Expression of cotton PLATZ1 in transgenic Arabidopsis reduces sensitivity to osmotic and salt stress for germination and seedling establishment associated with modification of the abscisic acid, gibberellin, and ethylene signalling pathways
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Zinc-finger transcription factors play central roles in plant growth, development and abiotic stress responses. PLATZ encodes a class of plant-specific zinc-finger transcription factor. However, biological functions or physiological mechanism controlled by PLATZ are currently limited.
GhPLATZ1 transcripts were considerably up-regulated by NaCl, mannitol, abscisic acid (ABA) and gibberellin (GA) treatments. Transgenic Arabidopsis by ectopic expression of GhPLATZ1 exhibited faster seed germination and higher seedling establishment under salt and mannitol stresses than those of wild type (WT), indicating enhanced osmotic insensitivity in GhPLATZ1 transgenic Arabidopsis. The ABA content in dry seeds of GhPLATZ1 transgenic Arabidopsis was lower than that of WT whereas the ABA content was not changed in germinating seeds under salt stress. Seed germination was faster than but the seedling establishment of transgenic Arabidopsis was similar to WT. Besides, GhPLATZ1 transgenic and WT Arabidopsis exhibited insensitivity to paclobutrazol (PAC), a GA biosynthesis inhibitor, whereas exogenous GA could eliminate the growth difference between GhPLATZ1 transgenic and WT Arabidopsis under salt stress. Moreover, exogenous 1-aminocyclopropane-1-carboxylic acid (ACC), an ethylene precursor, exerted similar effects to GA. Furthermore, ABI4 and ETO1 transcripts were significantly down-regulated, whereas ACS8 was up-regulated in GhPLATZ1 transgenic Arabidopsis under salt stress.
In conclusion, GhPLATZ1 had broad influence in responses to salt and mannitol stresses in transgenic Arabidopsis during seed germination and seedling establishment. The effect of GhPLATZ1 expression in transgenic Arabidopsis might be mediated by the ABA, GA, and ethylene pathways. Thus, this study provided new insights into the regulatory network in response to abiotic stresses in plants.
KeywordsGossypium hirtusum L PLATZ Abiotic stresses Ethylene ABA GAs
Ethylene-overproduction protein 1
Murashige and Skoog
Transgenic arabidopsis with high GhPLATZ1 overexpression
Impaired germination and postgermination growth are common among seeds exposed to salt and drought stresses. Plants can regulate and coordinate both growth and/or stress sensitivity to promote survival or escape from environmental stress by modifying the production, distribution, or signal transduction of hormones. Thus, identification of components involved in hormonal regulation during germination under abiotic stresses is essential.
A large number of genes encoding DNA-binding proteins, which play important roles in hormone mediated responses to abiotic stresses were identified in plants. For example, the major downstream components of abscisic acid (ABA) signaling, namely, ABA insensitive 3 (ABI3) , ABI4  and ABI5 [3, 4], are positive regulators of ABA, and they are crucial in seed maturation, seed germination and seedling growth . Fuctional loss of these genes causes fast germination under ABA and abiotic stresses. The GA signaling pathways depend on DELLA proteins including GA insensitive ones (GAI), repressor of ga1–3 (RGA), repressor of ga1–3-like (RGL) 1, RGL2 and RGL3 [6, 7]. GA destabilizes the DELLA proteins, which act as growth repressors, by targeting ubiquitination and degradation . EIN2 plays a key role in ethylene signaling and losing its function results in a hypersensitivity to salt and osmotic stress during germination and early seedling development in Arabidopsis . ERF genes might also play a pivotal role in ethylene responsiveness and germination regulation in tomato (Solanum lycopersicon); SlERF2 overexpression in transgenic lines causes premature seed germination .
Zinc-finger transcription factors are a relatively large family of plant transcription factors (approximately 15% of the total) and play central roles in plant growth and development [11, 12]. PLATZ1 was first isolated from pea . PLATZ1 and its paralogs from Arabidopsis and other species have two consensus signatures, namely, C-x2-H-x11-C-x2-C-x(4–5)-C-x2-C-x(3–7)-H-x2-H (CHC4H2) and C-x2-C-x(10–11)-C-x3-C. However, the two consensus signatures are different from those of previously characterized zinc-binding motifs, such as RING (C3HC4), LIM (C2HC5) , GATA finger (C-x2-C-x(17–18)-C-x2-C (C2C2)) [15, 16], COSTANS/CONSTANS-like (CO/COLs) , and the DNA-binding one finger (Dof) . Hence PLATZs encode a novel class of plant-specific zinc-finger transcription factors. Recently, Arabidopsis PLATZ1 and 2 were reported to positively regulate acquisition of dessication tolerance in seeds and vegetative tissues . Maize PLATZ protein FL3 is involved in tRNA and 5S rRNA transcription through interaction with RNA polymerase III . Multiple members of PLATZ genes exist in plants. For example, 12 PLATZ genes exist in the Arabidopsis genome (https://www.arabidopsis.org/servlets/Search?type=general&search_action=detail&method=1&show_obsolete=F&name=PLATZ&sub_type=gene&SEARCH_EXACT=4&SEARCH_CONTAINS=1/). Therefore, the roles of PLATZs remain largely unclear.
Cotton (Gossypium hirsutum) is one of the most important fibre and oil crops. Cotton seed germination and seedling establishment are severely impaired in abiotic stress conditions. The biological significance of cotton PLATZs has not yet been described. In this study, the first PLATZ form cotton, named as GhPLATZ1, was isolated and characterized. Our results indicated that the expression of GhPLATZ1 was induced by abiotic and hormone stimuli. Ectopic expression of GhPLATZ1 in Arabidopsis resulted in enhanced insensitivity to osmotic stresses, ABA and PAC. We deduced that GhPLATZ1 might play important roles in regulating hormone-mediated osmotic stress during cotton seed germination and seedling establishment.
Characterization of GhPLATZ1Transcription factor
We previously showed that a gene (GenBank ID: JQ837703) from cotton was significantly induced by salt stress . The deduced amino acid sequence was homologous to PLATZ1 from peas and PLATZs from Arabidopsis. Given that the gene was the first isolated PLATZ from cotton, we named it as GhPLATZ1. Genome-wide searching in G.hirtusium and Arabidopsis thaliana revealed that 9 PLATZ genes exist in cotton (https://phytozome.jgi.doe.gov) and 12 are in Arabidopsis [the Arabidopsis Information Resource (TAIR), https://www.arabidopsis.org/servlets/Search?type=general&search_action=detail&method=1&show_obsolete=F&name=PLATZ&sub_type=gene&SEARCH_EXACT=4&SEARCH_CONTAINS=1]. GhPLATZs showed high identity with each other (≥79.56%) (Additional file 1: Figure S1A), and all of them shared numerous similarities to a subfamily of AtPLATZs, including AtPLATZ3, AtPLATZ11, and AtPLATZ12 (Additional file 1: Figure S1B). However, the roles of GhPLATZs remain unclear.
GhPLATZ1 transgenic Arabidopsis enhances insensitivity to osmotic stresses
GhPLATZ1 inhibits ABA biosynthesis
GhPLATZ1 involves GA and ethylene-mediated salt stress responses
More than 10 years ago, PLATZ1 was isolated from pea and characterized as a plant-specific zinc-dependent transcription repressor . Recently, only Arabidopsis PLATZ1 and 2 , and maize PLATZ protein FL3  were reported to be involved in abiotic stress and seed development, respectively. Therefore, the roles of PLATZs remain largely unclear.
In the present study, we illustrated that the GhPLATZ1 expression was significantly induced by salt, mannitol, ABA and GA in 20-day-old plants and germinated seeds (Fig. 1a and b), thereby suggesting the involvement of GhPLATZ1 in multiple abiotic stress responses. GhPLATZ1 transgenic lines showed significantly enhanced osmotic, salt, ABA, and PAC insensitivity during seed germination and seedling establishment (Figs. 2, 3, 4 and 5). This function of GhPLATZ1 is similar to that of AtPLATZ1 and AtPLATZ2 whose mutants platz1 and platz2 increased sensitivity to ABA ; thus GhPLATZ1 might function similarly to AtPLATZ1 and AtLATZ2 during seed germination. However, GhPLATZ1 transgenic plants showed similar phenotypes to WT in vegetative tissues under normal, salt and mannitol conditions (data not shown), whereas constitutive expression of AtPLATZ1 conferred tolerance to low water availability . Therefore, PLATZs from different species may function similarly in some developing stages but differently in other developing stages in response to abiotic stresses.
Impaired germination and postgermination growth are common among seeds exposed to salt and drought stresses. Plants can regulate and coordinate both growth and/or stress tolerance to promote survival or escape from environmental stress by modifying the production, distribution, or signal transduction of hormones. The hormonal balance between ABA and GA in seed germination in response to environmental stimuli is well documented and discussed [5, 22, 23, 24]. ABA plays crucial roles in dormancy induction in developing seeds and in dormancy maintenance in seed imbibition, whereas GAs are involved in germination. Exogenous ABA application inhibits germination in a dose-dependent manner. Applying fluridone, an ABA biosynthesis inhibitor, substantially stimulates seed germination under salinity . The seeds of typical ABA-deficient mutants germinate faster than those of WT , and transgenic plants constitutively expressing the ABA biosynthesis gene maintain considerable seed dormancy [26, 27]. In contrast, GA3 enhances germination under NaCl stress . GA-deficient mutants, such as ga1 and ga2, show strong seed dormancy and fail to germinate without exogenous GA treatment . Mutants that are defective in GA 2-oxidases, which deactivate bioactive GA, show decreased seed dormancy . Compared with WT, our data indicated low levels of ABA in dry seeds of GhPLATZ1 transgenic Arabidopsis (Fig. 4a). This result may lead to the insensitivity of GhPLATZ1 transgenic Arabidopsis seeds to osmotic stress and ABA compared with WT. The down-regulation of ABI4 expression (Fig. 4c) confirmed the insensitivity of GhPLATZ1 transgenic Arabidopsis seeds to osmotic stress and ABA. By contrast, the different responses of GhPLATZ1 transgenic and WT Arabidopsis to PAC indicated the potential high GA in GhPLATZ1 transgenic Arabidopsis in response to salt stress. Therefore, the major active GA forms such as GA1 and GA4 need further investigated. The transcription of a key ABA biosynthetic gene, NCED6, and key GA catabolic gene, GA2ox7, is significantly enhanced by ABI4 overexpression by directly binding to their promoters; and ABA induces GA2ox7 transcription whereas GA represses NCED6 expression in an ABI4-dependent manner; and ABA stabilizes the ABI4 protein whereas GA promotes its degradation . Thus, GhPLATZ1 might function in ABA and GA antagonism by suppressing ABI4 transcription and inhibiting the activating expression of NCED6 and GA2ox7, thereby leading to decreased ABA and increased GA (Fig. 7).
In addition, ethylene accelerates seed germination by overcoming the inhibitory action of ABA or stimulating GA biosynthesis or its signaling pathway . Two results indicated that GhPLATZ1 increased ethylene production: first, ACS8, a gene that encodes ethylene biosynthesis, showed up-regulated expression in GhPLATZ1 transgenic lines compared with WT (Fig. 6c). ABI4 transcripts were significantly suppressed in GhPLATZ1 transgenic lines (Fig. 4c). Increasing evidence has revealed that ABI4 binds directly to promoters of ACS4, ACS8, and ACO2 to inhibit their transcription causing reduced ethylene production . Therefore, significantly suppressed ABI4 transcripts in GhPLATZ1 transgenic lines suggested the up-regulated expression of ethylene biosynthesis genes, such as ACS4, ACS8, and ACO2. Here, we detected the expression of ACS8, a member of a gene family encoding ethylene biosynthetic enzymes, was up-regulated in GhPLATZ1 in transgenic lines (Fig. 6c). Second, ETO1 showed significantly down-regulated expression in GhPLATZ1 transgenic lines (Fig. 6b). ETO1 is a component of the E3-ligase complex and interacts directly with ACS5 and Le-ACS3 for degradation in a proteasome-dependent manner [32, 33, 34, 35]. Mutated ETO1 forms result in increased ACS5 protein stability and ethylene overproduction . Therefore, the significantly down-regulation of ETO1 in GhPLATZ1 transgenic lines (Fig. 6b) also suggested increased ethylene levels in GhPLATZ1 transgenic lines. The results of ACC (the direct precursor of ethylene) application (Fig. 7a) further indicated the higher ethylene in GhPLATZ1 transgenic lines than WT. Thus, GhPLATZ1 might increase ethylene production by down-regulating the expression of ABI4 and ETO1 genes (Fig. 7).
In conclusion, this study discovered a new regulator, GhPLATZ1, which was induced by NaCl, mannitol, ABA and GA treatments. The model in Fig. 7 shows how GhPLATZ1 functions in osmotic stresses during seed germination and seedling establishment. First, GhPLATZ1 increases osmotic insensitivity of transgenic Arabidopsis by inhibiting ABI4 expression, which can induce the expression of NCED6 and GA2ox7. Second, GhPLATZ1 inhibits ABI4 and ETO1 expression, which can suppress ACS gene expression and decrease ACS protein stability, respectively. Therefore, GA and ethylene possibly increased and ABA decreases in GhPLATZ1 transgenic Arabidopsis to promote seed germination and seedling establishment under osmotic stress. However, overexpression of ABI4 and ETO1 in GhPATZ1 transgenic Arabidopsis will confirm this conclusion. However, GhPLATZ1 regulates the expression levels of ABI4 and ETO1, as well as what and how other signaling participate in GhPLATZ1-mediated pathways remains unknown.
Plant materials and treatments
Seeds of upland cotton (Gossypium hirtusium.L) cultivar ZM19 were bought from Chinese Academy of Agricultural Sciences. Seedlings were grown for 20 days in MS liquid medium in a growth chamber with 300 μM m− 2·s− 1 light intensity and day/night temperatures of 28 °C/20 °C. For each treatment, every 15 uniformly developed seedlings were transferred to MS media containing either 200 mM NaCl, 300 mM mannitol, 50 μM ABA or 50 μM GA3 for 12 h. In addition, seeds germinated in water for 2.5 days with 0.5 cm radicles were also treated with MS media containing either 200 mM NaCl, 300 mM mannitol, 50 μM ABA or 50 μM GA3 for 6 and 12 h, respectively. Twenty-day seedlings or 2.5-d germinated seeds transferred to MS media were used as control. Samples were harvested at the indicated points, frozen in liquid nitrogen, and stored at − 70 °C for RNA extraction. Each treatment was repeated three times.
Vector construction and transformation
To construct 35S::GhPLATZ1, the GhPLATZ1 coding sequence was amplified using cDNA by PCR with gene specific primers (Additional file 2: Table S1). The resulting PCR product was cloned into the SalI and KpnI sites of binary vector pBI121 under the control of a cauliflower mosaic virus 35S promoter.
The 35S::GhPLATZ1 was then introduced into Agrobacterium tumefaciens strain GV3101 to be transformed into Arabidopsis thaliana ecotype Columbia-0 by floral dipping . The transgenic plants were screened on 1/2 MS medium containing 50 mg·L− 1. kanamycin. Two generations of the corresponding T1 transgenic seedlings segregated at a ratio of 3:1 (resistant:sensitive) were selected to propagate T3 homozygous. Some of the transgenic Arabidopsis plants were confirmed by detecting the expression of GhPLATZ1 by PCR and used for further experiments. Primers are listed in Additional file 2: Table S1.
The total RNAs of different cotton samples used in this report were isolated using RNeasy Plant Mini Kit (QIAGEN). The total RNAs of 20-day-old seedlings and germinated seeds of different Arabidopsis transgenic lines were isolated using a Universal Plant Total RNA Extraction Kit (spin-column)-I (BioTeke Beijing China).
qRT-PCR was performed as previously described . Cotton GhUBI (EU604080) or Arabidopsis actin2 genes were used as the standard control. The relative GhPLATZ1 and AtPLATZs expression level was analyzed using the comparative CT method, and three replicates of each sample were analyzed. All of the primers used are listed in Additional file 2: Table S1. At least three independent experiments were carried out.
Roots from seven-day-old transgenic Arabidopsis containing 35S::GhPL-GFP were used and imaged by LSCM51 (Zeiss) at 488 nm for GFP.
Seed germination and cotyledon greening analysis
Seeds of each genotype were harvested from plants of the same age and stored for 4 weeks in the dark at 4 °C. For each comparison, seeds were surface-sterilized with 70% ethanol for 5 min, subsequently incubated in 2.6% sodium hypochlorite for 10 min, and washed five times with sterile water. At least 30 sterile seeds were plated on 1/2 MS medium plus 1% (w/v) sucrose with or without different concentrations of NaCl, KCl, Na2SO4, LiCl, mannitol, ABA, PAC, or NaCl combined with GA or ACC as indicated. Plates were chilled at 4 °C in the dark for 3 days (stratification) and moved to 22 °C with a 16-h-light/8-h-dark cycle. The percentage of seed germination was determined at indicated time points. Germination was defined as an obvious emergence of the radicle through the seed coat. The percentage of cotyledon greening was recorded at 14 days after the end of stratification. Cotyledon greening was defined as obvious cotyledon expansion and turning of cotyledon color into green. Three biological replications were performed.
ABA content measurements
To quantify ABA content, dry seeds and two-day germinated seeds of GhPLATZ1 overexpressing Arabidopsis and WT treated with or without 175 mM NaCl were ground in liquid nitrogen. Furthermore, 150 mg of seed powder was homogenized and extracted for 24 h in methanol containing D6-ABA (OIChemIm Co., Ltd.) as an internal standard. The mixture was purified with an Oasis Max solid-phase extract cartridge (150 mg/6 cc; waters) and eluted with 5% formic acid in methanol. The elution was dried and reconstituted. ABA content was measured by HPLC-MS-MS (Agilent 1290 Rapid-resolution Liquid chromatography, Agilent Technologies, Waldbronn, Germany; Sciex 6500 Q-Trap AB Technologies, USA). The mobile phase consisted of A:B (methyl alcohol/0.1% methanoic acid:H2O/0.1% methanoic acid). The elution gradient was 0–2 min, A = 20%; 2–14 min, A = 80%; and 15.1–20 min, A = 20%. The injection volume was 2 μL. The mass spectrometer conditions were as follows: spray voltage, 4500 V; atomizer pressure, 65 psi; assist device pressure, 70 psi; atomization temperature, 400 °C.
Data were subjected to data processing system and significant differences were established through one-way ANOVA. Differences at 5% and 1% levels were considered significant and denoted by single and double stars (*P < 0.05; **P < 0.01).
This work was supported by the National Natural Science Foundation of China (Grant number 31471425), the Natural Science Foundation of Shandong Province (Grant number ZR2015CM002).
Availability of data and materials
The data sets supporting the results of this article are included within the article and its additional files. Sequence data used in this manuscript can be found in the Arabidopsis Information Resource (TAIR, https://www.arabidopsis.org/servlets/Search?type=general&search_action=detail&method=1&show_obsolete=F&name=PLATZ&sub_type=gene&SEARCH_EXACT=4&SEARCH_CONTAINS=1) and The National Center for Biotechnology Information (https://blast.ncbi.nlm.nih.gov/Blast.cgi), under the following accession numbers: GhPLATZ1 (XP_016742770.1), GhPLATZ2 (XP_016736692.1), GhPLATZ3 (XP_016705363.1), GhPLATZ4 (XP_01672128.1), GhPLATZ5 (XP_012488860.1), GhPLATZ6 (XP_016670611.1), GhPLATZ7 (XP_016723269.1), GhPLATZ8 (XP_016728634.1), GhPLATZ9 (XP_016742383.1), AtPLATZ1.1 (AT1G21000.1), AtPLATZ1.2 (AT1G21000.2), AtPLATZ2 (AT1G76590.1), AtPLATZ3.1 (AT1G32700.1), AtPLATZ3.2 (AT1G32700.2), AtPLATZ4 (AT1G43000.1), AtPLATZ5 (AT1G31040.1), AtPLATZ6 (AT2G01818.1), AtPLATZ7 (AT2G12646.1), AtPLATZ8 (AT2G27930.1), AtPLATZ9 (AT3G50808.1), AtPLATZ10 (AT3G60670.1), AtPLATZ11.1 (AT4G17900.1), AtPLATZ11.2 (T4G17900.2), AtPLATZ12 (AT5G46710.1).
SCZ identified voucher specimen and carried out Arabidopsis transformation, majority of molecular studies and data analysis. SCZ also drafted the manuscript. RY, YQH, and SSL participated in phenotypic analysis, qRT-PCR and references editing. GDY, JGH and CCZ give some advices for experimental design. CAW conceived the study, participated in the design and coordination of this study and drafted the manuscript. All of the authors read and approved the final manuscript.
Ethics approval and consent to participate
Seeds of upland cotton (Gossypium hirtusium.L) cultivar ZM19 were bought from Chinese Academy of Agricultural Sciences.
Consent for publication
The authors declare that they have no competing interests.
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- 6.J.M. Daviere, P. Achard, Gibberellin signaling in plants, development (Cambridge, England), 140 (2013) 1147–1151.Google Scholar
- 12.Riechmann JL, Heard J, Martin G, Reuber L, Jiang C, Keddie J, Adam L, Pineda O, Ratcliffe OJ, Samaha RR, Creelman R, Pilgrim M, Broun P, Zhang JZ, Ghandehari D, Sherman BK, Yu G. Arabidopsis transcription factors: genome-wide comparative analysis among eukaryotes, science (New York). NY. 2000;290:2105–10.CrossRefGoogle Scholar
- 19.Gonzalez-Morales SI, Chavez-Montes RA, Hayano-Kanashiro C, Alejo-Jacuinde G, Rico-Cambron TY, de Folter S, Herrera-Estrella L. Regulatory network analysis reveals novel regulators of seed desiccation tolerance in Arabidopsis thaliana. Proc Natl Acad Sci U S A. 2016;113:E5232–41.CrossRefGoogle Scholar
- 25.Frey A, Effroy D, Lefebvre V, Seo M, Perreau F, Berger A, Sechet J, A. To, North HM, Marion-Poll A. Epoxycarotenoid cleavage by NCED5 fine-tunes ABA accumulation and affects seed dormancy and drought tolerance with other NCED family members. The Plant journal : for cell and molecular biology. 2012;70:501–12.CrossRefGoogle Scholar
- 34.M.J. Christians, D.J. Gingerich, M. Hansen, B.M. Binder, J.J. Kieber, R.D. Vierstra, The BTB ubiquitin ligases ETO1, EOL1 and EOL2 act collectively to regulate ethylene biosynthesis in Arabidopsis by controlling type-2 ACC synthase levels, Plant J : for cell and molecular biology, 57 (2009) 332–345.Google Scholar
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