Physiological and gene expression responses involved in teak (Tectona grandis L.) seedlings exposed to osmotic and salt stressors
- PMID: 37060520
- DOI: 10.1007/s11033-023-08437-x
Physiological and gene expression responses involved in teak (Tectona grandis L.) seedlings exposed to osmotic and salt stressors
Abstract
Background: Teak (Tectona grandis L.) is a forest tree having 2n = 2x = 36 diploid chromosomes. Plants are continually subjected to variety of abiotic stresses due to climate change, which alter their physiological processes and gene expression.
Methods and results: The current study sought to examine the physiological and differential gene expression of teak seedlings exposed to abiotic stresses (150 mM NaCl and 15% PEG-6000). Chlorophyll content, membrane stability index and relative water content were measured at 0, 2, 7 and 12 days after treatment. These parameters were initially numerically reduced, but they were significantly reduced during a longer period of treatment. Seedlings treated with 150 mM NaCl displayed more harmful effect on the plant than other treatments. The results showed that variety of stresses significantly affect the physiology of seedlings because they cause membrane damage, ROS generation, chlorophyll degradation, and reduction in water absorption. The gene expression of treated and control seedlings was also evaluated at 12 days after treatment. Ten stress-related genes were examined for their differential expression using RT-PCR under applied stress. The stress-treated seedlings' leaves showed an up-regulated expression of the genes MYB-3, HSP-1, BI-1 and CS-2.
Conclusion: Up-regulation of the genes confirmed the protective function of these genes in plants under abiotic stress. However, gene expression was affected by treatments, the extent of stress and the species of plant. This study came to the conclusion that physiological parameters could be utilized as marker indices to assess a tree's capability to withstand stress at seedling stage. The up-regulated genes will be further investigated and utilized to validate stress tolerance and susceptible teak seedlings.
Keywords: Abiotic stress; Gene expression profile; Physiological parameters; RT-PCR; Tectona grandis L..
© 2023. The Author(s), under exclusive licence to Springer Nature B.V.
Similar articles
-
Physiological and molecular responses to drought stress in teak (Tectona grandis L.f.).PLoS One. 2019 Sep 9;14(9):e0221571. doi: 10.1371/journal.pone.0221571. eCollection 2019. PLoS One. 2019. PMID: 31498810 Free PMC article.
-
Salicylic acid alleviates the adverse effects of salt stress in Torreya grandis cv. Merrillii seedlings by activating photosynthesis and enhancing antioxidant systems.PLoS One. 2014 Oct 10;9(10):e109492. doi: 10.1371/journal.pone.0109492. eCollection 2014. PLoS One. 2014. PMID: 25302987 Free PMC article.
-
Overexpression of TgERF1, a Transcription Factor from Tectona grandis, Increases Tolerance to Drought and Salt Stress in Tobacco.Int J Mol Sci. 2023 Feb 19;24(4):4149. doi: 10.3390/ijms24044149. Int J Mol Sci. 2023. PMID: 36835560 Free PMC article.
-
Seed priming and foliar application with jasmonic acid enhance salinity stress tolerance of soybean (Glycine max L.) seedlings.J Sci Food Agric. 2021 Mar 30;101(5):2027-2041. doi: 10.1002/jsfa.10822. Epub 2020 Oct 6. J Sci Food Agric. 2021. PMID: 32949013
-
Identification and validation of quantitative real-time reverse transcription PCR reference genes for gene expression analysis in teak (Tectona grandis L.f.).BMC Res Notes. 2014 Jul 22;7:464. doi: 10.1186/1756-0500-7-464. BMC Res Notes. 2014. PMID: 25048176 Free PMC article.
Cited by
-
Investigating the effect of chitosan on the expression of P5CS, PIP, and PAL genes in rapeseed (Brassica napus L.) under salt stress.BMC Plant Biol. 2025 Feb 18;25(1):215. doi: 10.1186/s12870-025-06187-5. BMC Plant Biol. 2025. PMID: 39966771 Free PMC article.
References
-
- Thakor MC, Fougat RS, Kumar S, Sakure AA (2019) Sequence-related amplified polymorphism (SRAP) analysis of teak (Tectona grandis L.) germplasm. Ecol Genet Genom 12:100041. https://doi.org/10.1016/j.egg.2019.100041 - DOI
-
- Maisuria HJ, Dhaduk HL, Kumar S, Sakure AA, Thounaojam AT (2022) Teak population structure and genetic diversity in Gujarat India. Curr Plant Biol 32:100267. https://doi.org/10.1016/j.cpb.2022.100267 - DOI
-
- Katwal R (2003) Teak in India: status, prospects and perspectives. In: Proceedings of the international conference on quality timber products of teak from sustainable forest management. Peechi, pp 2–5.
-
- Rosero C, Argout X, Ruiz M, Teran W (2011) A drought stress transcriptome profiling as the first genomic resource for white teak—Gamhar—(Gmelina arborea Roxb) and related species. BMC Proc 5(7):P178. https://doi.org/10.1186/1753-6561-5-S7-P178 - DOI - PMC
-
- Wang L (2014) Physiological and molecular responses to drought stress in rubber tree (Hevea brasiliensis Muell. Arg.). Plant Physiol Biochem 83:243–249. https://doi.org/10.1016/j.plaphy.2014.08.012 - DOI - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources