Dot Blot Assay for Assessing Trehalose-6-phosphate Synthase Gene Expression in a Maize Breeding Population under Water Stress

Main Article Content

Pischanan Lowantha
Pattama Hannok*

Abstract

Field maize is an important economic crop grown around the world and it has been mainly used in the animal feed industry. Maize yields have been inadequate for the demand due to drought events. One way to alleviate yield losses is to develop drought tolerant maize varieties for farmers. Trehalose-6-phosphate synthase (TPS) is an important enzyme involved in trehalose biosynthesis which has been found to increase plant tolerance to abiotic stresses. The aim of this research was to screen the levels of TPS gene expression in maize breeding materials under water stress via dot-blot hybridization using cDNA probe. To do so, 34 S2 maize families were grown and subjected to water stress condition. Leave samples were collected at 6 different days after planting (DAP) for a dot blot assay. The results showed that the level of TPS gene expression was highest at 4 days after stress (relative intensity at 64 DAP). However, dot blotting at 6 days after stress (relative intensity at 66 DAP) was effective to differentiate maize families. Furthermore, a moderate negative relationship between relative signal intensity at 66 DAP (RI66) and Smith index based on multi-phenotypic traits was found to be statistically significant. Our study showed that maize with high TPS gene expression tended to be less tolerant to water stress. It is noteworthy that the study of TPS gene expression in mature maize under stress in this study showed results that contrasted with previous reports on seedlings in many plant species. Furthermore, we found that 4 out of 34 S2 maize families may have potential for further use in our breeding program.


Keywords: cDNA probe; stay-green phenotype; S2 maize families; image processing; relative signal intensity


*Corresponding author: E-mail: [email protected]

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References

Thaitad, S., 2015. Research of Maize Breeding for Drought Tolerance. [online]. Available at: http://www.doa.go.th/research/attachment.php?aid=2093.

Zhang, H. and Zhou, C., 2013. Signal transduction in leaf senescence. Plant Molecular Biology, 82(6), 539-545.

Zhang, X., Lei, L., Lai, J., Zhao, H. and Song, W., 2018. Effects of drought stress and water recovery on physiological responses and gene expression in field maize seedlings. BMC Plant Biology, 18(1), 68, https://doi.org/10.1186/s12870-018-1281-x.

Bruce, W.B., Edmeades, G.O. and Barker, T.C., 2002. Molecular and physiological approaches to field maize improvement for drought tolerance. Journal of Experimental Botany, 53(336), 13-25.

Roberts, M.F., 2005. Organic compatible solutes of halotolerant and halophilic microorganisms. Saline Systems, 1, 5, https://doi.org/10.1186/1746-1448-1-5.

Wani, S.H., Singh, N.B., Haribhushan, A. and Mir, J.I., 2013. Compatible solute engineering in plants for abiotic stress tolerance - role of glycine betaine. Current Genomics, 14(3), 157-165.

Iordachescu, M. and Imai, R., 2008. Trehalose biosynthesis in response to abiotic stresses. Journal of Integrative Plant Biology, 50, 1223-1229.

Chen, D., Wang, S., Xiong, B., Cao, B. and Deng, X., 2015. Carbon/nitrogen imbalance associated with drought-induced leaf senescence in Sorghum bicolor. PLoS ONE, 10(8), 1-17.

Delorge, I., Janiak, M., Carpentier, S. and Van Dijck, P., 2014. Fine tuning of Trehalose biosynthesis and hydrolysis as novel tools for the generation of abiotic stress tolerant plants. Frontiers in Plant Science, 5(147), 1-9.

Grennan, A.K., 2007. The role of Trehalose biosynthesis in plants. Plant Physiology, 144(1), 3-5.

Carillo, P., Feil, R., Gibon, Y., Satoh-Nagasawa, N., Jackson, D., Bläsing, O.E., Stitt, M. and Lunn, J.E., 2013. A fluorometric assay for Trehalose in the picomole range. Plant Methods, 9(1), 21, https://doi.org/10.1186/1746-4811-9-21.

Cortina, C. and Culiáñez-Macià, F.A., 2005. Tomato abiotic stress enhanced tolerance by Trehalose biosynthesis. Plant Science, 169(1), 75-82.

Schluepmann, H., Dijken, A., Aghdasi, M., Wobbes, B., Paul, M. and Smeekens, S., 2004. Trehalose mediated growth inhibition of arabidopsis seedlings is due to Trehalose-6-phosphate accumulation. Plant Physiology, 135, 879-890.

Lin, Q., Yang, J., Wang, Q., Zhu, H., Chen, Z., Dao, Y. and Wang, K., 2019. Overexpression of the trehalose-6-phosphate phosphatase family gene AtTPPF improves the drought tolerance of Arabidopsis thaliana. BMC Plant Biology, 19(1), 381, https://doi.org/10.1186/s12870-019-1986-5.

Avonce, N., Leyman, B., Mascorro-Gallardo, J.O., Van Dijck, P., Thevelein, J.M. and Iturriaga, G., 2004. The arabidopsis Trehalose-6-p synthase AtTPS1 gene is a regulator of glucose, abscisic acid, and stress signaling. Plant Physiology, 136(3), 3649-3659.

Garg, A.K., Kim, J.-K., Owens, T.G., Ranwala, A.P., Choi, Y.D., Kochian, L.V. and Wu, R.J., 2002. Trehalose accumulation in rice plants confers high tolerance levels to different abiotic stresses. Proceedings of the National Academy of Sciences of the United States of America, 99(25), 15898-15903.

Li, H.-W., Zang, B.-S., Deng, X.-W. and Wang, X.-P., 2011. Overexpression of the Trehalose-6-phosphate synthase gene OsTPS1 enhances abiotic stress tolerance in rice. Planta, 234(5), 1007-1018.

Jang, I.-C., Oh, S.-J., Seo, J.-S., Choi, W.-B., Song, S.I., Kim, C.H., Kim, Y.S., Seo, H.-S., Choi, Y.D., Nahm, B.H. and Kim, J.-K., 2003. Expression of a bifunctional fusion of the Escherichia coli genes for Trehalose-6-phosphate synthase and Trehalose-6-phosphate phosphatase in transgenic rice plants increases Trehalose accumulation and abiotic stress tolerance without stunting growth. Plant Physiology, 131(2), 516-524.

Nicolau-Junior, N., Nicolau, M., Mantovanini, L. and Zingaretti, S., 2013. Expression analysis of two genes coding for Trehalose-6-Phosphate Synthase (TPS), in sugarcane (Saccharum spp.) under water stress. American Journal of Plant Sciences, 04, 91-99.

O'Hara, L.E., Paul, M.J. and Wingler, A., 2013. How do sugars regulate plant growth and development? New insight into the role of trehalose-6-phosphate. Molecular Plant, 6(2), 261-274.

Paul, M., Primavesi, L., Jhurreea, D. and Zhang, Y., 2008. Trehalose metabolism and signaling. Annual Review of Plant Biology, 59, 417-441.

Hannok, P., 2020. S2 Family Evaluation for Establishing a Base Population for Drought Tolerant Maize Breeding Program. Research Report. Maejo University, Thailand.

Abramoff, M.D., Magalhaes, P.J. and Ram, S.J., 2004. Image processing with imageJ. Biophotonics International, 11(7), 36-42.

Rasband, W., 2008. Dot Blot Analysis, ImageJ Documentation, Tutorial and Examples. [online]. Available at: http://image.bio.methods.free.fr/dotblot.html.

Smith, H.F., 1936. A discriminant function for plant selection. Annals of Eugenics, 7(3), 240-250.

Céron-Rojas, J.J. and Crossa, J., 2018. The linear phenotypic selection index theory. In J.J. Céron-Rojas and J. Crossa, eds. Linear Selection Indices in Modern Plant Breeding. Cham: Springer International Publishing, pp. 15-42.

Ángela, P., Sergio, P., Gregorio, A., Jesús, C., Francisco, R., José, C. and Juan, B., 2017. RIndSel Selection Indices for Plant Breeding. [online]. Available at: https://hdl.handle.net/11529/10854.

R Core Team, 2020. R: a Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna, Austria. [online]. Available at: https://www.R-project.org/.

IRRI, 2014. Biometrics and Breeding Informatics. Plant Breeding Genetics and Biotechnology Division, International Rice Research Institute, Los Baños, Laguna.

Anami, S., De Block, M., Machuka, J. and Lijsebettens, M., 2009. Molecular improvement of tropical maize for drought stress tolerance in sub-Saharan Africa. Critical Reviews in Plant Sciences, 28, 16-35.

Liu, X., Wang, X., Wang, X., Gao, J., Luo, N., Meng, Q. and Wang, P., 2020. Dissecting the critical stage in the response of maize kernel set to individual and combined drought and heat stress around flowering. Environmental and Experimental Botany, 179, 104213, https://doi.org/10.1016/j.envexpbot.2020.104213.

Sah, R.P., Chakraborty, M., Prasad, K., Pandit, M., Tudu, V.K., Chakravarty, M.K., Narayan, S.C., Rana, M. and Moharana, D., 2020. Impact of water deficit stress in maize: Phenology and yield components. Scientific Reports, 10(1), 29-44.

Rolando, J.L., Ramírez, D.A., Yactayo, W., Monneveux, P. and Quiroz, R., 2015. Leaf greenness as a drought tolerance related trait in potato (Solanum tuberosum L.). Environmental and Experimental Botany, 110, 27-35.

Betrán, F.J., Beck, D., Bänziger, M. and Edmeades, G.O., 2003. Secondary traits in parental inbreds and hybrids under stress and non-stress environments in tropical maize. Field Crops Research, 83(1), 51-65.

Bänziger, M., Edmeades, G.O., Beck, D.L. and Bellon, M.R., 2000. Breeding for Drought and Nitrogen Stress Tolerance in Maize: From Theory to Practice. Mexico: CIMMYT.

Campos, H., Cooper, M., Habben, J.E., Edmeades, G.O. and Schussler, J.R., 2004. Improving drought tolerance in maize: a view from industry. Field Crops Research, 90(1), 19-34.

Araus, J.L., Serret, M.D. and Edmeades, G., 2012. Phenotyping maize for adaptation to drought. Frontiers in Physiology, 3(305), https://doi.org/10.3389/fphys.2012.00305.

Bekavac, G., Stojaković, M., Ivanović, M., Jocković, Đ., Vasić, N., Purar, B., Boćanski, J., and Nastasić, A., 2002. Relationships of stay green trait in maize. Genetika, 34, 33-39.

Sun, J., Chen, T. and Tao, J., 2021. Single molecule, full-length transcript sequencing provides insight into the TPS gene family in Paeonia ostii. Peer Journal, 9, 1-22.

Fernandez, O., Vandesteene, L., Feil, R., Baillieul, F., Lunn, J.E. and Clément, C., 2012. Trehalose metabolism is activated upon chilling in grapevine and might participate in Burkholderia phytofirmans induced chilling tolerance. Planta, 236(2), 355-369.

Hu, X., Wu, Z.-D., Luo, Z.-Y., Burner, D. M., Pan, Y.-B. and Wu, C.-W., 2020. Genome-Wide Analysis of the Trehalose-6-phosphate synthase (TPS) gene family and expression profiling of ScTPS genes in Sugarcane. Agronomy, 10(7), 969, https://doi.org/10.3390/agronomy10070969.

Jiang, W., Fu, F.-L., Zhang, S.-Z., Wu, L. and Li, W.-C., 2010. cloning and characterization of functional trehalose 6 phosphate synthase gene in maize. Journal of Plant Biology, 53, 134-141.

Gan, S., 2003. Mitotic and postmitotic senescence in plants. Science of Aging Knowledge Environment, 2003(38), https://doi.org/10.1126/sageke.2003.38.re7.

Schluepmann, H., van Dijken, A., Aghdasi, M., Wobbes, B., Paul, M. and Smeekens, S., 2004. Trehalose mediated growth inhibition of Arabidopsis seedlings is due to Trehalose-6-phosphate accumulation. Plant Physiology, 135(2), 879-890.

Zhang, J., Fengler, K. A., Van Hemert, J. L., Gupta, R., Mongar, N., Sun, J., Allen, W.B., Wang, Y., Weers, B., Mo, H., Lafitte, R., Hou, Z., Bryant, A., Ibraheem, F., Arp, J., Swaminathan, K., Moose, S.P., Li, B. and Shen, B., 2019. Identification and characterization of a novel stay-green QTL that increases yield in maize. Plant Biotechnology Journal, 17(12), 2272-2285.

Wingler, A., 2002. The function of trehalose biosynthesis in plants. Phytochemistry, 60(5), 437-440.