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Article | Open Access

Analysis and Verification of the Conserved MYB Binding Element in the DFR Promoter in Compositae

Jialei Guo1,2Fengzhen Li2Guomin Shi3Weimin Zhao2Tao He1,2( )
State Key Laboratory of Plateau Ecology and Agriculture, Qinghai University, Xining, 810016, China
School of Ecol-Environmental Engineering, Qinghai University, Xining, 810016, China
Key Laboratory of Landscape Plants of Qinghai Province, Qinghai University, Xining, 810016, China
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Abstract

Anthocyanins, ubiquitous in the Compositae family, are regulated by MYB (v-myb avian myeloblastosis viral oncogene homolog), playing an important role in anthocyanin synthesis. In this study, we analyzed the regulation pathway in which the MYB protein of subgroup 6 promotes dihydroflavonol reductase (DFR) expression in Compositae, and validated this law in Saussurea medusa through yeast one-hybrid experiments. Our results showed that MYB and DFR underwent purification selection, DFR promoter analysis revealed the presence of MYB binding site (GAGTTGAATGG) and bHLH binding site (CANNTG) at the sense strand of 84–116 nucleotide residues from the start codon. These two motifs were separated by 9–10 nucleotide residues, as existed in the DFR promoters of many Compositae plants. Furthermore, the yeast one-hybrid experiment demonstrated that SmMYB1 can activate the promoter of SmDFR. Our results provide a reference for further functional study of DFR in Compositae.

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Phyton-International Journal of Experimental Botany
Pages 343-353

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Cite this article:
Guo J, Li F, Shi G, et al. Analysis and Verification of the Conserved MYB Binding Element in the DFR Promoter in Compositae. Phyton-International Journal of Experimental Botany, 2024, 93(2): 343-353. https://doi.org/10.32604/phyton.2024.047429

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Received: 05 November 2023
Accepted: 10 January 2024
Published: 27 February 2024
© The Author 2024.

This work is licensed under a Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.