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Flavonoid Synthesis Pathway Response to Low-Temperature Stress in a Desert Medicinal Plant, (Sandrice)

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2024 Sep 28
PMID 39336819
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Abstract

(L.) Moq. (), also known as sandrice, is an important medicinal plant widely distributed in dunes across all the deserts of China. Common garden trials have shown content variations in flavonoids among the ecotypes of sandrice, which correlated with temperature heterogeneity in situ. However, there have not been any environmental control experiments to further elucidate whether the accumulation of flavonoids was triggered by cold stress; This study conducted a four-day ambient 4 °C low-temperature treatment on three ecotypes along with an in situ annual mean temperature gradient (Dulan (DL), Aerxiang (AEX), and Dengkou (DK)); Target metabolomics showed that 12 out of 14 flavonoids in sandrice were driven by cold stress. Among them, several flavonoids were significantly up-regulated, such as naringenin and naringenin chalcone in all three ecotypes; isorhamnetin, quercetin, dihydroquercetin, and kaempferol in DL and AEX; and astragalin in DK. They were accompanied by 19 structural genes of flavonoid synthesis and 33 transcription factors were markedly triggered by cold stress in sandrice. The upstream genes, -, -, and -, were highly correlated with the enrichment of naringenin, which could be fine-tuned by -, - and -; This study sheds light on how desert plants like sandrice adapt to cold stress by relying on a unique flavonoid biosynthesis mechanism that regulating the accumulation of naringenin. It also supports the precise development of sandrice for the medicinal industry. Specifically, quercetin and isorhamnetin should be targeted for development in DL and AEX, while astragalin should be precisely developed in DK.

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References
1.
Shomali A, Das S, Arif N, Sarraf M, Zahra N, Yadav V . Diverse Physiological Roles of Flavonoids in Plant Environmental Stress Responses and Tolerance. Plants (Basel). 2022; 11(22). PMC: 9699315. DOI: 10.3390/plants11223158. View

2.
Jogawat A, Yadav B, Chhaya , Lakra N, Singh A, Narayan O . Crosstalk between phytohormones and secondary metabolites in the drought stress tolerance of crop plants: A review. Physiol Plant. 2021; 172(2):1106-1132. DOI: 10.1111/ppl.13328. View

3.
Castroverde C, Dina D . Temperature regulation of plant hormone signaling during stress and development. J Exp Bot. 2021; . DOI: 10.1093/jxb/erab257. View

4.
Wang C, Dong Y, Zhu L, Wang L, Yan L, Wang M . Comparative transcriptome analysis of two contrasting wolfberry genotypes during fruit development and ripening and characterization of the LrMYB1 transcription factor that regulates flavonoid biosynthesis. BMC Genomics. 2020; 21(1):295. PMC: 7147035. DOI: 10.1186/s12864-020-6663-4. View

5.
Jin H, Martin C . Multifunctionality and diversity within the plant MYB-gene family. Plant Mol Biol. 2000; 41(5):577-85. DOI: 10.1023/a:1006319732410. View