Sugar signaling is one of the most critical regulatory signals in plants, and its metabolic network contains multiple regulatory factors. Sugar signal molecules regulate cellular activities and organism development by combining with other intrinsic regulatory factors and environmental inputs. HXK, SnRK1, and TOR are three fundamental proteins that have a pivotal role in the metabolism of sugars in plants. HXK, being the initial glucose sensor discovered in plants, is renowned for its multifaceted characteristics. Recent investigations have unveiled that HXK additionally assumes a significant role in plant hormonal signaling and abiotic stress. SnRK1 serves as a vital regulator of growth under energy-depleted circumstances, whereas TOR, a large protein, acts as a central integrator of signaling pathways that govern cell metabolism, organ development, and transcriptome reprogramming in response to diverse stimuli. Together, these two proteins work to sense upstream signals and modulate downstream signals to regulate cell growth and proliferation. In recent years, there has been an increasing amount of research on these three proteins, particularly on TOR and SnRK1. Furthermore, studies have found that these three proteins not only regulate sugar signaling but also exhibit certain signal crosstalk in regulating plant growth and development. This review provides a comprehensive overview and summary of the basic functions and regulatory networks of these three proteins. It aims to serve as a reference for further exploration of the interactions between these three proteins and their involvement in co-regulatory networks.
Author contributions
Y.Z. wrote and approved the manuscript. GS.L. contributed to the revision of this review.
Data availability
Not applicable.
Conflict of interest
The authors declare no conflicts of interest.
| [1] |
Li L, Liu KH, Sheen J. Dynamic nutrient signaling networks in plants. Annu Rev Cell Dev Biol. 2021; 37 :341-67
|
| [2] |
Choudhary A, Kumar A, Kaur N. et al. Molecular cues of sugar signaling in plants. Physiol Plant. 2022; 174 :e13630
|
| [3] |
Aguilera-Alvarado GP, Sanchez-Nieto S. Plant hexokinases are multifaceted proteins. Plant Cell Physiol. 2017; 58 :1151-60
|
| [4] |
Kim HB, Cho JI, Ryoo N. et al. Role of rice cytosolic hexokinase OsHXK7 in sugar signaling and metabolism. J Integr Plant Biol. 2016; 58 :127-35
|
| [5] |
Zhao B, Qi K, Yi X. et al. Identification of hexokinase family members in pear ( Pyrus × bretschneideri ) and functional exploration of PbHXK1 in modulating sugar content and plant growth. Gene. 2019; 711 :143932
|
| [6] |
Moore B, Zhou L, Rolland F. et al. Role of the Arabidopsis glucose sensor HXK 1 in nutrient, light, and hormonal signaling. Science. 2003; 300 :332-6
|
| [7] |
Granot D, David-Schwartz R, Kelly G. Hexose kinases and their role in sugar-sensing and plant development. Front Plant Sci. 2013; 4 :44
|
| [8] |
Granot D, Kelly G, Stein O. et al. Substantial roles of hexokinase and fructokinase in the effects of sugars on plant physiology and development. J Exp Bot. 2014; 65 :809-19
|
| [9] |
Li L, Sheen J. Dynamic and diverse sugar signaling. Curr Opin Plant Biol. 2016; 33 :116-25
|
| [10] |
Li M, Feng F, Cheng L. Expression patterns of genes involved in sugar metabolism and accumulation during apple fruit development. PLoS One. 2012; 7 :e33055
|
| [11] |
Zhang C, Zhang H, Zhan Z. et al. Transcriptome analysis of sucrose metabolism during bulb swelling and development in onion ( Allium cepa L.). Front Plant Sci. 2016; 7 :1425
|
| [12] |
Ruan YL. Sucrose metabolism: gateway to diverse carbon use and sugar signaling. Annu Rev Plant Biol. 2014; 65 :33-67
|
| [13] |
Baena-Gonzalez E, Lunn JE. SnRK1 and trehalose 6-phosphate - two ancient pathways converge to regulate plant metabolism and growth. Curr Opin Plant Biol. 2020; 55 :52-9
|
| [14] |
Zhang Y, Primavesi LF, Jhurreea D. et al. Inhibition of SNF1-related protein kinase1 activity and regulation of metabolic pathways by trehalose-6-phosphate. Plant Physiol. 2009; 149 :1860-71
|
| [15] |
Xiong Y, McCormack M, Li L. et al. Glucose-TOR signalling reprograms the transcriptome and activates meristems. Nature. 2013; 496 :181-6
|
| [16] |
Hu DG, Sun CH, Zhang QY. et al. Glucose sensor MdHXK1 phosphorylates and stabilizes MdbHLH3 to promote anthocyanin biosynthesis in apple. PLoS Genet. 2016; 12 :e1006273
|
| [17] |
Belda-Palazon B, Adamo M, Valerio C. et al. A dual function of SnRK2 kinases in the regulation of SnRK1 and plant growth. Nat Plants. 2020; 6 :1345-53
|
| [18] |
Guo D, Liu P, Liu Q. et al. Legume-specific SnRK1 promotes malate supply to bacteroids for symbiotic nitrogen fixation. Mol Plant. 2023; 16 :1396-412
|
| [19] |
Stitz M, Kuster D, Reinert M. et al. TOR acts as a metabolic gatekeeper for auxin-dependent lateral root initiation in Arabidopsis thaliana. EMBO J. 2023; 42 :e111273
|
| [20] |
Fu L, Liu Y, Qin G. et al. The TOR-EIN2 axis mediates nuclear signalling to modulate plant growth. Nature. 2021; 591 :288-92
|
| [21] |
Çakir B. Identification and structure of six members of the hexokinase gene family in Vitis vinifera : cloning, expression, and functional analysis of a putative chloroplast stromal-type hexokinase. J Hortic Sci Biotechnol. 2014; 89 :663-73
|
| [22] |
Hayes MA, Davies C, Dry IB. Isolation, functional characterization, and expression analysis of grapevine (Vitis vinifera L.) hexose transporters: differential roles in sink and source tissues. J Exp Bot. 2007; 58 :1985-97
|
| [23] |
Rodriguez-Saavedra C, Morgado-Martínez LE, Burgos-Palacios A. et al. Moonlighting proteins: the case of the hexokinases. Front Mol Biosci. 2021; 8 :701975
|
| [24] |
Chen S, Tian Z, Guo Y. Characterization of hexokinase gene family members in Glycine max and functional analysis of GmHXK 2 under salt stress. Front Genet. 2023; 14 :1135290
|
| [25] |
Wu R, Lin X, He J. et al. Hexokinase 1: a glucose sensor involved in drought stress response and sugar metabolism depending on its kinase activity in strawberry. Front Plant Sci. 2023; 14 :1069830
|
| [26] |
Jaillon O, Aury JM, Noel B. et al. The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla. Nature. 2007; 449 :463-7
|
| [27] |
Xu WJ, Wei Y, Wang X. et al. Molecular cloning and expression analysis of hexokinase genes in peach fruit under postharvest disease stress. Postharvest Biol Technol. 2021; 172 :111377
|
| [28] |
Sarowar S, Lee JY, Ahn ER. et al. A role of hexokinases in plant resistance to oxidative stress and pathogen infection. J Plant Biol. 2008; 51 :341-6
|
| [29] |
Wang J, Wang X, Geng S. et al. Genome-wide identification of hexokinase gene family in Brassica napus : structure, phylogenetic analysis, expression, and functional characterization. Planta. 2018; 248 :171-82
|
| [30] |
Han P, Wei Y, Jiang S. et al. N-Acetyl-d-glucosamine inhibition of hexokinase results in downregulation of the phenylpropanoid metabolic pathway and decreased resistance to brown rot in peach fruit. J Agric Food Chem. 2022; 70 :3917-28
|
| [31] |
Shen C, Zhang Y, Li Q. et al. PdGNC confers drought tolerance by mediating stomatal closure resulting from NO and H2O2 production via the direct regulation of PdHXK 1 expression in Populus. New Phytol. 2021; 230 :1868-82
|
| [32] |
Jiao F, Chen Y, Zhang D. et al. Genome-wide characterization of soybean hexokinase genes reveals a positive role of GmHXK 15 in alkali stress response. Plants (Basel). 2023; 12 :3121
|
| [33] |
Perez-Diaz J, Batista-Silva W, Almada R. et al. Prunus hexokinase 3 genes alter primary C-metabolism and promote drought and salt stress tolerance in Arabidopsis transgenic plants. Sci Rep. 2021; 11 :7098
|
| [34] |
Wang H, Xin H, Guo J. et al. Genome-wide screening of hexokinase gene family and functional elucidation of HXK 2 response to cold stress in Jatropha curcas. Mol Biol Rep. 2019; 46 :1649-60
|
| [35] |
Jamsheer KM, Jindal S, Laxmi A. Evolution of TOR-SnRK dynamics in green plants and its integration with phytohormone signaling networks. J Exp Bot. 2019; 70 :2239-59
|
| [36] |
Broeckx T, Hulsmans S, Rolland F. The plant energy sensor: evolutionary conservation and divergence of SnRK 1 structure, regulation, and function. J Exp Bot. 2016; 67 :6215-52
|
| [37] |
Baena-Gonzalez E, Rolland F, Thevelein JM. et al. A central integrator of transcription networks in plant stress and energy signalling. Nature. 2007; 448 :938-42
|
| [38] |
Bhalerao RP, Salchert K, Bakó L. et al. Regulatory interaction of PRL1 WD protein with Arabidopsis SNF1-like protein kinases. Proc Natl Acad Sci USA. 1999; 96 :5322-7
|
| [39] |
Muranaka T, Banno H, Machida Y. Characterization of tobacco protein kinase NPK5, a homolog of Saccharomyces cerevisiae SNF 1 that constitutively activates expression of the glucose-repressible SUC2 gene for a secreted invertase of S. cerevisiae. Mol Cell Biol. 1994; 14 :2958-65
|
| [40] |
Alderson A, Sabelli PA, Dickinson JR. et al. Complementation of snf1, a mutation affecting global regulation of carbon metabolism in yeast, by a plant protein kinase cDNA. Proc Natl Acad Sci USA. 1991; 88 :8602-5
|
| [41] |
Lovas A, Sos-Hegedus A, Bimbo A. et al. Functional diversity of potato SNF1-related kinases tested in Saccharomyces cerevisiae. Gene. 2003; 321 :123-9
|
| [42] |
Lu CA, Lin CC, Lee KW. et al. The SnRK1A protein kinase plays a key role in sugar signaling during germination and seedling growth of rice. Plant Cell. 2007; 19 :2484-99
|
| [43] |
Yu W, Peng F, Wang W. et al. SnRK1 phosphorylation of SDH positively regulates sorbitol metabolism and promotes sugar accumulation in peach fruit. Tree Physiol. 2021; 41 :1077-86
|
| [44] |
Zhang S, Wang H, Luo J. et al. Peach PpSnRK1α interacts with bZIP11 and maintains trehalose balance in plants. Plant Physiol Biochem. 2021; 160 :377-85
|
| [45] |
Huang T, Yu D, Wang X. VvWRKY22 transcription factor interacts with VvSnRK1.1/VvSnRK1.2 and regulates sugar accumulation in grape. Biochem Biophys Res Commun. 2021; 554 :193-8
|
| [46] |
Luo J, Peng F, Zhang S. et al. The protein kinase FaSnRK1α regulates sucrose accumulation in strawberry fruits. Plant Physiol Biochem. 2020; 151 :369-77
|
| [47] |
Peixoto B, Moraes TA, Mengin V. et al. Impact of the SnRK1 protein kinase on sucrose homeostasis and the transcriptome during the diel cycle. Plant Physiol. 2021; 187 :1357-73
|
| [48] |
Liu H, Si X, Wang Z. et al. TaTPP-7A positively feedback regulates grain filling and wheat grain yield through T6P-SnRK1 signalling pathway and sugar-ABA interaction. Plant Biotechnol J. 2023; 21 :1159-75
|
| [49] |
Han C, Qiao Y, Yao L. et al. TOR and SnRK1 fine tune SPEECHLESS transcription and protein stability to optimize stomatal development in response to exogenously supplied sugar. New Phytol. 2022; 234 :107-21
|
| [50] |
Shi W, Wang L, Yao L. et al. Spatially patterned hydrogen peroxide orchestrates stomatal development in Arabidopsis. Nat Commun. 2022; 13 :5040
|
| [51] |
Viana AJC, Matiolli CC, Newman DW. et al. The sugar-responsive circadian clock regulator bZIP63 modulates plant growth. New Phytol. 2021; 231 :1875-89
|
| [52] |
Shin J, Sánchez-Villarreal A, Davis AM. et al. The metabolic sensor AKIN10 modulates the Arabidopsis circadian clock in a light-dependent manner. Plant Cell Environ. 2017; 40 :997-1008
|
| [53] |
Zhu T, Li L, Feng L. et al. Target of rapamycin regulates genome methylation reprogramming to control plant growth in Ara- bidopsis. Front Genet. 2020; 11 :186
|
| [54] |
Zhao Y, Wang XQ. The hot issue: TOR signalling network in plants. Funct Plant Biol. 2021; 48 :1-7
|
| [55] |
Fu L, Wang P, Xiong Y. Target of rapamycin signaling in plant stress responses. Plant Physiol. 2020; 182 :1613-23
|
| [56] |
Zhao Y, Wang XQ. In silico analysis of Vitis vinifera Cabernet Sauvignon TOR and its responses to sugar and abscisic acid signaling. Acta Bot Bras. 2022; 36 :e2020abb0482
|
| [57] |
Zhao Y, Wang XQ. VvTOR responds to ABA signal and affects sugar related genes expression in grape. Russ J Plant Physiol. 2022; 69 :1-8
|
| [58] |
Li D, Ding Y, Cheng L. et al. Target of rapamycin (TOR) regulates the response to low nitrogen stress via autophagy and hormone pathways in Malus hupehensis. Hortic Res. 2022; 9 :uhac143
|
| [59] |
Lamming DW, Ye L, Sabatini DM. et al. Rapalogs and mTOR inhibitors as anti-aging therapeutics. J Clin Invest. 2013; 123 :980-9
|
| [60] |
Xiong F, Dong P, Liu M. et al. Tomato FK506 binding protein 12KD (FKBP12) mediates the interaction between rapamycin and target of rapamycin (TOR). Front Plant Sci. 2016; 7 :1746
|
| [61] |
Schepetilnikov M, Kobayashi K, Geldreich A. et al. Viral factor TAV recruits TOR/S6K1 signalling to activate reinitiation after long ORF translation. EMBO J. 2011; 30 :1343-56
|
| [62] |
Ren M, Venglat P, Qiu S. et al. Target of rapamycin signaling regulates metabolism, growth, and life span in Arabidopsis. Plant Cell. 2012; 24 :4850-74
|
| [63] |
Ren M, Qiu S, Venglat P. et al. Target of rapamycin regulates development and ribosomal RNA expression through kinase domain in Arabidopsis. Plant Physiol. 2011; 155 :1367-82
|
| [64] |
Brunkard JO, Xu M, Scarpin MR. et al. TOR dynamically regulates plant cell-cell transport. Proc Natl Acad Sci USA. 2020; 117 :5049-58
|
| [65] |
Yuan X, Xu P, Yu Y. et al. Glucose-TOR signaling regulates PIN2 stability to orchestrate auxin gradient and cell expansion in Arabidopsis root. Proc Natl Acad Sci USA. 2020; 117 :32223-5
|
| [66] |
Xiong Y, Sheen J. Rapamycin and glucose-target of rapamycin (TOR) protein signaling in plants. J Biol Chem. 2012; 287 :2836-42
|
| [67] |
Ye R, Wang M, du H. et al. Glucose-driven TOR-FIE-PRC2 signalling controls plant development. Nature. 2022; 609 :986-93
|
| [68] |
Zhang N, Meng Y, Li X. et al. Metabolite-mediated TOR signaling regulates the circadian clock in Arabidopsis. Proc Natl Acad Sci USA. 2019; 116 :25395-7
|
| [69] |
Zhang H, Guo L, Li Y. et al. TOP1α fine-tunes TOR-PLT2 to maintain root tip homeostasis in response to sugars. Nat Plants. 2022; 8 :792-801
|
| [70] |
Zhang Z, Zhu JY, Roh J. et al. TOR signaling promotes accumulation of BZR1 to balance growth with carbon availability in Arabidopsis. Curr Biol. 2016; 26 :1854-60
|
| [71] |
Zhang W, Han L, Huang Y. et al. Unveiling the significance of target of rapamycin (TOR) signalling in grafting. Veg Res. 2024; 4 :e004
|
| [72] |
Sharma M, Sharma M, Jamsheer KM. et al. Jasmonic acid coordinates with light, glucose and auxin signalling in regulating branching angle of Arabidopsis lateral roots. Plant Cell Environ. 2022; 45 :1554-72
|
| [73] |
Zhao Y, Wang XQ. VvMYB1 potentially affects VvTOR gene expression by regulating VvTOR promoter and participates in glucose accumulation. J Plant Physiol. 2022; 272 :153668
|
| [74] |
Wang XQ, Li LM, Yang PP. et al. The role of hexokinases from grape berries (Vitis vinifera L.) in regulating the expression of cell wall invertase and sucrose synthase genes. Plant Cell Rep. 2014; 33 :337-47
|
| [75] |
Barbier FF, Cao D, Fichtner F. et al. HEXOKINASE1 signalling promotes shoot branching and interacts with cytokinin and strigolactone pathways. New Phytol. 2021; 231 :1088-104
|
| [76] |
Tong C, Li C, Cao XY. et al. Long-distance transport of sucrose in source leaves promotes sink root growth by the EIN3-SUC 2 module. PLoS Genet. 2022; 18 :e1010424
|
| [77] |
Cho YH, Yoo SD, Sheen J. Regulatory functions of nuclear hexokinase1 complex in glucose signaling. Cell. 2006; 127 :579-89
|
| [78] |
Sun MH, Ma QJ, Hu DG. et al. The glucose sensor MdHXK1 phosphorylates a tonoplast Na( + )/H( + ) exchanger to improve salt tolerance. Plant Physiol. 2018; 176 :2977-90
|
| [79] |
Liu Y, Bai Y, Li N. et al. HEXOKINASE1 forms a nuclear complex with the PRC2 subunits CURLY LEAF and SWINGER to regulate glucose signaling. J Integr Plant Biol. 2022; 64 :1168-80
|
| [80] |
Hanson J, Smeekens S. Sugar perception and signaling—an update. Curr Opin Plant Biol. 2009; 12 :562-7
|
| [81] |
Zhai Z, Keereetaweep J, Liu H. et al. Trehalose 6-phosphate positively regulates fatty acid synthesis by stabilizing WRINKLED1. Plant Cell. 2018; 30 :2616-27
|
| [82] |
Rodrigues A, Adamo M, Crozet P. et al. ABI1 and PP2CA phosphatases are negative regulators of Snf1-related protein kinase 1 signaling in Arabidopsis. Plant Cell. 2013; 25 :3871-84
|
| [83] |
Wang P, Zhao Y, Li Z. et al. Reciprocal regulation of the TOR kinase and ABA receptor balances plant growth and stress response. Mol Cell. 2018; 69 :100-112.e6
|
| [84] |
Liu XJ, Liu X, An XH. et al. An apple protein kinase MdSnRK1.1 interacts with MdCAIP 1 to regulate ABA sensitivity. Plant Cell Physiol. 2017; 58 :1631-41
|
| [85] |
Wang H, Han C, Wang JG. et al. Regulatory functions of cellular energy sensor SnRK 1 for nitrate signalling through NLP7 repression. Nat Plants. 2022; 8 :1094-107
|
| [86] |
Sun D, Fang X, Xiao C. et al. Kinase SnRK1.1 regulates nitrate channel SLAH 3 engaged in nitrate-dependent alleviation of ammonium toxicity. Plant Physiol. 2021; 186 :731-49
|
| [87] |
Simon NML, Kusakina J, Fernández-López Á. et al. The energy-signaling hub SnRK1 is important for sucrose-induced hypocotyl elongation. Plant Physiol. 2018; 176 :1299-310
|
| [88] |
Simon NML, Sawkins E, Dodd AN. Involvement of the SnRK1 subunit KIN10 in sucrose-induced hypocotyl elongation. Plant Signal Behav. 2018; 13 :e1457913
|
| [89] |
Jamsheer KM, Sharma M, Singh D. et al. FCS-like zinc finger 6 and 10 repress SnRK1 signalling in Arabidopsis. Plant J. 2018; 94 :232-45
|
| [90] |
Yang C, Li X, Zhou J. et al. Autophagy contributes to positive feedback regulation of SnRK 1 signaling in plants. Autophagy. 2023; 19 :3248-50
|
| [91] |
Liu XJ, An XH, Liu X. et al. MdSnRK1.1 interacts with MdJAZ 18 to regulate sucrose-induced anthocyanin and proanthocyanidin accumulation in apple. J Exp Bot. 2017; 68 :2977-90
|
| [92] |
Broucke E, Dang TTV, Li Y. et al. SnRK1 inhibits anthocyanin biosynthesis through both transcriptional regulation and direct phosphorylation and dissociation of the MYB/bHLH/TTG1 MBW complex. Plant J. 2023; 115 :1193-213
|
| [93] |
Zirngibl M-E, Araguirang GE, Kitashova A. et al. Triose phosphate export from chloroplasts and cellular sugar content regulate anthocyanin biosynthesis during high light acclimation. Plant Commun. 2023; 4 :100423
|
| [94] |
Margalha L, Elias A, Belda-Palazón B. et al. HOS 1 promotes plant tolerance to low-energy stress via the SnRK1 protein kinase. Plant J. 2023; 115 :627-41
|
| [95] |
Zhai Z, Liu H, Shanklin J. Phosphorylation of WRINKLED1 by KIN10 results in its proteasomal degradation, providing a link between energy homeostasis and lipid biosynthesis. Plant Cell. 2017; 29 :871-89
|
| [96] |
Kim GD, Cho YH, Yoo SD. Regulatory functions of cellular energy sensor SNF1-related kinase 1 for leaf senescence delay through ETHYLENE- INSENSITIVE3 repression. Sci Rep. 2017; 7 :3193
|
| [97] |
Jeong EY, Seo PJ, Woo JC. et al. AKIN10 delays flowering by inactivating IDD8 transcription factor through protein phosphorylation in Arabidopsis. BMC Plant Biol. 2015; 15 :110
|
| [98] |
Im JH, Cho YH, Kim GD. et al. Inverse modulation of the energy sensor Snf1-related protein kinase 1 on hypoxia adaptation and salt stress tolerance in Arabidopsis thaliana. Plant Cell Environ. 2014; 37 :2303-12
|
| [99] |
Muralidhara P, Weiste C, Collani S. et al. Perturbations in plant energy homeostasis prime lateral root initiation via SnRK1-bZIP63-ARF19 signaling. Proc Natl Acad Sci USA. 2021; 118 :e2106961118
|
| [100] |
Meng D, Cao H, Yang Q. et al. SnRK 1 kinase-mediated phosphorylation of transcription factor bZIP39 regulates sorbitol metabolism in apple. Plant Physiol. 2023; 192 :2123-42
|
| [101] |
Hu Y, Lin Y, Xia Y. et al. Overexpression of OsSnRK1a through a green tissue-specific promoter improves rice yield by accelerating sheath-to-panicle transport of nonstructural carbohydrates and increasing leaf photosynthesis. Plant Physiol Biochem. 2023; 203 :108048
|
| [102] |
Liu J, Nie B, Yu B. et al. Rice ubiquitin-conjugating enzyme OsUbc13 negatively regulates immunity against pathogens by enhancing the activity of OsSnRK1a. Plant Biotechnol J. 2023; 21 :1590-610
|
| [103] |
Morales-Herrera S. et al. Trehalose- 6- phosphate signaling regulates lateral root formation in Arabidopsis thaliana. Proc Natl Acad Sci USA. 2023; 120 :e2302996120
|
| [104] |
Marash I, Leibman-Markus M, Gupta R. et al. TOR inhibition primes immunity and pathogen resistance in tomato in a salicylic acid-dependent manner. Mol Plant Pathol. 2022; 23 :1035-47
|
| [105] |
Ahn CS, Lee DH, Pai HS. Characterization of Maf 1 in Arabidopsis : function under stress conditions and regulation by the TOR signaling pathway. Planta. 2019; 249 :527-42
|
| [106] |
Liu Y, Bassham DC. TOR is a negative regulator of autophagy in Arabidopsis thaliana. PLoS One. 2010; 5 :e11883
|
| [107] |
Pu Y, Luo X, Bassham DC. TOR-dependent and -independent pathways regulate autophagy in Arabidopsis thaliana. Front Plant Sci. 2017; 8 :1204
|
| [108] |
Suttangkakul A, Li F, Chung T. et al. The ATG1/ATG13 protein kinase complex is both a regulator and a target of autophagic recycling in Arabidopsis. Plant Cell. 2011; 23 :3761-79
|
| [109] |
Song Y, Li L, Yang Z. et al. Target of rapamycin (TOR) regulates the expression of lncRNAs in response to abiotic stresses in cotton. Front Genet. 2019; 9 :690
|
| [110] |
Wang L, Li H, Zhao C. et al. The inhibition of protein translation mediated by AtGCN1 is essential for cold tolerance in Arabidop- sis thaliana. Plant Cell Environ. 2017; 40 :56-68
|
| [111] |
Dong Y, Teleman AA, Jedmowski C. et al. The Arabidopsis THADA homologue modulates TOR activity and cold acclimation. Plant Biol (Stuttg). 2019; 21 :77-83
|
| [112] |
Sharma M, Banday ZZ, Shukla BN. et al. Glucose-regulated HLP1 acts as a key molecule in governing thermomemory. Plant Physiol. 2019; 180 :1081-100
|
| [113] |
Bakshi A, Moin M, Kumar MU. et al. Ectopic expression of Arabidopsis target of rapamycin (AtTOR) improves water-use efficiency and yield potential in rice. Sci Rep. 2017; 7 :42835
|
| [114] |
Rodriguez M, Parola R, Andreola S. et al. TOR and SnRK1 signaling pathways in plant response to abiotic stresses: do they always act according to the "yin-yang" model? Plant Sci. 2019; 288 :110220
|
| [115] |
Zhao Y, Wang XQ. VvTOR interacts with VvSnRK1.1 and regulates sugar metabolism in grape. Planta. 2022; 256 :56
|
| [116] |
Jamsheer KM, Jindal S, Sharma M. et al. A negative feedback loop of TOR signaling balances growth and stress-response trade-offs in plants. Cell Rep. 2022; 39 :110631
|
| [117] |
Saile J, Wießner-Kroh T, Erbstein K. et al. SNF1-RELATED KINASE 1 and TARGET OF RAPAMYCIN control light-responsive splicing events and developmental characteristics in etiolated Arabidopsis seedlings. Plant Cell. 2023; 35 :3413-28
|
| [118] |
Henry C, Watson-Lazowski A, Oszvald M. et al. Sugar sensing responses to low and high light in leaves of the C 4 model grass Setaria viridis. J Exp Bot. 2019; 71 :1039-52
|
| [119] |
Liao H-S, Chen Y-J, Hsieh W-Y. et al. Arabidopsis ACT DOMAIN REPEAT9 represses glucose signaling pathways. Plant Physiol. 2023; 192 :1532-47
|
| [120] |
Asim M, Guo M, Khan R. et al. Investigation of sugar signaling behaviors involved in sucrose-induced senescence initiation and progression in N. tabacum. Plant Physiol Biochem. 2022; 184 :112-25
|