Next Article in Journal
Center Degenerated Walking-Primer PCR: A Novel and Universal Genome-Walking Method
Previous Article in Journal
Special Issue “Molecules at Play in Neurological Diseases”
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
CIMB
Volume 47
Issue 8
10.3390/cimb47080601
cimb-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Research Progress on Responses and Regulatory Mechanisms of Plants Under High Temperature

by
Jinling Wang
1,2,
Yaling Wang
3,
Hetian Jin
2,
Yingzi Yu
2,
Kai Mu
2 and
Yongxiang Kang
1,*
1
College of Forestry, Northwest A&F University, Yangling 712100, China
2
Engineering Research Centre of Forestry Biotechnology of Jilin Province, College of Forestry, Beihua University, Jilin 132013, China
3
Xi’an Botanical Garden of Shaanxi, Xi’an 710061, China
*
Author to whom correspondence should be addressed.
Curr. Issues Mol. Biol. 2025, 47(8), 601; https://doi.org/10.3390/cimb47080601
Submission received: 8 June 2025 / Revised: 24 July 2025 / Accepted: 29 July 2025 / Published: 1 August 2025
(This article belongs to the Section Molecular Plant Sciences)
Browse Figure
Versions Notes

Abstract

Global warming has resulted in an increase in the frequency of extreme high-temperature events. High temperatures can increase cell membrane permeability, elevate levels of osmotic adjustment substances, reduce photosynthetic capacity, impair plant growth and development, and even result in plant death. Under high-temperature stress, plants mitigate damage through physiological and biochemical adjustments, heat signal transduction, the regulation of transcription factors, and the synthesis of heat shock proteins. However, different plants exhibit varying regulatory abilities and temperature tolerances. Investigating the heat-resistance and regulatory mechanisms of plants can facilitate the development of heat-resistant varieties for plant genetic breeding and landscaping applications. This paper presents a systematic review of plant physiological and biochemical responses, regulatory substances, signal transduction pathways, molecular mechanisms—including the regulation of heat shock transcription factors and heat shock proteins—and the role of plant hormones under high-temperature stress. The study constructed a molecular regulatory network encompassing Ca2+ signaling, plant hormone pathways, and heat shock transcription factors, and it systematically elucidated the mechanisms underlying the enhancement of plant thermotolerance, thereby providing a scientific foundation for the development of heat-resistant plant varieties.

1. Introduction

Temperature plays a crucial role in various plant physiological and developmental processes, including seed germination, vegetative growth, morphological structure development, and floral organ formation. Plant growth depends on an appropriate temperature range, with most species exhibiting optimal growth within a temperature range of 0 °C to 30 °C [1]. Different species demonstrate distinct adaptive capacities to temperature variations, and exceeding their optimal temperature thresholds can negatively impact plant growth and development. Due to global warming, global temperatures are on the rise, and this warming trend is also evident across various regions of China. In recent years, temperatures reaching 40 °C and above have increasingly occurred across various regions of the country, adversely affecting the normal growth and development of plants. High temperatures can compromise the stability of plant cell membranes, inducing physiological disorders and negatively impacting nutrient metabolism, photosynthesis, respiration, and other essential physiological processes [2,3,4]. Unlike animals, plants are unable to actively avoid exposure to high temperatures; however, they have evolved unique defense mechanisms to cope with such environmental stress. Upon exposure to high temperatures, plants enhance their antioxidant capacity and mitigate damage caused by elevated temperatures through a range of physiological and biochemical responses, cellular signal transduction pathways, and gene regulatory mechanisms.

2. Morphological and Leaf Anatomical Structural Alterations in Plants Under High-Temperature Stress

Leaves are vital organs responsible for photosynthesis, respiration, and transpiration in plants, and they demonstrate a more immediate and observable response to elevated temperatures. Therefore, leaves are widely regarded as the primary organs for studying heat resistance. Under high-temperature stress, leaves progressively exhibit various symptoms, including shrinkage, curling, marginal scorching, browning, and, in severe cases, desiccation. Moreover, newly emerged leaves are more prone to shrinkage and curling than mature leaves [5,6].
At room temperature, the cellular structures of leaves, such as the cell membrane, chloroplasts, mitochondria, and nucleus, exhibited a normal morphology. The intercellular spaces between plant cells were comparatively narrow. Chloroplasts displayed an elongated shape and were arranged adjacent to the cell wall. The grana were arranged in an orderly manner, and the plasma membrane, vacuolar membrane, and nuclear membrane were clearly distinguishable [7,8]. Under high-temperature conditions, the mesophyll cells underwent significant structural alterations, and plasmolysis became increasingly pronounced [9]. The plasma membrane and vacuolar membrane were disrupted, while the chloroplast membrane was either partially or even completely disintegrated. The thylakoid lamellae appeared loosely and haphazardly arranged, and the chloroplasts exhibited enlargement. Some displayed distorted and irregular shapes, gradually migrating toward the central region of the cell [7,8]. The spongy mesophyll tissue in the leaves was significantly shrunken, and the palisade mesophyll cells also showed signs of shrinkage, making the distinct palisade arrangement almost unrecognizable [10].

3. Effects of High Temperature on Plant Physiology and Biochemistry

The impacts of high temperature on plant physiology and biochemistry have consistently been a focal point of scientific research. Recently, studies on the effects of high-temperature stress on plants have expanded from model species (such as rice and Arabidopsis) [11,12] to a broader range of plant taxa [13,14,15]. The response mechanisms of various plants to high-temperature environments are increasingly being elucidated, offering valuable insights into the understanding of plant heat-tolerance mechanisms and providing a theoretical foundation for the development of heat-resistant crop varieties.

3.1. Effects of High-Temperature Stress on Photosynthesis

Generally, plant photosynthesis begins to decline when temperatures exceed 35 °C and typically ceases entirely within the temperature range of 40 °C to 50 °C. High-temperature stress can damage the structure of chloroplasts, mitochondria, and cytoplasm, degrade photosynthetic pigments, reduce chlorophyll content [16], inhibit photosynthesis, and, thereby, disrupt the normal functioning of plant photosynthetic processes. Under different high-temperature conditions, the factors contributing to the reduction in photosynthetic capacity varied. When the temperature ranged from 35 °C to 40 °C, the inhibition of photosynthesis was primarily attributed to stomatal limitations. However, when the temperature exceeded 40 °C, the decline in photosynthetic capacity was mainly due to non-stomatal factors [17,18]. However, in the study of maize net photosynthetic rate, it was observed that the net photosynthetic rate began to decline when leaf temperature exceeded 38 °C, and this reduction was not attributed to stomatal responses under high-temperature conditions [19].
Under high-temperature conditions, stomatal conductance (Gs) varies among different plant species. When the temperature increased from 30 °C to 40 °C, the stomatal conductance of Populus deltoides × nigra and Pinus taeda increases by 42% and 40%, respectively [20]. High-temperature stress led to a decrease in both the net photosynthetic rate (Pn) and stomatal conductance (Gs) in the leaves of kiwifruit [21] and Ficusconcinna var. Subsessilis [22]. Under high-temperature stress, the transpiration rate of plants exhibits corresponding changes. High temperature was observed to decrease the transpiration rate (Tr) of kiwifruit [21] and sesame leaves [23], whereas in Ficusconcinna var. Subsessilis [22] and grape [24], the transpiration rate initially increased rapidly under high-temperature conditions and subsequently stabilized.
Photosystem II (PSII) is highly sensitive to high temperatures and prone to damage [25]. Elevated temperatures impair the electron transport capacity of PSII. Under such conditions, the photochemical reactions in plant leaves are inhibited, resulting in reduced light energy absorption, quantum yield, and electron transfer efficiency of PSII. The maximal photochemical efficiency (Fv/Fm) exhibited a downward trend. High temperatures impeded energy transfer within the central thylakoids of PSII, resulting in irreversible inactivation [26,27]. The decrease in Fv/Fm in the heat-sensitive strain was significantly greater than that in the heat-resistant strain, indicating its potential as a marker for heat resistance [28,29].
Under short-term high-temperature stress (45 °C to 50 °C), the maximum photochemical efficiency of PSII (Fv/Fm) in Manglietia aromatica Dandy, Manglietia megaphylla Hu et Cheng, and Manglietia grandis Hu et Cheng decreased significantly, whereas the initial fluorescence (F0) increased [30]. However, certain Magnoliaceae species, such as Manglietiastrum sinicum, Magnolia biloba, Tsoongiodendron odorum, and Parakmeria yunnanensis, demonstrate strong adaptability to high-temperature environments and can be successfully introduced into regions with an average annual temperature of 20.6 °C and extreme maximum temperatures reaching up to 42 °C [31].

3.2. Effect of High Temperature on Regulatory Substances in Plants

Some osmolytes maintain physiological functions, facilitate osmoregulation, and protect subcellular structures. Moreover, certain osmolytes are capable of scavenging reactive oxygen species (ROS). Under high-temperature conditions, the levels of soluble sugars, proline (Pro), and malondialdehyde (MDA) in plants change dynamically to help regulate the plant’s response to temperature stress.
Under high-temperature conditions, the levels of malondialdehyde (MDA), proline (Pro), soluble sugars, soluble proteins, and electrolyte leakage (EL) in plants increased with rising temperatures [32,33,34]. However, there are differences among various plant varieties. Generally, heat-tolerant varieties exhibit higher proline content compared to heat-sensitive varieties [35]. When plants are subjected to high temperatures, osmotic substances play a role in regulating the plant defense system. However, as temperature rises, not all regulatory substances exhibit a corresponding increase. For instance, the soluble protein content in rose leaves was observed to initially increase and subsequently decrease with escalating temperatures [34]. This suggests that different plant species may employ distinct mechanisms in response to high-temperature stress.

4. Signal Transduction Under High-Temperature Conditions

As a key second messenger in cell signal transduction, Ca2+ plays essential roles in maintaining the structural integrity and physiological functions of plant cells. It contributes to the stabilization of the cell wall, cell membrane, and membrane-associated proteins [36], and is involved in the regulation of numerous physiological and biochemical processes in plants. Ca2+ are typically stored in various intracellular and extracellular organelles and are maintained at low concentrations [37,38]. When plants are subjected to high-temperature stress, the Ca2+ channel opens, resulting in an elevated intracellular Ca2+ concentration. This increase enables Ca2+ to bind with calmodulin (CaM), forming a Ca2+-CaM complex that activates specific target enzymes or proteins [39]. Consequently, this activation regulates various cellular processes, such as transcription, protein phosphorylation, and metabolic modifications, ultimately triggering appropriate physiological and biochemical responses. When the calcium signal has fulfilled its physiological role, cytosolic Ca2+ is transported out of the cell primarily through the plasma membrane Ca2+ ATPase (PMCA) and the Na+–Ca2+ exchanger (NCX). In parallel, Ca2+ can be resequestered into the endoplasmic reticulum via the sarco/endoplasmic reticulum Ca2+ ATPase (SERCA), which effectively restores the cytosolic Ca2+ concentration to its resting state level [40,41].
When exogenous Ca2+ levels increased, the damage caused by high temperatures to plants was alleviated, with improvements observed in chlorophyll content, total soluble protein levels, and antioxidant enzyme activity [42,43]. High temperature causes an influx of Ca2+, initiating downstream heat stress (HS) signaling pathways. At high temperatures, Ca2+ treatment triggers a significant and prolonged elevation of intracellular Ca2+ levels, thereby promoting the expression of rice CaM1–1 isoforms and nuclear small heat shock protein genes (sHSPC/N). Furthermore, the transient elevation of intracellular Ca2+ triggered by heat stress (HS) can be physiologically modulated in accordance with the intensity of the HS stimulus [44]. Elevated Ca2+ levels not only activate the calcium sensor calmodulin (CaM) but also trigger the activation of calcium-dependent protein kinases (CDPKs) and calcium/calmodulin-dependent protein kinases (CaMKs). Ca2+ can modulate the expression of stress-responsive genes by regulating the phosphorylation and dephosphorylation of specific transcription factors through the action of certain phosphatases [45]. Arabidopsis thaliana Calcium/Calmodulin-binding Kinase 3 (AtCBK3) phosphorylates heat shock factor AtHsfA1a to control the binding activity of heat shock factors (HSFs) to heat shock elements (HSEs), thereby regulating the transcription of heat shock protein (HSP) genes and the synthesis of HSPs [46]. CaM interacts with protein phosphatase 7 (PP7) to modulate HSF activity, thereby activating the expression of heat shock protein (HSP) genes. The expression levels of AtHSP70 and AtHSP101 were significantly upregulated in AtPP7 overexpression lines after heat shock treatment. These findings suggest that AtPP7 may play a role in regulating HSP gene expression and enhancing plant thermotolerance [47].
The Calmodulin-like (CML) gene family constitutes a plant-specific group of calcium sensors. When expressed at high levels in Arabidopsis, SlCML39—a CML gene isolated from tomato—exhibits inhibitory effects on germination rates and seedling growth under high-temperature-stress conditions. These findings suggest that SlCML39 plays a regulatory role in plant responses to heat stress [48]. The cyclic nucleotide-gated calcium channel (CNGC) is involved in the mechanism underlying the plant heat-stress response. Loss of function of CNGC2/CNGCb increases plant tolerance to heat stress, indicating that CNGC2/CNGCb negatively regulates plant thermotolerance [49].

5. Molecular Mechanism of High-Temperature Stress

5.1. Heat Shock Transcription Factor Regulation

The impact of temperature increase on plants extends beyond physiological effects to encompass molecular-level changes within the organism. When exposed to high temperatures, plants activate a series of stress responses, including the expression of relevant genes, the accumulation of transcriptional regulators, and the activation of heat shock proteins (HSPs), which help protect plants from damage or mitigate its severity [50,51,52,53,54].
After heat-stress treatment, the expression levels of ZmHsf and ZmHsp70 in maize were significantly upregulated, which contributed to the regulation of maize’s heat tolerance [55]. ZmHsf 23L and ZmHsf 23S are significantly upregulated under heat-stress conditions. Mutants deficient in ZmHsf23L or lacking both ZmHsf 23L and ZmHsf 23S exhibit increased sensitivity to heat stress. In contrast, the overexpression of ZmHsf 23S enhances heat tolerance in maize. Furthermore, the co-overexpression of ZmHsf 23L and ZmHsf 23S synergistically improves thermotolerance in transgenic plants [56].
The heat shock transcription factor HSFA1s is widely recognized as a central regulator of plant thermotolerance. Acting upstream of other key transcription factors such as HSFA2, HSFA7a/b, and DREB2A, HSFA1s plays a pivotal role in modulating the plant heat-stress response (HSR) [57]. Under high-temperature conditions, the rice heat shock transcription factor OsHsfA2b is markedly induced and expressed. Compared to the wild type, transgenic rice overexpressing OsHsfA2b exhibits significantly enhanced thermotolerance, characterized by reduced plant damage and an increased survival rate [58].
PeHSFA2 in Populus euphratica can significantly enhance plant heat tolerance by regulating the expression of PtoHSP19.9, PtoHSP21.3, PtoHSP21.8, and PtoHSP22.0 in Populus tomentosa. This gene exhibits considerable potential for the development of poplar varieties with markedly improved thermotolerance [59]. The expression levels of AtMBF1c, AtZAT12, AtAPX1, AtHSA32, and AtHSPs was significantly upregulated in PtHSFA4a transgenic plants of Populus trichocarpa. Moreover, PtHSFA4a directly binds to the promoters of AtAPX1 and AtHSPs under heat-stress conditions, thereby enhancing the heat resistance of leaves by upregulating the antioxidant defense system and maintaining protein-folding homeostasis in leaves [60]. Heat shock transcription factors (HSFs) regulate plant heat tolerance either individually or through interactions, and LlHSFC2 interacts with LlHSFA1, LlHSFA2, and LlHSFA3A. The overexpression of LlHSFA3A alone confers heat tolerance in lilies, whereas the co-overexpression of LlHSFC2 and LlHSFA3A further enhances the heat tolerance of transgenic plants [61].

5.2. Heat Shock Protein Regulation

When the ambient temperature exceeds the optimal range for normal plant growth, heat shock proteins (HSPs) are induced as a protective response in plants. In higher plants, short-term exposure to temperatures within the range of 38 °C to 40 °C is sufficient to induce the production of heat shock proteins (HSPs) [62]. Heat shock proteins (HSPs) are classified into five major families based on their molecular weight: HSP100, HSP90, HSP70, HSP60, and small heat shock proteins (sHSPs) [63]. The roles of various heat shock proteins in plants under high-temperature stress are becoming increasingly clear.
The expression of 14 heat shock protein (Hsp) genes in rice was upregulated under high-temperature conditions. Under natural high-temperature environments, the reduction in yield observed in knockout mutants of these 8 Hsp genes was primarily attributed to their effects on seed setting rate or grain weight [64]. HSP90 is a crucial member of the heat shock protein (HSP) family. It not only activates the expression of HSFA to enhance plant thermotolerance [65] but also participates in the high-temperature stress response mechanism in Arabidopsis thaliana through functional pathways such as ABA and Ca2+ signaling [66]. HSP90 can also actively regulate thermotolerance in tomatoes by activating the expression of other transcription factors [67]. In addition to HSP90, other heat shock proteins play a critical role in enabling cellular adaptation to heat shock.
Mutant plants in Arabidopsis, maize, and rice that lack the ClpB protein show increased sensitivity to heat stress compared to wild-type plants [50], and ClpB1-overexpressing transgenic tobacco exhibits significantly enhanced heat tolerance [68]. The HSP70/HSP40 molecular chaperone system plays a critical role in protecting plants from prolonged exposure to heat stress [52]. By modulating photosynthesis-related proteins, sHSPs provide a certain degree of protection to chloroplasts, thereby enhancing the heat tolerance of maize chloroplasts [69]. Overexpression of the HSP17.4 gene significantly improves the heat tolerance of soybean plants [70]. ZmHsf23S enhances thermotolerance by directly promoting the transcription of Hsp16.9, Hsp17.2, and Hsp18a [57].
There is a synergistic interaction among various heat shock proteins. Protein aggregates can be efficiently resolubilized by HSP100/Clp family chaperones and subsequently refolded with the assistance of the Hsp70 system; the final refolding of solubilized proteins into their native forms may be completed by members of the Hsp60 family (GroEL–GroES) [71]. The overexpression of PsHSP70b in Chlamydomonas not only enhanced its survival rate but also upregulated the transcription levels of HSF1, CrHSP20, and CrHSP70 genes [72].

6. Response of Plant Hormones to High Temperature

Under high-temperature stress, plant hormones can mitigate or enhance resistance to the adverse effects of high temperature on plants. The differential hormone metabolites in Loquat (Eriobotrya japonica) fruits under 40 °C stress were investigated. It was found that 37 hormone metabolites were differentially enriched in the fruits under high-temperature stress, including auxins, jasmonic acid, abscisic acid, salicylic acid, ethylene, and cytokinin [73].

6.1. Auxin

Auxins is a plant hormone that not only promotes growth but also plays a critical role in the plant’s response to heat stress. A total of 58 differentially expressed genes (DEGs) related to auxin signaling were identified in fruits exposed to high-temperature stress, and auxin-enriched hormone metabolites constituted 24.32% of the total metabolites [73]. These findings indicate that auxin is involved in the defense mechanisms activated by plants under high-temperature stress conditions.
The expression of the auxins receptor TIR1/AFB2 in rice spikelets was significantly downregulated under high-temperature stress. Exogenous IAA application could reduce membrane lipid peroxidation and ROS accumulation in spikelets [74], thereby alleviating high-temperature-induced damage. Auxins interact with HSP90 in Arabidopsis thaliana, which plays a role in regulating temperature-dependent seedling growth by stabilizing the auxin receptor TIR1. When the molecular chaperone HSP90 is present in plants, a slight increase in ambient temperature promotes the rapid accumulation of the auxin co-receptor TIR1. However, the inhibition of HSP90 activity leads to the degradation of TIR1 [75]. The auxin co-receptor TIR1 interacts with HOP proteins and plays a role in plant responses to high-temperature stress. In Arabidopsis triple mutants of hop1, hop2, and hop3, exposure to high temperatures inhibited plant growth, reduced auxin sensitivity, decreased TIR1 accumulation, and suppressed auxin-regulated transcriptional responses [76].

6.2. Abscisic Acid

Abscisic acid (ABA) is a stress-related hormone that mitigates membrane damage and promotes the accumulation of osmotic substances, thereby enhancing plant adaptability to various environmental stresses. Under high-temperature stress, the biosynthesis of endogenous ABA is upregulated, its degradation is reduced, or its bound form is released, leading to an increase in ABA concentration and improved plant resistance.
Abscisic acid regulates the synthesis of new stress-resistant proteins and enhances stress resistance by inducing the expression of stress-related genes. Additionally, abscisic acid promotes stomatal closure, reducing water loss, maintaining water balance, and minimizing stress damage [77]. ABA induces the expression of catalase (CAT1) through the MAPK signaling cascade mediated by AtMKK1 and AtMPK6, which also promotes H2O2 production. The overexpression of AtMKK1 and AtMPK6 significantly enhances the ABA-induced responses [78].
ABA can induce the expression of HSF and HSP genes. In tobacco, ABA treatment stimulates the expression of NtHSP70-1, which helps mitigate plant stress responses under adverse conditions [79]. Under high-temperature stress, NtHSP70-8b positively regulates the tobacco response to heat stress. In tobacco plants overexpressing NtHSP70-8b, the expression levels of genes involved in ABA synthesis and signaling pathways (NtNCED3 and NtAREB), stress defense mechanisms (NtERD10C and NtLEA5), and other heat shock proteins (NtHSP90 and NtHSP26a) were significantly upregulated [80]. ABA pretreatment induced the expression of heat-shock-related genes (OsHSP23.7, OsHSP17.7, OsHSF7, and OsHsfA2a), reduced cellular damage, and enhanced antioxidant defense capability [81]. Furthermore, ABA serves as an inducer of the transcription factors ERF74 and ERF75 under high-temperature conditions. These transcription factors form a complex regulatory network that modulates plant heat tolerance [82].
The synergistic effect of ABA and NO mitigated the damage caused by high-temperature stress in plants, decreased MDA content, and enhanced the activity of antioxidant enzymes. Exogenous ABA and NO treatment significantly alleviated these effects. Moreover, the ability of ABA to alleviate heat stress increased with rising levels of NO [83,84].

6.3. Ethylene

Ethylene (ET), a plant hormone, plays a critical role in regulating plant growth, development, and the response to heat stress. Under normal conditions, endogenous ethylene levels are maintained at a low concentration, allowing the ethylene receptor to remain active and sustain the kinase CTR1 in its active state, thereby suppressing ethylene signaling. However, upon exposure to high-temperature stress, ethylene biosynthesis is enhanced, leading to an increase in ethylene accumulation within the plant [73]. The membrane-anchored receptor family detects ethylene, and ligand binding leads to receptor inactivation, which subsequently inactivates CTR1 and activates EIN2. This process initiates a transcriptional cascade in which the EIN3/EIL and ERF transcription factors function in a sequential manner [85]. It then initiates the regulation of downstream genes in response to stress. Under high-temperature stress, the activities of ACS and ACO—key enzymes involved in ethylene synthesis—in the leaves of Rhododendron increase, leading to a higher release rate of endogenous ethylene. This, in turn, affects the heat resistance of Rhododendron by modulating the antioxidant system [86]. The basal thermotolerance of ethylene signaling-deficient mutants is reduced [82,87]. The AP2/ERF family transcription factors associated with ethylene response were upregulated following high-temperature stress [88]. Ethylene can also induce photosynthetically derived sugars, enhance photosynthesis and metabolism, and, thereby, promote plant growth and stress resistance [89].

6.4. Brassinosteroids

Brassinosteroids (BRs), one of the six major classes of plant hormones, function not only in promoting plant growth but also in enhancing stress resistance as key regulators of abiotic and biotic stress responses. The most well-known brassinosteroids include brassinolide (BL), castasterone (CS), and 24-epibrassinolide (EBL), among others.
Brassinosteroids exert their biological effects through signal transduction pathways. Specifically, brassinosteroids bind to the cell surface receptor kinase BRI1, which subsequently phosphorylates and activates two key downstream BR signaling kinases: brassinosteroid signaling kinase 1 (BSK1) and constitutive differential growth 1 (CDG1). This subsequently triggers the phosphorylation and activation of the protein serine/threonine phosphatase BRI1-Suppressor 1 (BSU1), thereby enhancing its enzymatic activity. Activated BSU1 dephosphorylates brassinosteroid-insensitive 2 (BIN2), which serves as a central negative regulator of BR signaling [90]. BIN2, located upstream of HsfA1d, attenuates plant heat tolerance by inhibiting the function of the HsfA1d protein. The removal of BIN2′s inhibitory effect facilitates the nuclear localization and DNA-binding activity of HsfA1d, thereby enhancing plant thermotolerance [91].
When the BR signal is perceived, the plasma membrane-associated NADPH oxidase (RBOH) is activated, leading to increased H2O2 production and enhanced enzymatic activity [92], thereby improving plant heat tolerance. MAP4K4/TOT3 (Mitogen-activated Protein Kinase Kinase Kinase Kinase 4/Target of Temperature 3) modulates the high-temperature stress response in Arabidopsis and wheat via BZR1-mediated signaling pathways [93]. EBR treatment improved the basal heat tolerance of plants. Under high-temperature stress, the exogenous application of brassinolide decreased MDA content while increasing the levels of soluble proteins and soluble sugars, along with enhancing SOD and CAT activities, thereby contributing to improved heat tolerance in Avena nuda [94]. The net CO2 assimilation rate, the maximum carboxylation rate of Rubisco, and the quantum yield of PSII electron transport were markedly increased by EBR application. Furthermore, the contents of sucrose, soluble sugars, and starch were significantly elevated, indicating that EBR enhances the CO2 assimilation capacity through promoting the Calvin cycle activity [95].

6.5. Jasmonic Acid

Jasmonic acid (JA) is a newly recognized type of endogenous plant hormone that plays a crucial role in regulating plant growth, development [96,97,98], and defense responses [99,100]. Jasmonic acid (JA) is synthesized from α-linolenic acid, which is released from the chloroplast membrane and serves as the initial substrate. The biosynthetic pathway of JA involves a series of sequential enzymatic reactions catalyzed by lipoxygenase (LOX), allene oxide synthase (AOS), allene oxide cyclase (AOC), and 12-oxophytodienoate reductase (OPR3). This is followed by three cycles of β-oxidation, ultimately leading to the formation of JA [101].
When plants are exposed to high temperatures, the synthesis of JA is induced, leading to the formation of the JA-Ile complex. This complex subsequently binds to the receptor coronatine-insensitive 1 (COI1). COI1 interacts with JAZ proteins, leading to their ubiquitination by the E3 ubiquitin ligase SCFCOI1 (Skp1/Cullin1/F-box) complex. The ubiquitinated JAZ proteins are subsequently recognized and degraded by the 26S proteasome, thereby releasing downstream transcription factors such as MYC, MYB, and NAC [102,103]. In turn, it regulates the transcription of JA response genes and activates the defense mechanisms in plants against external stress.
Under high-temperature stress conditions, OPR3, a key enzyme in JA synthesis, is activated, which promotes JA biosynthesis and subsequently activates the JA signaling pathway. Consequently, the expression of DREB2A is upregulated [104], leading to the regulation of plant responses to high temperatures, alleviation of heat-induced damage, and enhancement of plant thermotolerance.

6.6. Salicylic Acid

Salicylic acid (SA) is an endogenous plant hormone that is widely present in higher plants. It plays a crucial role not only in regulating plant growth but also in mediating the plant’s response to high-temperature stress. The two primary metabolic pathways involved in SA biosynthesis are the isochorismate synthase pathway (ICS pathway) and the phenylalanine ammonia-lyase pathway (PAL pathway) [105]. The PAL pathway plays a crucial role in the biosynthesis of SA and also serves as a key regulator of the steady-state stomatal aperture, thereby enhancing plant adaptability under stress conditions [106].
Exogenous SA can significantly alleviate heat-induced damage by reducing the heat injury index, decreasing electrolyte leakage and malondialdehyde content, and mitigating chlorophyll degradation in seedlings [107]. It increased the proline and soluble protein content, enhanced protein kinase activity, promoted protein phosphorylation, improved photosynthetic efficiency, elevated the activities of antioxidant enzymes (SOD, POD, CAT, and APX), reduced reactive oxygen species (ROS)-induced damage in plants, and alleviated the adverse effects of high-temperature stress [108,109]. Currently, salicylic acid has been extensively utilized as an effective approach to mitigate the adverse effects of high temperature on plant growth and development [110].

7. Regulatory Network for Plant Responses to High Temperature

When plants perceive elevated temperatures, calcium influx activates multiple regulatory pathways to coordinate the response to heat stress. These pathways interact synergistically, forming a complex signaling network that modulates plant responses to high-temperature conditions. JA, SA, ethylene, and abscisic acid have been shown to alleviate heat-induced damage in plants and improve their thermotolerance. Transcription factors such as HSF [111], DREB [112], MYB [113], WRKY [114], and MBF1C [115] play an important role in different metabolic pathways and play a role of connection and hub [116,117], for example, MBF1c acts upstream on SA and ethylene during heat stress [118]. Under high-temperature conditions, the Ca2+ regulatory network interacts with plant hormone signaling pathways and heat shock transcription factors to establish a comprehensive regulatory network. This network activates the expression of heat shock proteins (HSPs), thereby enhancing the thermotolerance of plants (Figure 1).

8. Strategies for Enhancing the Heat Tolerance of Plants

Climate change has resulted in an increasing number of plants being exposed to high temperatures, which severely affects their growth and survival. Under such conditions, plants can mitigate the adverse effects of high temperatures through self-regulatory mechanisms, demonstrating a survival strategy that involves adaptive responses to high temperatures [1]. However, the regulatory capacity of different plants in response to high-temperature damage varies, and certain strategies can be employed to alleviate the adverse effects of high temperatures on plants.

8.1. Effects of Heat Acclimation on Plant Responses to High-Temperature Stress

Different plant species exhibit varying responses to high temperatures. Plant heat tolerance is shaped by long-term interactions between plants and their environment throughout the evolutionary process. Through heat acclimation, plants can adjust their physiological and biochemical processes to enter an adaptive state, which enhances their capacity to withstand subsequent high temperatures, thereby enabling normal growth under such conditions.
Özlem Arslan demonstrated that heat acclimation mitigated the adverse effects of high-temperature stress on water content, chlorophyll and carotenoid levels, membrane integrity, photosynthetic efficiency, and the antioxidant defense system in Cicer arietinum L. Seedlings acclimated to high temperatures exhibited enhanced thermotolerance, as indicated by improved chlorophyll fluorescence parameters, which suggest a greater capacity to effectively manage the biochemical and physiological changes associated with heat stress [119]. Under high-temperature stress, the degree of decline in the relative water content (RWC) and the ultrastructural damage to chloroplasts in leaves subjected to heat acclimation was lower compared to non-acclimated leaves. Heat-acclimated leaves maintained higher membrane thermal stability, while exhibiting reduced lipid peroxidation as indicated by lower MDA content. Consequently, heat acclimation enhanced the heat resistance of the leaves [120].
This phenomenon of enhanced plant heat resistance through heat acclimation has also been observed in woody species. In Rhododendron hainanense, heat acclimation resulted in reduced damage to phenotypic traits, net photosynthetic rate, and membrane stability when compared to non-acclimated plants, thereby improving its tolerance to high temperatures. Furthermore, integrated omics analysis revealed that genes associated with photosynthesis were significantly enriched in heat-acclimated plants relative to their non-acclimated counterparts [121].

8.2. Application of Exogenous Substances to Enhance Plant Thermotolerance

The exogenous application of plant hormones and CaCl2 [42] as heat-resistant agents can significantly enhance plant heat tolerance. Commonly utilized plant hormones include abscisic acid (ABA) [84], salicylic acid (SA) [108], brassinolide (BR) [122], and ethylene (ET) [86], among others.
Rice seedlings were pretreated with sodium hyposilicate solution (Na2SiO3·9H2O), salicylic acid (SA) solution, calcium chloride solution (CaCl2·5H2O), and potassium dihydrogen phosphate (KH2PO4) solution before being exposed to high-temperature stress. The results demonstrated that the application of these four chemical agents significantly enhanced chlorophyll content, superoxide dismutase (SOD), peroxidase (POD), catalase (CAT) activity, and soluble protein levels in rice leaves, while effectively reducing malondialdehyde (MDA) content. This mitigated the adverse effects of high-temperature stress on rice leaves [123]. Under high-temperature stress conditions, the application of heat-resistant agents can effectively alleviate the decline in Fv/Fm values, thereby reducing damage to photosystem II (PSII), suppressing the rapid accumulation of malondialdehyde (MDA) in leaves, promoting the synthesis of free proline (Pro), decreasing the heat injury index, and, ultimately, enhancing the thermotolerance of Rhododendron [124,125].

9. Conclusions and Future Perspectives

Global warming is an undeniable reality in the present era. The frequency of extreme high-temperature events is increasing, which seriously affects the growth and development of plants. High temperature has become a critical factor constraining plant growth and development. High-temperature stress disrupts cell membrane integrity, decreases photosynthetic efficiency, accelerates chlorophyll degradation, and, ultimately, results in leaf browning, wilting, and even plant desiccation. When plants are subjected to heat stress, a Ca2+ influx across the cell membrane is triggered, activating the Ca2+ signaling pathway. This activation triggers the plant hormone regulatory pathway, leading to a significant accumulation of plant hormones. Subsequently, various transcription factors interact to form a regulatory network that activates the expression of heat shock proteins (HSPs). Together, these processes mitigate the detrimental effects of high temperatures on plants. At present, the research scope of the mechanism of the effect of high temperature on plants is expanding. Future research should focus more intensively on elucidating the regulatory network underlying the interactions among signal transduction, plant hormones, and heat shock transcription factors under high-temperature conditions, which regulates the heat tolerance mechanisms in plants. Additionally, future research should systematically and deeply explore the mystery of plants’ response to high temperature. Screening heat-resistant plant varieties can facilitate improvements in crop yield and broaden the selection range for landscaping tree species. Utilizing biotechnology to enhance plants’ adaptability to high-temperature stress provides a robust theoretical foundation for genetic breeding.

Author Contributions

Writing—original draft preparation, J.W.; conceptualization, Y.W.; investigation, H.J. and Y.Y.; visualization, K.M.; writing—review and editing, Y.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Wang, S.G.; Zong, X.F. Plant Resistance Biology; Xi’ an Normal University Press: Chongqing, China, 2015; pp. 1–113. [Google Scholar]
  2. Hong, E.M.; Xia, X.Z.; Ji, W.; Li, T.Y.; Xu, X.Y.; Chen, J.G.; Chen, X.; Zhu, X.T. Effects of high temperature stress on the physiological and biochemical characteristics of Paeonia ostii. Int. J. Mol. Sci 2023, 24, 11180. [Google Scholar] [CrossRef]
  3. Song, C.Y.; Liu, X.B.; Jin, C.X. Mechanisms of damage and acclimation of photosynthetic apparatus due to heat stress. Syst. Sci. Compr. Stud. Agric. 2002, 18, 252–255. [Google Scholar]
  4. Zhang, F.J.; Luo, F.; Tan, Y.Y.; Zhang, M.H.; Xing, W.; Jin, X.L. Effects of high temperature stress on the physiological characteristics and chlorophyll fluorescence parameters of Chinese Rose. J. Henan Agric. Sci. 2019, 48, 108–115. [Google Scholar]
  5. He, M.; Hu, Y.; Wang, T.; Xu, J.; Zeng, W.C.; Zhao, A. Physiological response of colored-leaved north American Begonia to high temperature. Acta Agric. Univ. Jiangxiensis 2019, 41, 664–672. [Google Scholar] [CrossRef]
  6. Yang, H.; Song, X.Z.; Wang, X.Y. Physiological responses of Rhododendron latoucheae to high temperature stress. J. For. Environ. 2020, 40, 284–289. [Google Scholar] [CrossRef]
  7. Liu, Y.P.; Huang, W.D.; Zhang, J.H. Effect of heat acclimation and SA pretreat on the ultra structure of mesophyll cell in grape plants under heat shock. Acta Hortic. Sin. 2006, 33, 491–495. [Google Scholar]
  8. Zhang, C.; Liu, H.; Xi, D.J.; Luo, H.F.; Pei, J.B.; Huang, K.K.; Ruan, R.X.; Lai, M.X.; Fan, H.F. Effects of high temperature on leaf physiological indexes of summit in seedlings sweet cherry. J. Fruit Sci. 2023, 40, 712–723. [Google Scholar]
  9. Hu, W.J.; Zhang, Q.X.; Pan, H.T.; Dong, L.L. Difference in ultrastructure of mesophyll cell between two Primula species with different thermotolerance under heat acclimation and heat stress. J. South China Agric. Univ. 2010, 31, 43–46. [Google Scholar]
  10. Liang, W.; Zhao, B.; Huang, W.M. Heat-resistance of Rhododendron with a heat acclimation pretreatment. J. Zhejiang AF Univ. 2018, 35, 284–290. [Google Scholar]
  11. Yang, D.S.; Peng, S.B.; Wang, F. Response of photosynthesis to high growth temperature was not related to leaf anatomy plasticity in Rice (Oryza sativa L.). Front. Plant Sci. 2020, 11, 26. [Google Scholar] [CrossRef]
  12. Kumar, A.; Li, C. Arabidopsis thaliana expressing a thermostable chimeric Rubisco activase exhibits enhanced growth and higher rates of photosynthesis at moderately high temperatures. Photosynth Res. 2009, 100, 143–153. [Google Scholar] [CrossRef] [PubMed]
  13. Zhang, Y.Z.; Cheng, Y.W.; Ya, H.Y.; Han, J.M.; Zheng, L. Identification of heat shock proteins viatranscriptome profiling of tree peony leafexposed to high temperature. Genet. Mol. Res. 2015, 14, 8431–8442. [Google Scholar] [CrossRef] [PubMed]
  14. Lu, A.X.; Ling, R.; Cheng, S.Y.; Zhai, J.W.; Zheng, Z.X.; Wu, S.S. Physiological and biochemical responses of eight Hydrangea Cultivars to high temperature stress. Chin. J. Trop. Crops 2022, 43, 816–828. [Google Scholar]
  15. Li, Z.Q.; Xing, W.; Luo, P.; Zhang, F.J.; Jin, X.L.; Zhang, M.H. Comparative transcriptome analysis of Rosa chinensis ‘Slater’s crimson China’ Tprovides insights into the crucial factors and signaling pathways in heatstress response. Plant Physiol. Biochem. 2019, 142, 312–331. [Google Scholar] [CrossRef]
  16. Liu, D.L.; Lai, W.N. Research on physio-biochemistry indexes of heat resistant of Prunus mume in summer. North. Hortic. 2012, 57–61. [Google Scholar]
  17. Zhang, X.; Wang, M.M.; Li, G.L.; Bai, Z.J.; Yao, F. Photosynthetic response of Quercus variabilis and Quercus aliena var. acuteserrata seedlings to high temperature stress. J. Beijing For. Univ. 2022, 44, 25–35. [Google Scholar]
  18. Yin, Z.P.; Lu, J.Z.; Gao, Z.H.; Qi, M.F.; Meng, S.D.; Li, T.L. Effects of photosynthetic, PSII electron transport and reactive oxygen species on short-term high temperature stress in tomato seedlings. North. Hortic. 2019, 1–11. [Google Scholar]
  19. Steven, J.C.; Michael, E.S. Sensitivity of photosynthesis in a C4 plant, maize, to heat stress. Plant Physiol. 2002, 129, 1773–1780. [Google Scholar] [CrossRef]
  20. Urban, J.; Ingwers, M.; McGuire, M.A.; Teskey, R.O. Stomatal conductance increases with rising temperature. Plant Signal. Behavior. 2017, 12, e1356534. [Google Scholar] [CrossRef]
  21. Zhang, W.B. Studies on Heat Resistance in ‘Ganmi 6’ Kiwifruit(Actinidia eriantha Benth); Jiangxi Agricultural University: Nanchang, China, 2017. [Google Scholar]
  22. Jin, S.H.; Li, X.Q.; Wang, J.G. Effects of high temperature stress on photosynthesis in Ficus concinna var. subsessilis. Chin. Agric. Sci. Bull. 2009, 25, 83–87. [Google Scholar]
  23. Su, X.Y.; Gao, T.M.; Li, F.; Wei, L.B.; Tian, Y.; Wang, D.Y.; Zhu, S.T.; Wei, S.L. Physiological response mechanism to high temperature stress in different heat-tolerant genotypes of sesame seedlings. Acta Agric. Boreali-Sin. 2021, 36, 96–105. [Google Scholar]
  24. Dou, F.F.; Zhang, L.P.; Wang, Y.K.; Yu, K.; Liu, H.F. Effects of high temperature stress on photosynthesis and gene expressionof different grape cultivars. J. Fruit Sci. 2021, 38, 871–883. [Google Scholar]
  25. Huan, L.; Gao, S.; Xie, X.J.; Tao, W.R.; Pan, G.H.; Zhang, B.Y.; Niu, J.F.; Lin, A.P.; He, L.W.; Wang, G.G. Specific photosynthetic and morphological characteristics allow macroalgae Gloiopeltis furcata (Rhodophyta) to survive in unfavorable conditions. Photosynthetica 2014, 52, 281–287. [Google Scholar] [CrossRef]
  26. Xu, C.; Wang, M.T.; Yang, Z.Q.; Han, W.; Zheng, S.H. Effects of high temperature on photosynthetic physiological characteristics of strawberry seedlings in greenhouse and construction of stress level. Chin. J. Appl. Ecol. 2021, 32, 231–240. [Google Scholar]
  27. Wu, J.Y.; Xu, G.X.; Li, H.F.; Zeng, X.Y.; Jiang, J.F.; Liu, Y.X.; Wei, Y.N.; Ren, H.S. Effects of heat stress on chlorophyll fluorescence and photosynthetic characteristic parameters in grape (Vitisvinifera L. Manicure finger). Xinjiang Agric. Sci. 2021, 58, 2274–2281. [Google Scholar] [CrossRef]
  28. Ashraf, M. Thermotolerance in plants: Potential physio-biochemical and molecular markers for crop improvement. Environ. Exp. Bot. 2021, 186, 104454. [Google Scholar] [CrossRef]
  29. Hameed, M.; Keitel, C.; Ahmad, N.; Mahmooda, T.; Trethowana, R. Screening of tomatoes germplasm for heat stress toleranceunder controlled conditions. Procedia Environ. Sci. 2015, 29, 173–174. [Google Scholar] [CrossRef]
  30. Li, Y.Y.; Dou, X.Y.; Peng, C.L. Response of photosynthesis in saplings of three endangered Magnolialia species to high temperature. Acta Ecol. Sin. 2008, 28, 3789–3797. [Google Scholar]
  31. Li, J.W.; Liu, X.Y.; Xiao, Z.B.; Huang, H.G. A Study on introduction and adaptation of Magnoliaceae plants and its landscape evaluation. For. Resour. Manag. 2020, 161–168. [Google Scholar] [CrossRef]
  32. Li, Y.Z.; Li, X.R.; Zhang, J.; Li, D.X.; Yan, L.J.; You, M.H.; Zhang, J.B.; Lei, X.; Chang, D.; Ji, X.F.; et al. Physiological and proteomic responses of contrasting alfalfa (Medicago sativa L.) varieties to high temperature stress. Front. Plant Sci. 2021, 12, 753011. [Google Scholar] [CrossRef]
  33. Wang, K.H.; Ling, J.H.; Zhang, L.H.; Liu, X.P.; Li, L. Analysis of principal components and subordinate function on heat tolerance of two seedlings of Rhododendron Subgenus Hymenanthes. J. Trop. Subtrop. Bot. 2011, 19, 412–418. [Google Scholar] [CrossRef]
  34. Peng, Y.Z.; Liu, Z.Y.; Zhu, X.F.; Du, X.W.; Ye, K.; Lu, Y.Q.; Qin, J.; Zeng, L. Physiological index changes and heat tolerance evaluation of five rose cultivars after high temperature treatment. J. Shanghai Jiaotong Univ. 2019, 37, 53–58. [Google Scholar]
  35. Han, Y.Y.; Fan, S.X.; Zhang, Q.; Wang, Y.A. Effect of heat stress on the MDA, proline and soluble sugars content in leaf lettuce seedlings. Agric. Sci. 2013, 4, 112–115. [Google Scholar] [CrossRef]
  36. Dong, Q.; Wallrad, L.; Almutairi, B.O.; Kudla, J. Ca2+ signaling in plant responses to abiotic stresses. J. Integr. Plant Biol. 2022, 64, 287–300. [Google Scholar] [CrossRef] [PubMed]
  37. Berridge, M.J. Unlocking the secrets of cell signaling. Annu. Rev. Physiol. 2005, 67, 1–21. [Google Scholar] [CrossRef]
  38. Zheng, Y.; Chen, Z.J. Organellar Calcium Signaling in Plants. Plant Physiol. J. 2015, 51, 1195–1203. [Google Scholar] [CrossRef]
  39. Zhou, J.J.; Xia, K.F. Study on Ca2+ signal transduction in plant. Gui Haia 2005, 25, 386–392. [Google Scholar]
  40. Pozzan, T.; Rizzuto, R.; Volpe, P.; Meldolesi, J. Molecular and cellular physiology of intracellular calcium stores. Physiol. Rev. 1994, 74, 595–636. [Google Scholar] [CrossRef]
  41. Blaustein, M.P.; Lederer, W.J. Sodium/calcium exchange: Its physiological implications. Physiol. Rev. 1999, 79, 763–854. [Google Scholar] [CrossRef]
  42. Shen, H.F.; Zhao, B.; Xu, J.J.; Zheng, X.Z.; Huang, W.M. Effects of salicylic acid and calcium chloride on heat tolerance in Rhododendron ‘Fen Zhen Zhu’. J. Amer. Soc. Hort. Sci. 2016, 141, 363–372. [Google Scholar] [CrossRef]
  43. Yang, H.G.; Yang, Y.M. Effect of exogenous calcium and calcium inhibitors on the heat tolerance in Phalaenopsis seedlings. Chin. J. Trop. Crops 2021, 42, 436–441. [Google Scholar] [CrossRef]
  44. Wu, H.C.; Jinn, T.L. Oscillation regulation of Ca2+/calmodulin and heat-stress related genes in response to heat stress in rice (Oryza sativa L.). Plant Signal. Behav. 2012, 7, 1056–1057. [Google Scholar] [CrossRef]
  45. Verma, V.; Ravindran, P.; Kumar, P.P. Plant hormone-mediated regulation of stress responses. BMC Plant Biol. 2016, 16, 86. [Google Scholar] [CrossRef] [PubMed]
  46. Liu, H.T.; Gao, F.; Li, G.L.; Han, J.L.; Liu, D.L.; Sun, D.Y.; Zhou, R.G. The calmodulin-binding protein kinase 3 is part of heat-shock signal transduction in Arabidopsis thaliana. Plant J. 2008, 55, 760–773. [Google Scholar] [CrossRef] [PubMed]
  47. Liu, H.T.; Li, G.L.; Chang, H.; Sun, D.Y.; Zhou, R.G.; Li, B. Calmodulin-binding protein phosphatase PP7 is involved in thermotolerance in Arabidopsis. Plant, Cell Environ. 2007, 30, 156–164. [Google Scholar] [CrossRef] [PubMed]
  48. Ding, H.D.; Qian, Y.; Fang, Y.F.; Ji, Y.R.; Sheng, J.R.; Ge, C.L. Characteristics of SlCML39, a tomato calmodulin-like gene, and its negative role in high temperature tolerance of Arabidopsis thaliana during germination and seedling growth. Int. J. Mol. Sci. 2021, 22, 11479. [Google Scholar] [CrossRef]
  49. Finka, A.; Cuendet, A.F.; Maathuis, F.J.; Saidi, Y.; Goloubinoff, P. Plasma membrane cyclic nucleotide gated calcium channels control land plant thermal sensing and acquired thermotolerance. Plant Cell 2012, 24, 3333–3348. [Google Scholar] [CrossRef]
  50. Mishra, R.C.; Grover, A. ClpB/Hsp100 proteins and heat stress tolerance in plants. Crit. Rev. Biotechnol. 2015, 36, 862–874. [Google Scholar] [CrossRef]
  51. Zai, W.S.; Miao, L.X.; Xiong, Z.L.; Zhang, H.L.; Ma, Y.R.; Li, Y.L.; Chen, Y.B.; Ye, S.G. Comprehensive identification and expression analysis of Hsp90s genefamily in Solanum lycopersicum. Genet. Mol. Res. 2015, 14, 7811–7820. [Google Scholar] [CrossRef]
  52. Wang, T.Y.; Wu, J.R.; Duong, N.K.; Lu, C.A.; Yeh, C.H.; Wu, S.J. HSP70-4 and farnesylated AtJ3 constitute a specific HSP70/HSP40-based chaperone machinery essential for prolonged heat stress tolerance in Arabidopsi. J. Plant Physiol. 2021, 261, 153430. [Google Scholar] [CrossRef]
  53. Haq, S.U.; Khan, A.; Ali, M.; Gai, W.X.; Zhang, H.X.; Yu, Q.H.; Yang, S.B.; Wei, A.M.; Gong, Z.H. Knockdown of CaHSP60-6 confers enhanced sensitivity to heat stressin pepper (Capsicum annuum L.). Planta. 2019, 250, 2127–2145. [Google Scholar] [CrossRef]
  54. Jiang, C.G.; Xu, J.Y.; Zhang, H.; Zhang, X.; Shi, J.; Li, M.; Ming, F. A cytosolic class I small heat shock protein, RcHSP17.8, of Rosa chinensis confers resistance to a variety of stressesto Escherichia coli, yeast and Arabidopsis thaliana. Plant Cell Environ. 2009, 32, 1046–1059. [Google Scholar] [CrossRef] [PubMed]
  55. Jiang, L.Y.; Hu, W.J.; Qian, Y.X.; Ren, Q.Y.; Zhang, J. Genome-wide identification, classification and expression analysis of the Hsf and Hsp70 gene families in maize. Gene 2021, 770, 145348. [Google Scholar] [CrossRef] [PubMed]
  56. Wang, J.; Song, N.; Qin, Q.; Su, A.; Si, W.; Cheng, B.; Wu, L.; Peng, X.; Jiang, H. Alternative splicing of ZmHsf23 modulates maize heat tolerance by regulating sHSPs and TIL1 expression. Crop J. 2025, 1–13. [Google Scholar] [CrossRef]
  57. Liu, H.C.; Liao, H.T.; Charng, Y.Y. The role of class A1 heat shock factors (HSFA1s) in response to heat and other stresses in Arabidopsis. Plant Cell Environ. 2011, 34, 738–751. [Google Scholar] [CrossRef]
  58. Zou, X.W.; Yue, J.N.; Li, Z.Y.; Dai, L.Y.; Li, W. Functional analysis of rice heat shock transcription factor HsfA2b regulating the resistance to abiotic stresses. Biotechnol. Bull. 2024, 40, 105–113. [Google Scholar] [CrossRef]
  59. Li, H.G.; Yang, Y.L.; Liu, M.Y.; Zhu, Y.H.; Wang, H.L.; Feng, C.H.; Niu, M.X.; Liu, C.; Yin, W.L.; Xia, X.L. The in vivo performance of a heat shock transcription factor from Populus euphratica, PeHSFA2, promises a prospective strategy toalleviate heat stress damage in poplar. Environ. Exp. Bot. 2022, 201, 104940. [Google Scholar] [CrossRef]
  60. Zhang, H.; Zhang, X.; Meng, M.; Di, H.; Wang, J. Populus trichocarpa PtHSFA4a enhances heat tolerance by regulating expression of APX1 and HSPs. Forests 2023, 14, 2028. [Google Scholar] [CrossRef]
  61. Wu, Z.; Li, T.; Ding, L.P.; Wang, C.P.; Cao, X.; Teng, N.J. Lily LlHSFC2 coordinates with HSFAs to balance heat stress response and improve thermotolerance. New Phytol. 2024, 241, 2124–2142. [Google Scholar] [CrossRef]
  62. Iba, K. Acclimative response to temperature stress in higher plants: Approaches of gene engineering for temperature tolerance. Annu. Rev. Plant Biol. 2002, 53, 225–245. [Google Scholar] [CrossRef]
  63. Waters, E.R.; Lee, G.J.; Vierling, E. Evolution, structure and functionof the small heat shock proteins in plants. J. Exp. Bot. 1996, 47, 325–338. [Google Scholar] [CrossRef]
  64. Wang, H.; Charagh, S.; Dong, N.; Lu, F.; Wang, Y.; Cao, R.; Ma, L.; Wang, S.; Jiao, G.; Xie, L.; et al. Genome-wide analysis of heat shock protein family and identification of their functions in rice quality and yield. Int. J. Mol. Sci. 2024, 25, 11931. [Google Scholar] [CrossRef]
  65. Yamada, K.; Fukao, Y.; Hayashi, M.; Fukazawa, M.; Suzuki, I.; Nishimura, M. Cytosolic HSP90 regulates the heat shock response that is responsible for heat acclimation in Arabidopsis thaliana. J. Biol. Chem. 2007, 282, 37794–37804. [Google Scholar] [CrossRef] [PubMed]
  66. Song, H.M.; Zhao, R.M.; Fan, P.X.; Wang, X.C.; Chen, X.Y.; Li, Y.X. Overexpression of AtHsp90.2, AtHsp90.5 and AtHsp90.7 in Arabidopsis thaliana enhances plant sensitivityto salt and drought stresses. Planta 2009, 229, 955–964. [Google Scholar] [CrossRef] [PubMed]
  67. Wang, J.Y.; Chen, C.; Wu, C.Z.; Meng, Q.W.; Zhuang, K.Y.; Ma, N.N. SlMYB41 positively regulates tomato thermotolerance by activating the expression of SlHSP90.3. Plant Physiol. Biochem. 2023, 204, 108106. [Google Scholar] [CrossRef] [PubMed]
  68. Panzade, K.P.; Vishwakarma, H.; Padaria, J.C. Heat stress inducible cytoplasmic isoform of ClpB1 from Z. nummularia exhibits enhanced thermotolerance in transgenic tobacco. Mol. Biol. Rep. 2020, 47, 3821–3831. [Google Scholar] [CrossRef]
  69. Rong, J.; Wang, P.W.; Wu, N.; Qu, J.; Yu, M.; Feng, Y.Q. Identification of heat tolerance of small heat shock protein gene HSP17. 4 from Soybean. J. Jilin Agric. Univ. 2018, 40, 568–576. [Google Scholar] [CrossRef]
  70. Li, N.N.; Yang, Y.F.; Zhao, F.Y.; Hu, X.L. Study on chloroplast proteins affected by small heat shock26(sHSP26) under heat stress in maize. J. Henan Agric. Univ. 2015, 49, 729–736. [Google Scholar] [CrossRef]
  71. Ben-Zvi, A.P.; Goloubinoff, P. Review: Mechanisms of disaggregation and refolding of stable protein aggregates by molecular chaperones. J. Struct. Biol. 2001, 135, 84–93. [Google Scholar] [CrossRef]
  72. Park, H.S.; Jeong, W.J.; Kim, E.C.; Jung, Y.G.; Lim, J.M.; Hwang, M.S.; Park, E.J.; Ha, D.S.; Choi, D.W. Heat shock protein gene family of the Porphyra seriata and enhancement of heat stress tolerance by PsHSP70 in Chlamydomonas. Mar. Biotechnol. 2012, 14, 332–342. [Google Scholar] [CrossRef]
  73. Chen, Y.P.; Deng, C.J.; Xu, Q.Z.; Chen, X.P.; Jiang, F.; Zhang, Y.L.; Hu, W.S.; Zheng, S.Q.; Su, W.B.; Jiang, J.M. Integrated analysis of the metabolome, transcriptome and miRNome reveals crucial roles of auxins and heat shock proteins in the heat stress response of loquat fruit. Sci. Hortic. 2022, 294, 110764. [Google Scholar] [CrossRef]
  74. Sharma, L.; Dalal, M.; Verma, R.K.; Kumar, S.V.; Yadava, S.K.; Pushkar, S.; Kushwaha, S.R.; Bhowmik, A.; Chinnusamy, V. Auxin protects spikelet fertility and grain yield under drought and heat Tstresses in rice. Environ. Exp. Bot. 2018, 150, 9–24. [Google Scholar] [CrossRef]
  75. Wang, R.H.; Zhang, Y.; Kieffer, M.; Yu, H.; Kepinski, S.; Estelle, M. HSP90 regulates temperature-dependent seedling growth in Arabidopsis by stabilizing the auxinsco-receptor F-box protein TIR1. Nat. Commun. 2016, 7, 10269, Erratum in Nat. Commun. 2016, 7, 11677. [Google Scholar] [CrossRef] [PubMed]
  76. Alfonso, M.; Silvina, M.; René, T.; Lourdes, F.C.; Juan, C.P.; Castellano, M.M. The co-chaperone HOP participates in TIR1 stabilisation and in auxins response in plants. Plant Cell Env. 2022, 45, 2508–2519. [Google Scholar] [CrossRef]
  77. Wen, T. Plant Physiology; China Agriculture Press: Beijing, China, 2018; pp. 1–348. [Google Scholar]
  78. Xing, Y.; Jia, W.S.; Zhang, J.H. AtMKK1 mediates ABA-induced CAT1 expression and H2O2 production via AtMPK6-coupled signaling in Arabidopsis. Plant J. 2008, 54, 440–451. [Google Scholar] [CrossRef]
  79. Cho, E.K.; Hong, B. Over-expression of tobacco NtHSP70-1 contributes to drought-stress tolerance in plants. Plant Cell Rep. 2006, 25, 349–358. [Google Scholar] [CrossRef]
  80. Zhang, X.Q.; Li, J.X.; Li, M.; Zhang, S.T.; Song, S.S.; Wang, W.M.; Wang, S.; Chang, J.B.; Xia, Z.L.; Zhang, S.T.; et al. NtHSP70-8b positively regulates heat tolerance and seed size in Nicotiana tabacum. Plant Physiol. Biochem. 2023, 201, 107901. [Google Scholar] [CrossRef]
  81. Liu, X.L.; Ji, P.; Yang, H.T.; Jiang, C.J.; Liang, Z.W.; Chen, Q.Z.; Lu, F.; Chen, X.; Yang, Y.Y.; Zhang, X.B. Priming effect of exogenous ABA on heat stress tolerance in rice seedlings is associated with the upregulation of antioxidative defense capability and heat shock-related genes. Plant Growth Regul. 2022, 98, 23–38. [Google Scholar] [CrossRef]
  82. Chen, Z.L.; Galli, M.; Gallavotti, A. Mechanisms of temperature-regulated growth and thermotolerance in crop species. Curr. Opin. Plant Biol. 2022, 65, 102134. [Google Scholar] [CrossRef]
  83. Prakash, V.; Singh, V.P.; Tripathic, D.K.; Sharma, S.; Corpas, F.J. Crosstalk between nitric oxide (NO) and abscisic acid (ABA) signalling molecules in higher plants. Environ. Exp. Bot. 2019, 161, 41–49. [Google Scholar] [CrossRef]
  84. Iqbal, N.; Sehar, Z.; Fatma, M.; Umar, S.; Sofo, A.; Khan, N.A. Nitric oxide and abscisic acid mediate heat stress tolerance through regulation of osmolytes and antioxidants to protect photosynthesis and growth in wheat plants. Antioxidants 2022, 11, 372. [Google Scholar] [CrossRef]
  85. Chen, Y.F.; Etheridge, N.; Schaller, G.E. Ethylene Signal Transduction. Ann. Bot. 2005, 95, 901–915. [Google Scholar] [CrossRef]
  86. Zhao, H.; Geng, X.M.; Wang, L.L.; Xu, S.D. Research on the effect of ethylene in heat resistance mechanism of Rhododendron. Acta Hortic. Sin. 2022, 49, 561–570. [Google Scholar] [CrossRef]
  87. Huang, J.Y.; Zhao, X.B.; Burger, M.; Wang, Y.R.; Chory, J. Two interacting ethylene response factors regulate heat stress response. Plant Cell 2021, 33, 338–357. [Google Scholar] [CrossRef] [PubMed]
  88. Fang, L.C.; Tong, J.; Dong, Y.F.; Xu, D.Y.; Mao, J.; Zhou, Y. De novo RNA sequencing transcriptome of Rhododendron obtusum identified the early heat response genes involved in the transcriptional regulation of photosynthesis. PLoS ONE 2017, 12, e0186376. [Google Scholar] [CrossRef] [PubMed]
  89. Eric, B.; Esha, D.; Brittani, H.; Lauren, H.W.; Daniel, M.R.; Brad, M.B. Ethylene-mediated metabolic priming increases photosynthesis and metabolism to enhance plant growth and stress tolerance. PNAS Nexus 2023, 2, 216. [Google Scholar] [CrossRef]
  90. Sadural, I.; Janeczko, A. Physiological and molecular mechanisms of brassinosteroid-induced tolerance to high and low temperature in plants. Biol. Plant. 2018, 62, 601–616. [Google Scholar] [CrossRef]
  91. Luo, J.Y.; Jiang, J.J.; Sun, S.Y.; Wang, X.L. Brassinosteroids promote thermotolerance through releasing BIN2-mediated phosphorylation and suppression of HsfA1 transcription factors in Arabidopsis. Plant Commun. 2022, 3, 100419. [Google Scholar] [CrossRef]
  92. Xia, X.J.; Wang, Y.J.; Zhou, Y.H.; Tao, Y.; Mao, W.H.; Shi, K.; Asami, T.D.; Chen, Z.X.; Yu, J.Q. Reactive oxygen species are involved in brassinosteroid-induced stress tolerancein cucumber. Plant Physiol. 2009, 150, 801–814. [Google Scholar] [CrossRef]
  93. Lam, D.V.; Xu, X.Y.; Zhu, T.T.; Pan, L.X.; Zanten, M.V.; Jong, D.D.; Wang, Y.W.; Vanremoortele, T.; Locke, A.M.; Cotte, B.; et al. The membrane-localized protein kinase MAP4K4/TOT3 regulates thermomorphogenesis. Nat. Commun. 2021, 12, 2842. [Google Scholar] [CrossRef]
  94. Wang, C.K.; Guo, M. Effects of brassinolide on growth morphology and physiological characters of Avena nuda under room and high temperature stresses. J. South. Agric. 2017, 48, 1173–1177. [Google Scholar] [CrossRef]
  95. Yu, J.Q.; Huang, L.F.; Hu, W.H.; Zhou, Y.H.; Mao, W.H.; Ye, S.F.; NogueÂs, S. A role for brassinosteroids in the regulation of photosynthesis in Cucumis sativus. J. Exp. Bot. 2004, 55, 1135–1143. [Google Scholar] [CrossRef]
  96. Guan, Y.X.; Ding, L.; Jiang, J.F.; Shentu, Y.Y.; Zhao, W.Q.; Zhao, K.K.; Zhang, X.; Song, A.; Chen, S.; Chen, F.D. Overexpression of the CmJAZ1-like gene delays flowering in Chrysanthemum morifolium. Hortic. Res. 2021, 8, 87. [Google Scholar] [CrossRef]
  97. Hu, R.L.; Wang, J.L.; Yang, H.Q.; Wei, D.Y.; Tang, Q.L.; Yang, Y.; Tian, S.B.; Wang, Z.M. Comparative transcriptome analysis reveals the involvement of an MYB transcriptional activator, SmMYB108, in anther dehiscence in eggplant. Front. Plant Sci. 2023, 14, 1164467. [Google Scholar] [CrossRef] [PubMed]
  98. Cheng, Y.Y.; Liang, C.L.; Qiu, Z.Y.; Zhou, S.Q.; Liu, J.L.; Yang, Y.Y.; Wang, R.; Yin, J.; Ma, C.H.; Cui, Z.H.; et al. Jasmonic acid negatively regulates branch growth in pear. Front. Plant Sci. 2023, 14, 1164467. [Google Scholar] [CrossRef] [PubMed]
  99. Wang, S.; Wang, Y.B.; Yang, R.; Cai, W.H.; Liu, Y.N.; Zhou, D.R.; Meng, L.; Wang, P.; Huang, B.Q. Genome-Wide identifcation and analysis uncovers the potential role of JAZ and MYC families in potato under abiotic stress. Int. J. Mol. Sci. 2023, 24, 6706. [Google Scholar] [CrossRef]
  100. Huang, Y.M.; Zeng, X.C. Effects of methyl jasmonate on physiological characteristics of rice leaves at heading and flowering stage under high temperature. Jiangsu Agric. Sci. 2023, 51, 66–71. [Google Scholar] [CrossRef]
  101. Wang, F. The functional characterization and regulatory mechanism analysis of jasmonate synthetic gene OPR3 in thermotolerance of Arabidopsis and Wheat (Triticum aestivum L.). China Agric. Univ. 2014, 1–67. [Google Scholar]
  102. Ji, D.L. Regulation Mechanism of Methyl Jasmonate on Panicle Morphogenesis in Rice Under High Temperature Stress During the Panicle Differentiation Stage; Yangzhou University: Yangzhou, China, 2024; pp. 1–118. [Google Scholar]
  103. Ruan, J.J.; Zhou, Y.X.; Zhou, M.L.; Yan, J.; Khurshid, M.; Weng, W.F.; Cheng, J.P.; Zhang, K.X. Jasmonic acid signaling pathway in plants. Int. J. Mol. Sci. 2019, 20, 2479. [Google Scholar] [CrossRef]
  104. Tian, X.J.; Wang, F.; Zhao, Y.; Lan, T.Y.; Yu, K.H.; Zhang, L.Y.; Qin, Z.; Hu, Z.R.; Yao, Y.Y.; Ni, Z.F.; et al. Heat shock transcription factor A1b regulates heat tolerance in wheat and Arabidopsis through OPR3 and jasmonate signalling pathway. Plant Biotechnol. J. 2020, 18, 1109–1111. [Google Scholar] [CrossRef]
  105. Li, J.J. Research Progress in Salicylic Acid Metabolism and Regulation in Plants. World Ecol. 2023, 12, 209–219. [Google Scholar] [CrossRef]
  106. Xu, L.; Zhao, H.Y.; Wang, J.B.; Wang, X.M.; Jia, X.Q.; Wang, L.; Xu, Z.; Li, R.L.; Jiang, K.; Chen, Z.X.; et al. AIM1-dependent high basal salicylic acid accumulation modulates stomatal aperture in rice. New Phytol. 2023, 238, 1420–1430. [Google Scholar] [CrossRef] [PubMed]
  107. Liu, J.Y.; Gao, Y.H.; Huang, J.S.; Zhang, Q. Effects of exogenous salicylic acid on physiological and electrical impedance parameters of trollius chinensis seedlings under high temperature stress. Bull. Bot. Res. 2020, 40, 543–551. [Google Scholar] [CrossRef]
  108. Jahan, M.S.; Wang, Y.; Shu, S.; Zhong, M.; Chen, Z.; Wu, J.Q.; Sun, J.; Guo, S.R. Exogenous salicylic acid increases the heat tolerance in tomato (Solanum lycopersicum L.) by enhancing photosynthesis efficiency and improving antioxidant defense system through scavenging of reactive oxygen species. Sci. Hortic. 2019, 247, 421–429. [Google Scholar] [CrossRef]
  109. Sun, J.L.; Zhao, B.L.; Yu, S.L. Study of exogenous salicylic acid(SA) on the heat tolerance in grape seedling under high temperature stress. J. Soil Water Conserv. 2014, 28, 290–294+299. [Google Scholar] [CrossRef]
  110. Ling, R.; You, L.; Wu, C.M.; Zheng, Z.X.; Zhai, J.W.; Wu, S.S. Effects of exogenous salicylic acidon heat-tolerance of two Hydrangea Cultivars. J. Northwest For. Univ. 2021, 36, 72–78. [Google Scholar] [CrossRef]
  111. Ding, M.H.; Xing, W.; Li, Z.Q.; Jin, X.; Yu, Q.X.; Sun, J.H. The class B heat shock factor RcHsf17 from Rosa chinensis enhances basal thermotolerance in Rosa rugosa. Environ. Exp. Bot. 2024, 225, 105832. [Google Scholar] [CrossRef]
  112. Bu, W.X.; Huang, Y.; Chen, L.J.; Zhang, M.H.; Luo, X.N.; Zheng, T.C.; Shao, F.X.; Lei, W.Q.; Xing, W.; Yang, X.Y. Transcriptome analysis of tree peony under high temperature treatment and functional verification of PsDREB2A gene. Plant Physiol. Biochem. 2025, 219, 109405. [Google Scholar] [CrossRef]
  113. Tian, X.J. Functional Analysis of Heat Stress Responsive Genes TaMBF1c and TaMYB in Wheat (Triticum aestivum L.); China Agricultureal University: Beijing, China, 2018; pp. 1–122. [Google Scholar]
  114. Li, S.J.; Fu, Q.T.; Chen, L.G.; Huang, W.D.; Yu, D.Q. Arabidopsis thaliana WRKY25, WRKY26, and WRKY33 coordinate induction of plant thermotolerance. Planta 2011, 233, 1237–1252. [Google Scholar] [CrossRef]
  115. Zou, L.F.; Yu, B.W.; Ma, X.L.; Cao, B.H.; Chen, G.J.; Chen, C.M.; Lei, J.J. Cloning and expression analysis of the BocMBF1c gene involved in heat tolerance in Chinese Kale. Int. J. Mol. Sci. 2019, 20, 5637. [Google Scholar] [CrossRef]
  116. Busch, W.; Wunderlich, M.; Schoffl, F. Identification of novel heat shock factor-dependent genes and biochemical pathways in Arabidopsis thaliana. Plant J. 2005, 41, 1–14. [Google Scholar] [CrossRef]
  117. Ding, L.P.; Wu, Z.; Teng, R.D.; Xu, S.J.; Cao, X.; Yuan, G.Z.; Zhang, D.H.; Teng, N.J. LlWRKY39 is involved in thermotolerance by activating LlMBF1c and interacting with LlCaM3 in lily (Lilium longiflorum). Hortic. Res. 2021, 8, 36. [Google Scholar] [CrossRef]
  118. Suzuki, N.; Bajad, S.; Shuman, J.; Shulaev, V.; Mittler, R. The transcriptional co-activator MBF1c is a key regulator of thermotolerance in Arabidopsis thaliana. J. Biol. Chem. 2008, 283, 9269–9275. [Google Scholar] [CrossRef] [PubMed]
  119. Arslan, Ö. The role of heat acclimation in thermotolerance of chickpea cultivars: Changes in photochemical and biochemical responses. Life 2023, 13, 233. [Google Scholar] [CrossRef] [PubMed]
  120. Xu, S.; Li, J.L.; Zhang, X.Q.; Wei, H.; Cui, L.J. Effects of heat acclimation pretreatment on changes of membrane lipid peroxidation, antioxidant metabolites, and ultrastructure of chloroplasts in two cool-season turfgrass species under heat stress. Environ. Exp. Bot. 2006, 56, 274–285. [Google Scholar] [CrossRef]
  121. Wang, X.Y.; Li, Z.; Liu, B.; Zhou, H.; Elmongy, M.S.; Xia, Y.P. Combined proteome and transcriptome analysis of heat-primed azalea reveals new insights into plant heat acclimation memory. Front. Plant Sci. 2020, 11, 1278. [Google Scholar] [CrossRef] [PubMed]
  122. Rhaman, M.S.; Imran, S.; Rauf, F.; Khatun, M.; Baskin, C.C.; Murata, Y.; Hasanuzzaman, M. Seed priming with phytohormones: An effective approach for the mitigation of abiotic stress. Plants 2021, 10, 37. [Google Scholar] [CrossRef]
  123. Jiang, X.D.; Jiang, L.L.; Hua, M.F.; Chen, H.L.; Lv, R.; Hu, N.; Yang, X.Y. Analysis the effect of different chemical agents on high temperature stress in rice leaves. Chin. J. Agrometeorol. 2018, 39, 92–99. [Google Scholar] [CrossRef]
  124. Zhao, B.; Fu, Y.M.; Ding, H.H.; Zhang, X.X.; Du, Y.K. Effects of Ca2+ on Tolerance of Rhododendron lapponicum in Qinling to Heat Stress. J. Northwest For. Univ. 2010, 25, 29–32. [Google Scholar]
  125. Wang, H.Q.; Qing, K.R.; Zhu, H.X.; Wang, W.L.; Wang, H.Y. Effect of exogenous heat-resistant agent on heat resistance of Rhododendron under high temperature stress. J. Southwest Univ. 2022, 44, 36–44. [Google Scholar] [CrossRef]
Cimb 47 00601 g001
Figure 1. Regulatory network for plant responses to high temperature.
Figure 1. Regulatory network for plant responses to high temperature.
Cimb 47 00601 g001
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Wang, J.; Wang, Y.; Jin, H.; Yu, Y.; Mu, K.; Kang, Y. Research Progress on Responses and Regulatory Mechanisms of Plants Under High Temperature. Curr. Issues Mol. Biol. 2025, 47, 601. https://doi.org/10.3390/cimb47080601

AMA Style

Wang J, Wang Y, Jin H, Yu Y, Mu K, Kang Y. Research Progress on Responses and Regulatory Mechanisms of Plants Under High Temperature. Current Issues in Molecular Biology. 2025; 47(8):601. https://doi.org/10.3390/cimb47080601

Chicago/Turabian Style

Wang, Jinling, Yaling Wang, Hetian Jin, Yingzi Yu, Kai Mu, and Yongxiang Kang. 2025. "Research Progress on Responses and Regulatory Mechanisms of Plants Under High Temperature" Current Issues in Molecular Biology 47, no. 8: 601. https://doi.org/10.3390/cimb47080601

APA Style

Wang, J., Wang, Y., Jin, H., Yu, Y., Mu, K., & Kang, Y. (2025). Research Progress on Responses and Regulatory Mechanisms of Plants Under High Temperature. Current Issues in Molecular Biology, 47(8), 601. https://doi.org/10.3390/cimb47080601

Article Metrics

Back to TopTop