Abstract
G proteins regulate shoot, root, and epidermis development, as well as biotic stress tolerance in plants; however, most studies have examined model plants and less attention has been paid to the function of G proteins in horticultural plants. Here, we identified a G protein, CsGPA1, from cucumber and studied its function in seedling development of cucumbers. CsGPA1 is a peptide of 392 amino acids with a predicted molecular mass of 44.6 kDa. Spatiotemporal expression analysis found that endogenous CsGPA1 was highly expressed in roots and young leaves. Immunohistochemical assay revealed that functional CsGPA1 was present in the plasma membranes of the epidermis and cortex, and in the cytosol of the endodermis, parenchyma, and vasculature of root meristematic cells. In comparison with wild-type seedlings, CsGPA1-overexpressing transgenic lines exhibited enhanced seed germination and earlier seedling development including hypocotyl elongation and root growth. In contrast, RNAi silencing of the CsGPA1 gene inhibited seedling growth and development. Further study showed that CsGPA1 controled hypocotyl elongation and root growth via promoting cell size and the meristem of hypocotyl and root tip cells of cucumber plants. Our study expands the roles of G proteins in plants and helps to elucidate the mechanism by which cucumber regulates early seedling development.
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Introduction
Heterotrimeric G proteins form a family of GTP-binding proteins and function as signaling molecules that are activated after binding to GTP1. These proteins are localized to the plasma membrane, where they interact with downstream effectors2. G proteins are involved in the transduction of extracellular signals into intracellular responses. In the inactive state, a G protein typically exists as a trimer consisting of an α-subunit (Gα) bound to GDP, a β-subunit (Gβ), and a γ-subunit (Gγ). When a ligand binds to a G protein-coupled receptor, a conformational change occurs in the G protein, resulting in the exchange of the GDP for a GTP and the dissociation of Gα-GTP from the Gβγ dimer. The G-protein subunits remain active until the intrinsic GTPase activity of Gα results in the hydrolysis of GTP to GDP and the reassociation of the inactive trimer. The Arabidopsis thaliana genome contains canonical Gα and Gβ genes, GPA1 and AGB1, and two genes that encode Gβγ, AGG1 and AGG21.
The Gα subunit is an important component of the heterotrimeric G-protein complex and is associated with the Ca2+/CaM signature, regulation of monomeric GTPases, phospholipase C- and D-mediated signaling, and the relay into secondary signaling pathways, which in turn lead to changes in the activity of specific proteins3,4. It plays important roles in the diverse process of plant growth and development. GPA1 in Arabidopsis is involved in seed germination and hypocotyl length5,6,7,8. gpa1 mutants display the phenotype of fewer lateral roots and a shorter hypocotyl and blades9,10. In rice, Gα is required for normal shoot elongation and seed growth11. The d1 mutant of rice exhibits dwarfism and produces erect leaves and small seeds12. Accumulating evidence indicates that GPA1 likely influences leaf, hypocotyl, and root growth by modulating cell division and proliferation. In addition, GPA1 is also involved in the response to drought, heat, and cold abiotic stresses by transmitting the signal through downstream effectors including ion channels, phospholipases, kinases/phosphatases, and other GTPases. The interaction between GPA1 and other signaling pathways such as S1P (sphingosine-1-phosphate)13 and the ABA signaling pathway has been recently uncovered.
Cucumber (Cucumis sativus L.) is one of the main vegetables cultivated in China. There are several stress conditions that significantly affect cucumber production, such as cold stress during the winter in the northern regions. Cucurbitaceae is one of only a few eudicot families with internal as well as external phloem, and thus cucumber requires individual study to maximize agricultural success. Although the Gα subunit has been the subject of study in model plants, the cucumber Gα subunit has not previously been characterized. In this study, we identified a G-protein from cucumber and investigated its function in seedling growth and development.
Materials and Methods
Plant materials and growth conditions
Cucumber (Cucumis sativus cv. Xintai Mici) seeds were immersed in hot water (55 °C) for 4 h. The seeds were then placed in 9-cm diameter Petri dishes containing two layers of filter paper moistened with 5 mL sterilized distilled water. Plates were incubated for 6 d at 30 °C in darkness. Cucumber seedlings with two true leaves were transferred to a growth chamber and grown under a 14-h light (28 °C)/10-h dark (18 °C) photoperiod (600 mmol m−2 s−1 photosynthetic photon flux density) with 70% relative humidity.
RNA extraction and cDNA synthesis
Total RNA was extracted from cucumber leaves using a total RNA isolation kit (Beijing Huayueyang, Beijing, China). The extracted RNA was treated with DNase A to remove residual DNA. First-strand cDNA was synthesized using a PrimeScript™ RT reagent Kit (TaKaRa Biotechnology, Dalian, China) with 2 µg RNA as the template. Quantitative real-time (qRT)-PCR was carried out using 96-well blocks in a 7500 Real Time PCR System (Applied Biosystems, Foster City, CA, USA). The 20-µL reaction volumes were prepared using SYBR® Green PCR Master Mix (Applied Biosystems) and appropriate primers (Supplementary Table 1). qRT-PCR was completed with 40 cycles of 95 °C for 5 s and 60 °C for 34 s. A melting curve analysis was used to verify the amplified product. The cycle threshold (Ct) values were converted to relative copy numbers using the ∆∆Ct method. Gene expression data were normalized against the expression of CsActin.
Gene cloning
Primers were designed to amplify the CsGPA1 gene using the published CsGPA1 consensus sequence and the Cucumber Genome Database (http://www.icugi.org/cgi-bin/ICuGI/index.cgi). A 1,179-bp fragment was amplified by a polymerase chain reaction (PCR) using PrimeSTAR Max DNA Polymerase (TaKaRa) with the prepared cDNA as the template. The PCR program was as follows: 95 °C for 3 min and 35 cycles of 95 °C for 30 s, 52 °C annealing for 45 s, and 72 °C for 2 min.
To generate the over-expression construct, the CsGPA1 coding region was PCR-amplified and cloned into the SmaI/XbaI sites of the pBI121 binary vector under the control of the 35 S promoter. To generate the RNA interference (RNAi) construct, a 129-bp sequence of CsGPA1 cDNA was PCR-amplified and cloned into the pFGC1008 binary vector. To investigate the subcellular localization of CsGPA1, the encoding region of CsGPA1 was PCR-amplified and inserted into the pUC vector (http://deepgreen.stanford.edu), through which a fusion protein comprising CsGPA1 and the green fluorescent protein (GFP) was generated. The sequences of the primers used to generate these constructs are listed in Supplementary Table 1.
Cucumber transformation
Cucumber (cv. Xintai Mici) plants were transformed with Agrobacterium tumefaciens, as previously described14. Briefly, 2-d-old cotyledons were cut into two pieces. After removing the germs, the cotyledons were incubated in MS liquid medium containing A. tumefaciens LBA4404 cells harboring pBI121-antisense-CsGPA1 and 35S::CsGPA1-GFP for 12 min at 28 °C. They were then placed on polarization medium (MS supplemented with 0.5 mg/L 6-BA and 1 mg/L ABA, pH 5.7–5.8). After culturing for 2 d at 28 °C in darkness, the cotyledons were transferred to polarization medium supplemented with 100 mg/L kanamycin and 500 mg/L carbenicillin. After 2–3 weeks, the shoots that differentiated from the cotyledons were transferred to rooting medium (MS supplemented with 100 mg/L kanamycin and 200 mg/L carbenicillin) to stimulate root growth. After 20–30 d, when the new roots were growing well in the rooting medium, the seedlings were exposed to weak light for 3–4 d and then transferred to pots containing vermiculite. The transgenic plants were cultivated in a phytotron under a 12-h light (25 °C)/12-h dark (18 °C) photoperiod (600 umol m−2s−1).
Phylogenetics
CLUSTAL W and MEGA7 software was used to analyze the phylogenetic relationships between the GPA1 genes from C. sativus, Zea mays, Oryza sativa subsp. indica (rice), O. sativa subsp. japonica, Pisum sativum (pea), Solanum lycopersicum (tomato), Solanum tuberosum (potato), Glycine max (soybean), Spinacia oleracea (spinach), Sasa veitchii, Chusquea spectabilis, Phyllostachys bambusoides (timber bamboo), Picea abies (Norway spruce), and Arabidopsis thaliana based on the encoded amino acid sequences (Thompson, Higgins & Gibson 1994). The phylogenetic tree was constructed using the neighbor-joining method of the MEGA7 software15.
Seed germination rate
To determine the germination rate of the seeds from different transgenic cucumber plants, the second and third fruits were collected 40 d after pollination and ripened for 5 d. Seeds were collected and 20–30 were placed in 9-cm diameter Petri dishes containing two layers of filter paper moistened with 5 mL sterilized distilled water. Plates were incubated for 2 d at 30 °C in darkness. Seeds were considered germinated if the emerging radicle grew to 3 mm. At least three replicates, with 30 plants per replicate, were used for the germination rate analysis.
Morphometry
The leaf blade width and hypocotyl length and area of 6-d-old cucumber plants were measured using ImageJ software (version 1.36b; http://rsb.info.nih.gov/ij). The root morphology was analyzed using an Epson Perfection 4990 Photo Scanner (Seiko Epson, Nagano, Japan). Root length, surface area, projArea (sum of the projection roots for all the merged images), and volume were analyzed using WinRHIZO software (2007 version; Saint Foy, Canada). Average number of cells per 0.5 mm2 in hypocotyl were counted16,17. Root meristem size was assessed as the cell number between the QC and the first elongating cell in the different transgenic cucumber plants18,19,20.
Microscopy
The hypocotyls of 6-d-old cucumber plants were fixed overnight in a 1:1:18 solution of formaldehyde, acetic acid, and 50% ethanol. The hypocotyls and tip roots were stained for 1 h with 1% safranin in 50% ethanol. After washing in 50% ethanol, the hypocotyls were incubated for 2 h in a solution consisting of 50 mM phosphate buffer (pH 7.2), 4% paraformaldehyde, and 0.25% glutaraldehyde. The samples were washed three times with phosphate-buffered saline (PBS), after which they were embedded in 5% agar containing saffron green. The samples were then sectioned using a vibrating microtome (0.5-cm sections) and visualized using a BX53 microscope (Olympus, Tokyo, Japan).
Subcellular localization
Strips of onion (Allium cepa) bulb epidermis were bombarded with gold particles containing the pUC 35S::CsGPA1-GFP plasmid using a PDS-1000/He particle delivery system (Bio-Rad, Hercules, CA, USA) and intraepidermal placed on MS medium and incubated for 24 h at 22 °C in darkness. The strips were then incubated in 3% (w/v) NaCl solution for a few seconds to induce plasmolysis and then analyzed for GFP fluorescence using a C1 confocal laser scanning microscope (Nikon, Tokyo, Japan) set to a 488-nm excitation wavelength.
Immunolocalization
Cucumber plants were grown until the eight- or nine-leaf stage. Transverse sections were prepared using 1-cm samples collected from the root tip and petiole region. The samples were cut into transverse or longitudinal paraffin sections and placed on microscope slides. After dewaxing, the sections were washed with 0.01 M PBS, pH 7.2–7.4 (137 mm NaCl, 2.7 mm KCl, 10 mm Na2HPO4, and 2 mm KH2PO4), containing 0.05% Tween-20. The sections were then incubated in serum blocking solution for 12 h at 4 °C, followed by a 4-h incubation in a solution of antibody that specifically targets CsGPA1 (1:100 dilution). The control sections were treated with pre-immune serum at the same dilution. The samples were washed three times with PBS and then incubated for 2 h in a solution containing a 1:1,000 dilution of alkaline phosphatase-conjugated anti-mouse IgG secondary antibody (PV9002, ZSGB-Bio Company, Beijing, China). The reaction was stopped by washing the sections with distilled water for 5 min. Finally, the stained sections were visualized using a BX53 microscope (Olympus). The N-terminal peptide of CsGPA1 (SRNRHYNEQDAEEKTQAC) was synthesized by Beijing Bormai Biotechnology Co. Ltd. (Beijing, China) and used to produce the antibody with CsGPA1 as the antigen.
Western blot
The membrane proteins were extracted using a plant membrane protein extraction kit.(Huayueyang Company, Beijing, China,) Briefly, the cucumber samples were ground with liquid nitrogen and then extracted with ice-cold plant lysis buffer with Complete Protease Inhibitor Cocktail Tablets (Roche, Basel, Switzerland). Extracts were incubated on ice for 30 min. Lysed samples were centrifuged at 4 °C at 13,000 g for 20 min to obtain the supernatants as total proteins. The protein level was determined by the BCA method. The same amount of total proteins and extracted membrane proteins were mixed with 5 × loading buffer, then electrophoresed in 10% sodium dodecyl sulfate polyacrylamide gel (SDS-PAGE) and then transferred onto a NC membrane (Millipore, Sigma, Burlington, MA). NC membranes were then blocked with 5% bovine serum albumin (BSA) for 1 h at room temperature. After thrice washing in Tris-buffered saline-Tween 20 (TBST), membranes were incubated with mouse anti-CsGPA1 primary antibody at 1:1000 dilution overnight at 4 °C. After washing in TBST, membranes were incubated with HRP-conjugated secondary antibodies at 1:5000 dilutions for 1 h at room temperature. Finally, proteins were detected using the ECL (Millipore) method. For all samples, protein level of actin was used as the loading control.
Results
Identification of CsGPA1
Using the public BLAST database for cucumber, we obtained a cDNA clone encoding a GPA1-like protein. The 5,879-kb full-length CsGPA1 gene encoded 392 amino acids with a predicted molecular mass of 44.6 kDa. CsGPA1 was located on chromosome 4 and comprised 13 exons and 12 introns, with one putative transmembrane domain (Supplementary Fig. 1a,b). A phylogenetic analysis of full-length amino acid sequences from different species found that the GPA1 genes could be divided into two clades. The first clade consisted of all genes, except for PsGPA1 and ZmGPA1, and showed that CsGPA1 possessed around 70% evolutionally homology with Arabidopsis, Solanum, Glycine max, Cucumis sativus (cucumber), Zea mays, Oryza sativa, and other species (Fig. 1a). Spatiotemporal expression analysis found endogenous CsGPA1 expression in all examined tissues, and it was particularly high in roots and young leaves (Fig. 1b).
Subcellular localization and immunohistochemical assay of CsGPA1
Transient expression assays using A. thaliana mesophyll protoplasts revealed that CsGPA1-GFP was mainly present in the plasma membrane (Fig. 2a). Similar results were obtained for chloroplast-free A. cepa epidermal cells (Fig. 2b). The positive control (pUC vector containing unfused GFP) showed fluorescence throughout the A. thaliana mesophyll protoplasts and A. cepa epidermal cells.
We also performed an immunohistochemical assay to investigate the subcellular localization of CsGPA1 in 4-leaf-old cucumber plants. Investigation on longitudinal sections of the root tips showed that CsGPA1 was present in the cortical, epidermal, and endodermal vasculature cells of the roots and quiescent center (Fig. 3a,b,f,h). In the magnified images, the immunolabeling signal was detected in the plasma membranes of epidermal, cortical and root cap cells. These findings agreed with the results of the GFP-assay. We also found signals in the cytosol of endodermal, parenchymal, and vasculature cells (Fig. 3a–h), suggesting that CsGPA1 might localize in the cytosol as well. No signal was detected in the nucleus. Investigation on cross sections of the roots also indicated that the CsGPA1 signal was present in the plasma membranes of the cortex and epidermal cells and was present in the cytosol of the endodermis and parenchyma but was excluded from the nucleus (Fig. 4a–c).
In 4-leaf-old cucumber plants, CsGPA1 immunolocalized primarily to the phloem, the companion cells of leaf veins, and to the external and internal phloem of stems (Fig. 4d–f). In particular, CsGPA1 localized to the membrane of sieve elements and the cytosol of companion cells (Fig. 4g). The association of CsGPA1 with the membranes of extension cells (i.e., epidermis, cortex) suggests that it may function in cell expansion and size extension.
CsGPA1 enhances cucumber seed germination and early seedling growth
To assess whether CsGPA1 contributes to cucumber growth, we constructed several CsGPA1-overexpressing (OE) and RNA interference(RNAi)lines (Fig. 5a–f). The qRT-PCR and western blot assays showed that mRNA levels correlated strongly with the levels of CsGPA1 in these six lines (Fig. 5c), and we thus selected them for further study.
We found a difference in germination rates between the OE, RNAi, and Wild-type(WT) lines in darkness (Fig. 5a). Analysis of samples incubated for 24 h under optimal conditions (30 °C in darkness) revealed that 100% of the WT and OE seeds had germinated, but only 49.3% of the RNAi seeds had germinated, although this percentage increased to 91.67% at 48 h (Fig. 4b). These results suggest that RNAi silencing of the CsGPA1 gene delayed speed and reduced rates of seed germination. The CsGPA1 gene and protein expression levels in the OE and RNAi lines were considerably higher and lower, respectively, than that in the WT plants at 6 d after germination (Fig. 5c).
To further clarify the effects of CsGPA1 on seed development and the morphology of young seedlings, we examined seed physiological traits (thousand-seed weight and seed length/weight) and morphological characteristics of 6-d-old seedlings (length, diameter, surface area, projected area, and volumes of the cotyledon, hypocotyl, and roots). We found that overexpression of CsGPA1 significantly enhanced seed development and resulted in the production of seeds that were larger and heavier than the WT seeds (Fig. 5d–f). After 6 d of incubation in darkness, the OE seedlings had larger cotyledons, longer hypocotyls, and more lateral roots than the WT or RNAi seedlings. Additionally, the lengths, diameters, surfArea, projArea, and volumes of the cotyledons, hypocotyls, and roots were all greater in the OE seedlings than in the WT or RNAi seedlings after 6 d of darkness incubation (Fig. 6a–l). Together, these observations suggest that CsGPA1 may affect cucumber seed development and early seedling growth in darkness by inducing the growth of the cotyledons, hypocotyl, and primary roots.
CsGPA1 positively regulates hypocotyl and root elongation
Plant growth involves both cell elongation and proliferation. We assessed the function of CsGPA1 in cell elongation and/or proliferation in the hypocotyls and roots of OE, WT, and RNAi seedlings (Fig. 6a–l). We examined transverse and longitudinal tissue sections of seedlings and hypocotyls. Epidermal, parenchymal, vascular bundle, and external phloem cell sizes were compared between the different lines using microscopic images. Analyses of the hypocotyl cross sections revealed that the external phloem cells were significantly larger in the OE seedlings than in the WT seedlings. Furthermore, the hypocotyls of OE plants had more epidermal and xylem cells than those of WT plants and had more loose cell layers (epidermis, parenchyma, vascular bundle, and external phloem) that were more disorganized (Fig. 7a,d,g). In contrast, the external phloem cells of the RNAi lines were smaller than those of the WT seedlings. In addition, the RNAi plants had fewer epidermal and xylem cells (Fig. 7b,e,and h) and had more tightly packed cell layers than did the WT hypocotyls (epidermis, parenchyma, vascular bundle, and external phloem; Fig. 7c,f,i–k).
An examination of the cotyledon and root longitudinal sections provided additional evidence of differences between the lines (Supplementary Fig. 2a–j). The cells of the OE seedlings expanded relatively quickly, resulting in larger but fewer cells in the meristem zone of the roots in comparison with the WT and RNAi lines (from QC to the first elongation cell) (Supplementary Fig. 3a–d). In contrast, the RNAi root and cotyledon cells divided and expanded relatively slowly. Analyses of the microscopic images suggested that the enlarged cotyledons, longer hypocotyls, and greater number of lateral roots in the OE lines might be the result of increased cell elongation. In contrast, the smaller cotyledons, shorter hypocotyls, and fewer lateral roots observed in the RNAi lines might be a consequence of decreased elongation. Thus, CsGPA1 may function as a positive regulator of seedling cell elongation in darkness, which then accelerates subsequent plant growth.
Discussion
Our study describes an entirely novel G protein from cucumber, a global food crop, and helps to elucidate the roles of G proteins in plants, particularly those both internal and external phloem. G-protein signaling pathways are known to affect many plant growth and development processes. Mutant analyses have shown that heterotrimeric G-proteins represent a critical nexus in the signal regulation of a variety of processes such as germination, cell division and elongation, stress responses, and plant morphology1. In this study, we found that the CsGPA1 gene was homologous to the GPA1 gene in other plant species. GPA1 is expressed in all stages of development and in all organs, with the exception of mature seeds21. Among the measured samples, expression was highest in the root, followed by the stem apex, hypocotyls, cotyledon, and leaf22, and levels in immature organs were higher than in mature organs21. Similarly, our study demonstrated the spatiotemporal expression of endogenous CsGPA1 (Fig. 1b). Previous studies showed that the Gα subunit was present in the plasma membranes of the pollen tube in other species23,24. Our study demonstrated that CsGPA1 is also present in the plasma membrane of the epidermis and cortex in cucumber (Fig. 3a–h), where it may help to regulate early seedling development. Immunohistochemical analyses showed that functional CsGPA1 acting in the epidermal and cortex membranes may affect seedling root growth. CsGPA1 was in the cytosol of the endodermal, parenchymal, vascular, and root meristematic cells (Fig. 4a–g). Gα-null mutations decrease root growth in Arabidopsis, rice, and maize25,26,27 and can lead to an increase in cell division to promote primary root elongation26 or to a decrease in cell division at the root apical meristem27. The results of our seed germination and seedling morphogenesis analyses in OE and RNAi plants showed that CsGPA1 affects seed germination and early seedling growth in the cotyledons, hypocotyl, and roots (Figs 5a–f and 6a–l). RNAi silencing of the CsGPA1 gene delayed the speed and reduced rates of seed germination (Fig. 5b), inhibited the size of the cotyledons, the lengths of the hypocotyl and the primary root, and the growth of lateral roots (Fig. 6c–l). Thus, we conclude that CsGPA1 is involved in regulation of seed germination and early seedling development in cucumber.
Cell division and elongation are two fundamental cellular processes in the life cycle of plants9 regulated in part by the Gα subunit. Mutations to Gα result in inhibition of cell division along the leaf length but not along the leaf width28,29 and can lead to dwarfism and etiolated seedling phenotypes in several species9,11,15. Maize Gα regulates and enlarges the shoot apical meristem (SAM)28, but gpa1 mutants display no obvious change in SAM height30. These findings suggest that the Gα subunit specifically mediates cell proliferation in the shoot apical meristem and leaf primordia but not at the leaf plate meristem. Our study showed that CsGPA1 helps facilitate the elongation of epidermal and parenchymal cells by positively regulating the hypocotyl and root meristem zone in early cucumber seedlings (Fig. 7a–g, Supplementary Figs 2a–i, and 3a–d). This may be conducive to the transport of nutrients from the roots to the upper leaves, as well as the transport of nutrients from the upper part of the cotyledon to the lower part of the roots, and may explain why the leaf areas and root volumes were greater in the OE seedlings than in the WT seedlings. In contrast, the relatively low abundance of CsGPA1 in the RNAi seedlings inhibited the development of the hypocotyl tissue, in particular parenchymal cells surrounding the vascular bundles. This inhibition likely hindered the transport of nutrients through the hypocotyl and suppressed leaf and root growth.
In conclusion, we infer that CsGPA1 is involved in the regulation of meristem cell elongation in the early seedling stage by regulating hypocotyl elongation and root growth. Strong development of early seedlings will be useful for alleviating abiotic stress and enhancing stress tolerance in the cucumber production process in greenhouses during the winter31, and thus additional work is required in this direction. Further study of CsGPA1 will be required to elucidate its precise function and will provide insights into the relationship between signal transduction and growth and the development of cucumber. This additional work will serve to increase global food security by creating a more reliable growth system for cucumber and other crops32,33,34,35,36,37.
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Acknowledgements
This work was supported by the earmarked fund for National Nature Science Foundation of China (31601796) and Science and Technology Innovation Program of the Chinese Academy of Agricultural Sciences (CAAS-ASTIP-IVFCAAS) and the support by the Key Laboratory of Horticultural Crop Biology and Germplasm Innovation, Ministry of Agriculture, China. We thank Shelley Robison, PhD, from Liwen Bianji, Edanz Editing China (www.liwenbianji.cn/ac) for editing the English text of a draft of this manuscript.
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Conceived and designed the experiments: Y.Y., L.G. and X.Y. Conducted the experiments: Y.Y., Y.-S.L., C.H. Analyzed the data: Y.Y. and W.Z. Wrote a draft of the manuscript: Y.Y. and W.Z.
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Yan, Y., Zhang, W., Li, Y. et al. Functions of CsGPA1 on the hypocotyl elongation and root growth of cucumbers. Sci Rep 8, 15583 (2018). https://doi.org/10.1038/s41598-018-33782-4
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DOI: https://doi.org/10.1038/s41598-018-33782-4
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