant roots, causing disruptions in cellular balance, nutrient deficiencies, and hampered growth. Specific ion transporters and channels play crucial roles in maintaining a low Na+/K+ ratio in root cells which is pivotal for salt tolerance. The family of high-affinity potassium transporters, recently characterized in Avicennia officinalis, contributes to K+ homeostasis in transgenic Arabidopsis plants even under high-salt conditions. The salt overly sensitive pathway and genes related to vacuolar-type H+-ATPases hold promise for expelling cytosolic Na+ and sequestering Na+ in transgenic plants, respectively. Aquaporins contribute to mangroves’ adaptation to saline environments by regulating water uptake, transpiration, and osmotic balance. Antioxidant enzymes mitigate oxidative damage, whereas genes regulating osmolytes, such as glycine betaine and proline, provide osmoprotection. Mangroves exhibit increased expression of stress-responsive transcription factors such as MYB, NAC, and CBFs under high salinity. Moreover, genes involved in various metabolic pathways, including jasmonate synthesis, triterpenoid production, and protein stability under salt stress, have been identified. This review highlights the potential of mangrove genes to enhance salt tolerance of crops. Further research is imperative to fully comprehend and apply these genes to crop breeding to improve salinity resilience.
Similar content being viewed by others
Data availability
Data sharing is not applicable to this article as no datasets were generatedor analyzed during the current review study.
References
Acosta-Motos JR, Ortuño MF, Bernal-Vicente A, Diaz-Vivancos P, Sanchez-Blanco MJ, Hernandez JA (2017) Plant responses to salt stress: adaptive mechanisms. Agronomy 7:18. https://doi.org/10.3390/agronomy7010018
Lawrence J, Mackey B, Chiew F, Costello MJ, Hennessy K, Lansbury N et al (2022) Australasia. In: Pörtner H-O, Roberts DC, Tignor M et al (eds) Climate change 2022: impacts, adaptation and vulnerability. Contribution of working group II to the sixth assessment report of the intergovernmental panel on climate change. Cambridge University Press, Cambridge, UK and New York, pp 1581–1688. https://doi.org/10.1017/9781009325844.013.
Shabala S (2013) Learning from halophytes: physiological basis and strategies to improve abiotic stress tolerance in crops. Ann Bot 112:1209–1221. https://doi.org/10.1093/aob/mct205
Zhu JK (2016) Abiotic Stress Signaling and responses in plants. Cell 167:313–324. https://doi.org/10.1016/j.cell.2016.08.029
Isayenkov SV, Maathuis FJ (2019) Plant salinity stress: many unanswered questions remain. Front Plant Sci 10:435515. https://doi.org/10.3389/fpls.2019.00080
Maathuis FJ, Ahmad I, Patishtan J (2014) Regulation of Na+ fluxes in plants. Front Plant Sci 5:105882. https://doi.org/10.3389/fpls.2014.00467
Yokoi S, Quintero FJ, Cubero B, Ruiz MT, Bressan RA, Hasegawa PM, Pardo JM (2002) Differential expression and function of Arabidopsis thaliana NHX Na+/H+ antiporters in the salt stress response. Plant J 30:529–539. https://doi.org/10.1046/j.1365-313x.2002.01309.x
Flowers TJ, Colmer TD (2015) Plant salt tolerance: adaptations in halophytes. Ann Bot 115:327–331. https://doi.org/10.1093/aob/mcu267
Nizam A, Meera SP, Kumar A (2021) Genetic and molecular mechanisms underlying mangrove adaptations to intertidal environments. iScience 25:103547. https://doi.org/10.1016/j.isci.2021.103547
Lugo AE, Snedaker SC (1974) The ecology of mangroves. Ann Rev Ecol Syst 5:39–64. https://doi.org/10.1146/annurev.es.05.110174.000351
Nabeelah Bibi S, Fawzi MM, Gokhan Z, Rajesh J, Nadeem N, Kannan RRR et al (2019) Ethnopharmacology, phytochemistry, and global distribution of mangroves - a comprehensive review. Mar Drugs 17:231. https://doi.org/10.3390/md17040231
Kathiresan K, Bingham BL (2001) Biology of mangroves and mangrove ecosystems. Adv Mar Biol 40:81–251. https://doi.org/10.1016/S0065-2881(01)40003-4
Zhou Y, Wen L, Liao L, Lin S, Zheng E, Li Y, Zhang Y (2022) Comparative transcriptome analysis unveiling reactive oxygen species scavenging system of Sonneratia caseolaris under salinity stress. Front Plant Sci 13:953450. https://doi.org/10.3389/fpls.2022.953450
Prashanth SR, Sadhasivam V, Parida A (2008) Overexpression of cytosolic copper/zinc superoxide dismutase from a mangrove plant Avicennia marina in indica rice var Pusa Basmati-1 confers abiotic stress tolerance. Transgenic Res 17:281–291. https://doi.org/10.1007/s11248-007-9099-6
Kavitha K, George S, Venkataraman G, Parida A (2010) A salt-inducible chloroplastic monodehydroascorbate reductase from halophyte Avicennia marina confers salt stress tolerance on transgenic plants. Biochimie 92:1321–1329. https://doi.org/10.1016/j.biochi.2010.06.009
Ganesan G, Sankararamasubramanian HM, Harikrishnan M, Ganpudi A, Parida A (2012) A MYB transcription factor from the grey mangrove is induced by stress and confers NaCl tolerance in tobacco. J Exp Bot 63:4549–4561. https://doi.org/10.1093/jxb/ers135
Jing X, Hou P, Lu Y, Deng S, Li N, Zhao R et al (2015) Overexpression of copper/zinc superoxide dismutase from mangrove Kandelia Candel in tobacco enhances salinity tolerance by the reduction of reactive oxygen species in chloroplast. Front Plant Sci 5:23. https://doi.org/10.3389/fpls.2015.00023
Xu S, He Z, Zhang Z, Guo Z, Guo W, Lyu H, Shi S (2017) The origin, diversification and adaptation of a major mangrove clade (Rhizophoreae) revealed by whole-genome sequencing. Natl Sci Rev 4:721–734. https://doi.org/10.1093/nsr/nwx065
Friis G, Vizueta J, Smith EG, Nelson DR, Khraiwesh B, Qudeimat E et al (2021) A high-quality genome assembly and annotation of the gray mangrove, Avicennia marina. G3 (Bethesda) 11:jkaa025. https://doi.org/10.1093/g3journal/jkaa025
Natarajan P, Murugesan AK, Govindan G, Gopalakrishnan A, Kumar R, Duraisamy P et al (2021) A reference-grade genome identifies salt-tolerance genes from the salt-secreting mangrove species Avicennia marina. Commun Biol 4:851. https://doi.org/10.1038/s42003-021-02384-8
Munns R, Tester M (2008) Mechanisms of salinity tolerance. Annu Rev Plant Biol 59:651–681. https://doi.org/10.1146/annurev.arplant.59.032607.092911
Plett DC, Møller IS (2010) Na+ transport in glycophytic plants: what we know and would like to know. Plant Cell Environ 33:612–626. https://doi.org/10.1111/j.1365-3040.2009.02086.x
Cabot C, Sibole JV, Barceló J, Poschenrieder C (2014) Lessons from crop plants struggling with salinity. Plant Sci 226:2–13. https://doi.org/10.1016/j.plantsci.2014.04.013
Assaha DV, Ueda A, Saneoka H, Yaish MW (2017) The role of Na+ and K+ transporters in salt stress adaptation in glycophytes. Front Physiol 8:275169. https://doi.org/10.3389/fphys.2017.00509
Tester M, Davenport R (2003) Na+ tolerance and Na+ transport in higher plants. Ann Bot 91:503–527. https://doi.org/10.1093/aob/mcg058
Hanin M, Ebel C, Ngom M, Laplaze L, Masmoudi K (2016) New insights on plant salt tolerance mechanisms and their potential use for breeding. Front Plant Sci 7:209523. https://doi.org/10.3389/fpls.2016.01787
Ali A, Raddatz N, Pardo JM, Yun DJ (2021) HKT sodium and potassium transporters in Arabidopsis thaliana and related halophyte species. Physiol Plant 171:546–558. https://doi.org/10.1111/ppl.13166
Ali Z, Park HC, Ali A, Oh H, Aman R, Kropornicka A et al (2012) TsHKT1;2, a HKT1 homolog from the extremophile Arabidopsis relative Thellungiella salsuginea, shows K+ specificity in the presence of NaCl. Plant Physiol 158:1463–1474. https://doi.org/10.1104/pp.111.193110
Ali A, Raddatz N, Aman R, Kim S, Park HC, Jan M et al (2016) A single amino-acid substitution in the sodium transporter HKT1 associated with plant salt tolerance. Plant Physiol 171:2112–2126. https://doi.org/10.1104/pp.16.00569
Ali A, Khan IU, Jan M, Khan HA, Hussain S, Nisar M, Chung WS, Yun DJ (2018) The high-affinity potassium transporter EpHKT1;2 from the extremophile Eutrema parvula mediates salt tolerance. Front Plant Sci 9:1108. https://doi.org/10.3389/fpls.2018.01108
Krishnamurthy P, Mohanty B, Wijaya E, Lee D, Lim T, Lin Q, Kumar PP (2017) Transcriptomics analysis of salt stress tolerance in the roots of the mangrove Avicennia Officinalis. Sci Rep 7:1–19. https://doi.org/10.1038/s41598-017-10730-2
Krishnamurthy P, Amzah NRB, Kumar PP (2023) High-affinity potassium transporter from a mangrove tree Avicennia Officinalis increases salinity tolerance of Arabidopsis thaliana. Plant Sci 336:111841. https://doi.org/10.1016/j.plantsci.2023.111841
Shi H, Quintero FJ, Pardo JM, Zhu J (2002) The putative plasma membrane Na+/H+ antiporter SOS1 controls long-distance Na+ transport in plants. Plant Cell 14:465–477. https://doi.org/10.1105/tpc.010371
Qiu Q, Guo Y, Dietrich MA, Schumaker KS, Zhu J (2002) Regulation of SOS1, a plasma membrane Na+/H+ exchanger in Arabidopsis thaliana, by SOS2 and SOS3. Proc Natl Acad Sci USA 99:8436–8441. https://doi.org/10.1073/pnas.122224699
Quintero FJ, Villalta I, Jiang X, Kim W, Ali Z, Fujii H et al (2011) Activation of the plasma membrane Na/H antiporter salt-overly-sensitive 1 (SOS1) by phosphorylation of an auto-inhibitory C-terminal domain. Proc Natl Acad Sci USA 108:2611–2616. https://doi.org/10.1073/pnas.1018921108
Halfter U, Ishitani M, Zhu J (2000) The Arabidopsis SOS2 protein kinase physically interacts with and is activated by the calcium-binding protein SOS3. Proc Natl Acad Sci 97:3735–3740. https://doi.org/10.1073/pnas.97.7.3735
Gong D, Guo Y, Schumaker KS, Zhu JK (2004) The SOS3 family of calcium sensors and SOS2 family of protein kinases in Arabidopsis. Plant Physiol 134:919–926. https://doi.org/10.1104/pp.103.037440
Zhou Y, Yin X, Duan R, Hao G, Guo J, Jiang X (2015) SpAHA1 and SpSOS1 coordinate in transgenic yeast to improve salt tolerance. PLoS ONE 10:e0137447. https://doi.org/10.1371/journal.pone.0137447
Fan Y, Yin X, Xie Q, Xia Y, Wang Z, Song J, Zhou Y, Jiang X (2019) Co-expression of SpSOS1 and SpAHA1 in transgenic Arabidopsis plants improves salinity tolerance. BMC Plant Biol 19(1):74. https://doi.org/10.1186/s12870-019-1680-7
Zhou Y, Zhu Y, Li W et al (2023) Heterologous expression of Sesuvium portulacastrum SOS-related genes confer salt tolerance in yeast. Acta Physiol Plant 45:58. https://doi.org/10.1007/s11738-023-03518-7
Futai M, Sun-Wada GH, Wada Y, Matsumoto N, Nakanishi-Matsui M (2019) Vacuolar-type ATPase: a proton pump to lysosomal trafficking. Proc Jpn Acad Ser B 95:261–277. https://doi.org/10.2183/pjab.95.018
Dietz KJ, Tavakoli N, Kluge C, Mimura T, Sharma SS, Harris GC, Chardonnens AN, Golldack D (2001) Significance of the V-type ATPase for the adaptation to stressful growth conditions and its regulation on the molecular and biochemical level. J Exp Bot 52:1969–1980. https://doi.org/10.1093/jexbot/52.363.1969
Ho C-L, Nguyen PD, Harikrishna JA, Rahim RA (2008) Sequence analysis and characterization of vacuolar-type H+-ATPase proteolipid transcript from Acanthus ebracteatus Vahl. DNA Seq 19:73–77. https://doi.org/10.1080/10425170701445501
Bhardwaj R, Sharma I, Kanwar M, Sharma R, Handa N, Kaur H, Kapoor D, Poonam (2013) Aquaporins: role under salt stress in plants. In: Ahmad P, Azooz M, Prasad M (eds) Ecophysiology and responses of plants under salt stress. Springer, New York, pp 213–248. https://doi.org/10.1007/978-1-4614-4747-4_8
Krishnamurthy P, Tan XF, Lim TK, Lim TM, Kumar PP, Loh CS, Lin Q (2014) Proteomic analysis of plasma membrane and tonoplast from the leaves of mangrove plant Avicennia Officinalis. Proteomics 14:2545–2557. https://doi.org/10.1002/pmic.201300527
Tan WK, Lin Q, Lim TM, Kumar P, Loh CS (2013) Dynamic secretion changes in the salt glands of the mangrove tree species Avicennia officinalis in response to a changing saline environment. Plant Cell Environ 36:1410–1422. https://doi.org/10.1111/pce.12068
Tan WK, Lim TK, Loh CS, Kumar P, Lin Q (2015) Proteomic characterisation of the salt gland-enriched tissues of the mangrove tree species Avicennia Officinalis. PLoS ONE 10:e0133386. https://doi.org/10.1371/journal.pone.0133386
Jyothi-Prakash P, Mohanty B, Wijaya E, Lim T, Lin Q, Loh C-S, Kumar P (2014) Identification of salt gland-associated genes and characterization of a dehydrin from the salt secretor mangrove Avicennia Officinalis. BMC Plant Biol 14:291. https://doi.org/10.1186/s12870-014-0291-6
Guo Z, Ma D, Li J, Wei M, Zhang L, Zhou L et al (2022) Genome-wide identification and characterization of aquaporins in mangrove plant Kandelia obovata and its role in response to the intertidal environment. Plant Cell Environ 45:1698–1718. https://doi.org/10.1111/pce.14286
Guo Z, Wei M, Xu C, Wang L, Li J, Liu J et al (2024) Genome-wide identification of Avicennia marina aquaporins reveals their role in adaptation to intertidal habitats and their relevance to salt secretion and vivipary. Plant Cell Environ 47:832–853. https://doi.org/10.1111/pce.14769
Gill SS, Anjum NA, Gill R, Yadav S, Hasanuzzaman M, Fujita M, Tuteja N (2015) Superoxide dismutase-mentor of abiotic stress tolerance in crop plants. Environ Sci Pollut Res 22:10375–10394. https://doi.org/10.1007/s11356-015-4532-5
Takemura T, Hanagata N, Dubinsky Z, Karube I (2002) Molecular characterization and response to salt stress of mRNAs encoding cytosolic Cu/Zn superoxide dismutase and catalase from Bruguiera gymnorrhiza. Trees 16:94–99. https://doi.org/10.1007/s00468-001-0154-2
Jithesh MN, Prashanth SR, Sivaprakash KR, Parida A (2006) Monitoring expression profiles of antioxidant genes to salinity, iron, oxidative, light and hyperosmotic stresses in the highly salt-tolerant grey mangrove, Avicennia marina (Forsk.) Vierh. By mRNA analysis. Plant Cell Rep 25:865–876. https://doi.org/10.1007/s00299-006-0127-4
Yang E, Yi S, Bai F, Niu D, Zhong J, Wu Q, Wang F (2016) Cloning, characterization and expression pattern analysis of a cytosolic copper/zinc superoxide dismutase (SaCSD1) in a highly salt tolerant mangrove (Sonneratia alba). Int J Mol Sci 17:4. https://doi.org/10.3390/ijms17010004
Wang F, Wu Q, Zhang Z, Chen S, Zhou R (2013) Cloning, expression, and characterization of iron superoxide dismutase in Sonneratia alba, a highly salt tolerant mangrove tree. Protein J 32:259–265. https://doi.org/10.1007/s10930-013-9482-5
Anjum NA, Sharma P, Gill SS, Hasanuzzaman M, Khan EA, Kachhap K et al (2016) Catalase and ascorbate peroxidase-representative H2O2-detoxifying heme enzymes in plants. Environ Sci Pollut Res Int 23:19002–19029. https://doi.org/10.1007/s11356-016-7309-6
Jithesh MN (2004) Isolation and characterization of two cDNA isoforms for catalase gene from Avicennia marina (Forsk.) Vierh and its expression in transgenic system. Dissertation, University of Madras
Sofo A, Scopa A, Nuzzaci M, Vitti A (2015) Ascorbate peroxidase and catalase activities and their genetic regulation in plants subjected to drought and salinity stresses. Int J Mol Sci 16:13561–13578. https://doi.org/10.3390/ijms160613561
Nguyen P, Ho CL, Harikrishna J, Wong M, Rahim R (2006) Generation and analysis of expressed sequence tags from the mangrove plant, Acanthus ebracteatus Vahl. Tree Genet Genomes 2:196–201. https://doi.org/10.1007/s11295-006-0044-2
Sultana S, Khew CY, Morshed N, Namasivayam P, Napis S, Chai L (2012) Overexpression of monodehydroascorbate reductase from a mangrove plant (AeMDHAR) confers salt tolerance on rice. Plant Mol Biol Rep 30:311–318. https://doi.org/10.1016/j.jplph.2011.09.004
Sakamoto A, Murata N (2002) The role of glycine betaine in the protection of plants from stress: clues from transgenic plants. Plant Cell Environ 25:163–171. https://doi.org/10.1046/j.0016-8025.2001.00790.x
Hibino T, Meng Y-L, Kawamitsu Y, Uehara N, Matsuda N, Tanaka Y et al (2001) Molecular cloning and functional characterization of two kinds of betaine-aldehyde dehydrogenase in betaine-accumulating mangrove Avicennia marina (Forsk.) Vierh. Plant Mol Biol 45:353–363. https://doi.org/10.1023/A:1006497113323
Zhang N, Si H-J, Wen G, Du H-H, Liu B-L, Wang D (2011) Enhanced drought and salinity tolerance in transgenic potato plants with a BADH gene from spinach. Plant Biotechnol Rep 5:71–77. https://doi.org/10.1007/s11816-010-0160-1
Bhat BA, Mir RA, Mir WR, Hamdani SS, Mir MA (2024) Transcription factors-golden keys to modulate the plant metabolism to develop salinity tolerance. Plant Stress 11:100409. https://doi.org/10.1016/j.stress.2024.100409
Feng X, Xu S, Li J et al (2020) Molecular adaptation to salinity fluctuation in tropical intertidal environments of a mangrove tree Sonneratia alba. BMC Plant Biol 20:178. https://doi.org/10.1186/s12870-020-02395-3
Ambawat S, Sharma P, Yadav NR, Yadav RC (2013) MYB transcription factor genes as regulators for plant responses: an overview. Physiol Mol Biol Plants 19:307–321. https://doi.org/10.1007/s12298-013-0179-1
Wilkins O, Nahal H, Foong J, Provart NJ, Campbell MM (2009) Expansion and diversification of the Populus R2R3-MYB family of transcription factors. Plant Physiol 149:981–993. https://doi.org/10.1104/pp.108.132795
Chen Z, Newman I, Zhou M, Mendham N, Zhang G, Shabala S (2005) Screening plants for salt tolerance by measuring K+ flux: a case study for barley. Plant Cell Environ 28:1230–1246. https://doi.org/10.1111/j.1365-3040.2005.01393.x
Pradhan S, Shyamli PS, Suranjika S, Parida A (2021) Genome wide identification and analysis of the R2R3-MYB transcription factor gene family in the mangrove Avicennia marina. Agronomy 11:123. https://doi.org/10.3390/agronomy11010123
Olsen AN, Ernst HA, Leggio LL, Skriver K (2005) NAC transcription factors: structurally distinct, functionally diverse. Trends Plant Sci 10:79–87. https://doi.org/10.1016/j.tplants.2004.12.010
Puranik S, Sahu PP, Srivastava PS, Prasad M (2012) NAC proteins: regulation and role in stress tolerance. Trends Plant Sci 17:369–381. https://doi.org/10.1016/j.tplants.2012.02.004
Nakashima K, Tran LS, Van Nguyen D, Fujita M, Maruyama K, Todaka D et al (2007) Functional analysis of a NAC-type transcription factor OsNAC6 involved in abiotic and biotic stress-responsive gene expression in rice. Plant J 51:617–630. https://doi.org/10.1111/j.1365-313X.2007.03168.x
Murugesan AK, Somasundaram S, Mohan H, Parida AK, Alphonse V, Govindan G (2020) Ectopic expression of AmNAC1 from Avicennia marina (Forsk.) Vierh. Confers multiple abiotic stress tolerance in yeast and tobacco. Plant Cell Tiss Organ Cult 142:51–68. https://doi.org/10.1007/s11240-020-01830-5
Riechmann JL, Meyerowitz EM (1998) The AP2/EREBP family of plant transcription factors. Biol Chem 379:633–646. https://doi.org/10.1515/bchm.1998.379.6.633
Yamaguchi-Shinozaki K, Shinozaki K (1993) The plant hormone abscisic acid mediates the drought-induced expression but not the seed-specific expression of rd22, a gene responsive to dehydration stress in Arabidopsis thaliana. Mol Gen Genet 238:17–25. https://doi.org/10.1007/bf00279525
Huang GT, Ma SL, Bai LP, Zhang L, Ma H, Jia P et al (2012) Signal transduction during cold, salt, and drought stresses in plants. Mol Biol Rep 39:969–987. https://doi.org/10.1007/s11033-011-0823-1
Peng YL, Wang YS, Cheng H, Sun CC, Wu P, Wang LY, Fei J (2013) Characterization and expression analysis of three CBF/DREB1 transcriptional factor genes from mangrove Avicennia marina. Aquat Toxicol 140:68–76. https://doi.org/10.1016/j.aquatox.2013.05.014
Peng YL, Wang YS, Cheng H, Wang LY (2015) Characterization and expression analysis of a gene encoding CBF/DREB1 transcription factor from mangrove Aegiceras corniculatum. Ecotoxicology 24:1733–1743. https://doi.org/10.1007/s10646-015-1485-x
Peng YL, Wang YS, Fei J, Cheng H, Sun CC (2020) Isolation and expression analysis of a CBF transcriptional factor gene from the mangrove Bruguiera gymnorrhiza. Ecotoxicology 29:726–735. https://doi.org/10.1007/s10646-020-02215-2
Han G, Lu C, Guo J, Qiao Z, Sui N, Qiu N et al (2020) C2H2 zinc finger proteins: Master regulators of abiotic stress responses in plants. Front Plant Sci 11:500889. https://doi.org/10.3389/fpls.2020.00115
Wang K, Ding Y, Cai C, Chen Z, Zhu C (2019) The role of C2H2 zinc finger proteins in plant responses to abiotic stresses. Physiol Plant 165:690–700. https://doi.org/10.1111/ppl.12728
Xie M, Sun J, Gong D, Kong Y (2019) The roles of Arabidopsis C1-2i subclass of C2H2-type zinc-finger transcription factors. Genes 10:653. https://doi.org/10.3390/genes10090653
Wang F, Tong W, Zhu H, Kong W, Peng R, Liu Q, Yao Q (2016) A novel Cys2/His2 zinc finger protein gene from sweetpotato, IbZFP1, is involved in salt and drought tolerance in transgenic Arabidopsis. Planta 243:783–797. https://doi.org/10.1007/s00425-015-2443-9
Yuan S, Li X, Li R, Wang L, Zhang C, Chen L, Zhou X (2018) Genome-wide identification and classification of soybean C2H2 zinc finger proteins and their expression analysis in legume-rhizobium symbiosis. Front Microbiol 9:287812. https://doi.org/10.3389/fmicb.2018.00126
Hu X, Zhu L, Zhang Y, Xu L, Li N, Zhang X, Pan Y (2019) Genome-wide identification of C2H2 zinc-finger genes and their expression patterns under heat stress in tomato. PeerJ 7:e7929. https://doi.org/10.7717/peerj.7929
Mittler R, Kim Y, Song L, Coutu J, Coutu A, Ciftci-Yilmaz S et al (2006) Gain- and loss-of-function mutations in Zat10 enhance the tolerance of plants to abiotic stress. FEBS Lett 580:6537. https://doi.org/10.1016/j.febslet.2006.11.002
Gao H, Song A, Zhu X, Chen F, Jiang J, Chen Y et al (2012) The heterologous expression in Arabidopsis of a chrysanthemum Cys2/His2 zinc finger protein gene confers salinity and drought tolerance. Planta 235:979–993. https://doi.org/10.1007/s00425-011-1558-x
Yu Z, Yan H, Liang L, Zhang Y, Yang H, Li W, Deng S (2021) A C2H2-type zinc-finger protein from Millettia pinnata, MpZFP1, enhances salt tolerance in transgenic Arabidopsis. Int J Mol Sci 22:10832. https://doi.org/10.3390/ijms221910832
Abbasi F, Komatsu S (2004) A proteomic approach to analyze salt-responsive proteins in rice leaf sheath. Proteomics 4:2072–2081. https://doi.org/10.1002/pmic.200300741
Yang X, Liang Z, Wen X, Lu C (2008) Genetic engineering of the biosynthesis of glycinebetaine leads to increased tolerance of photosynthesis to salt stress in transgenic tobacco plants. Plant Mol Biol 66:73–86. https://doi.org/10.1007/s11103-007-9253-9
Tada Y, Kashimura T (2009) Proteomic analysis of salt-responsive proteins in the mangrove plant, Bruguiera gymnorhiza. Plant Cell Physiol 50:439–446. https://doi.org/10.1093/pcp/pcp002
Per TS, Khan MIR, Anjum NA, Masood A, Hussain SJ, Khan NA (2018) Jasmonates in plants under abiotic stresses: crosstalk with other phytohormones matters. Environ Exp Bot 145:104–120. https://doi.org/10.1016/j.envexpbot.2017.11.004
Yamada A, Saitoh T, Mimura T, Ozeki Y (2002a) Expression of mangrove allene oxide cyclase enhances salt tolerance in Escherichia coli, yeast, and tobacco cells. Plant Cell Physiol 43:903–910. https://doi.org/10.1093/pcp/pcf108
Yu X, Kikuchi A, Shimazaki T, Yamada A, Ozeki Y, Matsunaga E, Watanabe KN (2013) Assessment of the salt tolerance and environmental biosafety of Eucalyptus camaldulensis harboring a mangrin transgene. J Plant Res 126:141–150. https://doi.org/10.1007/s10265-012-0503-9
Abe I, Rohmer M, Prestwich GD (1993) Enzymatic cyclization of squalene and oxidosqualene to sterols and triterpenes. Chem Rev 93:2189–2206. https://doi.org/10.1021/cr00022a009
Basyuni M, Baba S, Kinjo Y, Putri LA, Hakim L, Oku H, Tamaki M (2012) Proteome analysis of salt-responsive proteins in the mangrove plant, Bruguiera gymnorhiza. Proteome Sci 10:47. https://doi.org/10.1186/1477-5956-10-47
Robinson C, Klösgen RB (1994) Targeting of proteins into and across the thylakoid membrane-a multitude of mechanisms. Plant Mol Biol 26:15–24. https://doi.org/10.1007/bf00039516
Sugihara K, Hanagata N, Dubinsky Z, Baba S, Karube I (2000) Molecular characterization of cDNA encoding oxygen-evolving enhancer protein 1 increased by salt treatment in the mangrove Bruguiera gymnorrhiza. Plant Cell Physiol 41:1279–1285. https://doi.org/10.1093/pcp/pcd061
Wang L, Liu X, Liang M, Tan F, Liang W, Chen Y, Chen W (2014) Proteomic analysis of salt-responsive proteins in the leaves of mangrove Kandelia candel during short-term stress. PLoS ONE 9:e83141. https://doi.org/10.1371/journal.pone.0083141
Zhu Z, Chen J, Zheng HL (2012) Physiological and proteomic characterization of salt tolerance in a mangrove plant, Bruguiera gymnorrhiza (L.) Lam. Tree Physiol 32:1378–1388. https://doi.org/10.1093/treephys/tps097
Yamada A, Sekiguchi M, Mimura T, Ozeki Y (2002b) The role of plant CCT α in salt- and osmotic-stress tolerance. Plant Cell Physiol 43:1043–1048. https://doi.org/10.1093/pcp/pcf120
Mehta PA, Sivaprakash K, Parani M, Venkataraman G, Parida AK (2005) Generation and analysis of expressed sequence tags from the salt-tolerant mangrove species Avicennia marina (Forsk) Vierh. Theor Appl Genet 110:416–424. https://doi.org/10.1007/s00122-004-1801-y
Miyama M, Shimizu H, Sugiyama M, Hanagata N (2006) Sequencing and analysis of 14,842 expressed sequence tags of Burma mangrove, Bruguiera gymnorrhiza. Plant Sci 171:234–241. https://doi.org/10.1016/j.plantsci.2006.03.015
Fu X, Huang Y, Deng S, Zhou R, Yang G, Ni X et al (2005) Construction of a SSH library of Aegiceras corniculatum under salt stress and expression analysis of four transcripts. Plant Sci 169:147–154. https://doi.org/10.1016/j.plantsci.2005.03.009
Wong Y-Y, Ho C-L, Nguyen PD, Teo S-S, Harikrishna JA, Rahim RA, Wong MCVL (2007) Isolation of salinity tolerant genes from the mangrove plant, Bruguiera Cylindrica by using suppression subtractive hybridization (SSH) and bacterial functional screening. Aquat Bot 86:117–122. https://doi.org/10.1016/j.aquabot.2006.09.009
Zeng H-C, Deng L-H, Zhang C-F (2006) Cloning of salt tolerance-related cDNAs from the mangrove plant Sesuvium portulacastrum L. J Integr Plant Biol 48:952–957. https://doi.org/10.1111/j.1744-7909.2006.00287.x
Funding
No funding was received for conducting this study.
Author information
Authors and Affiliations
Contributions
PM conceived the idea. GG, HP, VA wrote the first draft. PM and GG refined and finalized the draft. All authors reviewed and approved the final manuscript.
Corresponding author
Ethics declarations
Ethical approval
Not applicable.
Conflict of interest
Authors have no conflict of interest to declare.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Govindan, G., Harini, P., Alphonse, V. et al. From swamp to field: how genes from mangroves and its associates can enhance crop salinity tolerance. Mol Biol Rep 51, 598 (2024). https://doi.org/10.1007/s11033-024-09539-w
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s11033-024-09539-w