INTRASPECIFIC VARIABILITY OF THE Sus1 SUCROSE SYNTHASE GENE IN Pisum sativum ACCESSIONS
https://doi.org/10.18699/VJ18.338
Abstract
The pea Pisum sativum is widely cultivated in Russia as well as over the world. Pea productivity depends on the ability of the pea plant to get into a symbiosis with nodule bacteria. It was previously shown that the strength of the symbiotic activity depends on the activity of plant sucrose cleavage enzymes. Sucrose synthase Sus1 is one of the most important enzymes involved in carbohydrate metabolism. Sucrose synthase cleaves sucrose into UDP-glucose and fructose. This paper is devoted to characterization of Sus1 gene intraspecific variability in 14 Pisum sativum accessions. The length of the identified Sus1 gene varied from 3514 bp to 3532 bp. All identified genes had a similar structure and contained 13 exons and 12 introns. According to their structure, they were assigned to the SUS1-group of dicotyledonous plants. In nucleotide sequences, 125 SNPs were identified. In addition to SNPs, intron sequences contained six indels, thus their length varied from 1093 bp to 1111 bp. The most variable was the intron III. In coding sequences, 47 SNPs were found, wherein the most variable was the exon II. 16 exon SNPs led to amino acid substitutions. Six of them were deleterious and may potentially influence protein folding and stability. All the conservative motifs and active sites were detected in the translated amino acid sequences. It was shown that their sequences were invariable in all the tested accessions. Computational analysis of the amino acid sequences has predicted Sus1 tertiary structure. The protein is a tetramer and each subunit in its turn consists of three domains. The phylogenetic analysis using identified Pisum Sus1 sequences and homologous sucrose synthase genes revealed that the Sus1 and Sus3 genes are closer to each other than to Sus2. It was also proposed that the sucrose synthase family genes had diverged before legumes split into species.
Keywords
About the Authors
E. A. DyachenkoRussian Federation
Moscow
M. A. Slugina
Russian Federation
References
1. Barratt D.H.P., Barber L., Kruger N.J., Smith A.M., Wang T.L., Martin C. Multiple, distinct isoforms of sucrose synthase in pea. Plant Physiol. 2001;127:655-664.
2. Baud S., Vaultier M.-N., Rochat C. Structure and expression profile of the sucrose synthase multigene family in Arabidopsis. J. Exp. Bot. 2004;55(396):397-409.
3. Choi M.-K., Le M.T., Nguyen D.T., Choi H., Kim W., Kim J.-H., Chun J., Hyeon J., Seo K., Park C. Genome-level identification, gene expression, and comparative analysis of porcine β-defensin genes. BMC Genetics. 2012;13:98-107.
4. Dahl W.J., Foster L.M., Tyler R.T. Review on the health benefits of peas (Pisum sativum L). Br. J. Nutr. 2012;108:3-10.
5. Dyachenko E.A., Boris K.V., Kochieva E.Z. Identification and polymorphism of the sucrose synthase gene Sus1 in Pisum fulvum. Molekulyarnaya biologia = Molecular Biology (Moscow). 2015;49(4):700704. (in Russian)
6. Harada T., Satoh S., Yoshioka T., Ishizawa K. Expression of sucrose synthase genes involved in enhanced elongation of pondweed (Potamogeton distinctus) turions under anoxia. Ann. Botany. 2005;96: 683-692.
7. Horst I., Welham T., Kelly S., Kaneko T., Sato S., Tabata S., Parniske M., Wang T.L. Tilling mutants of Lotus japonicus reveal that nitrogen assimilation and fixation can occur in the absence of nodule-enhanced sucrose synthase. Plant Physiol. 2007;144:806820.
8. Jiang Q., Hou J., Hao C., Wang L., Ge H., Dong Y., Zhang X. The wheat (T. aestivum) sucrose synthase 2 gene (TaSus2) active in endosperm development is associated with yield traits. Funct. Integr. Genomics. 2011;11:49-61.
9. Kelley L.A., Mezulis S., Yates C.M., Wass M.N., Sternberg M.J. The Phyre2 web portal for protein modeling, prediction and analysis. Nat. Protoc. 2015;10(6):845-858.
10. Kumar S., Stecher G., Tamura K. MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 2016;33:1870-1874.
11. Lairson L.L., Henrissat B., Davies G.J., Withers S.G. Glycosyltransferases: structures, functions, and mechanisms. Annu. Rev. Biochem. 2008;77:521-555.
12. Rohrig H., Schmidt J., Miklashevichs E., Schell J., John M. Soybean ENOD40 encodes two peptides that bind to sucrose synthase. Proc. Natl. Acad. Sci. USA. 2002;99(4):1915-1920.
13. Ryzhova N.N., Slugina M.A., Kochieva E.Z., Skryabin K.G. Polymorphism and structural variation of rps16 group II intron in the Solanum species. Genetika = Genetics (Moscow). 2013;49(7):824-829. (in Russian)
14. Silvente S., CamasA., Lara M. Heterogeneity of sucrose synthase genes in bean (Phaseolus vulgaris L.): evidence for a nodule-enhanced sucrose synthase gene. J. Exp. Bot. 2003;54:749-755.
15. Zhang J., Arro J., Chen Y., Ming R. Haplotype analysis of sucrose synthase gene family in three Saccharum species. Genomics. 2013;14: 314. DOI 10.1186/1471-2164-14-314.
16. Zheng Y., Anderson S., Zhang Y., Garavito R.M. The structure of sucrose synthase-1 from Arabidopsis thaliana and its functional implications. J. Biol. Chem. 2011;286(41):36108-36118.