TOR-SnRK1 são modulados por uma sinalização upstream para regular o crescimento e o desenvolvimento in vitro do porta-enxerto de ameixeira ‘Myrobalan 29C’

rbf Revista Brasileira de Fruticultura Rev. Bras. Frutic. 0100-2945 1806-9967 Sociedade Brasileira de Fruticultura Resumo O objetivo deste estudo foi: (i) compreender como a sinalização upstream modula o nexo TOR-SnRK1; e (ii) estabelecer uma interação entre o nexo SnRK1-TOR, disponibilidade de açúcar, atividades de enzimas sucrolíticas, nível de expressão de genes-chave relacionados à sinalização e metabolismo de açúcar, incluindo trealose, em porta-enxertos de ameixeira ‘Myrobalan 29C’ (Prunus cerasifera) cultivados in vitro. Explantes foram cultivados em meio Murashigue e Skoog (MS) com trealose (0; 1,0 e 10 mM). Aos 3 dias, o papel antagônico de PcSnRK1 e PcTOR foi confirmado em plantas tratadas com trealose 10mM, possivelmente indicando que ‘Myrobalan 29C’ não estava em uma condição de estresse. Além disso, foi observada uma regulação positiva do gene PcTREA, que pode levar ao acúmulo de glicose, que por sua vez é um precursor da síntese de sorbitol. Em relação aos parâmetros de crescimento avaliados após 21 dias de cultivo in vitro, o maior número de brotações e de comprimento do explante foi observado em resposta a trealose 10mM. Tais respostas positivas podem ser devido ao aumento do teor de glicose e UDPGlc, produtos diretos da enzima sacarose sintase (SuSy). Consistente com este resultado, a maior disponibilidade dessas moléculas pode ser o sinal upstream para ativação de TOR. Interessantemente, nesta mesma condição, foi observado um acúmulo de sacarose, o que também pode ter contribuído para o aumento da expressão do gene PcTOR e para a melhora nos parâmetros de crescimento. Introduction Sugars regulate many aspects of plant growth and development. In this sense, the trehalose (non-reducing disaccharide) is used as an energy source, as storage and transport molecule for glucose, and despite of the physiological effects it is found in very low amounts in plants, pointing to a role in the signaling process (TSAI et al. 2016). Trehalose is synthesized from UDP-glucose and glucose-6-phosphate by trehalose-phosphate synthase (TPS) and then dephosphorylated by trehalose-phosphate phosphatase (TPP) and can be hydrolysed to glucose by trehalase (TREA) (CABIB; LELOIR,1958). Some studies have shown the role of the precursor of trehalose, trehalose-6-phosphate (T6P), as an important signaling molecule (FIGUEROA et al. 2018) that regulates growth and development, however, the regulation mechanism is unknown. Recent studies have shown that T6P inhibits the activity of the Sucrose non-fermenting-1 (SNF1)- relatedkinase 1 (BAENA-GONZALEZ et al. 2017, 2020; WINGLER; HENRIQUES, 2022). According to Fichtner et al. (2021) SnRK1 and Target of Rapamycin (TOR) are conserved protein kinases that act as sensors of energy availability in order to maintain energy homeostasis. The TOR is activated in favorable conditions, while SnRK1 under nutrient and energy starvation (TOMÉ et al. 2014; MARGALHA et al. 2019). The TOR-SnRK1 nexus has emerged as crucial in regulating the perception and responses to energy/sugar levels in the cells/tissues (RODRIGUEZ et al. 2019) and to adjust plants to the environments (BAENA-GONZALEZ; HANSON, 2017). Although it is widely accepted that both kinases (SnRK1 and TOR) exert control on growth and stress responses (MARGALHA et al. 2019; WINGLER; HENRIQUES, 2022), an overview of regulatory networks on its activation mechanisms is still missing. In a sense, the in vitro plant culture, through the possibility of manipulating the culture medium, may help to define the physiological, biochemical and molecular roles of trehalose and the complexity of this regulation exerts on putative targets, such as SnRK1 and TOR. In contrast with the advances made in discovering functions of TOR-SnRK1 nexus, the upstream signals of TOR-SnRK1 remain widely unknown (SONG et al. 2021), as well as the role of trehalose as a mediating molecule of perception and signaling in plants. To fill this gap, the aim of this study was: (i) understand how upstream signaling modulated TOR-SnRK1 nexus; and (ii) establish an interplay between SnRK1-TOR, trehalose metabolism, enzyme activity and their associated sugar content in in vitro-grown ‘Myrobalan 29C’plum rootstock (Prunus cerasifera). Material and methods As a plant material ‘Myrobalan 29C (Prunus cerasifera) rootstock were used. This rootstock is mainly used for Japanese Plum and Prune, and it was selected in California from an open-pollinated seedling of P. cerasifera. It has as main characteristics the resistance to root-knot nematode (Meloidogyne spp.), grow vigorously and makes large tree with low suckers and good anchorage, promoting good yields and fruit quality (OKYE et al. 1987). Explants (2.0 cm long) were cultivated in flasks containing MS (MURASHIGUE; SKOOG, 1962) medium and different trehalose concentrations (0, 1 and 10 mM) supplemented with BAP 0.4 mg L-1, IBA 0.05 mg L-1 and GA3 0.3 mg L-1 of, 7 g L-1 agar and pH 5.2. In vitro cultures were incubated in a growth room (25 ± 2°C) with a photosynthetic photon flux density of 48 μmol photon m−2 s−1 and 16 h light/8 h dark. After 3 and 21 days, leaves were collected for biochemical and molecular analysis. The number and lenght of shoots and leaves were assessed in a non-destructive way. For gene expression analysis, total RNA was obtained by the Lithium Chloride method modified by Chang et al. (1993). Total RNA was isolated, quantified and checked quality and integrity. Two micrograms of total RNA were used to obtain cDNA with a final volume of 20 μL. Primers were designed based on coding sequences of Prunus persica deposited in the Genome Database for Rosaceae (https://www.rosaceae.org/), using the Primer Designing tool, from the NCBI database, and in detail described in Table 1. The reference gene Elongation factor 1-α (EF 1-α) was applied for data normalization, according to previous studies. The gene expression results were presented as a heatmap (Figure 1). The relative quantification (RQ) was calculated with the 2-△△Ct method (LIVAK; SCHMITTGEN, 2001). Three technical repetitions were performed for each biological replicate, including samples for the control treatment as template-free controls. Table 1 Primer sequences to RT-qPCR analysis of the genes assayed in plum rootstocks ‘Myrobalan 29C’. GENE Putative name Primer foward (5'-3') Primer reverse (5'-3') Reference Tm CINV1 Alkaline/neutral invertase1 TGAATGGTGAGCCTGAGA GGATAGGGTCGTGAAGAA ZHANG et al. (2013) 82.0 CINV2 Alkaline/neutral invertase2 TATGATTGATAGACGGATGG CTAAGTCGGTTATTGATTGC ZHANG et al. (2013) 80.5 Susy Sucrose synthase ATTGGAAATGGCGTTGAGT TTGCCCTTGTAGCAGTGAA ZHANG et al. (2013) 82.5 CWINV Cell wall acid invertase GTCACAGCAGCACAGGCAG CCAATACGAGTAACCCGAAT ZHANG et al. (2013) 81.0 HXK Hexokinase 1 AGATGTGGTGGGAGAGCTGA GTGCCCAATATCACAGCAGC - 80.5 SPS Sucrose phosphate synthase CATACCCCAAACACCACAA TATCAACAGGACCCCC ZHANG et al. (2013) 80.0 S6PDH Sorbitol-6-phosphate dehydrogenase ACATGGCACGACATGGAAAAGAC AATTGGCTCACTTGAGGCTTGAT JIMENEZ et al. (2013) 80.5 SDH Sorbitol dehydrogenase CGAAGTTGGTAGCTTGGTGAAGA CTTGCACTGCTCACATCTCCA JIMENEZ et al. (2013) 83.5 TPP trehalose phosphate phosphatase GTCGAGCACCCTTCTGCATT TTGGTGAAAGGGTCCCATCG - 79.5 TPS trehalose phosphate synthase AGAACACCGCGGTCTCATTT ATTGGGCCTGTCCACAGATG - 79.0 TREA trehalase CAACAAAAGCCTCGTCAGCC TTTTCCAAAAGTGGCGAGCG - 83.0 SnRK1 Sucrose non-fermenting 1-related kinase1 GCTCTAGAATGGATGGATCGGTTG GCGTCGACTTAAAGGACCCG - 79.0 TOR Target of Rapamycin TGGAAGAAGAAGCCCGTGAC TTCTCCGCAACATCACTGCT - 80.5 EF-1α Elongantion factor 1-alpha AATTGCCTTTGTTCCCATCTCTG TGGGCTCCTTCTAATCTCCTTA XU et al. (2008) 84 Figure 1 Heatmap showing the expression levels of genes involved in sugar signaling and carbohydrate metabolism in 'Myrobalan 29-C' plum rootstocks cultured in vitro with different concentrations of trehalose (0, 1, and 10mM) for 3 and 21 days. The color scale refers to Log2FC. The red scale refers to up-regulated genes and the blue scale refers to down-regulated genes. For quantification of starch, the method used was described by Graham and Smydzuk (1965), while that for sucrose was proposed by Handel (1968), with some modifications. Absorbance readings for Starch and Sucrose were determined at 620nm using a Ultrospec® 7000/7000PC UV–Visible spectrophotometer. Besides, for the quantification of starch, the values obtained for soluble sugar total were corrected by factor 0.9, according to McCready et al. (1950). Additionally, sucrolytic enzymes activities were measured. For that, leaves samples from the explants (about 0.4 g) were ground until a fine powder. The extraction of the neutral/alkaline invertase (CINV) and the acid invertase enzymes (CWINV and VINV) followed the methodology described by Zeng et al. (1999), with minor modifications. The supernatant solution was collected to measure soluble invertase activity (VINV and CINV) and the precipitate was collected to measure insoluble invertase (CWINV). The aliquots were collected after 10 and 40 min to determine enzymatic activity. Enzymatic activity was evaluated by quantifying reducing sugars produced according to the dinitrosalicylic acid (DNS) method, previously described by Miller (1959). Sucrose Synthase (Susy) and Sucrose Phosphate Synthase (SPS) activity were determined according to Lowell et al. (1989), with some modifications. The protein content was determined using Bradford’s (1976) method. Half of the extracts were boiled for 10 min, and the other half were incubated for 1 h at 37°C and then boiled for 10 min. The sucrose formed was measured with the anthrone method (GRAHAM AND SMYDZUK 1965). All enzyme activities were determined in triplicate and expressed in micromoles of glucose per gram of fresh weight per min (μmol glucose g−1 FW min−1), except to SPS that was expressed in micromoles of sucrose per gram of fresh weight per hour (μmol sucrose g−1 FW h−1). The experiment was repeated three times and was set up in a completely randomized factorial design with three treatments (trehalose concentrations) and each treatment was constituted by five flasks with four explant per flask. Results correspond to mean ± standard deviation. For statistical analysis, ANOVA and Tukey Test at the 5% probability level (P < 0.05) were performed to calculate for significant differences among treatments using the Sisvar 5.0 software (FERREIRA, 2011). Results and discussion In spite of the multiple roles that have been proposed to trehalose, such as compatible solutes, stress protecting and regulation of plant growth and development (ALMEIDA et al. 2007; LLORENTE et al. 2007), limited information are available about the effects that exogenous trehalose induce on morphology, sugar metabolism and signalling in woody fruit trees (in vitro and ex vitro conditions). Furthermore, it is extremely necessary to optimize the amount of trehalose required to development of in vitro plants. Previous studies showed that trehalose allows the plants to tolerate adverse in vitro conditions (LLORENTE et al. 2007). Thus, the aim of this study was to explore the exogenous Trehalose: as a source energy, carbon storage and sugar signal in ‘Myrobalan 29C’ after 3 and days 21 of in vitro culture. The regulation of trehalose biosynthetic genes in response to trehalose-treated in ‘Myrobalan 29C’ was studied. The highest exogenous trehalose (10mM) provided up-regulation of the PcTPP (2.14±0.05) and PcTREA genes (2.14± 0.04) after 3 days in vitro culture, on the other hand, PcTPS (0.55±0.08) and PcSnRK1 (0.18±0.07) were down-regulated (Figure 1). Trehalose-6- phosphate (T6P) and SnRK1 inhibits Susy and SPS activity (FEDOSEJEVS et al. 2018; WANG et al. 2022). In our experiment, PcTPS and PcSnRK1 were down-regulated, possibly contributing to regulation of PcSusy and PcSPS genes. Extensive studies have demonstrated that sugar signals can be translated by protein kinases, such SnRK1 and TOR (SONG et al. 2021, WINGLER; HENRIQUES, 2022). In this study, the expression patterns of PcSnRK1 and PcTOR genes were down- and up-regulated in trehalose 10mM, supporting their globally antagonistic roles (MARGALHA et al. 2019; FICHTNER et al. 2021). SnRK1 is activated in response to energy decline; conversely, TOR is activated and promotes growth and biosynthetic processes in high-energy availability (Figure 3) (BAENA-GONZALEZ; HANSON, 2017; WINGLER; HENRIQUES, 2022). Figure 3 Regulatory loop showing interplay between trehalose metabolism in different organelles and SnRK1-TOR nexus in 'Myrobalan 29-C' plum rootstocks cultured in vitro with trehalose 10mM for 3 days. Enzymatic flow is depicted as arrows from substrates to products. Enzymes catalyzing each step are shown into each arrow. Upward arrows in black indicated up-regulation, whereas those red downward arrows represent down-regulation. Taking into account the earlier studies and the results of our experiment, it is possible to infer that in this condition ‘Myrobalan 29C’ was not in a stress condition (by sugar supply), especially because it was in the culture medium for 3 days and with the supplementation of 10mM of trehalose. Although this study focused more on the effect of the trehalose on the signaling process, it is impossible to rule out its role as a stress-protective molecule since it is also considered a compatible solute (KOSAR et al. 2019). The increased expression of PcTREA gene (trehalose degradation) observed in this study can lead to glucose accumulation and signaling to activate PcTOR, that in its turn had the expression increased 3-fold in this condition. Besides, this accumulation of glucose, can be used as precursor for sorbitol synthesis. In the Rosaceae family, sorbitol represents the main form of carbon transported from source to sink tissues (YANG et al. 2018). Sorbitol-synthesizing species raises an interesting question as to how the trehalose interact with sugar signalling and metabolism in woody fruit trees, since the available information is mostly in Arabidopsis and cereal crops. Genes encoding the key enzymes of sorbitol synthesis (S6PDH) and degradation (SDH) were measured. Our results showed an up-regulation of PcS6PDH (4.07±0.40) and PcSDH (2.78±0.06) genes in response to trehalose 10mM. This revealed that exogenous trehalose influences on sorbitol metabolism, however, further studies are needed to better unravel its effects. Zhang et al. (2017) suggested that Tre6P is more closely related to sorbitol than other soluble sugars. A more recent study showed that SnRK1 is involved in sorbitol metabolism in peach fruits, in which the SnRK1 activated SDH (sorbitol dehydrogenase), and it also regulated the activities of SuSy (sucrose synthase) and SPS (sucrose phosphate synthase), enhancing sucrose accumulation (YU et al. 2021). Regarding to glycolytic enzymes, PcHXK gene expression was stable. Based on that, glucose and fructose can be accumulated in cytoplasm or can also be stored in the vacuoles, rather than converted to hexose-phosphate (G6P and F6P) for ATP production via glycolysis. This suggestion is further supported by up-regulation of the PcTREA, sucrose hydrolytic enzymes (PcCINV1, PcCINV2 and PcCWINV), and PcSusy (cleavage) that were up-regulated in response to trehalose 10mM. On the oth- er hand, it is not supported by their activity (Figure 2A-C). Figure 2 Activity determination of sucrose synthesis and degradation enzymes in 'Myrobalan 29-C' plum rootstocks cultured in vitro with different concentrations of trehalose (0, 1 and 10mM) for 3 and 21 days. (A) neutral/alkaline invertase (NINV), (B) cell wall acid invertase (CWINV), (C) Vacuolar acid invertase (AINV), (D) sucrose synthase (Susy) and (E) sucrose phosphate synthase (SPS). Error bars represent the standard deviation (n=3). Columns with different uppercase letters indicate differences between times (3 and 21 days) for the same concentration, while different lowercase letters indicate differences between concentrations for the same time. Significant differences based on ANOVA followed by Tukey test P=0.05. T6P (intermediate of trehalose biosynthesis) plays a key control between low carbon and high carbon signaling in the form of sucrose (GRIFFITHS et al. 2016; ZHANG et al. 2017). Overall, the T6P accumulation occurs in response to high sucrose content (SCHLUEPMANN et al. 2011). In our study no differences were observed between treatments for sucrose content after 3 days of the in vitro culture, suggesting that the levels observed were not sufficient to provide an up-regulation of PcTPS gene (synthesis enzyme of T6P). Starch metabolism is one of the most striking examples of regulation by trehalose (PAUL et al. 2008). In this sense, trehalose has been shown to regulate starch breakdown in plastids (PONNU et al. 2011) and T6P seems to activate the ADP-Glc pyrophosphorylase (AGPase) enzyme (thioredoxin- dependent redox mechanism), in response to high sucrose (SCHLUEPMANN et al. 2011). Interestingly, our results show a decrease and stability in starch and sucrose content, respectively (Table 2) which may be related to low T6P levels and with PcTPP up-regulation (see chloroplast in Figure 3). Table 2 Sugar content in in 'Myrobalan 29-C' plum rootstocks cultured in vitro with different concentrations of trehalose (0. 1 and 10mM) for 3 and 21 days. Trehalose (mM) Soluble Sugar total *Sucrose Starch 3 days 21 days 3 days 21 days 3 days 21 days 0 50.44ns 47.98ns 0.20±0.04Aa 0.21±0.00Ab 9.48±0.15Aa 0.49±0.14Bb 1 0.16±0.01Aa 0.12±0.01Ab 2.78±0.08Bb 6.05±0.09Aa 10 0.22±0.03Ba 1.20±0.14Aa 2.70±0.29Bb 5.55±0.14Aa CV% 23.31 22.91 24.90 * *mg/g-1 MF Columns with different capital letters indicate differences between times (3 and 21 dys) for the same concentration, while different lowercase letters indicate differences between concentrations for the same time. Significant differences were based on ANOVA, followed by the Tukey test at P = 0.05. Regarding the growth parameters, the greatest number of shoots and explant length was observed at 10mM trehalose (Table 3). Table 3 Growth parameters evaluated in 'Myrobalan 29-C' 'Myrobalan 29-C' plum rootstocks cultured in vitro with different trehalose concentrations (0, 1 and 10mM) for 21 days. Trehalose (mM) *Shoot number *Leaf number *Leaf lenght (cm) *Explant lenght (cm) 0 2.778±0.064 b 27.333ns 1.446ns 2.294±0.047 b 1 3.333±0.112 ab 2.289±0.053 b 10 4.334±0.192 a 2.644±0.017 a VC% 11.51 2.99 8.48 5.22 1 Different lowercase letters in the column represent differences between concentrations. Significant differences based on ANOVA followed by Tukey test P=0.05. * per explant Similar results were found to Llorent et al. (2007) in Simmondsia chinensis where trehalose promoted the shoot growth. This improved in plant growth in response to trehalose may be due to increase in Glucose and UDP-Glc content, direct products of SuSy enzyme. In our study showed PcSusy gene was up-regulated about 12-fold (12.69±0.38) when compared to the control plants to same condition (Figure 1). However, an increase in Susy activity was not observed (Figure 2D). The sucrose content was about 6-fold higher than that observed in the control plants (Table 2), in response to 10mM trehalose, what may have contributed to the up-regulation of PcTOR gene (Figure 1). TOR which in turn positively regulates the growth and development in response to high sugar availability (RODRIGUEZ et al. 2019). The causal relationship between high sucrose content, PcTOR gene upregulated, and ameliorates in growth parameters supported this statement (Figure 3). Besides, Glc and sucrose are activators of TOR signaling (LI et al. 2017) and responsible for development of shoot apical (SONG et al. 2021). In a physiological context, Glc-TOR signaling activates Brasinosteroids (plant hormone) pathway by phosphorylates BIN2, a negative regulator of Brasinosteroids (BR), thus promoting growth (ZHANG et al. 2016). Overall, the highest availability of sucrose and glucose may be the upstream signal for TOR-activation (hexose-signal) and an indirect repressor of SnRK1 (Figure 4). Thus, our data also are consistent with the hypothesis that SnRK1 is not activated and therefore it is not blocking the in vitro growth and development of shoots of ‘Myrobalan 29C’ (Figure 3). Figure 4 Overview of regulatory networks to low and high carbon (signaling pathways) and trehalose metabolism in ‘Myrobalan 29C’. SnRK1 activity is found to be inhibited by diverse sugar phosphates, including trehalose-6-phosphate (T6P). In addition, T6P inhibits Susy and SPS activity. TOR-SnRK1 nexus signals to permissive or restrictive growth decisions. Trehalose synthesis involves a twostep, catalysed by trehalose-6-phosphate synthase (TPS) and trehalose 6-phosphate phosphatase (TPP) and degraded by trehalase (TREA) (In blue). The increase in sucrose content observed in this study is accompanied to increase in PcSPS gene expression and activity, and additionally of the up-regulation of the PcSusy gene (about 12-fold). The products of sucrose cleavage by SuSy are available for many metabolic pathways, in case, UDP-Glc and ADP-Glc to trehalose and starch synthesis, respectively. Although UDP-Glc be the main nucleotide phosphate, ADP-Glc also is product of Susy (BAROJA-FERNANDEZ et al. 2012). Some evidence suggesting that Susy is involved in starch synthesis pathway, and Stein and Granot et al. (2019) proposed a model in which starch accumulation is determined by SuSy activity. Based on this, we suggested that the increasing in starch content observed in this condition is related with sucrose cleavage by Susy that yields ADP-Glc. Overall, our results implied that Susy was acting as a cleavage enzyme and sucrose synthesis occurring by SPS pathway. In recent studies, Wang et al. (2022) pointed that accumulated sucrose in peach trehalose- treated is associated with the decrease in expression of PpSnRK1 and increases in the expression and activity of the SPS (Figure 1 and 2E). This is in agreement with the findings of this study. Regarding the expression of trehalose biosynthetic genes, it was possible to observe in response to 10mM trehalose, the PcTPP (0.28 ± 0.03) and PcTREA (0.35 ± 0.04) genes were down-regulated, on the other hand, PcTPS and PcSnRK1 genes showed stability in their expression (Figure 1). According to Schluepmann et al. (2011) and Griffiths et al. (2016) T6P functions as an inhibitor of the kinase SnRK1. However, the molecular mechanisms thereof remain unknown (PEIXOTO; BAENA-GONZÁLEZ, 2022; ONWE et al. 2022). Our results therefore suggest that the lack of T6P caused by the stable expression of the synthesis gene (PcTPS) observed in this study did not provide the inhibition of PcSnRK1 in ‘Myrobalan 29C’. Besides, SnRK1 up-regulated is related with low-energy responses (TOMÉ et al. 2014; BAENA-GONZALEZ; LUNN, 2020). Interestingly, no harmful effects were observed in the explants growth in this condition (Table 3), supporting the hypothesis that the explants are in optimal growth conditions and promoting processes for carbon utilization and anabolism. Overall, T6P/SnRK1 are essential on regulation plant growth and development as proposed by GRIFFITHS et al. (2016). Taking all the results obtained in the present study, we suggest that trehalose not only interacts with the sucrose, but also with sorbitol and starch metabolism. Furthermore, we postulate for the first time the mechanism that SnRK1-TOR nexus uses to modulate together with trehalose the growth of sorbitol- synthesizing species. Future studies will be needed to evaluate the role of trehalose and of the regulators of energy homeostasis, SnRK1-TOR in plants under stress conditions (heat temperature, drought, flooding and salinity), since it is accepted in the literature that SnRK1-TOR mechanism operates differently in these conditions (MARGALHA et al. 2019; RODRIGUEZ et al. 2019). Conclusion The glucose is an upstream signal to SnRK1- TOR in order to maintain in vitro growth and development of ‘Myrobalan 29C’ plum rootstock in response to exogenous application of trehalose. Besides, the sorbitol metabolism was modulated by exogenous trehalose. The regulatory loop, which involves trehalose and starch metabolism in different organelles and the SnRK1-TOR nexus has been proposed. Exogenously applied trehalose do not cause harmful effects in growth and developmental of ‘Myrobalan 29C’ plum rootstock. Remarkably this may be due to finely tuned of SnRK1-TOR. Acknowledgements The authors gratefully acknowledge the CNPq (Conselho Nacional de Desenvolvimento Cientifíco e Tecnológico) for their financial support and research fellowship VJB, as well as the FAPERGS (Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul). This study was financed in part by CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior—Brasil—Finance Code 001. ALMEIDA, A.M.; CARDOSO, L.A.; SANTOS, D.M.; TORNÉ, J.M.; FEVEREIRO, P.S. Trehalose and its applications in plant biotechnology. In Vitro Cellular e Developmental Biology – Plant, Wallingford, v.43, p.167-77, 2007. ALMEIDA A.M. CARDOSO L.A. SANTOS D.M. Trehalose and its applications in plant biotechnology. In Vitro Cellular e Developmental Biology – Plant Wallingford 43 2007 167 77 BAENA-GONZALEZ, E.; HANSON, J. Shaping plant development through the SnRK1–TOR metabolic regulators. Current Opinion in Plant Biology, Oxford, v.35, p.152-7, 2017. BAENA-GONZALEZ E. HANSON J. 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