Strigolactones are carotenoid-derived phytohormones that impact plant growth and development in diverse ways. However, the roles of strigolactones in the responses to temperature stresses are largely unknown. Here, we demonstrated that strigolactone biosynthesis is induced in tomato (Solanum lycopersicum) by heat and cold stresses. Compromised strigolactone biosynthesis or signaling negatively affected heat and cold tolerance, while application of the synthetic strigolactone analog GR245DS enhanced heat and cold tolerance. Strigolactone-mediated heat and cold tolerance was associated with the induction of abscisic acid (ABA), heat shock protein 70 (HSP70) accumulation, C-REPEAT BINDING FACTOR 1 (CBF1) transcription, and antioxidant enzyme activity. Importantly, a deficiency in ABA biosynthesis compromised the GR245DS effects on heat and cold stresses and abolished the GR245DS-induced transcription of HSP70, CBF1, and antioxidant-related genes. These results support that strigolactones positively regulate tomato heat and cold tolerance and that they do so at least partially by the induction of CBFs and HSPs and the antioxidant response in an ABA-dependent manner.
Plants encounter stressful conditions that adversely impact growth, metabolism, and productivity throughout their life cycles. Extreme high or low temperature, drought, salinity, floods, pollutants, and radiation are the main stress factors that limit the productivity of many crops of economic importance1. These stresses disrupt many physiological processes through the excessive generation of reactive oxygen species (ROS), which results in serious injury to DNA and proteins in plants2,3. To avoid oxidative damage, plants activate ROS-scavenging enzymes, including glutathione reductase (GR), superoxide dismutase (SOD) and ascorbate peroxidase (APX), and make use of nonenzymatic antioxidants, including glutathione and ascorbate3,4. The induction of the antioxidant system is considered a crucial mechanism to enhance extreme temperature tolerance in plants, as transcript suppression or deficiency of the genes encoding antioxidants results in increased sensitivity to temperature stresses5,6.
Plants have evolved a complex network of interconnected signaling pathways allowing them to flexibly acclimate to and overcome these stress conditions. In addition to the induction of the antioxidant system, plants have also evolved other mechanisms to prevent cellular damage in response to temperature stresses7,8. Heat shock proteins (HSPs) are significantly induced by heat stress to protect cellular proteins against irreversible damage9. HSP70s comprise a subset of HSPs and function as molecular chaperones to bind and release unfolded/nonnative proteins. Several studies have shown that HSP70s are pivotal for the survival of plants under heat stress conditions and the induction of thermotolerance9,10,11. In contrast, plants can also activate the transcription of C-REPEAT BINDING FACTOR (CBF), subsequently leading to the induction of many COLD-RESPONSIVE (COR) genes modulating cold stress responses7,12.
Plant hormones such as abscisic acid (ABA) are actively involved in stress responses13. In response to stresses, plants accumulate more ABA in leaves, which can promote stomatal closure, enhance water balance, and induce antioxidant defense systems to alleviate oxidative injury13,14. Moreover, ABA can activate numerous cellular responses in plants through a series of signal transduction pathways and induction of HSP and CBF, promoting plant tolerance against stresses11,15. Furthermore, ABA can interact with other plant hormones, such as gibberellins, jasmonic acid and strigolactones, which makes it a hub in the responses to various abiotic stresses7,16,17.
Strigolactones are a group of terpenoid lactone hormones. To date, several genes involved in the biosynthesis of strigolactones, such as CAROTENOID CLEAVAGE DIOXYGENASE 7 (CCD7), CCD8, and MORE AXILLARY GROWTH 1 (MAX1), have been identified18,19,20. In Arabidopsis, for example, after perception of the strigolactone signal via the strigolactone-specific receptor DWARF14 (D14), downstream proteins such as the F-box protein MAX2 participate in various physiological processes21,22. Deficiency or suppressed transcription of strigolactone biosynthesis or signaling genes has been shown to affect multiple processes in plants, such as leaf senescence, root growth, shoot branching, and responses to external stimuli, including pathogens, nutrient deficiency, drought, and salinity23,24,25,26,27,28. Strigolactone biosynthesis is induced under adverse growth conditions such as phosphate deficiency29. Strigolactone-deficient and/or strigolactone-insensitive mutants are hypersensitive to stresses such as salt, drought and osmotic stress26,30,31, and exogenous strigolactone treatment rescues the phenotype of wild-type plants and strigolactone-deficient max mutants (max3-11, max4-7) under drought stress in Arabidopsis26, implying that strigolactones positively regulate abiotic stress tolerance. Notably, decreased stress tolerance in strigolactone-related mutants is associated with lower ABA levels and/or slower ABA-mediated stomatal closure in stressed shoots of several species, while exogenous strigolactones increase the sensitivity of guard cells to ABA in tomato, Lotus japonicus, and Arabidopsis26,30,31,32. Therefore, the crosstalk between strigolactones and ABA may play a critical role in the plant response to stresses.
Strigolactones are mainly produced in roots but can be transported to shoots or secreted into the rhizosphere33,34. To date, several studies have shown that strigolactone biosynthesis or signaling is important for plants to acclimate to temperature stresses. Cooper et al.35 demonstrated that there is a more significant decrease in the CO2 assimilation rate in several strigolactone biosynthesis or signaling mutants of pea and Arabidopsis after a dark chill. Similarly, Hu et al.36 found that application of strigolactones attenuates heat suppression at leaf elongation, which is associated with the increased transcript levels of cell cycle-related genes and decreased transcript levels of genes involved in auxin transport in elongating leaves of tall fescue. Most recently, Liu et al.17 showed that rice dwarf27 mutants deficient in strigolactone biosynthesis display lower ABA contents with decreased transcript levels of ABA-responsive genes and impaired cold resistance. In the present work, we report that strigolactone biosynthesis and signaling play crucial roles in the responses to heat and cold stresses in tomato. The results show that strigolactones act as positive regulators of tolerance to heat and cold stresses by activating the transcription of CBF and HSP and antioxidant enzyme activity at least partially in an ABA-dependent manner.
Strigolactones accumulate in the roots in response to heat and cold stresses
To explore the role of strigolactones under extreme temperatures, a time course of the transcript levels of strigolactone biosynthesis (CCD7, CCD8, and MAX1) and signaling (MAX2) genes in the roots of wild-type tomato plants was carried out after the whole plants were transferred to hot (42 °C) or cold (4 °C) conditions. As shown in Fig. 1a, either high or low growth temperature significantly induced the transcription of CCD7, CCD8, MAX1, and MAX2 in the roots at 3 h after heat or at 6 h after cold stress. Afterward, the transcript levels of these genes decreased gradually to levels similar to those before the stresses. Among the four genes examined, the increases in the transcript levels of CCD7 and CCD8 were more notable than those of MAX1 and MAX2 under either high- or low-temperature conditions. Additional experiments showed that transcript levels of strigolactone biosynthesis genes in the leaves were also induced in response to heat or cold stress, and the levels were, however, much lower than those in the roots under optimal growth conditions, and hot and cold conditions (Figs. 1a and S1). In addition, changes in the accumulation of three principal strigolactones, orobanchol, solanacol, and didehydro-orobanchol, in the roots were examined (Fig. 1b, c). While the levels of orobanchol and didehydro-orobanchol were not significantly altered, solanacol significantly increased under either high- or low-temperature conditions by 68.7% at 3 h after heat stress and by 107.8% at 6 h after cold stress (Fig. 1b, c). These results indicate that strigolactone biosynthesis is induced at the early stage of heat or cold stress.
Strigolactones play a positive role in the heat stress response and HSP70 protein accumulation under heat stress
To examine whether strigolactones regulate heat responses, virus-induced gene silencing (VIGS) experiments were conducted, and we generated CCD7-, CCD8-, MAX1-, and MAX2-silenced plants with a reduction in the respective gene transcript levels in the roots by 79.8%, 77.4%, 76.2%, and 79.9% as well as a reduction in the gene transcript levels of CCD7, CCD8, and MAX1 in the leaves by 74.1%, 73.7%, and 71.7% in CCD7-, CCD8-, and MAX1-silenced plants, respectively, compared with those in the control plants (pTRV) (Fig. S2a, b). In addition to the decreasing effects on stimulating the germination of Phelipanche aegyptiaca seeds, the contents of orobanchol, didehydro-orobanchol, and solanacol in root extracts of the CCD7-, CCD8-, and MAX1-silenced plants was significantly lower than that of the pTRV plants (Fig. S2c, d). However, root extracts of MAX2-silenced plants did not show altered accumulation of these strigolactones or result in changed germination of P. aegyptiaca seeds (Fig. S2c, d). Therefore, strigolactone biosynthesis was partially suppressed in CCD7-, CCD8-, and MAX1-silenced plants but not in MAX2-silenced plants. Moreover, all the VIGS plants at the 6~7-leaf stage were shorter (Fig. S3a) and had increased root weight with little change in shoot weight (Fig. S3c) compared with the pTRV plants. Moreover, increased lateral branches were found in all VIGS plants at the 10~12-leaf stage (Fig. S3b). Additionally, detached leaves from the VIGS plants exhibited increased sensitivity to dehydration, as indicated by the increased water loss under dehydration conditions and higher stomatal conductance than that in the pTRV plants (Fig. S4). Interestingly, higher leaf water loss rates during dehydration and increased stomatal conductance were found in MAX2-silenced plants than those in CCD7-, CCD8-, and MAX1-silenced plants (Fig. S4b, c). Therefore, suppression of either strigolactone biosynthesis or signaling was sufficient to alter plant architecture and water dynamics in tomato plants.
After 48 h of heat stress at 42 °C, the pTRV plants exhibited slight dehydration symptoms (Fig. S5). In comparison, leaves on the VIGS plants showed severe wilting after the same heat treatment (Fig. S5). Moreover, higher malondialdehyde (MDA) contents were observed in these VIGS plants than in the pTRV plants (Fig. 2a). Relative electrolyte leakage (REL) increased slightly in the leaves of the VIGS plants at 22 °C (Fig. 2b). Heat stress caused a more significant increase in the REL values in VIGS plants, and this increase was especially significant in pTRV-CCD7 and pTRV-CCD8 plants (Fig. 2b). Moreover, an increased level of oxidized proteins was observed after 12 h of heat stress in the VIGS plants compared with that in the pTRV plants (Fig. 2c).
To substantiate the role of strigolactones in the heat response, we supplied the roots of wild-type plants with a GR245DS solution of 1, 3, or 9 µM or with distilled water containing an equal amount of acetone as the 1 µM GR245DS solution as a control at 24 h before the start of heat stress at 42 °C. After heat exposure for 48 h, the GR245DS-treated WT plants exhibited reduced sensitivity to heat, as evidenced by the less severe wilting and lower REL values and MDA contents in the leaves than those in the leaves of control plants (Fig. S6a–c). Additionally, after 12 h of heat exposure, the accumulation of oxidized proteins triggered by heat stress was attenuated in the GR245DS-treated plants, especially in the plants pretreated with GR245DS at 9 µM (Fig. S6d). Moreover, root application of GR245DS at different concentrations differentially induced the accumulation of HSP70 protein after 12 h of heat stress (Fig. S6e).
We then generated transgenic CRISPR-ccd7 mutants, and homozygous ccd7 T2 progenies with a 2 bp (TA) deletion were used. In comparison to WT plants, the ccd7 mutant plants displayed increased lateral branches, decreased plant height, 58–63% less orobanchol, solanacol and didehydro-orobanchol, and higher stomatal conductance (Fig. S7). We then treated the roots of WT and ccd7 plants with GR245DS at 3 µM at 24 h before they were exposed to heat stress at 42 °C. Heat-induced plant wilting was alleviated by the application of GR245DS in both WT and ccd7 plants (Fig. S8a). Under optimal conditions, no significant differences were found in the actual quantum efficiency of PSII photochemistry (ФPSII), the maximum quantum yield of PSII (Fv/Fm), and REL among these plants (Figs. 2d, e and S8b). Heat stress resulted in more significant decreases in ФPSII and Fv/Fm, as well as a more significant increase in REL in ccd7 plants relative to the WT plants after 48 h of heat exposure. However, the values of these parameters did not significantly differ between the heat-exposed WT and ccd7 plants in the presence of GR245DS (Figs. 2d, e and S8b). Moreover, less accumulation of the HSP70 protein was induced by heat stress in ccd7 plants than in WT plants; however, application of GR245DS substantially increased the accumulation of HSP70 protein in both WT plants and ccd7 plants after heat exposure for 12 h (Fig. 2f). Thus, it is likely that strigolactones induce heat stress tolerance in tomato, which is associated with an increased level of HSP70 protein in the leaves of plants.
Strigolactones are crucial for the induction of the CBF transcript and the cold response
To establish whether strigolactones also play a role in the cold response, 5-week-old CCD7-, CCD8-, MAX1-, and MAX2-silenced plants were exposed to cold conditions at 4 °C. After 7 days (d) of cold exposure, the pTRV plants exhibited slight wilting; in contrast, the VIGS plants showed severe wilting (Fig. S9a). At 22 °C, there were no differences in ФPSII (Fig. 3a) and Fv/Fm (Fig. S9b) among these plants. After 7 d of cold exposure, the leaves of the VIGS plants had lower Fv/Fm and ФPSII than the pTRV leaves (Figs. 3a and S9b). Moreover, exposure to cold resulted in more significant increases in the REL value and MDA accumulation in the VIGS plants than in the pTRV plants (Figs. 3b and S9c). Importantly, the cold-induced transcription of CBF1, which acts as a pivotal regulator in cold responses, was significantly attenuated in the leaves of VIGS plants (Fig. 3c).
We then applied GR245DS to the roots of plants and exposed these plants to cold conditions at 4 °C. In addition to severe wilting, leaves of ccd7 plants showed lower Fv/Fm and ФPSII than those of the WT plants after cold stress in the absence of GR245DS (Figs. 3d and S10). However, there were no significant differences in ФPSII and Fv/Fm between the leaves of WT plants and ccd7 plants when the roots were pretreated with GR245DS before the exposure of plants to cold stress (Figs. 3d and S10b). In agreement with the above results, the leaves of ccd7 plants had higher REL and lower transcript levels of CBF1 compared to those of the WT plants in the absence of GR245DS under cold conditions (Fig. 3e, f). Importantly, GR245DS application led to a significant decrease in REL and an increase in the transcript levels of CBF1 in both ccd7 mutants and WT plants after stress (Fig. 3e, f). Therefore, our results reveal that strigolactones act as positive regulators in cold tolerance and the induction of CBF transcript levels under cold stress.
Strigolactones induce ABA biosynthesis and ABA-dependent transcriptional responses under heat and cold stresses
ABA participates in the regulation of abiotic stresses, especially dehydration stress37. To explore whether ABA is associated with strigolactone-induced heat or cold responses in tomato, we determined the ABA content and the transcript accumulation of several genes related to ABA biosynthesis and signaling in the leaves of both ccd7 plants and GR245DS-treated plants. In the absence of stress, mutation of CCD7 did not significantly alter ABA accumulation (Fig. 4a, c). Notably, the ABA content increased after heat or cold stress in both WT and ccd7 plants, and this effect was more obvious with the application of GR245DS (Fig. 4a, c). Although heat and cold induced the accumulation of ABA in ccd7 plants, their ABA content was still significantly lower than that in WT plants at 42 and 4 °C, respectively (Fig. 4a, c).
We next analyzed the transcript accumulation of genes involved in ABA biosynthesis and signaling. The mutation of CCD7 did not significantly change the transcript levels of the ABA biosynthesis gene 9-CIS EPOXY CAROTENOID DIOXYGENASE 6 (NCED6) or of the ABA-responsive genes Lycopersicon esculentum DEHYDRIN 4 (Le4) and ABA-RESPONSIVE ELEMENT BINDING FACTOR 4 (ABF4) at 22 °C (Fig. 4b, d). Heat stress and cold stress both significantly upregulated the transcript levels of NCED6, Le4, and ABF4 in WT and ccd7 plants, except for the transcript levels of Le4 in ccd7 plants under hot conditions and ABF4 in ccd7 plants under cold conditions (Fig. 4b, d). Importantly, treatment with GR245DS increased the transcript levels of NCED6, Le4, and ABF4 in both WT and ccd7 plants under heat or cold stress conditions. However, transcript levels of these genes were always lower in ccd7 mutants than in WT plants (Fig. 4b, d). This evidence demonstrates that strigolactones participate in modulating ABA biosynthesis and ABA-dependent transcriptional responses under heat and cold stress conditions.
Strigolactones enhance antioxidant responses under heat and cold stress
To determine whether strigolactones are associated with antioxidant responses under heat and cold stresses, we determined hydrogen peroxide (H2O2) accumulation in the leaves after 48 h of heat stress or 7 d of cold stress. After heat or cold exposure, ccd7 mutants accumulated more H2O2 than WT plants. However, root application of GR245DS significantly reduced H2O2 concentrations in both WT and ccd7 plants under stress conditions (Fig. S11). Then, we measured the antioxidant enzyme (SOD, APX, GR, MDAR, and DHAR) activity in WT and ccd7 plants after 12 h of heat or cold stress. At 22 °C, no obvious differences in the activity of these enzymes were found between WT and ccd7 plants (Fig. 5). Their activity increased significantly under heat and cold stresses in WT plants but not in ccd7 plants. Finally, root application of GR245DS significantly increased their activity under optimal growth conditions or stress conditions in both WT and ccd7 plants (Fig. 5). Consistent with the changes in the activity of these enzymes, no obvious differences were found in the transcript levels of Cu/Zn-SOD, APX, GR, MDAR, and DHAR between WT and ccd7 plants under optimal conditions (Fig. S12). While heat and cold stresses significantly induced the transcription of these genes in WT plants, such inductions were not observed in ccd7 plants (Fig. S12). Similarly, root application of GR245DS significantly increased the transcript levels of Cu/Zn-SOD, APX, GR, MDAR, and DHAR under optimal or stress conditions in both WT and ccd7 plants (Fig. S12). Thus, these data reveal that strigolactones are generally involved in the regulation of the enzymatic antioxidant response under both optimal and stress conditions in tomato plants.
ABA mediates strigolactone-induced heat and cold stress responses
We next determined the effects of GR245DS on heat and cold responses in the ABA-deficient mutant notabilis (not). After 48 h of heat exposure or 7 d of cold exposure, most of the leaves on the not plants showed severe wilting symptoms (Fig. S13a, c) accompanied by decreased values of ФPSII and increased REL relative to those in the WT plants (Fig. 6a–d). While GR245DS significantly increased the values of ФPSII and decreased the values of REL in the WT plants, such effects were abolished in the not plants after heat (Fig. 6a, b) or cold treatment (Fig. 6c, d). After 12 h of heat exposure, heat-induced ABA accumulation and transcription of HSP70, HSP90, Cu/Zn-SOD, APX, GR, MDAR, DHAR, Le4, and ABF4 were substantially attenuated in the not plants (Figs. 7a, S13b, and S14a, b). Similarly, ABA accumulation and transcription of CBF1, CBF3, Cu/Zn-SOD, APX, GR, MDAR, DHAR, Le4, and ABF4 were significantly compromised in the not plants after 12 h of cold stress (Figs. 7b, S13d, and S14c, d). Moreover, GR245DS failed to induce the accumulation of ABA and the transcription of HSP70, HSP90, antioxidant genes, and ABA-responsive genes in response to heat and that of CBF1, CBF3, antioxidant genes, and ABA-responsive genes in response to cold stress, respectively, in not mutants (Figs. 7a, b, S13b, d, and S14). Similarly, the effect of heat and GR245DS on the induction of the HSP70 protein was less noticeable in not plants (Fig. 7c). Thus, ABA mediates at least a subset of strigolactone-induced heat and cold stress responses.
Recently, strigolactones have been found to positively modulate dark chilling resistance in pea and Arabidopsis35 and cold tolerance in rice17, and alleviate heat-induced adverse effects on leaf growth in tall fescue36. Several studies have demonstrated the critical role of strigolactones in the drought response in Arabidopsis, L. japonicus, and tomato26,30,31,32 and the induction of HSP transcript levels in Arabidopsis26. In this study, we demonstrate that strigolactones act as positive regulators in plant responses to heat and cold stresses in tomato. Importantly, we found that strigolactone-induced tolerance against heat and cold stresses is linked to the induction of CBFs, HSPs and antioxidant metabolism in a largely ABA-dependent manner.
Strigolactones play a positive role in both heat and cold responses in tomato
Studies have revealed that plants deficient in strigolactone biosynthesis or signaling-related genes show decreased stress tolerance in several species, while application of a synthetic strigolactone analog increases tolerance to drought stress in Arabidopsis and wheat17,26,27,31,35,38,39. Here, multiple lines of evidence were provided to indicate that strigolactones positively regulate responses to heat and cold stresses in tomato. First, the transcript accumulation of both strigolactone biosynthesis genes (CCD7, CCD8, MAX1) and the signaling gene MAX2, as well as the accumulation of solanacol, all increased under heat or cold stress in tomato roots (Fig. 1); however, strigolactone biosynthesis is repressed by osmotic-related stresses, such as drought and salinity, in the roots of nonmycorrhizal dicot plants, including tomato, lettuce, and L. japonicus30,31,40,41, implying that different environmental stimuli may have different effects on the regulation of strigolactone biosynthesis. In addition, the transcriptional activation of the pathway in the leaves (Fig. S1) suggests that the observed phenotypes may be at least in part due to locally produced strigolactones; however, since the accumulation of strigolactones is very low and undetectable in the shoots of plants such as Arabidopsis and tomato22,31, this point cannot be solved analytically at this stage. Second, disruption of CCD7 or silencing of CCD7, CCD8, MAX1, or MAX2 enhanced the susceptibility to heat and cold stresses, as indicated by the increased values of REL and MDA in these plants relative to those in the control plants (Figs. 2, 3, S5, and S8–S10). Third, root application of the strigolactone analog GR245DS mitigated the damage against heat and cold stresses (Figs. 2, 3, and S6). These data strongly indicate that strigolactones are important in both heat and cold stress responses in tomato.
We found that mutation of CCD7 decreased while application of GR245DS increased the accumulation of the HSP70 protein in response to heat stress (Fig. 2f). There is evidence that the transcript levels of HSP and HEAT SHOCK TRANSCRIPTION FACTOR A6B (HSFA6B) are responsive to strigolactones under stress26 or normal conditions42. HSPs can protect cellular proteins against severe injury under hot conditions, which is essential for plant survival under heat stress9,11. In agreement with this, an increased and a decreased accumulation of oxidized proteins were observed in the VIGS plants and the GR245DS-treated WT plants, respectively, after exposure to heat stress (Fig. 2c and S6d). On the other hand, CBF1 plays a pivotal role in cold responses by inducing COR genes7,12. Chromatin immunoprecipitation sequencing (ChIP-seq) assays show that the transcription factor SUPPRESSOR OF MAX2-LIKE 6 (SMXL6) involved in strigolactone signaling directly binds to the CBF promoter42. In agreement with this, we found that silencing CCD7, CCD8, MAX1 or MAX2, or disruption of CCD7 partially compromised cold-induced transcript accumulation of CBF1, while application of GR245DS had the opposite effects on the WT and strigolactone-deficient plants (Fig. 3c, f). Therefore, strigolactones activate CBF1 transcription in the cold response.
ABA participates in strigolactone-induced heat and cold responses
ABA is known to be involved in plant responses to abiotic stresses such as salinity, drought, heat, and cold5,15,37. When encountering these stresses, plants accumulate ABA with the induction of stomatal closure and increase in antioxidant capacity13,14. ABA can crosstalk with other plant hormones, such as gibberellins and strigolactones, involved in plant growth, development, and stress responses16,17. Recently, several research groups have found that strigolactone-related mutants of Arabidopsis, L. japonicus, and tomato show decreased accumulation of ABA or exhibit increased water loss rates under dehydration and/or reduced ABA responsiveness compared with WT plants26,27,30,31,38. Interestingly, the rice d3 (dwarf3), d10, and d17 mutants are more drought tolerant, with increased ABA contents, compared to the WT plants, while the d27 mutants exhibit reduced drought tolerance with decreased ABA accumulation43. The compromised stress tolerance observed in the max2-3 mutant is linked to the downregulation of numerous stress- and/or ABA-responsive genes in Arabidopsis26. Moreover, the application of GR24 can induce the transcription of ABA catabolic genes and alleviate stress-induced seed dormancy44,45,46. Therefore, strigolactones can alter ABA homeostasis and ABA sensitivity. Consistent with previous studies in Arabidopsis and tomato26,31, silencing of strigolactone biosynthesis genes or MAX2 resulted in increased water loss in detached leaves and higher stomatal conductance (Fig. S4). The increased stomatal conductance and sensitivity of pTRV-MAX2 leaves to dehydration relative to pTRV-CCD7, pTRV-CCD8, and pTRV-MAX1 leaves is probably due to the role of MAX2 linked not only to the strigolactone pathway but also to the (KARRIKIN INSENSITIVE 2) KAI2-dependent signaling47. Moreover, ccd7 plants had decreased transcript levels of ABA biosynthesis gene and ABA-responsive genes NCED6, Le4, and ABF4 with a decreased accumulation of ABA in the leaves under heat or cold stress conditions, while exogenous GR245DS treatment increased the transcription of these genes and induced ABA accumulation in both WT and ccd7 plants (Fig. 4). In addition, we found that cold-induced transcription of CBF1 and heat-induced HSP70 protein accumulation were linked to strigolactones and that these effects were partially ABA-dependent under heat or cold stress conditions (Figs. 2f, 3f, and 7); however, it remains to be studied how ABA biosynthesis is induced by strigolactones and how ABA regulates CBF1 transcription and the HSP70 protein under temperature stresses.
Strigolactones participate in the upregulation of the antioxidant system in response to heat and cold stresses
One of the findings of this study is the role of strigolactones in regulating the antioxidant system in stress responses. When suffering from stresses, plants accumulate ROS, which cause oxidative damage to cells and tissues3. In this study, tomato plants showed an increased accumulation of ROS, oxidized proteins, and MDA with decreases in Fv/Fm and ФPSII in the ccd7 mutants or silenced plants after heat or cold exposure (Figs. 2, 3, and S8–S11). To protect cells against oxidative damage, plants activate ROS-scavenging systems, including antioxidant enzymes (DHAR, MDAR, SOD, GR, and APX)3,4. It seems likely that their activity is regulated by multiple hormones, such as ABA and brassinosteroids14,48. However, our understanding of the role of strigolactones in scavenging ROS is very limited. In rapeseed, GR24 application increases the activity of peroxidase and SOD and decreases lipid peroxidation under salt stress49. Moreover, treatment with GR24 enhances drought tolerance by increasing the activity of antioxidant enzymes (SOD, peroxidase, catalase, and APX) and decreasing lipid peroxidation39. Under heat and cold stresses, induction of both the activity of antioxidant enzymes (SOD, APX, GR, MDAR and DHAR) and the transcript levels of the corresponding genes was attenuated in ccd7 mutants compared with those in WT plants, which is consistent with stronger oxidative stress in ccd7 plants under heat and cold stresses (Figs. 5, S11–S12). Enzyme activity is regulated at several levels: gene transcription, protein turnover, and stability. In agreement with this, we found that the activity of antioxidant enzymes and/or the transcription of antioxidant genes were affected by the changes in the growth temperature and the strigolactone level (Figs. 5 and S12). These results suggest that strigolactones participate in the activation of ROS-scavenging systems. This conclusion is also substantiated by the results of the GR245DS application experiment (Figs. 5 and S12). Until now, both downregulation50 and upregulation26,28 of the transcript levels of many photosynthesis-related genes have been observed in strigolactone-related mutants. In our study, the alleviation of oxidative stress by strigolactones was followed by increased Fv/Fm and ФPSII, suggesting that strigolactones may prevent stress-induced photoinhibition (Fv/Fm) and decrease of photosynthetic electron transport at PSII (ФPSII) by alleviating oxidative stress. However, we could not exclude the direct role of strigolactones in the regulation of photosynthesis, as strigolactones have been found to potentially regulate light harvesting in tomato plants50.
As an antistress hormone, ABA enhances antioxidant capacity in response to stress14. Consistent with this, heat- and cold-induced transcription of the Cu/Zn-SOD, APX, GR, MDAR, and DHAR genes was compromised in the ABA-deficient mutant not (Figs. 7a, b and S13b, d). While GR245DS induced a significant increase in the transcript levels of Cu/Zn-SOD, APX, GR, MDAR, and DHAR in WT plants, this effect was again abolished in not plants (Figs. 7a, b and S13b, d). Therefore, the role of strigolactones in the activation of the antioxidant response in our study was partially dependent on ABA. Strigolactones are known to affect the sensitivity of guard cells to ABA in tomato, Arabidopsis, and L. japonicus26,30,31. Here, we found that the transcript levels of the ABA-responsive genes Le4 and ABF4 in ABA-deficient not plants did not increase in response to GR245DS under stress (Fig. S14b, d). Further study on the relationship of strigolactones and ABA is highly warranted.
Materials and methods
The tomato (Solanum lycopersicum) lines used in this study were the cultivar Ailsa Craig (wild type, WT), the ABA-deficient mutant notabilis (not; in the Ailsa Craig background)51, and Condine Red (WT). The tomato ccd7 mutant on the Condine Red background was generated by a clustered, regularly interspaced, short palindromic repeat (CRISPR)/CRISPR-associated 9 (Cas9) technique52. The target sequence (ATTAACATTGCCTAGCCACG) was selected using the CRISPR-P program53 and subsequently synthesized, annealed and introduced into an AtU6-sgRNA-AtUBQ-Cas9 vector at the BbsI site. Then, we inserted the reconstructed vectors into the pCAMBIA1301 binary vector at the HindIII and KpnI sites. After confirmation by sequencing, the resulting CCD7 CRISPR/Cas9 vector was transformed into Agrobacterium tumefaciens strain EHA105 and subsequently introduced into tomato seeds (Condine Red) according to a previously described method54. The homozygous line of ccd7 mutants with a 2 bp deletion was identified and used (Fig. S7).
Virus-induced gene silencing (VIGS) experiments were carried out to silence the genes CCD7, CCD8, MAX1, and MAX2 (Solyc12g010900.1.1, with a protein sequence similarity of 57% to the MAX2 protein in Arabidopsis)55. To specifically silence these target genes, 200~500 bp of the 3ʹ UTR was PCR-amplified with the specific primers listed in Table S1 and ligated into pTRV2 at the EcoRI and BamHI sites. After sequencing confirmation, the reconstructed vector was electroporated into A. tumefaciens strain GV3101. The virus infection mediated by Agrobacterium was conducted as previously described56. Empty pTRV2 was also inoculated into tomato plants, which served as a control (pTRV). The plants were placed at 22/19 °C. Approximately 2~3 weeks later, root samples from the target-gene-silenced plants were collected to verify the silencing efficiency of their respective target genes with reverse transcription-quantitative PCR (RT-qPCR).
Growth conditions and treatments
Seeds were germinated at 28 °C for 48 h, and then germinated seeds were grown in a mixture of vermiculite and peat (1:2, v/v). Growth conditions: 12 h photoperiod, 600 μmol m−2 s−1 photosynthetic photon flux density (PPFD), and 22/19 °C (day/night) temperature.
For the dehydration treatment, leaves of the CCD7-, CCD8-, MAX1-, and MAX2-silenced plants were detached and placed on a piece of weighing paper on a laboratory bench and weighed at the indicated time. Finally, the leaf water loss percentage (%) was determined. Stomatal conductance was determined on the fourth expanded leaves using an LI-6400 Portable Photosynthesis System (LI-COR, Lincoln, NE, USA). The PPFD was set at 1000 μmol m−2 s−1. Stomatal conductance was measured between 10:00 a.m. and 12:00 noon on six plants per silenced line or per treatment as reported by Liu et al.30. Both experiments were repeated three times, and each replication had six leaves.
For the strigolactone treatment, at 24 h before heat or cold stress, the roots of 5-week-old tomato plants were treated with GR245DS solution (StrigoLab S.r.l., Torino, Italy). A stock solution of GR245DS at 25 mM was dissolved in pure acetone (≥99.5%, AR, Sinopharm Chemical Reagent Co., Ltd.). After that, GR245DS was diluted to 1, 3, or 9 µM in distilled water for the heat response, in which water solution (distilled water containing an equal amount of acetone as the 1 µM GR245DS solution) served as a control (Fig. S6). For the other GR245DS treatments, a 3 µM concentration was adopted, and distilled water containing an equal amount of acetone was used as a control. A solution of 15 mL was applied to the roots of each plant.
Analysis of heat and cold stress tolerance
For the heat or cold stress, 60~70 uniform 5-week-old plants for each genotype were divided into 6 groups and placed into 6 growth chambers (10~12 per chamber for each genotype) at 22/19 °C for 3 d. After that, the growth temperature was switched to a stable state of 42 °C (heat treatment) for 2 d or 4 °C (cold treatment) for 7 d in 3 growth chambers while another 3 growth chambers were maintained at 22 °C. The plants of each genotype were randomly placed with plants of other genotypes in the growth chambers.
REL in the leaves, which is an important index of cell membrane permeability, was determined as previously described57. The level of leaf lipid peroxidation was examined by determining the accumulation of MDA as described58. The actual quantum efficiency of PSII photochemistry (ФPSII) and the maximum quantum yield of PSII (Fv/Fm) were detected via an IMAGING-PAM chlorophyll fluorometer (IMAG-MAXI; Heinz Walz, Germany) after a 30 min dark acclimation for the whole plants. The fifth leaf from the bottom was collected for assays.
Purification of root extracts and germination bioassays
Root extracts were purified as described previously29,59. The seeds of P. aegyptiaca were obtained from Dr Jinxia Cui (Shihezi University, China). The bioassays of P. aegyptiaca seed germination were conducted according to our earlier study59.
Detection of oxidized proteins and HSP70 protein by western blotting
The total soluble proteins of tomato leaves were determined according to our previous study60 via a BCA Protein Assay Kit (Pierce, USA). Oxidized protein levels in the soluble protein fraction were measured via an OxyBlot protein oxidation detection kit (Chemicon International, USA). The HSP70 protein samples were separated by 10% SDS-PAGE and examined using an anti-HSP70 polyclonal antibody (Beijing Protein Innovation Co., Ltd., China) and a horseradish peroxidase-linked secondary antibody (Cell Signaling Technology, USA). Then, the antigen–antibody signal was observed via a chemiluminescence kit (Perkin Elmer, USA) in accordance with the manufacturer’s protocol.
Measurements of hydrogen peroxide (H2O2) levels
To detect the accumulation of leaf H2O2, 0.3 g fresh tissue was homogenized in 3 mL 1 M HClO4 according to a previously described method61.
Assays of antioxidant enzyme activity
To detect the enzyme activity, 0.3 g leaf tissue was homogenized with 2 mL 50 mM phosphate buffer (pH 7.8) containing 2 mM L-ascorbic acid, 2% (w/v) polyvinylpyrrolidone K30, and 0.2 mM EDTA. After centrifugation at 12,000g for 20 min, supernatants were collected for analysis. The activity of SOD was measured by detecting the capacity to suppress the photochemical reduction of nitroblue tetrazolium (NBT) according to Stewart and Bewley62. The enzyme activity that results in a 50% inhibition of NBT photochemical reduction is defined as one unit. The activities of APX and DHAR were detected by a decrease and an increase at A290 and A265, respectively, and separately, following a previously described method63. The activities of GR and MDAR were both assayed by a decrease at A340 following previous protocols64,65. The units of enzyme (APX, DHAR, GR, and MDAR) activities were calculated according to Noctor et al.66. Spectrophotometric experiments were carried out on a UV-2410PC spectrophotometer (Shimadzu, Japan).
For strigolactone measurements, 0.5 g frozen roots were homogenized with 500 µL 40% acetone/water. The homogenate was centrifuged at 12,000g for 5 min at 4 °C, and then the supernatant was removed. Afterward, the remaining pellet was eluted with 500 µL 50% acetone/water and centrifuged again. The analysis and quantification of strigolactones were performed as described previously29,59.
For ABA measurements, leaves were sampled for quantification at 12 h after exposure to heat or cold stress. Phytohormone extraction from tomato leaves and ABA analysis were conducted following the methods of Wang et al.7. Generally, 0.1 g frozen tomato leaves were extracted with 1 mL ethyl acetate, in which the internal standard D6-ABA (CDN Isotopes Inc., Canada) was added. After centrifugation at 18,000g for 10 min at 4 °C, the resulting pellet was once again extracted with 1 mL ethyl acetate. Supernatants collected twice were merged and evaporated to dryness under N2 gas. The residue was then resuspended in 500 µL 70% methanol (v/v) and centrifuged. Finally, the supernatant was analyzed via a liquid chromatography tandem mass spectrometry system (Varian 320-MS LC/MS, Agilent Technologies, the Netherlands).
RNA isolation and quantitative PCR (qPCR) analysis
Total RNA was isolated from the tomato leaves or roots with an RNA extraction kit (Tiangen, Beijing, China) following the manufacturer’s protocol. Total RNA (1 µg) was reverse transcribed to the cDNA template via a ReverTra Ace qPCR RT Kit (Toyobo, Osaka, Japan). qPCR was conducted using a LightCycler 480 detection machine (Roche, Basel, Switzerland). qPCR procedures: denaturation at 95 °C for 3 min, followed by 45~50 cycles of denaturation at 95 °C for 30 s, annealing at 57 °C for 20 s, and extension at 72 °C for 30 s. The ACTIN gene, which is suitable for heat67 and cold7 responses in tomato, was used as an internal reference. Specific primers are shown in Table S2. The relative expression of genes was analyzed according to the methods of Livak and Schmittgen68.
There were three replicates, and each replicate within a growth chamber consisted of 10~12 plants. For the determination of Fv/Fm and ФPSII, 15 leaves from 10 independent plants were used (n = 15). For other measurements, at least three biological samples were used. Statistical analysis of bioassays was conducted using Statistics Analysis System (SAS) software, version 8 (SAS Institute). The means were analyzed by using Tukey’s test (P < 0.05), except for pairwise comparisons, in which Student’s t-test was adopted (P < 0.05).
Sequence data in this study are available in the Sol Genomics Network (https://solgenomics.net/) according to the following accession numbers: ACTIN (Solyc11g005330), CCD7 (Solyc01g090660), CCD8 (Solyc08g066650), MAX1 (Solyc08g062950), MAX2 (Solyc12g010900), Cu/Zn-SOD (Solyc11g066390), APX (Solyc01g111510), GR (Solyc09g091840), MDAR (Solyc08g081530), DHAR (Solyc05g054760), CBF1 (Solyc03g026280), CBF3 (Solyc03g026270), HSP70 (Solyc04g011440), HSP90 (Solyc12g015880), NCED6 (Solyc05g053530), Le4 (Solyc02g084850), and ABF4 (Solyc11g044560).
Reddy, A. R., Chaitanya, K. V. & Vivekanandan, M. Drought-induced responses of photosynthesis and antioxidant metabolism in higher plants. J. Plant Physiol. 161, 1189–1202 (2004).
Apel, K. & Hirt, H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 55, 373–399 (2004).
Gill, S. S. & Tuteja, N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem. 48, 909–930 (2010).
Mittler, R., Vanderauwera, S., Gollery, M. & Van Breusegem, F. Reactive oxygen gene network of plants. Trends Plant Sci. 9, 490–498 (2004).
Larkindale, J., Hall, J. D., Knight, M. R. & Vierling, E. Heat stress phenotypes of Arabidopsis mutants implicate multiple signaling pathways in the acquisition of thermotolerance. Plant Physiol. 138, 882–897 (2005).
Suzuki, N. & Mittler, R. Reactive oxygen species and temperature stresses: a delicate balance between signaling and destruction. Physiol. Plant. 126, 45–51 (2006).
Wang, F. et al. Phytochrome A and B function antagonistically to regulate cold tolerance via abscisic acid-dependent jasmonate signaling. Plant Physiol. 170, 459–471 (2016).
Chi, C. et al. Brassinosteroids act as a positive regulator of NBR1-dependent selective autophagy in response to chilling stress in tomato. J. Exp. Bot. 71, 1092–1106 (2020).
Boston, R. S., Viitanen, P. V. & Vierling, E. Molecular chaperones and protein folding in plants. Plant Mol. Biol. 32, 191–222 (1996).
Lee, J. H. & Schöffl, F. An Hsp70 antisense gene affects the expression of HSP70/HSC70, the regulation of HSF, and the acquisition of thermotolerance in transgenic Arabidopsis thaliana. Mol. Gen. Genet. 252, 11–19 (1996).
Li, H. et al. Hydrogen peroxide mediates abscisic acid-induced HSP70 accumulation and heat tolerance in grafted cucumber plants. Plant Cell Environ. 37, 2768–2780 (2014).
Gilmour, S. J. et al. Low temperature regulation of the Arabidopsis CBF family of AP2 transcriptional activators as an early step in cold-induced COR gene expression. Plant J. 16, 433–442 (1998).
Lee, S. C. & Luan, S. ABA signal transduction at the crossroad of biotic and abiotic stress responses. Plant Cell Environ. 35, 53–60 (2012).
Jiang, M. Y. & Zhang, J. H. Water stress-induced abscisic acid accumulation triggers the increased generation of reactive oxygen species and up-regulates the activities of antioxidant enzymes in maize leaves. J. Exp. Bot. 53, 2401–2410 (2002).
Knight, H., Zarka, D. G., Okamoto, H., Thomashow, M. F. & Knight, M. R. Abscisic acid induces CBF gene transcription and subsequent induction of cold-regulated genes via the CRT promoter element. Plant Physiol. 135, 1710–1717 (2004).
Nir, I. et al. The tomato DELLA protein PROCERA acts in guard cells to promote stomatal closure. Plant Cell 29, 3186–3197 (2017).
Liu, X. et al. ζ-Carotene isomerase suppresses tillering in rice through the coordinated biosynthesis of strigolactone and abscisic acid. Mol. Plant 13, 1784–1801 (2020).
Vogel, J. T. et al. SlCCD7 controls strigolactone biosynthesis, shoot branching and mycorrhiza-induced apocarotenoid formation in tomato. Plant J. 61, 300–311 (2010).
Kohlen, W. et al. The tomato CAROTENOID CLEAVAGE DIOXYGENASE8 (SlCCD8) regulates rhizosphere signaling, plant architecture and affects reproductive development through strigolactone biosynthesis. New Phytol. 196, 535–547 (2012).
Zhang, Y. et al. Rice cytochrome P450 MAX1 homologs catalyze distinct steps in strigolactone biosynthesis. Nat. Chem. Biol. 10, 1028–1033 (2014).
Yao, R. F. et al. DWARF14 is a non-canonical hormone receptor for strigolactone. Nature 536, 469–473 (2016).
Lv, S. et al. Strigolactone-triggered stomatal closure requires hydrogen peroxide synthesis and nitric oxide production in an abscisic acid-independent manner. New Phytol. 217, 290–304 (2018).
Agusti, J. et al. Strigolactone signaling is required for auxin-dependent stimulation of secondary growth in plants. Proc. Natl Acad. Sci. USA 108, 20242–20247 (2011).
Kapulnik, Y. et al. Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis. Planta 233, 209–216 (2011).
de Jong, M. et al. Auxin and strigolactone signaling are required for modulation of Arabidopsis shoot branching by nitrogen supply. Plant Physiol. 166, 384–395 (2014).
Ha, C. V. et al. Positive regulatory role of strigolactone in plant responses to drought and salt stress. Proc. Natl Acad. Sci. USA 111, 851–856 (2014).
Torres-Vera, R., García, J. M., Pozo, M. J. & López-Ráez, J. A. Do strigolactones contributes to plant defence? Mol. Plant Pathol. 15, 211–216 (2014).
Woo, H. R. et al. ORE9, an F-box protein that regulates leaf senescence in Arabidopsis. Plant Cell 13, 1779–1790 (2001).
López-Ráez, J. A. et al. Tomato strigolactones are derived from carotenoids and their biosynthesis is promoted by phosphate starvation. New Phytol. 178, 863–874 (2008).
Liu, J. et al. Osmotic stress represses strigolactone biosynthesis in Lotus japonicus roots: exploring the interaction between strigolactones and ABA under abiotic stress. Planta 241, 1435–1451 (2015).
Visentin, I. et al. Low levels of strigolactones in roots as a component of the systemic signal of drought stress in tomato. New Phytol. 212, 954–963 (2016).
Visentin, I. et al. A novel strigolactone-miR156 module controls stomatal behaviour during drought recovery. Plant Cell Environ. 43, 1613–1624 (2020).
Xie, X., Yoneyama, K. & Yoneyama, K. The strigolactone story. Annu. Rev. Phytopathol. 48, 93–117 (2010).
Kohlen, W. et al. Strigolactones are transported through the xylem and play a key role in shoot architectural response to phosphate deficiency in nonarbuscular mycorrhizal host Arabidopsis. Plant Physiol. 155, 974–987 (2011).
Cooper, J. W. et al. Strigolactones positively regulate chilling tolerance in pea and in Arabidopsis. Plant Cell Environ. 41, 1298–1310 (2018).
Hu, Q. N., Zhang, S. X. & Huang, B. R. Strigolactones promote leaf elongation in tall fescue through upregulation of cell cycle genes and downregulation of auxin transport genes in tall fescue under different temperature regimes. Int. J. Mol. Sci. 20, 1836 (2019).
Zhu, J. K. Salt and drought stress signal transduction in plants. Annu. Rev. Plant Biol. 53, 247–273 (2002).
Li, W. Q. et al. Comparative functional analyses of DWARF14 and KARRIKIN INSENSITIVE 2 in drought adaptation of Arabidopsis thaliana. Plant J. 103, 111–127 (2020).
Sedaghat, M., Tahmasebi-Sarvestani, Z., Emam, Y. & Mokhtassi-Bidgoli, A. Physiological and antioxidant responses of winter wheat cultivars to strigolactone and salicylic acid in drought. Plant Physiol. Biochem. 119, 59–69 (2017).
Aroca, R. et al. Arbuscular mycorrhizal symbiosis influences strigolactone production under salinity and alleviates salt stress in lettuce plants. J. Plant Physiol. 170, 47–55 (2013).
Ruiz-Lozano, J. M. et al. Arbuscular mycorrhizal symbiosis induces strigolactone biosynthesis under drought and improves drought tolerance in lettuce and tomato. Plant Cell Environ. 39, 441–452 (2016).
Wang, L. et al. Transcriptional regulation of strigolactone signalling in Arabidopsis. Nature 583, 272–281 (2020).
Haider, I. et al. The interaction of strigolactones with abscisic acid during the drought response in rice. J. Exp. Bot. 69, 2403–2414 (2018).
Lechat, M. M. et al. PrCYP707A1, an ABA catabolic gene, is a key component of Phelipanche ramosa seed germination in response to the strigolactone analogue GR24. J. Exp. Bot. 63, 5311–5322 (2012).
Toh, S. et al. Thermoinhibition uncovers a role for strigolactones in Arabidopsis seed germination. Plant Cell Physiol. 53, 107–117 (2012).
Ferrero, M. et al. Exogenous strigolactone interacts with abscisic acid-mediated accumulation of anthocyanins in grapevine berries. J. Exp. Bot. 69, 2391–2401 (2018).
De Cuyper, C. et al. Strigolactones, karrikins and beyond. Plant Cell Environ. 40, 1691–1703 (2017).
Xia, X. J. et al. Reactive oxygen species are involved in brassinosteroid-induced stress tolerance in cucumber. Plant Physiol. 150, 801–814 (2009).
Ma, N. et al. Strigolactones improve plant growth, photosynthesis, and alleviate oxidative stress under salinity in rapeseed (Brassica napus L.) by regulating gene expression. Front. Plant Sci. 8, 1671 (2017).
Mayzlish-Gati, E. et al. Strigolactones are positive regulators of light-harvesting genes in tomato. J. Exp. Bot. 61, 3129–3136 (2010).
Burbidge, A. et al. Characterization of the ABA-deficient tomato mutant notabilis and its relationship with maize Vp14. Plant J. 17, 427–431 (1999).
Pan, C. et al. CRISPR/Cas9-mediated efficient and heritable targeted mutagenesis in tomato plants in the first and later generations. Sci. Rep. 6, 24765 (2016).
Lei, Y. et al. CRISPR-P: a web tool for synthetic single-guide RNA design of CRISPR-system in plants. Mol. Plant 7, 1494–1496 (2014).
Fillatti, J. J., Kiser, J., Rose, R. & Comai, L. Efficient transfer of a glyphosate tolerance gene into tomato using a binary Agrobacterium tumefaciens vector. Nat. Biotechnol. 5, 726–730 (1987).
Challis, R. J., Hepworth, J., Mouchel, C., Waites, R. & Leyser, O. A role for MORE AXILLARY GROWTH1 (MAX1) in evolutionary diversity in strigolactone signaling upstream of MAX2. Plant Physiol. 161, 1885–1902 (2013).
Ekengren, S. K., Liu, Y., Schiff, M., Dinesh-Kumar, S. P. & Martin, G. B. Two MAPK cascades, NPR1, and TGA transcription factors play a role in Pto-mediated disease resistance in tomato. Plant J. 36, 905–917 (2003).
Cao, W. H. et al. Modulation of ethylene responses affects plant salt-stress responses. Plant Physiol. 143, 707–719 (2007).
Ogweno, J. O. et al. Detached leaves of tomato differ in their photosynthetic physiological response to moderate high and low temperature stress. Sci. Hortic. 123, 17–22 (2009).
Xu, X. C. et al. Strigolactones positively regulate defense against root-knot nematodes in tomato. J. Exp. Bot. 70, 1325–1337 (2019).
Zhou, J. et al. NBR1-mediated selective autophagy targets insoluble ubiquitinated protein aggregates in plant stress responses. PLoS Genet. 9, e1003196 (2013).
Willekens, H. et al. Catalase is a sink for H2O2 and is indispensable for stress defence in C3 plants. EMBO J. 16, 4806–4816 (1997).
Stewart, R. R. C. & Bewley, J. D. Lipid peroxidation associated with accelerated aging of soybean axes. Plant Physiol. 65, 245–248 (1980).
Nakano, Y. & Asada, K. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol. 22, 867–880 (1981).
Foyer, C. H. & Halliwell, B. The presence of glutathione and glutathione reductase in chloroplasts: a proposed role in ascorbic acid metabolism. Planta 133, 21–25 (1976).
Hossain, M. A., Nakano, Y. & Asada, K. Monodehydroascorbate reductase in spinach chloroplasts and its participation in regeneration of ascorbate for scavenging hydrogen peroxide. Plant Cell Physiol. 25, 385–395 (1984).
Noctor, G., Mhamdi, A. & Foyer, C. H. Oxidative stress and antioxidative systems: recipes for successful data collection and interpretation. Plant Cell Environ. 39, 1140–1160 (2016).
Yin, Y. L. et al. BZR1 transcription factor regulates heat stress tolerance through FERONIA receptor-like kinase-mediated reactive oxygen species signaling in tomato. Plant Cell Physiol. 59, 2239–2254 (2018).
Livak, K. J. & Schmittgen, T. D. Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCt Method. Methods 25, 402–408 (2001).
This work was supported by the National Key Research and Development Program of China (2018YFD1000800) and the State Key Program of National Natural Science Foundation of China (31430076). We are grateful to the Tomato Genetics Resource Center at the University of California, Davis, for supplying mutants. We also thank Dr Jinxia Cui (Shihezi University, Xinjiang, China) for providing P. aegyptiaca seeds.
Conflict of interest
The authors declare no competing interests.
About this article
Cite this article
Chi, C., Xu, X., Wang, M. et al. Strigolactones positively regulate abscisic acid-dependent heat and cold tolerance in tomato. Hortic Res 8, 237 (2021). https://doi.org/10.1038/s41438-021-00668-y