» Articles » PMID: 32958560

HEAT SHOCK FACTOR A8a Modulates Flavonoid Synthesis and Drought Tolerance

Overview
Journal Plant Physiol
Specialty Physiology
Date 2020 Sep 22
PMID 32958560
Citations 54
Authors
Affiliations
Soon will be listed here.
Abstract

Drought is an important environmental factor affecting the growth and production of agricultural crops and fruits worldwide, including apple (). Heat shock factors (HSFs) have well-documented functions in stress responses, but their roles in flavonoid synthesis and the flavonoid-mediated drought response mechanism remain elusive. In this study, we demonstrated that a drought-responsive HSF, designated MdHSFA8a, promotes the accumulation of flavonoids, scavenging of reactive oxygen species, and plant survival under drought conditions. A chaperone, HEAT SHOCK PROTEIN90 (HSP90), interacted with MdHSFA8a to inhibit its binding activity and transcriptional activation. However, under drought stress, the MdHSP90-MdHSFA8a complex dissociated and the released MdHSFA8a further interacted with the APETALA2/ETHYLENE RESPONSIVE FACTOR family transcription factor RELATED TO AP2.12 to activate downstream gene activity. In addition, we demonstrated that MdHSFA8a participates in abscisic acid-induced stomatal closure and promotes the expression of abscisic acid signaling-related genes. Collectively, these findings provide insight into the mechanism by which stress-inducible MdHSFA8a modulates flavonoid synthesis to regulate drought tolerance.

Citing Articles

Biological Functions and Health Benefits of Flavonoids in Fruits and Vegetables: A Contemporary Review.

Zheng X, Zhang X, Zeng F Foods. 2025; 14(2).

PMID: 39856822 PMC: 11765039. DOI: 10.3390/foods14020155.


Genome-Wide Analysis of the Hsf Gene Family in and Function in Thermotolerance.

Kang Y, Sun P, Yang Y, Li M, Wang H, Sun X Int J Mol Sci. 2025; 26(1.

PMID: 39796142 PMC: 11719701. DOI: 10.3390/ijms26010287.


Integrative metabolomics and transcriptomics profiling reveals differential expression of flavonoid synthesis in Ophiopogon japonicus (L. f.) Ker-Gawl. in adaptation to drought.

Cheng T, Lin J, Zhou X, Wang H, Zhou X, Huang X PLoS One. 2025; 20(1):e0313580.

PMID: 39774546 PMC: 11706389. DOI: 10.1371/journal.pone.0313580.


Transcriptional Profiling Analysis Providing Insights into the Harsh Environments Tolerance Mechanisms of .

Zhang H, Wang Y, Ma B, Bu X, Dang Z, Wang Y Int J Mol Sci. 2024; 25(22).

PMID: 39595960 PMC: 11594238. DOI: 10.3390/ijms252211891.


Integrating gene expression analysis and ecophysiological responses to water deficit in leaves of tomato plants.

Bortolami G, de Werk T, Larter M, Thonglim A, Mueller-Roeber B, Balazadeh S Sci Rep. 2024; 14(1):29024.

PMID: 39578554 PMC: 11584733. DOI: 10.1038/s41598-024-80261-0.


References
1.
Furihata T, Maruyama K, Fujita Y, Umezawa T, Yoshida R, Shinozaki K . Abscisic acid-dependent multisite phosphorylation regulates the activity of a transcription activator AREB1. Proc Natl Acad Sci U S A. 2006; 103(6):1988-93. PMC: 1413621. DOI: 10.1073/pnas.0505667103. View

2.
Bian X, Li W, Niu C, Wei W, Hu Y, Han J . A class B heat shock factor selected for during soybean domestication contributes to salt tolerance by promoting flavonoid biosynthesis. New Phytol. 2019; 225(1):268-283. DOI: 10.1111/nph.16104. View

3.
Zou J, Guo Y, Guettouche T, Smith D, Voellmy R . Repression of heat shock transcription factor HSF1 activation by HSP90 (HSP90 complex) that forms a stress-sensitive complex with HSF1. Cell. 1998; 94(4):471-80. DOI: 10.1016/s0092-8674(00)81588-3. View

4.
Andre C, Schafleitner R, Legay S, Lefevre I, Aliaga C, Nomberto G . Gene expression changes related to the production of phenolic compounds in potato tubers grown under drought stress. Phytochemistry. 2009; 70(9):1107-1116. DOI: 10.1016/j.phytochem.2009.07.008. View

5.
Littlefield O, NELSON H . A new use for the 'wing' of the 'winged' helix-turn-helix motif in the HSF-DNA cocrystal. Nat Struct Biol. 1999; 6(5):464-70. DOI: 10.1038/8269. View