Genome Level And Epigenetic Changes Induced by Tissue Culture

Main Article Content

Dr. Sandip. N. Chavan, Kapil Shankar Pawar, Uttam Shivram Mahale,Smarnika Dileep Korde

Abstract

Plant tissue culture is one of the basic methods in plant biotechnology in clonal propagation, disease free plant production, genetic transformation and improved production of secondary metabolites. But, in vitro environments like disturbed hormone ratios, osmotic stress, and non-physiological nutrient composition may cause genomic instability and epigenetic re-programming, which is seen as somaclonal variation. The paper compared the genome level changes, DNA methylation, transposon activation, and somaclonal variation between callus culture, organogenesis, and somatic embryogenesis in rice, maize, sugarcane and banana. Cytogenetic examination showed that, callus cultures were the most genetically unstable with chromosomal aberration (42.5%), aneuploidy (35.2%), and structure rearrangement (27.8%), and organogenesis retained the best of clonal fidelity. The global hypomethylation in control groups was frequent (38.6 percent) in callus cultures, and was associated with high transposon mobilization (31.2 percent), and low organogenesis levels (12.7 percent) and intermediate levels in somatic embryogenesis. Phenotypic and molecular analysis showed more somaclonal variation in polyploid crops (banana and sugarcane) than in diploid cereals (rice and maize) and is indicative of the effect of genome complexity on variability induced by tissue culture. These findings highlight the importance of the regeneration pathway, the genome architecture of the species, and the epigenetic processes in shaping the nature of somaclonal variation, implying that callus culture, although yielding new phenotypes, presents fidelity problems to genetic faithfulness, whereas organogenesis offers stability to clonal propagation. The results guide the best tissue culture approaches to crop improvement and breeding and biotechnological use and propose the future research that would examine locus-specific epigenetic modifications and heritability of induced variants.

Article Details

How to Cite
Dr. Sandip. N. Chavan, Kapil Shankar Pawar, Uttam Shivram Mahale,Smarnika Dileep Korde. (2025). Genome Level And Epigenetic Changes Induced by Tissue Culture. International Journal of Advanced Research and Multidisciplinary Trends (IJARMT), 2(4), 77–87. Retrieved from https://ijarmt.com/index.php/j/article/view/524
Section
Articles

References

Alonso-Curbelo, D., Ho, Y. J., Burdziak, C., Maag, J. L., Morris IV, J. P., Chandwani, R., … & Lowe, S. W. (2021). A gene–environment-induced epigenetic program initiates tumorigenesis. Nature, 590(7847), 642–648. https://doi.org/10.1038/s41586-021-03228-2

Bednarek, P. T., & Orłowska, R. (2020). Plant tissue culture environment as a switch-key of (epi)genetic changes. Plant Cell, Tissue and Organ Culture (PCTOC), 140(2), 245–257. https://doi.org/10.1007/s11240-019-01727-2

Bjørklund, G., Aaseth, J., Chirumbolo, S., Urbina, M. A., & Uddin, R. (2018). Effects of arsenic toxicity beyond epigenetic modifications. Environmental Geochemistry and Health, 40(3), 955–965. https://doi.org/10.1007/s10653-017-0014-0

Cong, W., Miao, Y., Xu, L., Zhang, Y., Yuan, C., Wang, J., … & Ou, X. (2019). Transgenerational memory of gene expression changes induced by heavy metal stress in rice (Oryza sativa L.). BMC Plant Biology, 19(1), 282. https://doi.org/10.1186/s12870-019-1916-0

Ghosh, A., Igamberdiev, A. U., & Debnath, S. C. (2021). Tissue culture-induced DNA methylation in crop plants: A review. Molecular Biology Reports, 48(1), 823–841. https://doi.org/10.1007/s11033-020-05883-4

Hamilton, P. J., & Nestler, E. J. (2019). Epigenetics and addiction. Current Opinion in Neurobiology, 59, 128–136. https://doi.org/10.1016/j.conb.2019.03.011

Kakoulidou, I., Avramidou, E. V., Baránek, M., Brunel-Muguet, S., Farrona, S., Johannes, F., … & Maury, S. (2021). Epigenetics for crop improvement in times of global change. Biology, 10(8), 766. https://doi.org/10.3390/biology10080766

Lee, K., & Seo, P. J. (2018). Dynamic epigenetic changes during plant regeneration. Trends in Plant Science, 23(3), 235–247. https://doi.org/10.1016/j.tplants.2017.11.009

Li, J., Wang, M., Li, Y., Zhang, Q., Lindsey, K., Daniell, H., … & Zhang, X. (2019). Multi-omics analyses reveal epigenomics basis for cotton somatic embryogenesis through successive regeneration acclimation process. Plant Biotechnology Journal, 17(2), 435–450. https://doi.org/10.1111/pbi.12992

Loyola-Vargas, V. M., & Ochoa-Alejo, N. (2018). An introduction to plant tissue culture: Advances and perspectives. In V. M. Loyola-Vargas & N. Ochoa-Alejo (Eds.), Plant cell culture protocols (pp. 3–13). Humana Press. https://doi.org/10.1007/978-1-4939-8711-2_1

Mani, S., Ghosh, J., Coutifaris, C., Sapienza, C., & Mainigi, M. (2020). Epigenetic changes and assisted reproductive technologies. Epigenetics, 15(1–2), 12–25. https://doi.org/10.1080/15592294.2019.1705334

Migliore, L., & Coppedè, F. (2022). Gene–environment interactions in Alzheimer disease: The emerging role of epigenetics. Nature Reviews Neurology, 18(11), 643–660. https://doi.org/10.1038/s41582-022-00690-w

Perez, S., Kaspi, A., Domovitz, T., Davidovich, A., Lavi-Itzkovitz, A., Meirson, T., … & Gal-Tanamy, M. (2019). Hepatitis C virus leaves an epigenetic signature post cure of infection by direct-acting antivirals. PLoS Genetics, 15(6), e1008181. https://doi.org/10.1371/journal.pgen.1008181

Rajaee Behbahani, S., Iranbakhsh, A., Ebadi, M., Majd, A., & Ardebili, Z. O. (2020). Red elemental selenium nanoparticles mediated substantial variations in growth, tissue differentiation, metabolism, gene transcription, epigenetic cytosine DNA methylation, and callogenesis in bittermelon (Momordica charantia); an in vitro experiment. PLoS ONE, 15(7), e0235556. https://doi.org/10.1371/journal.pone.0235556

Sotoodehnia-Korani, S., Iranbakhsh, A., Ebadi, M., Majd, A., & Ardebili, Z. O. (2020). Selenium nanoparticles induced variations in growth, morphology, anatomy, biochemistry, gene expression, and epigenetic DNA methylation in Capsicum annuum; an in vitro study. Environmental Pollution, 265, 114727. https://doi.org/10.1016/j.envpol.2020.114727

Tao, Y., Kang, B., Petkovich, D. A., Bhandari, Y. R., In, J., Stein-O'Brien, G., … & Easwaran, H. (2019). Aging-like spontaneous epigenetic silencing facilitates Wnt activation, stemness, and BrafV600E-induced tumorigenesis. Cancer Cell, 35(2), 315–328. https://doi.org/10.1016/j.ccell.2018.12.013

Verheijen, M., Lienhard, M., Schrooders, Y., Clayton, O., Nudischer, R., Boerno, S., … & Caiment, F. (2019). DMSO induces drastic changes in human cellular processes and epigenetic landscape in vitro. Scientific Reports, 9(1), 4641. https://doi.org/10.1038/s41598-019-41256-1

Wang, K., Liu, H., Hu, Q., Wang, L., Liu, J., Zheng, Z., … & Liu, G. H. (2022). Epigenetic regulation of aging: Implications for interventions of aging and diseases. Signal Transduction and Targeted Therapy, 7(1), 374. https://doi.org/10.1038/s41392-022-01212-0

Wijerathna-Yapa, A., Ramtekey, V., Ranawaka, B., & Basnet, B. R. (2022). Applications of in vitro tissue culture technologies in breeding and genetic improvement of wheat. Plants, 11(17), 2273. https://doi.org/10.3390/plants11172273

Wójcikowska, B., Wójcik, A. M., & Gaj, M. D. (2020). Epigenetic regulation of auxin-induced somatic embryogenesis in plants. International Journal of Molecular Sciences, 21(7), 2307. https://doi.org/10.3390/ijms21072307.

Similar Articles

1 2 > >> 

You may also start an advanced similarity search for this article.