Description of new naturally transgenic plants enables estimation of the time intervals of horizontal gene transfer from agrobacterium to plants
- Authors: Shaposhnikov A.D.1, Matveeva T.V.1,2
-
Affiliations:
- Saint Petersburg State University
- All-Russian Research Institute of Plant Protection
- Issue: Vol 24, No 1 (2026)
- Pages: 15-28
- Section: Genetically modified organism.history, achievements, social and environmental risks.
- Submitted: 17.10.2025
- Accepted: 19.11.2025
- Published: 31.03.2026
- URL: https://journals.eco-vector.com/ecolgenet/article/view/693516
- DOI: https://doi.org/10.17816/ecogen693516
- EDN: https://elibrary.ru/ZBWJTR
- ID: 693516
Cite item
Abstract
BACKGROUND: Horizontal gene transfer from Agrobacterium to dicotyledonous plants leads to the emergence of naturally transgenic species containing DNA fragments known as cellular T-DNA. Such plants are also referred to as naturally genetically modified organisms (GMOs). The continuous expansion of nucleotide sequence databases and advances in bioinformatics methods have made it possible to systematically identify natural transgenes in deposited genomes of various dicot species, thereby expanding the list of known natural GMOs. Detailed investigation of horizontally transferred sequences opens opportunities for their comparative analysis.
AIM: To search for and analyze sequences homologous to Agrobacterium T-DNA in the genomes of dicotyledonous plants and subsequently estimate the timing of horizontal gene transfer events based on comparisons of extended inverted repeats of cellular T-DNA.
METHODS: Data from the WGS and TSA nucleotide sequence databases were used, together with BLAST alignment algorithms.
RESULTS: A total of 93 new species of naturally transgenic plants were identified. Based on the analysis of cellular T-DNA sequences present as inverted repeats, approximate timing of horizontal gene transfer events was estimated for 28 species of natural GMOs. The analysis revealed numerous common features in the evolution of transgenes between the newly identified natural GMOs and other examples of horizontal gene transfer. It was established that the transfer events occurred between 0.62 and 24 million years ago, spanning three periods of the Cenozoic era.
CONCLUSION: The obtained results may be used to investigate the evolutionary role of cellular T-DNA and horizontal gene transfer in naturally transgenic plants.
Full Text
About the authors
Anton D. Shaposhnikov
Saint Petersburg State University
Author for correspondence.
Email: st096319@student.spbu.ru
ORCID iD: 0009-0002-7905-2999
SPIN-code: 5145-8352
Russian Federation, Saint Petersburg
Tatiana V. Matveeva
Saint Petersburg State University; All-Russian Research Institute of Plant Protection
Email: radishlet@gmail.com
ORCID iD: 0000-0001-8569-6665
SPIN-code: 3877-6598
Dr. Sci. (Biology), Professor
Russian Federation, Saint Petersburg; Saint PetersburgReferences
- Soucy SM, Huang J, Gogarten JP. Horizontal gene transfer: building the web of life. Nat Rev Genet. 2015;16(8):472–482. doi: 10.1038/nrg3962
- Matveeva T. New naturally transgenic plants: 2020 update. BioComm. 2021;66(1):105. doi: 10.21638/spbu03.2021.105
- White FF, Garfinkel DJ, Huffman GA, et al. Sequences homologous to Agrobacterium rhizogenes T-DNA in the genomes of uninfected plants. Nature. 1983;301(5898):348–350. doi: 10.1038/301348a0
- Intrieri MC, Buiatti M. The horizontal transfer of Agrobacterium rhizogenes genes and the evolution of the genus Nicotiana. Mol Phylogenet Evol. 2001;20(1):100–110. doi: 10.1006/mpev.2001.0927
- Matveeva TV, Bogomaz DI, Pavlova OA, et al. Horizontal gene transfer from genus Agrobacterium to the plant Linaria in nature. Mol Plant Microbe Interact. 2012;25(12):1542–1551. doi: 10.1094/MPMI-07-12-0169-R
- Kyndt T, Quispe D, Zhai H, et al. The genome of cultivated sweet potato contains Agrobacterium T-DNAs with expressed genes: An example of a naturally transgenic food crop. PNAS USA. 2015;112(18):5844–5849. doi: 10.1073/pnas.1419685112
- Chen K, Dorlhac De Borne F, Sierro N, et al. Organization of the TC and TE cellular T-DNA regions in Nicotiana otophora and functional analysis of three diverged TE-6b genes. Plant J. 2018;94(2):274–287. doi: 10.1111/tpj.13853
- Matveeva TV, Bogomaz OD, Golovanova LA, et al. Homologs of the rolC gene of naturally transgenic toadflaxes Linaria vulgaris and Linaria creticola are expressed in vitro. Vavilov Journal of Genetics and Breeding. 2018;22(2):273–278. doi: 10.18699/VJ18.359 EDN: YSOQJV
- Matveeva TV, Otten L. Widespread occurrence of natural genetic transformation of plants by Agrobacterium. Plant Mol Biol. 2019;101(4–5): 415–437. doi: 10.1007/s11103-019-00913-y
- Matveeva TV. Why do plants need agrobacterial genes? Ecological genetics. 2021;19(4):365–375. doi: 10.17816/ecogen89905 EDN: CPNOPB
- Matveeva TV. Agrobacterium-mediated transformation in the evolution of plants. In: Gelvin S, editor. Agrobacterium biology. Current topics in microbiology and immunology. Vol. 418. Springer, Cham; 2018. P. 421–441. doi: 10.1007/82_2018_80
- Matveeva TМ. Natural GMOs: a history of research. Ecological genetics. 2022;20(1S):7–8. doi: 10.17816/ecogen112371 EDN: BFCWSH
- Zhidkin RR, Matveeva TV. Phylogeny problems of the genus Vaccinium L. and ways to solve them. Ecological genetics. 2022; 20(2):151–164. doi: 10.17816/ecogen109142 EDN: PMZCQM
- Zhidkin R, Zhurbenko P, Bogomaz O, et al. Biodiversity of rolB/C-like natural transgene in the genus Vaccinium L. and its application for phylogenetic studies. IJMS. 2023;24(8):6932. doi: 10.3390/ijms24086932
- Chen K, Zhurbenko P, Danilov L, et al. Conservation of an Agrobacterium cT-DNA insert in Camellia section Thea reveals the ancient origin of tea plants from a genetically modified ancestor. Front Plant Sci. 2022;13:997762. doi: 10.3389/fpls.2022.997762
- Matveeva TV. Naturally transgenic plants as a model for the study of delayed environmental risks of cultivation of GMOs. Ecological genetics. 2015;13(2):118–126. doi: 10.17816/ecogen132118-126 EDN: TYRKIL
- Lipatov PYu, Bogomaz FD, Gosudarev KD, et al. New cellular T-DNAs in naturally transgenic plants. Ecological genetics. 2022;20(1S):40–41. doi: 10.17816/ecogen112352 EDN: MPRCSO
- Altschul SF, Madden TL, Shaffer AA, et al. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997;25(17):3389–3402. doi: 10.1093/nar/25.17.3389
- The Angiosperm Phylogeny Group. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV. Bot J Linn Soc. 2016;181(1):1–20. doi: 10.1111/boj.12385
- Gaut BS, Morton BR, McCaig BC, Clegg MT. Substitution rate comparisons between grasses and palms: synonymous rate differences at the nuclear gene Adh parallel rate differences at the plastid gene rbcL. PNAS USA. 1996;93(19):10274–10279. doi: 10.1073/pnas.93.19.10274
- Bogomaz FD, Matveeva TV. Expression sequences of opine synthase genes in natural GMOs based on analysis of their transcriptomes. Plant Biotechnology and Breeding. 2022;5(3):15–24. doi: 10.30901/2658-6266-2022-3-o2 EDN: BSIJRA
- Pavlova OA, Matveeva TV, Lutova LA. Genome of Linaria dalmatica contains the homolog of Agrobacterium rhizogenes rolC gene. Ecological genetics. 2013;11(2):10–15. doi: 10.17816/ecogen11210-15 EDN: RBXNXH
- Chen K, Dorlhac De Borne F, Szegedi E, Otten L. Deep sequencing of the ancestral tobacco species Nicotiana tomentosiformis reveals multiple T-DNA inserts and a complex evolutionary history of natural transformation in the genus Nicotiana. Plant J. 2014;80(4):669–682. doi: 10.1111/tpj.12661
- Otten L, Liu H, Meeprom N, et al. Accumulation of numerous cellular T-DNA sequences in the genus Diospyros by multiple rounds of natural transformation. Plant J. 2025;122(3):e70202. doi: 10.1111/tpj.70202
- Van Kregten M, De Pater S, Romeijn R, et al. T-DNA integration in plants results from polymerase-θ-mediated DNA repair. Nat Plants. 2016;2(11):16164. doi: 10.1038/nplants.2016.164
- Husnik F, McCutcheon JP. Functional horizontal gene transfer from bacteria to eukaryotes. Nat Rev Microbiol. 2018;16(2):67–79. doi: 10.1038/nrmicro.2017.137
- Li W-H, Gojobori T, Nei M. Pseudogenes as a paradigm of neutral evolution. Nature. 1981;292(5820):237–239. doi: 10.1038/292237a0
- Alsmark C, Foster PG, Sicheritz-Ponten T, et al. Patterns of prokaryotic lateral gene transfers affecting parasitic microbial eukaryotes. Genome Biol. 2013;14(2):R19. doi: 10.1186/gb-2013-14-2-r19
- Chen R, Huangfu L, Lu Y, et al. Adaptive innovation of green plants by horizontal gene transfer. Biotechnol Adv. 2021;46:107671. doi: 10.1016/j.biotechadv.2020.107671
- Weisberg AJ, Davis EW II, Tabima J, et al. Unexpected conservation and global transmission of agrobacterial virulence plasmids. Science. 2020;368(6495):eaba5256. doi: 10.1126/science.aba5256
Supplementary files








