Polymorphism of Sdr genes regulating seed dormancy in Triticum persicum Vav. and Triticum aethiopicum Jakubz.
https://doi.org/10.18699/VJ19.573
Abstract
Preharvest sprouting of wheat grain, sporadically observed in many regions of cultivation of this crop, leads to deterioration of its food and sowing qualities. Seed dormancy is considered to be the main component of resistance to preharvest sprouting. This physiological state of seeds is regulated by many genes, and it depends heavily on environmental conditions. One of the regulators of seed dormancy in cereals is the Sdr4 gene (Seed dormancy 4), which was first studied in rice. In common wheat, the homologues of this gene (TaSdr-A1 and TaSdr-B1) are also involved in the regulation of seed dormancy. The search for valuable alleles in local varieties and endemic forms is a promising area of research aimed at increasing the resistance of crops to adverse environmental factors. In this study, Sdr genes were sequenced in several accessions of two tetraploid wheat species with limited cultivation areas: Persian wheat (Triticum persicum Vav.) and Ethiopian wheat (Triticum aethiopicum Jakubz.). As a result, the same Sdr-A1 and Sdr-B1 variants that had been found in common wheat were detected in these species. The Persian wheat accessions possessed only the Sdr-A1a allele, while Ethiopian ones, only Sdr-A1b. The analysis of F2 hybrids obtained from crossing these tetraploid species showed that the Sdr-A1b allele was associated with a lower germination index of grains than Sdr-A1a. This result was inconsistent with earlier association studies. Previously unknown polymorphisms were found in the promoter of the Sdr-B1 gene in the studied accessions. A deletion of 16 nucleotides was detected in the 3’-terminal region of the TraesCS2B02G215200 gene, located on the complementary DNA chain close to the 3’-end of the Sdr-B1 gene. Possible effects of the detected polymorphisms on the expression of Sdr genes are discussed.
About the Authors
M. S. BazhenovRussian Federation
Moscow
E. D. Guseva
Russian Federation
Moscow
V. S. Rubets
Russian Federation
Moscow
References
1. Alaux M., Rogers J., Letellier T., Flores R., Alfama F., Pommier C., Mohellibi N., Durand S., Kimmel E., Michotey C., Guerche C., Loaec M., Laine M., Steinbach D., Choulet F., Rimbert H., Leroy P., Guilhot N., Salse J., Feuillet C. Linking the International Wheat Genome Sequencing Consortium bread wheat reference genome sequence to wheat genetic and phenomic data. Genome Biol. 2018; 19(1):111. DOI 10.1186/s13059-018-1491-4.
2. Badaeva E.D., Shishkina A.A., Dragovich A.Y., Kudriavtsev A.M., Goncharov N.P., Zuev E.V., Lysenko N.S., Mitrofanova O.P. Evolution of Triticum aethiopicum Jakubz. from the position of chromosome analysis. Russ. J. Genet. 2018;54(6):629-642. DOI 10.1134/S1022795418060029.
3. Dorofeev V.F., Filatenko A.A., Migushova E.F., Udachin R.A., Jakubtsiner M.M. Cultural Flora of the USSR. Vol. 1. Wheat. Leningrad: Kolos, 1979. (in Russian)
4. Doyle P.J. DNA Protocols for Plants. Molecular Techniques in Taxonomy. 1991;57(1):283-293. DOI 10.1007/978-3-642-83962-7.
5. Hoang H.H., Sechet J., Bailly C., Leymarie J., Corbineau F. Inhibition of germination of dormant barley (Hordeum vulgare L.) grains by blue light as related to oxygen and hormonal regulation. Plant Cell Environ. 2014;37(6):1393-1403. DOI 10.1111/pce.12239.
6. Lescot M., Dehais P., Thijs G., Marchal K., Moreau Y., Van de Peer Y., Rouze P., Rombauts S. PlantCARE, a database of plant cis-acting regulatory elements and a portal to tools for in silico analysis of promoter sequences. Nucleic Acids Res. 2002;30(1):325-327.
7. Nakamura S. Grain dormancy genes responsible for preventing pre-harvest sprouting in barley and wheat. Breed. Sci. 2018;68(3):295-304. DOI 10.1270/jsbbs.17138.
8. Olaerts H., Courtin C.M. Impact of preharvest sprouting on endogenous hydrolases and technological quality of wheat and bread: a review. Compr. Rev. Food Sci. Food Safety. 2018;17(3):698-713. DOI 10.1111/1541-4337.12347.
9. Sugimoto K., Takeuchi Y., Ebana K., Miyao A., Hirochika H., Hara N., Ishiyama K., Kobayashi M., Ban Y., Hattori T., Yano M. Molecular cloning of Sdr4, a regulator involved in seed dormancy and domestication of rice. Proc. Natl. Acad. Sci. USA. 2010;107(13):5792-5797. DOI 10.1073/pnas.0911965107.
10. Vetch J.M., Stougaard R.N., Martin J.M., Giroux M. Allelic impacts of TaPHS1, TaMKK3, and Vp1B3 on preharvest sprouting of northern great plains winter wheats. Crop Sci. 2018;59(1):140-150. DOI 10.2135/cropsci2018.05.0341.
11. Walker-Simmons M. Enhancement of ABA responsiveness in wheat embryos by high temperature. Plant Cell Environ. 1988;11(8):769-775. DOI 10.1111/j.1365-3040.1988.tb01161.x.
12. Xu Q., Truong T.T., Barrero J.M., Jacobsen J.V., Hocart C.H., Gubler F. A role for jasmonates in the release of dormancy by cold stratification in wheat. J. Exp. Bot. 2016;67(11):3497-3508. DOI 10.1093/jxb/erw172.
13. Zhang Y., Miao X., Xia X., He Z. Cloning of seed dormancy genes (TaSdr) associated with tolerance to pre-harvest sprouting in common wheat and development of a functional marker. Theor. Appl. Genet. 2014;127(4):855-866. DOI 10.1007/s00122-014-2262-6.
14. Zhang Y., Xia X., He Z. The seed dormancy allele TaSdr-A1a associated with pre-harvest sprouting tolerance is mainly present in Chinese wheat landraces. Theor. Appl. Genet. 2017;130(1):81-89. DOI 10.1007/s00122-016-2793-0.