Preview

Proceedings on applied botany, genetics and breeding

Advanced search

Influence of allelic polymorphism in the 3’ untranslated region of the StTCP23 gene on the tolerance of potato cultivars to the potato spindle tuber viroid

https://doi.org/10.30901/2227-8834-2023-1-137-143

Abstract

Background. It is known that the pathological phenotype of potato plants can be mediated by complementary interactions between the genomic RNA of PSTVd and mRNA of some regulatory genes, which consequently lead to RNA interference, the synthesis of small interfering RNAs (vd-sRNA PSTVd), and impaired morphogenesis. At the same time, symptoms caused by the viroid may vary in different potato cultivars. Here we predict the interactions between the 3’ UTRs of various alleles of the StTCP23 transcription factor gene and the complementary regions in PSTVd genomic RNA.
Materials and methods. We selected eight commercial potato cultivars with different symptoms of viroid infection and disease. For each cultivar, six clones of each cDNA amplicon of StTCP23 with a 3’ UTR were identified, and the allelic compositions of the target regions within their 3’ UTRs were characterized.
Results. In total, 11 types of alleles of the 3’ UTR StTCP23 segment complementary to the vd-sRNA PSTVd were identified. Cultivars with the A allele (‘Gala’, ‘Colomba’, ‘Favorit’, and ‘Fioletovy’) identical to the reference genome or a high dose of the C allele with a deletion of four nucleotides (cv. ‘Impala’) were characterized by high susceptibility already at the primary (firstyear) infection with the PSTVd. Cvs. ‘Krepysh’, ‘Labadia’ and ‘Riviera’, classified as tolerant during primary inoculation, on the contrary, were characterized by the absence of the A allele and the presence of cultivar-specific mutant alleles.
Conclusion. A high degree of polymorphism in the target site (3’ UTR region) of StTCP23 indicates a possible selection pressure on this locus. It can be assumed that cultivars with shorter alleles, which have fewer bases complementary to vd-sRNA in hypothetical duplexes and therefore less likely to induce target gene silencing, are more tolerant to the PSTVd upon primary viroid infection.

About the Authors

N. V. Mironenko
All-Russian Research Institute of Plant Protection
Russian Federation

Dr.Sci. (Biology),Leading Researcher

3 Podbelskogo Hwy., Pushkin, St. Petersburg 196608, Russia 



A. V. Kochetov
Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences; Novosibirsk State Agrarian University
Russian Federation

Dr. Sci. (Biology), Professor of the RAS, Director

10 Akademika Lavrentyeva Ave., Novosibirsk 630090 Russia

160 Dobrolyubova St., Novosibirsk 630039, Russia, 



O. S. Afanasenko
All-Russian Research Institute of Plant Protection
Russian Federation

Dr. Sci. (Biology), Professor of the RAS, Chief Researcher

3 Podbelskogo Hwy., Pushkin, St. Petersburg 196608, Russia 



References

1. Adkar-Purushothama C.R., Brosseau C., Giguère T., Sano T., Moffett P., Perreault J.P. Small RNA derived from the virulence modulating region of the potato spindle tuber viroid silences callose synthase genes of tomato plants. The Plant Cell. 2015;27(8):2178-2194. DOI: 10.1105/tpc.15.00523

2. Adkar-Purushothama C.R., Perreault J.P. Alterations of the viroid regions that interact with the host defense genes attenuate viroid infection in host plant. RNA Biology. 2018;15(7):955-966. DOI: 10.1080/15476286.2018.1462653

3. Afanasenko O.S., Lashina N.M., Mironenko N.V., Kyrova E.I., Rogozina E.V., Zubko N.G. et al. Evaluation of responses of potato cultivars to potato spindle tuber viroid and to mixed viroid/viral infection. Agronomy. 2022;12(12):2916. DOI: 10.3390/agronomy12122916

4. Aviña-Padilla K., Rivera-Bustamante R., Kovalskaya N.Y., Hammond R.W. Pospiviroid infection of tomato regulates the expression of genes involved in flower and fruit development. Viruses. 2018;10(10):516. DOI: 10.3390/v10100516

5. Bao S., Owens R.A., Sun Q., Song H., Liu Y., Eamens A.L. et al. Silencing of transcription factor encoding gene StTCP23 by small RNAs derived from the virulence modulating region of potato spindle tuber viroid is associated with symptom development in potato. PLoS Pathogens. 2019a;15(12):e1008110. DOI: 10.1371/journal.ppat.1008110

6. Bao S., Zhang Z., Lian Q., Sun Q., Zhang R. Evolution and expression of genes encoding TCP transcription factors in Solanum tuberosum reveal the involvement of StTCP23 in plant defence. BMC Genetics. 2019b;20(1):91. DOI: 10.1186/s12863-019-0793-1

7. Doebley J., Stec A., Hubbard L. The evolution of apical dominance in maize. Nature. 1997;386(6624):485-488. DOI: 10.1038/386485a0

8. El-Sappah A.H., Yan K., Huang Q., Islam M.M., Li Q., Wang Y. et al. Comprehensive mechanism of gene silencing and its role in plant growth and development. Frontiers in Plant Science. 2021;12:705249. DOI: 10.3389/fpls.2021.705249

9. Fang Y., Zheng Y., Lu W., Li J., Duan Y., Zhang S. et al. Roles of miR319-regulated TCPs in plant development and response to abiotic stress. The Crop Journal. 2021;9(1):17-28. DOI: 10.1016/j.cj.2020.07.007

10. Katsarou K., Wu Y., Zhang R., Bonar N., Morris J., Hedley P.E. et al. Insight on genes affecting tuber development in potato upon Potato spindle tuber viroid (PSTVd) infection. PLoS One. 2016;11(3):e0150711. DOI: 10.1371/journal.pone.0150711

11. Keese P., Symons R.H. Domains in viroids: evidence of intermolecular RNA rearrangements and their contribution to viroid evolution. Proceedings of the National Academy of Sciences of the United States of America. 1985;82(14):4582-4586. DOI: 10.1073%2Fpnas.82.14.4582

12. Kosugi S., Ohashi Y. PCF1and PCF2 specifically bind to cis elements in the rice proliferating cell nuclear antigen gene. The Plant Cell. 1997;9(9):1607-1619. DOI: 10.1105/tpc.9.9.1607

13. Luo D., Carpenter R., Vincent C., Copsey L., Coen E. Origin of floral asymmetry in Antirrhinum. Nature. 1996; 383(6603):794-799. DOI: 10.1038/383794a0.

14. Manrique-Carpintero N.C., Coombs J.J., Pham G.M., Laimbeer F.P.E., Braz G.T., Jiang J. et al. Genome reduction in tetraploid potato reveals genetic load, haplotype variation, and loci associated with agronomic traits. Frontiers in Plant Science. 2018;9:944. DOI: 10.3389/fpls.2018.00944

15. Martín-Trillo M., Cubas P. TCP genes: a family snapshot ten years later. Trends in Plant Science. 2010;15(1):31-39. DOI: 10.1016/j.tplants.2009.11.003

16. Navarro B., Flores R., Serio F.D. Advances in viroid–host interactions. Annual Review of Virology. 2021;8(1):305-325. DOI: 10.1146/annurev-virology-091919-092331

17. Nicolas M., Cubas P. TCP factors: new kids on the signaling block. Current Opinion in Plant Biology. 2016;33:33-41. DOI: 10.1016/j.pbi.2016.05.006

18. Ohnishi Y., Tamura Y., Yoshida M., Tokunaga K., Hohjoh H. Enhancement of allele discrimination by introduction of nucleotide mismatches into siRNA in allele-specific gene silencing by RNAi. PLoS One. 2008;3(5):e2248. DOI: 10.1371/journal.pone.0002248

19. Pham G.M., Newton L., Wiegert-Rininger K., Vaillancourt B., Douches D.S., Buell C.R. Extensive genome heterogeneity leads to preferential allele expression and copy numberdependent expression in cultivated potato. The Plant Journal. 2017;92(4):624-637. DOI: 10.1111/tpj.13706

20. Ren L., Wu H., Zhang T., Ge X., Wang T., Zhou W. et al. Genomewide identification of TCP transcription factors family in sweet potato reveals significant roles of miR319-targeted TCPs in leaf anatomical morphology. Frontiers in Plant Science. 2021;12:686698. DOI: 10.3389/fpls.2021.686698

21. Sano T. Progress in 50 years of viroid research – Molecular structure, pathogenicity, and host adaptation. Proceedings of the Japan Academy. Series B: Physical and Biological Sciences. 2021;97(7):371-401. DOI: 10.2183/pjab.97.020

22. Sevestre F., Facon M., Wattebled F., Szydlowski N. Facilitating gene editing in potato: a Single-Nucleotide Polymorphism (SNP) map of the Solanum tuberosum L. cv. Desiree genome. Scientific Reports. 2020;10(1):2045. DOI: 10.1038/s41598-020-58985-6

23. Watanabe K. Potato genetics, genomics, and applications. Breeding Science. 2015;65(1):53-68. DOI: 10.1270/jsbbs.65.53


Review

For citations:


Mironenko N.V., Kochetov A.V., Afanasenko O.S. Influence of allelic polymorphism in the 3’ untranslated region of the StTCP23 gene on the tolerance of potato cultivars to the potato spindle tuber viroid. Proceedings on applied botany, genetics and breeding. 2023;184(1):137-143. (In Russ.) https://doi.org/10.30901/2227-8834-2023-1-137-143

Views: 398


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2227-8834 (Print)
ISSN 2619-0982 (Online)