Mechanism of CsGPA1 in regulating cold tolerance of cucumber

Yan Yan , Mintao Sun , Si Ma , Qian Feng , Yijia Wang , Qinghua Di , Mengdi Zhou , Chaoxing He , Yansu Li , Lihong Gao , Xianchang Yu

Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) : uhac109

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Horticulture Research ›› 2022, Vol. 9 ›› Issue (1) :uhac109 DOI: 10.1093/hr/uhac109
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Mechanism of CsGPA1 in regulating cold tolerance of cucumber
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Abstract

G proteins function directly in cold tolerance of plants. However, the framework of the G α subunit in regulating cold tolerance remains to be explored. Here, we used protein interaction techniques to elucidate cold-related pathways regulated by CsGPA1. Suppression of CsGPA1 decreased the cold tolerance of cucumber. Further protein interaction experiments showed that CsGPA1 interacted with Csa_4G663630.1 located in the cell membrane and nucleus and with CsCOR413PM2 located in the cell membrane. Csa_4G663630.1 was named CsCDL1 due to its 71% protein sequence similarity to AtCDL1, a positive brassinolide signal gene. Suppression of CsGPA1 decreased the expression of most of brassinolide-related genes (including CsCDL1) under cold stress. Principal component and linear regression analyses showed that expressions of CsGPA1 and brassinolide-related genes were positively correlated. Suppression of CsCOR413PM2 also decreased cold tolerance of cucumber. The expression and protein content of CsCOR413PM2 and CsGPA1 in CsGPA1-RNAi and CsCOR413PM2-RNAi lines were determined under cold tolerance. Only CsGPA1 silencing affected the expression and protein content of CsCOR413PM2 during cold stress. Moreover, suppression of CsGPA1 or CsCOR413PM2 decreased Ca2+ influx at low temperature and then decreased the expression of CsICECsCBF. These results indicated that the CsGPA1CsCOR413PM2–Ca2+ axis regulated the expression of CsICECsCBF during cold stress. In conclusion, Our results provide the first framework of CsGPA1 in regulating cold tolerance of cucumber, laying the foundation for further mechanistic studies of cold tolerance for G α in cucumber.

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Yan Yan, Mintao Sun, Si Ma, Qian Feng, Yijia Wang, Qinghua Di, Mengdi Zhou, Chaoxing He, Yansu Li, Lihong Gao, Xianchang Yu. Mechanism of CsGPA1 in regulating cold tolerance of cucumber. Horticulture Research, 2022, 9 (1) : uhac109 DOI:10.1093/hr/uhac109

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References

[1]

Gookin TE, Assmann SM . Significant reduction of BiFC nonspecific assembly facilitates in planta assessment of heterotrimeric G-protein interactors. Plant J. 2014; 80: 553-67.

[2]

Yan Y, Zhang W, Li Y et al. Functions of CsGPA1 on the hypocotyl elongation and root growth of cucumbers. Sci Rep. 2018; 8: 15583.

[3]

Yan Y, Sun M, Li Y et al. The CsGPA1-CsAQPs module is essential for salt tolerance of cucumber seedlings. Plant Cell Rep. 2020; 39: 1301-16.

[4]

Pandey S. Heterotrimeric G-protein signaling in plants: conserved and novel mechanisms. Annu Rev Plant Biol. 2019; 70: 213-38.

[5]

Ma Y, Dai X, Xu Y et al. COLD1 confers chilling tolerance in rice. Cell. 2015; 160: 1209-21.

[6]

Tunc-Ozdemir M, Tang C, Ishka MR et al. A cyclic nucleotide-gated channel (CNGC16) in pollen is critical for stress tolerance in pollen reproductive development. Plant Physiol. 2013; 161: 1010-20.

[7]

Jiang Z, Zhou X, Tao M et al. Plant cell-surface GIPC sphingolipids sense salt to trigger Ca2+ influx . Nature. 2019; 572: 341-6.

[8]

Zhu JK . Abiotic stress signaling and responses in plants. Cell. 2016; 167: 313-24.

[9]

Eremina M, Unterholzner SJ, Rathnayake AI et al. Brassinosteroids participate in the control of basal and acquired freezing tolerance of plants. Proc Natl Acad Sci USA. 2016; 113: E5982-91.

[10]

Ye K, Li H, Ding Y et al. BRASSINOSTEROID-INSENSITIVE2 negatively regulates the stability of transcription factor ICE1 in response to cold stress in Arabidopsis . Plant Cell. 2019; 31: 2682-96.

[11]

Xia XJ, Gao CJ, Song LX et al. Role of H2O2 dynamics in brassinosteroid-induced stomatal closure and opening in Solanum lycopersicum . Plant Cell Environ. 2014; 37: 2036-50.

[12]

Fang P, Yan M, Chi C et al. Brassinosteroids act as a positive regulator of photoprotection in response to chilling stress. Plant Physiol. 2019; 180: 2061-76.

[13]

Xia XJ, Wang YJ, Zhou YH et al. Reactive oxygen species are involved in brassinosteroid-induced stress tolerance in cucumber. Plant Physiol. 2009; 150: 801-14.

[14]

Cui JX, Zhou YH, Ding JG et al. Role of nitric oxide in hydrogen peroxide-dependent induction of abiotic stress tolerance by brassinosteroids in cucumber. Plant Cell Environ. 2011; 34: 347-58.

[15]

Jiang YP, Huang LF, Cheng F et al. Brassinosteroids accelerate recovery of photosynthetic apparatus from cold stress by balancing the electron partitioning carboxylation and redox homeostasis in cucumber. Physiol Plant. 2013; 148: 133-45.

[16]

Guy CL, Niemi KJ, Brambl R . Altered gene expression during cold acclimation of spinach. Proc Natl Acad Sci USA. 1985; 82: 3673-7.

[17]

Yamaguchi-Shinozaki K, Shinozaki K . A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought low-temperature or high-salt stress . Plant Cell. 1994; 6: 251-64.

[18]

Shi Y, Ding Y, Yang S . Molecular regulation of CBF signaling in cold acclimation. Trends Plant Sci. 2018; 23: 623-37.

[19]

Stockinger EJ, Gilmour SJ, Thomashow MF . Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit . Proc Natl Acad Sci USA. 1997; 94: 1035-40.

[20]

Gilmour SJ, Zarka DG, Stockinger EJ 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. 1998; 16: 433-42.

[21]

Liu Q, Kasuga M, Sakuma Y et al. Two transcription factors DREB1 and DREB2 with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought- and low-temperature-responsive gene expression respectively in Arabidopsis . Plant Cell. 1998; 10: 1391-406.

[22]

Vogel JT, Zarka DG, Van Buskirk HA et al. Roles of the CBF2 and ZAT12 transcription factors in configuring the low temperature transcriptome of Arabidopsis . Plant J. 2005; 41: 195-211.

[23]

Park S, Lee CM, Doherty CJ et al. Regulation of the Arabidopsis CBF regulon by a complex low-temperature regulatory network. Plant J. 2015; 82: 193-207.

[24]

Li H, Ye K, Shi Y et al. BZR1 positively regulates freezing tolerance via CBF-dependent and CBF-independent pathways in Arabidopsis . Mol Plant. 2017; 10: 545-59.

[25]

Ding Y, Shi Y, Yang S . Advances and challenges in uncovering cold tolerance regulatory mechanisms in plants. New Phytol. 2019; 222: 1690-704.

[26]

Zhang L, Guo X, Zhang Z et al. Cold-regulated gene LeCOR413PM2 confers cold stress tolerance in tomato plants. Gene. 2021; 764: 145097.

[27]

Lee SY, Boon NJ, Webb AA et al. Synergistic activation of RD29A via integration of salinity stress and abscisic acid in Arabidopsis thaliana . Plant Cell Physiol. 2016; 57: 2147-60.

[28]

Okawa K, Nakayama K, Kakizaki T et al. Identification and characterization of Cor413im proteins as novel components of the chloroplast inner envelope. Plant Cell Environ. 2008; 31: 1470-83.

[29]

Breton G, Danyluk J, Charron JBF et al. Expression profiling and bioinformatic analyses of a novel stress-regulated multispanning transmembrane protein family from cereals and Arabidopsis . Plant Physiol. 2003; 132: 64-74.

[30]

Lin C, Thomashow MF . DNA sequence analysis of a complementary DNA for cold-regulated Arabidopsis gene COR15 and characterization of the COR15 polypeptide. Plant Physiol. 1992; 99: 519-25.

[31]

Su C, Chen K, Ding Q et al. Proteomic analysis of the function of a novel cold-regulated multispanning transmembrane protein COR413-PM1 in Arabidopsis . Int J Mol Sci. 2018; 19: 2572.

[32]

Zhou A, Liu E, Li H et al. PsCOR413pm2, a plasma membrane-localized cold-regulated protein from Phlox subulata, confers low temperature tolerance in Arabidopsis . Int J Mol Sci. 2018; 19: 2579.

[33]

Guo X, Zhang L, Dong G et al. A novel cold-regulated protein isolated from Saussurea involucrata confers cold and drought tolerance in transgenic tobacco (Nicotiana tabacum) . Plant Sci. 2019; 289: 110246.

[34]

Yu JQ, Zhou YH, Huang LF et al. Chill-induced inhibition of photosynthesis: genotypic variation within Cucumis sativus . Plant Cell Physiol 2002; 43: 1182-8.

[35]

Chakraborty N, Singh N, Kaur K et al. G-protein signaling components GCR1 and GPA1 mediate responses to multiple abiotic stresses in Arabidopsis . Front Plant Sci. 2015; 6: 1000.

[36]

Guo X, Li J, Zhang L et al. Heterotrimeric G-protein α subunit (LeGPA1) confers cold stress tolerance to processing tomato plants (Lycopersicon esculentum Mill) . BMC Plant Biol. 2020; 20: 1-16.

[37]

Kim TW, Guan S, Burlingame AL et al. The CDG1 kinase mediates brassinosteroid signal transduction from BRI1 receptor kinase to BSU1 phosphatase and GSK3-like kinase BIN2. Mol Cell. 2011; 43: 561-71.

[38]

Wei L, Deng XG, Zhu T et al. Ethylene is involved in brassinosteroids induced alternative respiratory pathway in cucumber (Cucumis sativus L.) seedlings response to abiotic stress . Front Plant Sci. 2015; 6: 982.

[39]

Liu Q, Ding Y, Shi Y et al. The calcium transporter ANNEXIN1 mediates cold-induced calcium signaling and freezing tolerance in plants. EMBO J. 2020; 40: e104559.

[40]

Liang W, Wang M, Ai X . The role of calcium in regulating photosynthesis and related physiological indexes of cucumber seedlings under low light intensity and suboptimal temperature stress. Sci Hortic. 2009; 123: 34-8.

[41]

Zhang Z, Wuab P, Zhang W et al. Calcium is involved in exogenous NO-induced enhancement of photosynthesis in cucumber (Cucumis sativus L.) seedlings under low temperature . Sci Hortic. 2020; 261: 108953.

[42]

Huang C, Hu G, Li F et al. Nbphan, a myb transcriptional factor, regulates leaf development and affects drought tolerance in Nicotiana benthamiana . Physiol Plant. 2013; 149: 297-309.

[43]

Murshed R, Lopez-Lauri F, Sallanon H . Microplate quantification of enzymes of the plant ascorbate-glutathione cycle. Anal Biochem. 2008; 383: 320-2.

[44]

Jiang MY, Zhang JH . Effect of abscisic acid on active oxygen species antioxidative defence system and oxidative damage in leaves of maize seedlings. Plant Cell Physiol. 2001; 42: 1265-73.

[45]

Li Y, Jia Y, Bian Y et al. Autocrine motility factor promotes endometrial cancer progression by targeting gper-1. Cell Commun Signal. 2019; 17: 22.

[46]

Hu X, Qian Q, Xu T et al. The U-box E3 ubiquitin ligase TUD1 functions with a heterotrimeric G α subunit to regulate brassinosteroid-mediated growth in rice . PLoS Genet. 2013; 9: e1003391.

[47]

Wang L, Xu YY, Ma QB et al. Heterotrimeric G protein alpha subunit is involved in rice brassinosteroid response. Cell Res. 2006; 16: 916-22.

[48]

Li X, Ma D, Lu SX et al. Blue light and low temperature-regulated COR27 and COR28 play roles in the Arabidopsis circadian clock. Plant Cell. 2016; 28: 2755-69.

[49]

Thomashow MF . PLANT COLD ACCLIMATION: freezing tolerance genes and regulatory mechanisms. Annu Rev Plant Physiol Plant Mol Biol. 1999; 50: 571-99.

[50]

Zhao C, Zhang Z, Xie S et al. Mutational evidence for the critical role of CBF transcription factors in cold acclimation in Arabidopsis . Plant Physiol. 2016; 171: 2744-59.

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