The NAC Protein from Tamarix hispida, ThNAC7, Confers Salt and Osmotic Stress Tolerance by Increasing Reactive Oxygen Species Scavenging Capability

Abstract

Plant specific NAC (NAM, ATAF1/2 and CUC2) transcription factors (TFs) play important roles in response to abiotic stress. In this study, we identified and characterized a NAC protein, ThNAC7, from Tamarix hispida. ThNAC7 is a nuclear localized protein and has transcriptional activation activity. ThNAC7 expression was markedly induced by salt and osmotic stresses. Transiently transformed T. hispida seedlings overexpressing ThNAC7 (OE) or with RNA interference (RNAi) silenced ThNAC7 were generated to investigate abiotic stress tolerance via the gain- and loss- of function. Overexpressing ThNAC7 showed an increased reactive oxygen species (ROS) scavenging capabilities and proline content, which was accomplished by enhancing the activities of superoxide dismutase (SOD) and peroxidase (POD) in transiently transformed T. hispida and stably transformed Arabidopsis plants. Additionally, ThNAC7 activated these physiological changes by regulating the transcription level of P5CS, SOD and POD genes. RNA-sequencing (RNA-seq) comparison between wild-type and ThNAC7-transformed Arabidopsis showed that more than 40 known salt tolerance genes might regulated by ThNAC7, including stress tolerance-related genes and TF genes. The results indicated that ThNAC7 induces the transcription level of genes associated with stress tolerance to enhance salt and osmotic stress tolerance via an increase in osmotic potential and enhanced ROS scavenging.

1. Introduction

Environmental constraints, including cold, salt and drought, which negatively affect the growth and development of plants, are leading large agricultural production losses worldwide [1]. Plants have evolved a wide range of adaptations to abiotic and biotic stresses, involving stress perception coupled with signal transduction and amplification [2]. In progress, TFs can regulate the expression of downstream functional genes involved in biotic or abiotic stress tolerance [3]. Recently, many researches have reported that a battery of TFs or functional genes involved in abiotic stress responses. For instance, overexpression of AtbHLH112 increased salt and drought tolerance via increasing the expression level of PODs and SODs to improve ROS scavenging ability in Arabidopsis [4]. Overexpression of BplMYB46 in transgenic Betula platyphylla improved abiotic tolerance via enhancing the ROS scavenging and proline level [5]. Overexpressing of VvWRKY30 improved salinity stress resistance via regulating osmoticum accumulation and ROS scavenging in Arabidopsis [6]. Besides, the overexpression of OsDhn1 increased drought and salt tolerance via reducing ROS accumulation in transgenic rice [7]. The overexpression of AnnSp2 enhanced salt and drought tolerance by ABA synthesis and the elimination of ROS in transgenic tomato [8].

The NAC TF family is a plant specific TF family and includes 117 members in Arabidopsis thaliana, 163 in Populus trichocarpa, 151 in Oryza sativa, and 152 in both Nicotiana tabacum and Glycine max [9]. NAC proteins possess a nuclear localization signal sequence, which have variable C-terminal domain in addition to highly conserved N-terminal binding domain [10].

In recent years, many studies have reported that a number of NAC TFs involved in biotic [11,12] and abiotic [12,13] stress responses in plants. A relatively large proportion of rice and Arabidopsis NAC TFs under different abiotic and biotic stresses showed differential expression patterns by transcriptional analysis. [14,15]. Moreover, NAC TFs confer abiotic stress tolerance to transgenic plants. For instance, AtNAC72, AtNAC109, and AtNAC55 contribute to drought tolerance by promoting the detoxification of aldehydes in the glyoxalase pathway [16,17]. Transgenic rice plants overexpressing OsNAC2, OsNAC3, OsNAC6, or OsNAC14 enhanced drought tolerance [18,19,20,21]. The overexpression of OsNAC6 induced tolerance to high salt, drought and blast disease in rice [22]. Overexpression of TaNAC69 improved the expression of stress-related genes and drought tolerance in transgenic wheat plants [23]. Overexpression of TsNAC1 in both Thellungiella halophila and Arabidopsis could enhance abiotic stress resistance, particularly salt stress tolerance [24]. MusaNAC68 positively regulates salt and drought stress tolerance in transgenic banana plants [25]. Overexpression of MdNAC1 enhanced drought stress tolerance via enhancing photosynthesis and ROS scavenging in apple transgenic plants [26]. Although a variety of NAC proteins in different plant species have been identified and reported to play key roles in abiotic stress, few studies have been performed about the biological functions of NAC TFs in halophytic woody plants.

Tamarix hispida, belong to the genus Tamarix, is a woody halophyte that it can grow better than other plants in drought and saline soils. T. hispida has properly effective stress defense system and is appropriately used to study abiotic stress tolerance. Previous study identified 16 NAC TFs in transcriptomes of T. hispida [27]. Among these NACs, we further identified a NAC gene, ThNAC7, which can respond to high levels of salt stress. Therefore, we selected ThNAC7 for further study. The results demonstrated that ThNAC7 regulates osmotic and salt stress tolerance via modulating the transcription levels of genes that may activate a number of physiological variations, containing ROS scavenging and changes in osmotic potential, in both transiently transformed T. hispida and stably transformed Arabidopsis plants. The present study offers new insights into the functions of NAC TFs in abiotic stress tolerance.

2. Results

2.1. Bioinformatics Analysis of ThNAC7

The open reading frame (ORF) of ThNAC7 is 1737 bp, encodes 578 amino acids with 65.13 kDa molecular weight. Multiple sequence alignment analysis indicated that ThNAC7 and NAC proteins of other plant species shared highly conserved binding domain at the N-terminal. ThNAC7 contains a classic NAC domain that is the basic characteristic of the NAC family (Supplementary Figure S1). Phylogenetic tree was constructed in order to study the evolutionary relationships between ThNAC7 and other 105 NACs from Arabidopsis. The results showed that ThNAC7 is most similar to two Arabidopsis NAC proteins, ANAC091 (AT5G24590) and ANAC062 (AT3G49530) from NAC subfamily VI (Figure 1), indicating that ThNAC7 should also belong to the NAC subfamily VI.

Figure 1.

Phylogenetic analysis between ThNAC7 and the NAC proteins from Arabidopsis. The phylogenetic relationship of ThNAC7 and the NAC proteins from Arabidopsis. The ThNAC7 and 105 Arabidopsis NACs were aligned; the unrooted NJ tree was constructed using MEGA 6.06.

ThNAC7 and 88 NACs from the transcriptomes of T. hispida were used for another phylogenetic tree to study the phylogenetic relationships of the NAC TF family in T. hispida. All NACs could be divided into 10 subfamilies (I–X), and ThNAC7 was most similar to ThNAC35, and belongs to NAC subfamily I (Figure S2).

2.2. ThNAC7 Is a Nuclear Localization Protein with Transactivation Activity

The 35S::ThNAC7-GFP (green fluorescent protein) or 35S::GFP plasmid was respectively imported into onion epidermal cells via particle bombardment. Microscopic observation indicated that the 35S::ThNAC7-GFP fusion protein was observed exclusively in nucleus, while the 35S::GFP protein in the control was uniformly distributed throughout the cytoplasm and nucleus (Figure 2A). The results indicate d that ThNAC7 is a nuclear localization protein.

Figure 2.

Subcellular localization and transcriptional activation of ThNAC7. (A): Subcellular localization analysis of ThNAC7. The onion nuclei were visualised through DAPI (4′,6-diamidino-2-phenylindole) staining. Bars, 50 μm. (B): Transactivation assay of ThNAC7 (a, b: NAC domain). A diagram of the pGBKT7 constructs for expressing different truncated ThNAC7 proteins in yeast cells. Transactivation assay of the intact or truncated ThNAC7 proteins. Full length or truncated CDSs of ThNAC7 were constructed into pGBKT7 vector and transformed into Y2HGold cells, and grown on SD/-Trp or SD/-Trp/-His/X-α-gal mediums to assess their transcriptional activation.

To confirm the transactivation activity of ThNAC7, full length or truncated CDSs of ThNAC7 were constructed to pGBKT7 vector and transformed into Y2HGold cells to detect their transactivation activity (Figure 2B). All transformants could grow normally on the SD/-Trp plates, showing that they had been transformed in Y2HGold cells. The yeast cells containing the full-length CDS of ThNAC7 grew well and appeared blue on the SD/-Trp-His/X-a-Gal plates, suggesting that this protein is capable of transcriptional activation. Furthermore, we noticed that the yeast cells transformed with the assumed C-terminal activation domain (dc2, amino acids 146–578) of ThNAC7 thrived and became blue, whereas cells expressing the N-terminal domain (dc1, amino acid 1–435) of ThNAC7 could not grow, showing that the C-terminal of ThNAC7 has transactivation activity. The truncated CDSs expressing amino acids 146–290 and 291–435 retained the transactivation activity, whereas cells expressing the 436–578 fragment had completely abolished transactivation activity. Moreover, the smallest fragment of ThNAC7 that retained transactivation activity was located respectively in amino acids 216–290, 291–360, and 361–435. Taken together, the results indicated that ThNAC7 has transcriptional activation with three independent activation domains: aa 216–290, 291–360 and 361–435, respectively.

2.3. The Expression of ThNAC7 Is Induced by Osmotic and Salt Stress

QRT-PCR assay proved that the expression of ThNAC7 was markedly induced by osmotic (400 mM mannitol) or salt (300 mM NaCl) stress in both roots and leaves of T. hispida (Figure 3). Under salt stress conditions, ThNAC7 was highly induced at 12 h in root tissue; meanwhile, it was highly induced at 24 h in leaf tissue (Figure 3A,B). Under osmotic stress conditions, ThNAC7 was highly induced at 12 h in leaf tissue and at 6 h in root tissue (Figure 3C,D). These results showed that the expression of ThNAC7 is induced by osmotic and salt stress, implying that ThNAC7 plays roles in osmotic and salt stress responses.

Figure 3.

The expression level of ThNAC7 in response to osmotic or salt stress in T. hispida. The expression patterns of ThNAC7 in roots or leaves of T. hispida plants in response to treatment with NaCl (300 mM) (A,B) or mannitol (400 mM) (C,D). The expression of ThNAC7 in normal conditions (0 h) was designed as 1 to standardize the expression level of ThNAC7 in salt or osmotic conditions.

2.4. Overexpression of ThNAC7 in Arabidopsis Confers Osmotic and Salt Stress Tolerance

Nine independent T₃ homozygous lines overexpressing ThNAC7 were obatined to verify the molecular function of ThNAC7 in salt and osmotic stress tolerance. RT-PCR and qRT-PCR results showed that the transgenic Arabidopsis successfully expressed the exogenous ThNAC7 (Figure S3). Moreover, the transcription of ThNAC7 in OE2 and OE5 lines was higher than that in other lines, so these two lines were chosen for further study (Figure S3C). In normal conditions, the OE2 and OE5 had no substantial distinction in growth phenotype compared to that of the Col-0 plants (control) (Figure 4A–C). However, OE2 and OE5 showed greatly enhanced root growth and fresh weight in osmotic or salt stress compared with those in the Col-0 (Figure 4A–C). Col-0 and transgenic Arabidopsis plants had approximately the same chlorophyll contents before treatment, whereas the OE2 and OE5 lines both had markedly higher chlorophyll contents than Col-0 plants in salt or osmotic stress (Figure 4D). In addition, phenotypic growth and fresh weight analyses of the plants growing in soil also indicated that OE2 and OE5 grew much better and had higher fresh weights than Col-0 plants (Figure 4E,F). The results suggested that ThNAC7 plays positive regulatory roles in the regulation of salt and osmotic stress.

Figure 4.

Stress tolerance of overexpressing ThNAC7 in Arabidopsis. (A): Growth phenotype of transgenic and Col-0 plants under normal (1/2 MS), salt (150 mM NaCl), or osmotic (150 mM mannitol) stress. (B): Root length assay. (C): Analysis of fresh weight. (D): Chlorophyll content assay. The plants were cultured in 1/2 MS (as control) or 1/2 MS containing 150 mM NaCl or 150 mM mannitol for 14 days for the above analysis. (E): Growth phenotype of Arabidopsis plants. (F): Fresh weight of Arabidopsis seedlings. Three weeks old Arabidopsis seedlings in soil were treated with 400 mM mannitol or 250 mM NaCl for 2 weeks, then took a photograph of their phenotypes. Control: Plants growing in normal conditions. The asterisks (p < 0.05) show * significant differences compared to Col-0 Arabidopsis. Col-0: wild-type Arabidopsis plants; OE2 and 5: Arabidopsis lines 2 and 5 transformed with ThNAC7.

2.5. Transient Overexpression or Knockdown of ThNAC7 in T. hispida Plants

To further study the role of ThNAC7 using gain- and loss- of function studies, we confirmed the expression level of ThNAC7 in overexpressing ThNAC7 (OE), RNAi-silenced ThNAC7 (IE), and control plants (transfected with pROKII) using qRT-PCR. We used the transcription level of ThNAC7 in plants transformed for 48 hours in control plants as the standard (designated as 1) to standardize the corresponding expression of ThNAC7 in the other T. hispida seedlings. The OE plants showed markedly enhanced levels of ThNAC7 transcripts, while they were dramatically reduced in the IE plants in comparison with those in the control T. hispida plants (Figure S4), which indicated that ThNAC7 had been successfully overexpressed or knocked down; therefore, these transgenic plants were suitable to study the gain- and loss-of-function of ThNAC7.

2.6. The ROS Scavenging Capability Was Improved by Overexpressing ThNAC7

Reactive oxygen species (ROS) accumulation is a substantial indicator to detect the degree of stress tolerance [26]. To determine ROS accumulation, two major ROS species, superoxide anion (O₂⁻) and hydrogen peroxide (H₂O₂) were stained using nitroblue tetrazolium (NBT) and diaminobenzidine (DAB) in situ, respectively. Under salt and osmotic stress conditions, both NBT and DAB histochemical staining of T. hispida plants indicated that the OE T. hispida plants had the lowest levels of O₂⁻ and H₂O₂; while the IE had the highest levels (Figure 5A,B). Consistent with the DAB staining results, the determined content of H₂O₂ in the OE T. hispida plants was the lowest; and the IE T. hispida plants showed the highest H₂O₂ content in salt and osmotic stress environment (Figure 5C). The above analyses were repeated in Arabidopsis. Under salt or osmotic stress environment, NBT and DAB histochemical staining and H₂O₂ content assay verified that ROS contents were markedly decreased in OE lines rather than in Col-0 plants (Figure S5A,B). SOD and POD activities, the two primary ROS scavenging enzymes, were further researched in T. hispida plants. In normal growth conditions, the POD and SOD activities of OE plants were not significantly different from those of IE and control plants (Figure 5D,E). However, under salt or osmotic stress environment, markedly higher activities of POD and SOD were detected in OE plants; while the IE plants had greatly lower POD and SOD activities compared to those in the control plants (Figure 5D,E). These analyses were repeated in Arabidopsis plants. The SOD and POD activity analysis showed that the OE plants had markedly enhanced the SOD and POD activities compared to those of the Col-0 Arabidopsis plants in osmotic and salt stress environment (Figure S5D,E). These results showed that ThNAC7 expression results in reduced ROS accumulation in plant cells, mediated by increased POD and SOD activities.

Figure 5.

Analysis of ROS accumulation and the activities of SOD and POD among OE, IE, and control T. hispida plants. (A,B): T. hispida plants treated with NaCl (150 Mm) or mannitol (200 mM), and stained with DAB to visualise H₂O₂ level (A), or stained with NBT to visualise O₂⁻ (B). (C): Measurement of H₂O₂ levels in T. hispida. (D,E): Measurement of the POD (D) and SOD (E) activity. OE: T. hispida plants overexpressing ThNAC7; IE: ThNAC7 RNAi-silenced T. hispida seedlings; Control: T. hispida plants transformed with pROKII.

2.7. The Expression Levels of SODs and PODs Are Induced by ThNAC7

We further analysed the transcription levels of SODs and PODs to confirm whether overexpression of the SOD and POD genes could increase SOD and POD activities. We analyzed 3 ThSOD genes (GenBank numbers: KF756930–KF756932) and 3 ThPOD genes (GenBank numbers: KF756934–KF756936). The results indicated that compared to that in control T. hispida, the OE plants indicated markedly increased expression of all the analysed PODs and SODs in osmotic and salt stress environment, while their expression were markedly reduced in the IE plants (Figure 6). Three Arabidopsis PODs (AT2G18140, AT5G58400 and AT1G14550) and three Arabidopsis SOD genes (AT2G28190, AT3G10920 and AT1G08830) were assessed to test the expression patterns of them in Arabidopsis seedlings. Compared with the expression levels of the Col-0 plants, the SODs and PODs of all the studies were markedly advanced in transgenic lines in both salt and osmotic stress environments (Figure S6). The results showed that the expression of SODs and PODs could be induced by ThNAC7, which would result in enhanced SOD and POD enzyme activities.

Figure 6.

The expression patterns of the PODs and SODs in OE, IE, and control T. hispida seedlings. The expression of PODs (A) and SODs (B) were analyzed in control, OE, and IE T. hispida in response to salt (150 mM NaCl) or osmotic (200 mM mannitol) stress. The transcription level of a gene in control under normal growth conditions was designed as 1 to standardize its relative expression values. OE: T. hispida seedlings overexpressed ThNAC7; IE: ThNAC7 RNAi-silenced T. hispida seedlings; Control: T. hispida seedlings transformed with pROKII. * Significant (p < 0.05) difference compared to the control plants.

2.8. Overexpression of ThNAC7 Reduces Water Loss Rate, Cell Death and Malondialdehyde Contents

Electrolyte leakage is associated with plant stress response, and stress-induced electrolyte leakage is often associated with the accumulation of ROS, usually leading to PCD (programmed cell death) [28]. The electrolyte leakage rates were measured to monitor cell death in T. hispida under different environment. They had not substantial difference in electrolyte leakage rates of the OE, IE, and control T. hispida plants in normal growth conditions, while the electrolyte leakage rates showed marked differences under osmotic and salt stress environment. The highest electrolyte leakage rates appeared in the IE plants, then in the control, and the lowest in OE plants (Figure 7A). The water loss assay indicated that the water loss rates of OE plants were lower than those in the control, while that of IE plants were the highest (Figure 7B). Moreover, the MDA contents were similar among the control, OE, and IE T. hispida plants in normal growth environment. Nevertheless, the highest MDA level was appeared in the IE plants, followed by the control plants, and the lowest levels were recorded in the OE T. hispida plants in osmotic and salt stress (Figure 7C). In addition, the electrolyte leakage rate, MDA content and water loss rate in transgenic Arabidopsis seedlings were all markedly decreased compared to those in Col-0 Arabidopsis plants under osmotic and salt stress (Figure S7). The results were richly consistent with the results from the T. hispida seedlings, proving that overexpression of ThNAC7 could decrease the water loss rate, cell death, and MDA content in osmotic and salt stress environments to protect plants.

Figure 7.

Detection of cell death, water loss rates, and MDA level in OE, IE, and control T. hispida seedlings. (A): Electrolyte leakage rates assay. (B): Water loss rates. (C): MDA content. The T. hispida plants were treated with H₂O (as control), NaCl (150 mM), or mannitol (200 mM) for 24 h. Data are means ± SD from 3 independent experiments. * Significant (p < 0.05) difference compared to the control. OE: T. hispida overexpressing ThNAC7; IE: ThNAC7 RNAi-silenced T. hispida; Control: T. hispida plants transformed with pROKII.

2.9. ThNAC7 Positively Affects Proline Biosynthesis

We next studied whether ThNAC7 is involved in proline biosynthesis in salt or osmotic stress environment. The proline contents were measured in comparison of the control, OE, and IE T. hispida seedlings. There was no difference in proline contents among the above three T. hispida seedlings in normal environment; whereas, there were substantial differences in the proline contents among the OE, IE, and control T. hispida plants in osmotic or salt stress. The order of the proline contents from highest to lowest was the OE plants, the control plants, and the IE T. hispida plants (Figure 8A). We further studied whether the altered proline contents were caused by changes in expression of proline biosynthesis genes, including ThP5CS genes (delta 1-pyrroline-5-carboxylate synthetase, GenBank number: KM101096 and KM101097). There was no difference in expression of ThP5CS1 and ThP5CS2 among all 3 types of plants in normal conditions. Under osmotic or salt stress, overexpression of ThNAC7 induced the transcription levels of proline biosynthesis related genes, including ThP5CS1 and ThP5CS2 (Figure 8B,C).

Figure 8.

Analysis of the effect of ThNAC7 on the biosynthesis of proline. (A): Analysis of proline contents in OE, IE, and control T. hispida seedlings in response to osmotic (200 mM Mannitol) or salt (150 mM NaCl)stresses. (B,C): The expression levels of proline biosynthesis related genes. The relative expression levels were log2 transformed. Asterisk indicate significant (p < 0.05) difference compared to the control. OE: T. hispida plants overexpressing ThNAC7; IE: ThNAC7 RNAi-silenced T. hispida seedlings; Control: T. hispida plants transformed with pROKII.

To confirm the role of ThNAC7 in proline biosynthesis, we repeated the above analyses on Arabidopsis transformed with Col-0 and ThNAC7Arabidopsis plants. In normal growth environment, the Col-0 and OE plants had similar proline contents. By contrast, under salt or osmotic stress, the proline levels in OE2 and OE5 lines were markedly increased compared with the Col-0 (Figure S8A). We further studied the gene expression related to proline biosynthesis, i.e., AtP5CS1 (AT2G39800) and AtP5CS2 (AT3G55610). Under the salt or osmotic stress conditions, both AtP5CS1 and AtP5CS2 showed markedly higher expression in OE2 and OE5 lines than in Col-0 plants (Figure S8B,C). These outcomes are in accordance with the results in T. hispida.

2.10. Identification of the Genes Regulated by ThNAC7 Using RNA-Seq

The ThNAC7-overexpressing Arabidopsis plants displayed higher tolerance than Col-0 Arabidopsis plants in salt stress; therefore, we performed an RNA-seq analysis of OE5 and Col-0 to verify the down-stream target genes of ThNAC7 responsible for enhancing salt tolerance.

Under normal conditions, between OE5 and Col-0, a total of 272 differentially expressed genes (DEGs, log2 ratio >1, FDR < 0.05) were obtained, and 185 were upregulated and 87 were downregulated (Table S4). Total of 673 DEGs were obtained, including 453 that were induced by ThNAC7 and 220 that were inhibited by ThNAC7 under salt stress (Table S5). Among the DEGs upregulated under salt stress conditions with functional information, we found that over 40 encoded proteins and multiple TF genes that respond to salt stress (Table 1), such as peroxidase; lipid transfer protein; MAP kinase; late embryogenesis abundant protein; aquaporin; ethylene-responsive TF genes; and MYB, HSF, DREB, TCP, NAC, bZIP, and WRKY TF genes.

Table 1.

List of DEGs upregulated in response to salt stress in ThNAC7-overexpression line OE5 compared with Col-0 Arabidopsis plants.

Locus ID	Gene Name	FDR	Fold Change	Annotations-Description
AT5G42180	PER64	2.62 × 10−8	6.65	peroxidase
AT1G43160	RAP2.6	6.88 × 10−16	4.12	ethylene-responsive transcription factor RAP2-6
AT1G09540	MYB61	1.02 × 10−6	3.44	myb domain protein 61
AT5G64750	ABR1	8.68 × 10−20	3.04	ethylene-responsive transcription factor ABR1
AT2G45180	LTP	1.23 × 10−21	2.78	lipid transfer protein (LTP) family protein
AT2G32510	MAPKKK17	5.09 × 10−9	2.38	mitogen-activated protein kinase kinasekinase 17
AT1G52690	LEA	0.004977	2.31	Late embryogenesis abundant protein (LEA) family protein
AT1G21910	DREB26	2.03 × 10−6	2.24	ethylene-responsive transcription factor ERF012
AT4G29930	bHLH27	1.36 × 10−7	2.2	transcription factor bHLH27
AT1G05100	MAPKKK18	0.008566	2.18	mitogen-activated protein kinase kinasekinase 18
AT4G22470	LTP	6.33 × 10−10	2.12	lipid transfer protein (LTP) family protein
AT5G59310	LTP4	1.96 × 10−7	2.11	non-specific lipid-transfer protein 4
AT2G37180	RD28	6.49 × 10−44	2.1	aquaporin PIP2-3
AT5G12020	HSP17.6II	0.008487	2.1	class II heat shock protein 17.6
AT2G20880	ERF053	0.00016	2.09	ethylene-responsive transcription factor ERF053
AT2G40340	DREB2C	0.000646	2.04	dehydration-responsive element-binding protein 2C
AT5G61890	ERF114	0.001014	2.03	ethylene-responsive transcription factor ERF114
AT4G05100	AtMYB74	2.65 × 10−7	2.01	myb domain protein 74
AT3G18550	BRC1	0.000907	1.93	transcription factor TCP18
AT4G18170	WRKY28	2.97 × 10−7	1.75	DNA binding-like protein
AT5G13330	RAP2.6L	3.84 × 10−12	1.71	ethylene-responsive transcription factor ERF113
AT1G67260	TCP1	2.94 × 10−7	1.71	transcription factor TCP1
AT1G71030	ATMYBL2	2.28 × 10−8	1.64	putative myb family transcription factor
AT5G39610	ATNAC2	9.09 × 10−6	1.63	NAC-domain transcription factor
AT2G22200	ERF056	4.68 × 10−5	1.63	ethylene-responsive transcription factor ERF056
AT1G75490	DREB2D	0.001527	1.6	dehydration-responsive element-binding protein 2D
AT4G23400	PIP1D	3.65 × 10−11	1.57	putative aquaporin PIP1-5
AT5G40630	-	0.001874	1.56	ubiquitin family protein
AT2G22770	bHLH020	6.89 × 10−6	1.44	putative bHLH transcription factor
AT2G26150	ATHSFA2	2.19 × 10−6	1.43	heat stress transcription factor A-2
AT3G53420	PIP2A	1.95 × 10−13	1.4	aquaporin PIP2-1
AT5G56550	OXS3	1.04 × 10−10	1.37	protein OXIDATIVE STRESS 3
AT2G21650	MEE3	0.006908	1.36	MYB transcription factor RSM1
AT4G27410	RD26	6.73 × 10−5	1.33	NAC transcription factor RD26
AT5G60890	ATMYB34	1.14 × 10−7	1.31	myb domain protein 34
AT1G56650	PAP1	2.41 × 10−5	1.28	transcription factor MYB75
AT1G54100	ALDH7B4	1.61 × 10−8	1.28	aldehyde dehydrogenase 7B4
AT5G28770	ATbZIP63	1.08 × 10−13	1.27	basic leucine zipper 63
AT5G50915	bHLH137	3.16 × 10−5	1.21	transcription factor bHLH137
AT2G36830	TIP	2.04 × 10-10	1.21	aquaporin TIP1-1

GO (Gene ontology) analyses showed that these DEGs were primarily related to 1 molecular function, 12 biological processes and three cellular components. Most were categorized in “metabolic process”, “single-organism process”, “cell part”, “cell”, and “organelle”. The other genes were assigned to “cell process”, “response to stimulus”, “biological regulation”, “cellular component organization or biogenesis”, “localization”, “development process”, “signaling”, “reproductive process”, “multicellular organismal process”, “reproduction”, “binding”, and “catalytic activity” (Figure S9).

Furthermore, we randomly selected 12 DEGs related to salt stress (six upregulated and six downregulated) and compared their expression levels between Col-0 and OE5 Arabidopsis plants by qRT-PCR (Table 2 and Table S6). As shown in Figure 9 and Figure S10, all these genes had similar expression patterns to those decided using RNA-seq, proving the reliability of the RNA-seq results.

Table 2.

The expression values of RNA-seq for validation of the selected DEGs.

Locus ID	FDR	Fold Change	Annotations-Description
AT5G42180	2.62 × 10−8	6.65	peroxidase
AT5G24240	0.01	4.44	phosphatidylinositol 3- and 4-kinase/ubiquitin family protein
AT5G57550	3.65 × 10−20	4.35	probable xyloglucan endotransglucosylase/hydrolase protein 25
AT1G75750	3.37 × 10−38	4.26	GA-responsive GAST1 protein-like protein
AT2G38240	2.86 × 10−13	4.21	2-oxoglutarate (2OG) and Fe (II)-dependent oxygenase-like protein
AT1G43160	6.88 × 10−16	4.12	ethylene-responsive transcription factor RAP2-6
AT4G22485	5.48 × 10−4	−4.81	protease inhibitor/seed storage/LTP family protein
AT2G34390	6.8 × 10−14	−4.7	aquaporin NIP2-1
AT1G50750	5.5 × 10−9	−3.71	plant mobile domain family protein
AT2G26010	1.24 × 10−5	−3.07	plant defensin 1.3
AT4G29610	2.42 × 10−14	−2.73	cytidine/deoxycytidylate deaminase family protein
AT5G52750	2.14 × 10−8	−1.36	alpha/beta-hydrolases superfamily protein

Figure 9.

Comparison of the expression patterns between RNA-seq and qRT-PCR. A: Twelve highly differentially regulated genes were randomly selected for qRT-PCR assay. B: Correlation: correlation analysis of the results between qRT-PCR and RNA-sequencing; the correlation coefficient R² is 0.910. * Significant (p < 0.05) difference compared with the control plants.

3. Discussion

Previously, we identified 16 NAC TFs that are involved in the differential response to NaHCO₃ stress [27]. Furthermore, we confirmed that ThNAC7 was greatly induced by salt stress; therefore, we selected ThNAC7 for further research. Transactivation assays indicated that ThNAC7 has transcriptional activation that lies within three independent activation domains: aa 216–290, 291–360, and 361–435, respectively (Figure 2B). The full-length ThNAC7 protein showed strong transcriptional activation activity without the N-terminal domain (dc1, 1–435), containing three activation domains, abolished the transcriptional activation activity. These results indicated that ThNAC7 might possess a transcriptional repression domain in N-terminal 1–145 amino acids. The transactivation activity of NAC TFs might depend upon the interaction between the NAC activation domain and repression domain [29]. Therefore, whether ThNAC7 is a transcriptional activator or repressor depends on its interactions with other TFs or target genes.

The expression of ThNAC7 was greatly induced by osmotic or salt stress conditions in T. hispida (Figure 3), indicating that ThNAC7 plays roles in abiotic stress responses. To analyze the molecular function of ThNAC7 in resistance to abiotic stress, two independent ThNAC7 transgenic lines (OE2 and OE5) lines were used in further study. The overexpression of ThNAC7 in transgenic Arabidopsis improved root growth (Figure 4A,B), fresh weight (Figure 4C), and chlorophyll contents (Figure 4D). Therefore, ThNAC7 plays a positive role in osmotic or salt stress tolerance in plants.

ROS scavenging is crucial in resistance to plant abiotic stress [30,31,32,33]. We found that overexpression of ThNAC7 could reduce excess ROS accumulation in this study (Figure 5 and Figure S5), indicating that ThNAC7 is related to ROS scavenging. In addition, ThNAC7 can induce the transcription levels of PODs and SODs in transiently transformed T. hispida and stably transformed Arabidopsis (Figure 6 and Figure S6), thereby improving their activities (Figure 6 and Figure S6). Additionally, overexpression of ThNAC7 could decrease cell death, water loss rate, and the MDA content in osmotic or salt stress (Figure 7 and Figure S7). These data showed that ThNAC7 could elevate the transcription levels of ROS scavenging genes for improving stress tolerance. NAC TFs could enhance stress tolerance and modulate the expression level of ROS scavenging genes, which is accordance with previous studies [34,35,36,37]. Overexpression of ThNAC13 enhanced the osmotic and salt stress tolerances via controlling the transcriptional levels of PODs and SODs to enhance the ROS scavenging ability [34]. In this study, we found that both ThNAC7 and ThNAC13 belong to NAC subfamily I in T. hispida (Figure S2).

Proline is not only an osmotic agent, but also a radical scavenger. It can maintain photosynthetic activity and defend cells from harm in abiotic stress environments, allowing plants to maintain stable growing conditions under long term stress [38,39]. We found that the transcription levels of P5CSs were induced by ThNAC7 in T. hispida (Figure 8) and Arabidopsis (Figure S8). In addition, the transcription levels of P5CSs were positively related to the proline content (Figure 8). This result demonstrated that ThNAC7 activates proline biosynthesis to increase the proline content, which consequently increases abiotic stress tolerance by elevating the osmotic potential and ROS scavenging ability.

The RNA-seq analyses revealed that more than 40 upregulated genes are related to salt stress, including four aquaporins (AQPs) and three lipid transfer proteins LTPs (Table 1). Many AQPs in the PIP subfamilies affect the expression levels of mRNA transcripts or/and proteins under salt, drought, or cold stresses [40]. In transgenic Arabidopsis, the overexpression of OsPIP1 and OsPIP2 improved drought and salt tolerance [41]. LTPs are responsive to many abiotic stresses [42,43,44]. These results suggested that ThNAC7 might improve abiotic stress tolerance via inducing the transcription levels of AQPs and LTPs.

In addition, ThNAC7 regulated multiple TFs involved in abiotic stress. Seven ERFs were up-regulated by ThNAC7 in salt conditions. For instance, RAP2.6 can response to high cold, salt, osmotic and ABA stresses [45]. Overexpression of RAP2.6L in Arabidopsis had no impact on phenotype, but it could improve drought and salt stresses tolerance [46]. The ABR1 gene could response to drought, salt, cold and ABA stresses [47]. Therefore, the ERF TFs mediated by ThNAC7 might play a vital role in salt stress tolerance. Moreover, other TF families were differentially expressed, such as MYB, bHLH, HSP, DREB, TCP, NAC, bZIP, and WRKY. Arabidopsis DREB2C plays vital roles in salt stress tolerance and the regulating of several genes related to abiotic stress [48]. The co-expression of AtWRKY28 and AtbHLH17 enhances resistance to NaCl, Mannitol, and oxidative stress in Arabidopsis [49]. ATNAC2 and ANAC092 are highly affected by salinity and can positively regulate the leaf senescence [50]. These results suggested that ThNAC7 may directly or indirectly regulate these stress-related TFs to improve salt stress resistance in plants.

4. Materials and Methods

4.1. Plant Materials and Growth Conditions

Seeds of T. hispida were planted in containers with a mixture of turf peat and sand (3:1 v/v), were grown in the greenhouse maintained at 24 °C, with 70–75% relative humidity and a 14 h light/10 h dark photocycle. Seeds of Arabidopsis thaliana Columbia (Col-0) were directly seeded into containers with a mixture of perlite and soil (2:1 v/v) in the greenhouse at 22 °C, with 65–70% relative humidity and a 16 h light/8 h dark photocycle.

4.2. Plasmid Construction and Plant Transformation

In our previous study, eight transcriptomes were obtained from T. hispida [27]. The open reading frame (ORF) sequence of ThNAC7 (GenBank number: JQ974961) was obtained using the transcriptome data. Multiple sequence alignments of ThNAC7 and 10 NAC proteins from different species were performed using ClustalW. The NAC proteins of Arabidopsis were obtained from UniPort (http://www.uniport.org/). Phylogenetic tree analysis was generated between ThNAC7 and 105 NAC proteins from Arabidopsis using the MEGA6.06 program (Tokyo Metropolitan University and 1 Research Center for Genomics and Bioinformatics, Tokyo, Japan). Another phylogenetic tree was generated using MEGA6.06 between ThNAC7 and 88 NAC proteins from T. hispida.

The ORF of ThNAC7 was inserted into plasmid pROKII following the CaMV 35S promoter. The inverted repeat cDNA sequence of ThNAC7 was cloned to the pFGC5941 RNAi vector (pFGC::ThNAC7) to knockdown the expression of ThNAC7. All the primers used in the experiments are listed in Table S1. The highly efficient transient transformation of T. hispida plants were performed as previously described by Ji et al. [51]. We constructed three kinds of transgenic T. hispida plants: OE (overexpression) plants (transformed with 35S::ThNAC7), IE (inhibited expression) plants (transformed with pFGC::ThNAC7), and control T. hispida plants with the empty pROKII plasmid. The 35S::ThNAC7 plasmid was stably transformed into Arabidopsis by the Agrobacterium mediated floral dip transformation method to obtain ThNAC7 overexpressed plants [52]. T₃ homozygous transgenic Arabidopsis were used in further study.

4.3. Subcellular Location of ThNAC7 Proteins

The coding sequence (CDS) of ThNAC7 with no termination codon was fused with the C-terminus of the GFP following the CaMV 35S promoter. 35S::GFP was used as control. All primer used are listed in Table S1. The 35S::ThNAC7-GFP and 35S::GFP plasmids was respectively imported into onion epidermal cells by particle bombardment (Bio-Rad, Hercules, CA, USA). The nuclei were stained using 4′,6-diamidino-2-phenylindole (DAPI) (10 μg·mL⁻¹) with phosphate buffered saline for 5 min. The transformed onion epidermal cells were visualised by LSM700 confocal laser scanning microscopy (Zeiss, Jena, Germany).

4.4. Transactivational Activity of ThNAC7

To evaluate the transcriptional activity of ThNAC7 and determine its transactivation domain, the full length or various truncated ThNAC7 fragments were fused to the yeast GAL4 DNA binding domain of the pGBKT7 (Clontech, Palo Alto, CA, USA) using Infusion enzyme (Clontech) and transformed in Y2HGold cells. The procedure was performed according to the Matchmaker™ Gold Yeast Two-Hybrid System instructions. In the transactivation assay, the transformed yeast cells were grown on SD/-Trp-His/X-α-gal medium for 3–5 days. All primers were listed in Table S2. Three independent experiments were performed.

4.5. Stress Tolerance Assays

The T₃ generation ThNAC7 transgenic Arabidopsis lines were used as the materials for stress tolerance analyses. After culturing in 1/2 MS medium for 5 days, the germinated Arabidopsis seeds were separately transferred to 1/2 MS or 1/2 MS containing 150 mM mannitol or 150 mM NaCl for two weeks. The fresh weight and root length of Arabidopsis were determined. The chlorophyll contents of excised leaves were measured as described by Lichtenthaler [53]. Arabidopsis seeds cultured in 1/2 MS plates for five days were planted in soil. The three-week seedlings were watered using 400 mM mannitol or 250 mM NaCl for 2 weeks; the fresh weights of plants were also determined. Three independent experiments were performed.

4.6. Physiological Measurements

T. hispida seedlings were cultured in 1/2 MS or 1/2 MS with 200 mM mannitol or 150 mM NaCl for 24 hours were for physiological assays. Arabidopsis grown into soil for 3 weeks were watered with 200 mM mannitol or 150 mM salt (NaCl) solution at 24 h for physiological assay. The seedlings were treated with 200 mM mannitol or 150 mM NaCl solution for 2 hours. The leaves of T. hispida or Arabidopsis plants was stained by nitroblue tetrazolium (NBT) and diaminobenzidine (DAB) using the methods of Fryer et al. [54,55]. The SOD and POD activities, and the MDA content were determined using the methods of Wang et al. [56]. The H₂O₂ level was detected according to the method of Dal Santo et al. [57]. An electrolyte leakage assay was determined via the method of Ji et al. [51]. The water loss rate was measured using the method of Zhang et al. [55]. The proline content was determined according to the method of Bates et al. [58]. Three independent experiments were performed.

4.7. qRT-PCR Assay

The total RNA of T. hispida was obtained using the Universal Plant Total RNA Extraction Kit (BioTeke). Arabidopsis total RNA was isolated using the Trizol reagent (Invitrogen, Waltham, MA, USA). Then RNA (2 μg) was reversely transcribed into cDNA as PCR templates. Actin (GenBank number: FJ618517) and β-tubulin (GenBank number: FJ618519) were used as reference genes for T. hispida analysis (Table S3). For Arabidopsis analysis, α-tubulin (AT1G50010) and Actin3 (AT3G53750) were used as reference genes (Table S3). The reaction system included 2 μL of cDNA template, 0.5 μM each of primer, and 10 μL of SYBR Green Real time PCR Master Mix (Toyobo) in the volume of 20 μL. The procedure involved the following: 94 °C/30 s; followed by 45 cycles at 94 °C/12 s, 60 °C/30 s, and 72 °C/40 s; followed by 1 s at 82 °C for plate reading. The qRT-PCR was performed using an Opticon 2 System (Bio-Rad, Hercules, CA, USA). For each sample, the melting curve evaluated the purity of the PCR products. The expression levels of genes were treated using the 2^−ΔΔCt method [59]. Three independent experiments were performed.

4.8. RNA-Sequencing Analysis

Total RNA from four-week-old ThNAC7-overexpression line OE5 and Col-0 Arabidopsis, without treatment or treated with NaCl (150 mM) for 6 hours, were used for RNA-sequencing, and three biological replicates were performed. Total RNAs were extracted using the Trizol reagent, and purified using AMPure beads (Agencourt, CA, USA). The preparation of the sequencing library and PCR amplification used a TruSeq PE Cluster Kit and a TruSeq™ DNA Sample Prep Kit-Set A, respectively (Illumina, San Diego, CA, USA). RNA-seq was analyzed on the Illumina HiSeq 2000 platform. The relative expression levels were obtained under salt and normal conditions. All the relative expression levels were calculated using log₂. With a log-fold expression change of |log₂FC| ≥ 1, and the threshold of false discovery rate (FDR < 0.05), DEGs were identified via the DEGSeq algorithm [60]. The correlation between qRT-PCR and digital genes expression (DGE) was evaluated statistically by calculating the Pearson correlation coefficient. Gene ontology (GO) classification was executed using the molecule annotation system (MAS). The RNA-seq data was uploaded to the NCBI (PRJNA525176).

4.9. Statistical Analyses

Statistical analyses were accomplished with SPSS (IBM SPSS 22, IBM Corp., Armonk, NY, USA). Data were calculated using student’s t-test. p < 0.05 was statistically significant. * represents p < 0.05 in the figures. Three biological replicates were carried out for statistical analyses.

5. Conclusions

A NAC TF from Tamarix hispida, ThNAC7, is a nuclear localization protein with transactivation activity. Overexpression of ThNAC7 markedly increased proline levels and enhanced the POD and SOD activities to increase the ROS scavenging ability in both transiently transformed T. hispida and stably transformed Arabidopsis. ThNAC7 positively regulated a series of genes that enhance osmotic and salt stress tolerance, including salt tolerance genes and many TF genes. Taken together, ThNAC7 promotes the expression level of genes related to stress tolerance in order to enhance osmotic and salt stress tolerance by improving the osmotic potential and increasing ROS scavenging. The results of the present study enrich the molecular mechanism of ThNAC7 involved in salt and osmotic stresses.

Supplementary Materials

The following are available online at https://www.mdpi.com/2223-7747/8/7/221/s1. Figure S1. Multiple sequence alignment analysis of NAC proteins from 10 other species. ThNAC7: Tamarix hispida (AFN55267.2); PpNAC17: Prunus persica (XP_007201176.1); PaNAC17: Prunus avium (XP_021820479.1); JrNAC17: Juglans regia (XP_018848079.1); MeNAC17: Manihot esculenta (XP_021603416.1); JcNAC17: Jatropha curcas (XP_012073984.1); NaNAC17: Nicotiana attenuate (XP_019238422.1); NtNAC17: Nicotiana tabacum (XP_016438196.1); PtNAC17: Populus trichocarpa (AOF43232.1); NnNAC17: Nelumbo nucifera (XP_010243336.1); and ANAC91: Arabidopsis (AT5G24590.1). Figure S2. Phylogenetic analysis between ThNAC7 and the NAC proteins from T. hispida. The phylogenetic relationship of ThNAC7 and the NAC proteins from the transcriptome of T. hispida. The amino acid sequences of ThNAC7 and 88 T. hispida NAC proteins were aligned; the un-rooted NJ tree was constructed using MEGA 6.06. Figure S3. RT-PCR and qRT-PCR analysis of the expression level of exogenous ThNAC7 in transgenic Arabidopsis lines. Col-0: wild-type Arabidopsis plants; OE1–9: Arabidopsis lines transformed with ThNAC7, M: DL2000 marker. Figure S4. Expression of ThNAC7 in OE, IE and control T. hispida plants. T. hispida were cultured in 1/2 MS (normal conditions) or 1/2 MS medium containing 150 mM NaCl or 200 mM mannitol for 24 h to determine the expression level of ThNAC7. The expression level of ThNAC7 after 48 h of transformation in the control plants was regarded as a calibrator (designated as 1) to standardize the expression of ThNAC7 in the other plants. Control: T. hispida plants transformed with empty pROKII; OE: T. hispida plants overexpressing ThNAC7; IE: ThNAC7 RNAi-silenced plants. Asterisks indicate * significant (p < 0.05) difference compared with the control plants. Figure S5. Analysis of ROS accumulation and the activities of POD and SOD in OE and Col-0 Arabidopsis plants. A, B: Arabidopsis plants treated with 150 mM NaCl or 200 mM mannitol, and stained with DAB to visualize H2O2 (A), or stained with NBT to visualize O2- (B). C: Measurement of H2O2 levels in Arabidopsis plants. D, E: Measurement of POD (D) and SOD (E) activities. Col-0: wild-type Arabidopsis plants; OE2 and 5: Arabidopsis lines 2 and 5 transformed with ThNAC7. Figure S6. The expression of the PODs and SODs in OE and Col-0 Arabidopsis plants. Analysis of POD (A) and SOD (B) gene expression was carried out in Arabidopsis OE and Col-0 plants in response to NaCl (150 mM) or Mannitol (200 mM) stress treatments. The expression levels of the genes in Col-0 plants grown in the normal condition were regarded as a calibrator (designed as 1) to standardize the relative transcript values. Col-0: wild-type Arabidopsis plants; OE2, 5: the Arabidopsis lines transformed with ThNAC7. Figure S7. Detection of cell death, water loss rates, and MDA content in OE and Col-0 Arabidopsis plants. A: Comparison of electrolyte leakage rates. B: Water loss rates. C: MDA content. The plants were treated with water (control), 150 mM NaCl (NaCl), or 200 mM Mannitol for 24 h for analyses. Data are means ± SD from three independent experiments. * Significant (p < 0.05) difference compared with Col-0 plants. Col-0: wild-type Arabidopsis plants; OE2 and 5: lines 2 and 5 of Arabidopsis transformed with ThNAC7. Figure S8. Analysis of the biosynthesis of proline in OE and Col-0 Arabidopsis plants. A: Analysis of proline levels in OE and Col-0 plants in response to NaCl (150 mM) or Mannitol (200 mM) stress treatments. B, C: The expression of proline biosynthesis and degradation-related genes. The relative expression levels were log2 transformed. * Significant (p < 0.05) difference compared with Col-0 plants. Col-0: wild-type Arabidopsis plants; OE2, 5: the Arabidopsis lines transformed with ThNAC7. Figure S9. GO classification of the annotated DEGs in salt stress. Figure S10. Comparison of the expression profiles between RNA-seq and qRT-PCR. Table S1. Primer sequences used to construct recombinant plasmids. Table S2. Primer sequences used to construct yeast recombinant plasmids. Table S3. Primer sequences used in qRT-PCR. Table S4. List of differentially expressed genes in the OE5 compared to Col-0 Arabidopsis plants under normal conditions. Table S5. List of differentially expressed genes in the OE5 compared to Col-0 Arabidopsis plants under salt stress conditions. Table S6. The primer sequences of qRT-PCR for validation of the selected DEGs.

Author Contributions

X.J. and Y.W. designed the research. Z.H., Z.L., H.L., and L.H. performed the experiments. Z.H., Z.L., H.L., and Z.W. analyzed the data. Z.H. and X.J. wrote the article.

Funding

This work was supported by The Fundamental Research Funds for the Central Universities (No. 2572017DA01), the National Natural Science Foundation of China (No. 31500535), and The Heilongjiang Province Science Foundation (No. QC2018017).

Conflicts of Interest

The authors declare no conflicts of interest.