Poplar PdPTP1 Gene Negatively Regulates Salt Tolerance by Affecting Ion and ROS Homeostasis in Populus

High concentrations of Na+ in saline soil impair plant growth and agricultural production. Protein tyrosine phosphorylation is crucial in many cellular regulatory mechanisms. However, regulatory mechanisms of plant protein tyrosine phosphatases (PTPs) in controlling responses to abiotic stress remain limited. We report here the identification of a Tyrosine (Tyr)-specific phosphatase, PdPTP1, from NE19 (Populus nigra × (P. deltoides × P. nigra). Transcript levels of PdPTP1 were upregulated significantly by NaCl treatment and oxidative stress. PdPTP1 was found both in the nucleus and cytoplasm. Under NaCl treatment, transgenic plants overexpressing PdPTP1 (OxPdPTP1) accumulated more Na+ and less K+. In addition, OxPdPTP1 poplars accumulated more H2O2 and O2·−, which is consistent with the downregulation of enzymatic ROS-scavengers activity. Furthermore, PdPTP1 interacted with PdMAPK3/6 in vivo and in vitro. In conclusion, our findings demonstrate that PdPTP1 functions as a negative regulator of salt tolerance via a mechanism of affecting Na+/K+ and ROS homeostasis.


Introduction
Soil salinity is one of the major abiotic stresses that imposes severe threats to the growth and yield of diverse plants. More than 6% of the world's total land area suffers from overabundance of salt that impedes plant absorption of water and nutrients from the soil [1]. Salt stress is associated with ionic stress, osmotic stress, and secondary oxidative stress in plants [2]. Therefore, primary strategies for plants adapting to salt conditions are to regulate ionic and osmotic homeostasis, as well as detoxification [3].
Genetic analyses have indicated that the salt overly sensitive (SOS) pathway is crucial in regulating ionic homeostasis and helps plants adapt to salt stress. In this pathway, exposure to NaCl would elicit a transit increase in cytosolic Ca 2+ concentrations, which is perceived by a calcium-binding protein, SOS3. SOS3 physically translates to Ser/Thr protein kinase SOS2. The SOS2-SOS3 complex phosphorylate and activate Na + /H + exchanger SOS1 located in the plasma membrane, finally transporting Na + out of the cytosol [2][3][4]. In glycophytes, excessive Na + often leads to K + deficiency under salt stress [5]. As a major osmoticum, the maintenance of high cytosolic K + concentrations is crucial for plant salinity tolerance [1,6]. Therefore, maintaining a suitable K + /Na + is an important mechanism used by plants to adapt to salt stress.
Salt-induced secondary oxidative stresses generate ROS, including superoxide anion radical (O 2 · − ), hydroxyl radicals (·OH), and hydrogen peroxide (H 2 O 2 ). Low ROS concentrations have been Overexpression of PdPTP1 reduced salinity tolerance in poplar, as a consequence of impairing re-establishment of cellular ionic and ROS homeostasis. Furthermore, we also provided evidence that PdPTP1 interacts with the stress-responsive kinase PdMAPK3/6. This study provides important new information for engineering salt-tolerant poplar.

PdPTP1 Encodes a Tyr-Specific PTP in Populus
Based on the CDS sequences of the P. trichocarpa PtPTP1 gene, the PdPTP1 gene in NE19 was isolated by using the polymerase chain reaction (PCR) approach, using the specific primers (Table S1). The full-length nucleotide sequence of cDNA is 1020 bp that encodes a protein of 339 amino acids. PdPTP1 shares high identity with Arabidopsis (Arabidopsis thaliana, 65.64%) AtPTP1, soybean (Glycine max, 64.51%) GmPTP1, and pea (Pisum sativum, 62.82%) PsPTP1, suggesting that PdPTP1 may be a member of Tyr-specific PTPs. The phylogenetic tree of PdPTP1 protein and other PTPs from eukaryotes was constructed ( Figure 1A, Table S2). Furthermore, an amino acid sequence alignment of the PdPTP1 with PTPs from plants, human, and rats shows that PdPTP1 contains an amino acid sequence motif "(I/V)HCXAGXXR(S/T)G" characteristic for many active PTPs and the KNRY and the WPD motifs specific to Tyr-specific PTPs ( Figure S1). Moreover, PdPTP1 contains the IHNT domain of Tyr-specific PTPs, but not MKP domain "AYLM" of dual-specificity PTPs, by comparing the conserved catalytic domains between Tyr-specific and dual-specificity PTPs in plants ( Figure 1B). These results suggested that PdPTP1 is a novel member of the Tyr-specific PTP in poplar.

PdPTP1 Localized to both the Cytosol and Nucleus
In order to investigate the subcellular localization of PdPTP1 in polar, we performed transient expression assays by using tobacco leaves, tobacco and poplar leaf protoplasts, with constructs expressing the green fluorescent protein (GFP)-PdPTP1 fusion protein, and then the transformed protoplasts, tobacco, and transgenic poplar leaves were observed by laser confocal fluorescence microscopy. The green fluorescence protein was observed in both the cytosol and nucleus (Figure 2A,B), indicating that PdPTP1 is localized in cytosol and nucleus.

Expression Patterns of PdPTP1 in Response to Salt and Oxidative Stress
In order to determine expression patterns of PdPTP1, the expression levels of PdPTP1 in various tissues were evaluated by qRT-PCR. PdPTP1 was expressed in all tissues tested with the highest mRNA level in roots ( Figure 3A). Furthermore, we determined the transcript level of PdPTP1 under the 350 mM NaCl treatment for 0, 1, 4, 6, 12, and 24 h. Quantitative RT-PCR analysis showed salt-stress induced PdPTP1 expression within 1 h, reaching the highest transcript level at 6 h. The upregulation of PdPTP1 decreased afterward, up to 24 h ( Figure 3B). Because salt stress could induce oxidative stress, the effect of 100 µM methylviologen (MV) on PdPTP1 transcription also was examined. The results showed that PdPTP1 expression was induced to increase during the entire 24 h period and reached a maximum at 24 h, after MV treatment ( Figure 3C). These results suggested that the PdPTP1 gene may be involved in salt-related stress response. . Each column is a mean of three replicates ± SD. Asterisks indicate significant differences: ** p < 0.01, * p < 0.05.

Identification of Transgenic Poplar
In order to investigate the function of PdPTP1 proteins, transgenic poplar overexpressing PdPTP1 (OxPdPTP1) was produced by introducing the construct pSuper:PdPTP1:GFP into poplar 84K. Putative transgenic plants were selected for confirming the integration of transgene by PCR analysis, using the primers of the hygromycin phosphotransferase gene (Hyg) ( Figure S2A). Furthermore, transgenic lines harboring PdPTP1 were verified by qRT-PCR analysis and fluorescence signals detection ( Figure S2B,C). Three transgenic lines with different level of PdPTP1 expression (OxPdPTP1-1, OxPdPTP1-2, and OxPdPTP1-6) were selected for further functional analysis.

Overexpression of PdPTP1 Increased Sensitivity to NaCl in Transgenic Poplar
Since PdPTP1 was a salt induced gene, it is probable that PdPTP1 functions in a plant's response to salt. To confirm this assumption, we next treated WT and OxPdPTP1 poplars with 350 mM of NaCl. After five days, OxPdPTP1 poplars showed more severe shrinking of the leaves than WT poplars ( Figure 4A). Similar results were observed when Arabidopsis overexpressing PdPTP1 was treated with 200 mM of NaCl ( Figure S3). The Photosynthesis and Maximal PSII quantum yield (Fv/Fm) have the potential of evaluating overall quantum yield and capacity [27]. We measured photosynthetic rate and Fv/Fm of WT and OxPdPTP1 poplars after exposure to 350 mM of NaCl. As expected, salt stress resulted in a decrease in photosynthetic rate in all lines, with the effect being most pronounced in OxPdPTP1 poplars ( Figure 4B). Changes in Fv/Fm in response to 350 mM of NaCl were also compared between the WT and OxPdPTP1 poplars. The OxPdPTP1 poplars leaves had relatively lower Fv/Fm than those of WT poplars after salinity exposure ( Figure 4C). Furthermore, leaf RWC was measured in the OxPdPTP1 and WT plants upon exposure to salt stress. Consistently, OxPdPTP1 poplars exhibited an obvious decrease in leaf RWC than that in WT plants ( Figure 4D).
The REL and MDA are used as an indicator of tolerance to abiotic stresses, such as drought, salinity, and extreme temperatures [9]. To further evaluate the effects of salt stress on the performance of OxPdPTP1 poplars, we thus compared the levels of REL and MDA in the leaves of OxPdPTP1 poplar under 350 mM NaCl stress with those in WT. Under normal growth conditions, the physiological levels of the total REL and MDA were similar between . Each column is a mean of three replicates ± SD. Asterisks indicate significant differences: ** p < 0.01, * p < 0.05.

Identification of Transgenic Poplar
In order to investigate the function of PdPTP1 proteins, transgenic poplar overexpressing PdPTP1 (OxPdPTP1) was produced by introducing the construct pSuper:PdPTP1:GFP into poplar 84K. Putative transgenic plants were selected for confirming the integration of transgene by PCR analysis, using the primers of the hygromycin phosphotransferase gene (Hyg) ( Figure S2A). Furthermore, transgenic lines harboring PdPTP1 were verified by qRT-PCR analysis and fluorescence signals detection ( Figure  S2B,C). Three transgenic lines with different level of PdPTP1 expression (OxPdPTP1-1, OxPdPTP1-2, and OxPdPTP1-6) were selected for further functional analysis.

Overexpression of PdPTP1 Increased Sensitivity to NaCl in Transgenic Poplar
Since PdPTP1 was a salt induced gene, it is probable that PdPTP1 functions in a plant's response to salt. To confirm this assumption, we next treated WT and OxPdPTP1 poplars with 350 mM of NaCl. After five days, OxPdPTP1 poplars showed more severe shrinking of the leaves than WT poplars ( Figure 4A). Similar results were observed when Arabidopsis overexpressing PdPTP1 was treated with 200 mM of NaCl ( Figure S3). The Photosynthesis and Maximal PSII quantum yield (Fv/Fm) have the potential of evaluating overall quantum yield and capacity [27]. We measured photosynthetic rate and Fv/Fm of WT and OxPdPTP1 poplars after exposure to 350 mM of NaCl. As expected, salt stress resulted in a decrease in photosynthetic rate in all lines, with the effect being most pronounced in OxPdPTP1 poplars ( Figure 4B). Changes in Fv/Fm in response to 350 mM of NaCl were also compared between the WT and OxPdPTP1 poplars. The OxPdPTP1 poplars leaves had relatively lower Fv/Fm than those of WT poplars after salinity exposure ( Figure 4C). Furthermore, leaf RWC was measured in the OxPdPTP1 and WT plants upon exposure to salt stress. Consistently, OxPdPTP1 poplars exhibited an obvious decrease in leaf RWC than that in WT plants ( Figure 4D). withstand environmental stresses. TTC reduction assay is commonly used to access the vitality of root [28]. To evaluate the effects of salt stress on the root vitality of OxPdPTP1 poplars, TTC reduction assay was performed. Under normal condition, OxPdPTP1 and WT roots had similar TTC reduction activity ( Figure 4G). Following 350 mM NaCl stress, OxPdPTP1 roots had lower TTC reduction activity than that of WT. Together, these results indicated that overexpression of PdPTP1 poplars made them more sensitive to salt stress.

Overexpression of PdPTP1 Poplar Increased ROS Levels and Inhibited ROS Scavenger Activities in Response to Salt Stress
For localization and quantification of H2O2 and O2· − in vivo, WT and OxPdPTP1 poplar leaves and roots were treated with 350 mM of NaCl for zero and three days and then stained with diaminobenzidine (DAB) (dark brown) ( Figure 5A,C) and nitrotetrazolium blue chloride (NBT) (dark blue) ( Figure 5B,D). The OxPdPTP1 plants clearly exhibited higher intensities of DAB and NBT staining in leaves and roots compared with WT plants ( Figure 5C,D) after 350 mM NaCl treatment for three days, indicating a higher level of H2O2 and O2· − accumulation. Additionally, H2O2 content in the leaves and roots of OxPdPTP1 and WT plants were measured. The result showed that H2O2 content of the leaves and roots was similar in WT and OxPdPTP1 poplars under normal growth condition, while salt treatment increased the amount of H2O2 by an average of 17.28% and 63.21% in leaves and roots of WT poplars, respectively, but by an average of 45.09% and 79.44% in leaves and roots of OxPdPTP1 poplars ( Figure 5E). Furthermore, we examined the activities of ROS scavengers and found there was a significant decrease in CAT activity of OxPdPTP1 leaves but not roots, compared with WT ( Figure 5F). The REL and MDA are used as an indicator of tolerance to abiotic stresses, such as drought, salinity, and extreme temperatures [9]. To further evaluate the effects of salt stress on the performance of OxPdPTP1 poplars, we thus compared the levels of REL and MDA in the leaves of OxPdPTP1 poplar under 350 mM NaCl stress with those in WT. Under normal growth conditions, the physiological levels of the total REL and MDA were similar between OxPdPTP1 and WT plants. Following salt stress, the total REL averagely increased by 52.07% in WT poplars, but 74.96%, 79.96%, and 80.00% in OxPdPTP1-1, OxPdPTP1-2, and OxPdPTP1-6 poplars, respectively ( Figure 4E). Higher contents in the MDA were also obtained from these transgenic plants after salt treatment ( Figure 4F). The effect of salt stress on plants first acts on the roots. The vitality of root directly affects plant growth and reflects the ability of plants to withstand environmental stresses. TTC reduction assay is commonly used to access the vitality of root [28]. To evaluate the effects of salt stress on the root vitality of OxPdPTP1 poplars, TTC reduction assay was performed. Under normal condition, OxPdPTP1 and WT roots had similar TTC reduction activity ( Figure 4G). Following 350 mM NaCl stress, OxPdPTP1 roots had lower TTC reduction activity than that of WT. Together, these results indicated that overexpression of PdPTP1 poplars made them more sensitive to salt stress.

Overexpression of PdPTP1 Poplar Increased ROS Levels and Inhibited ROS Scavenger Activities in Response to Salt Stress
For localization and quantification of H 2 O 2 and O 2 · − in vivo, WT and OxPdPTP1 poplar leaves and roots were treated with 350 mM of NaCl for zero and three days and then stained with diaminobenzidine (DAB) (dark brown) ( Figure 5A,C) and nitrotetrazolium blue chloride (NBT) (dark blue) ( Figure 5B,D). The OxPdPTP1 plants clearly exhibited higher intensities of DAB and NBT staining in leaves and roots compared with WT plants ( Figure 5C,D) after 350 mM NaCl treatment for three days, indicating a higher level of H 2 O 2 and O 2 · − accumulation. Additionally, H 2 O 2 content in the leaves and roots of OxPdPTP1 and WT plants were measured. The result showed that H 2 O 2 content of the leaves and roots was similar in WT and OxPdPTP1 poplars under normal growth condition, while salt treatment increased the amount of H 2 O 2 by an average of 17.28% and 63.21% in leaves and roots of WT poplars, respectively, but by an average of 45.09% and 79.44% in leaves and roots of OxPdPTP1 poplars ( Figure 5E). Furthermore, we examined the activities of ROS scavengers and found there was a significant decrease in CAT activity of OxPdPTP1 leaves but not roots, compared with WT ( Figure 5F). SOD activity in both leaves and roots of OxPdPTP1 poplars was lower than that of WT poplars after exposure to 350 mM of NaCl ( Figure 5G). Taken together, these data indicated the high level of ROS in OxPdPTP1 poplars under salt stress might be caused by inactivated ROS scavengers. SOD activity in both leaves and roots of OxPdPTP1 poplars was lower than that of WT poplars after exposure to 350 mM of NaCl ( Figure 5G). Taken together, these data indicated the high level of ROS in OxPdPTP1 poplars under salt stress might be caused by inactivated ROS scavengers.

Overexpression of PdPTP1 Polar Compromised Ion Homeostasis in Response to Salt Stress
To assess the effect of PdPTP1 overexpression on ion homeostasis, the Na + and K + contents of OxPdPTP1 and WT plants were measured after exposure to 350 mM of NaCl for five days. Under nonstress growing condition, there was no significant variation in the Na + and K + contents between OxPdPTP1 and WT plants ( Figure 6A,B). After NaCl treatment, Na + content of OxPdPTP1 was significantly higher than that of WT in leaves and stems but not in roots ( Figure 6C). Generally, OxPdPTP1 poplars had a slightly lower K + content in stems, leaves, and roots than that in WT plants after salt treatment ( Figure 6D). Taken together, our data suggested that OxPdPTP1 negatively regulates Na + and K + homoeostasis under salt stress.
Int. J. Mol. Sci. 2020, 21, 1065 9 of 20 roots ( Figure 6C). Generally, OxPdPTP1 poplars had a slightly lower K + content in stems, leaves, and roots than that in WT plants after salt treatment ( Figure 6D). Taken together, our data suggested that OxPdPTP1 negatively regulates Na + and K + homoeostasis under salt stress. Figure 6. Na + and K + contents in WT and OxPdPTP1 lines. (A) Na + contents and (B) K + contents in leaf, stem, and root under 0 mM NaCl treatment for five days. (C) Na + contents and (D) K + contents in leaf, stem, and root under 350 mM of NaCl for five days. Each column is a mean of three replicates ± SD. Asterisks indicate significant differences: ** p < 0.01.

Overexpression of PdPTP1 Reduced Salt-Stress Tolerance in Transgenic Poplar under Long-Term Salt Stress
To further explore the effects of OxPdPTP1 on poplar during salt stress, Greenhouse experiment was applied to WT and OxPdPTP1 plants under 0 and 200 mM NaCl condition for a four-week period. As shown in Figure 7, compared with WT plants, OxPdPTP1 plants' growth was severely limited under 200 mM NaCl treatment ( Figure 7A). OxPdPTP1 poplars showed a significantly lower plant height and stem height growth rate during the period of salt treatment. Interestingly, under nonstress growing conditions, OxPdPTP1 poplars had a slightly greater plant height and stem height growth rate than WT plants ( Figure 7B,C). Consistent with the growth phenotype under 200 mM NaCl treatment, OxPdPTP1 poplars had a significantly lower photosynthetic rate than WT plants during salt stress ( Figure 7D). Furthermore, the REL and leaf RWC of OxPdPTP1 plants were similar to that of WT plants under normal growth conditions, while the OxPdPTP1 poplars showed higher REL and lower leaf RWC than WT poplars after exposure to 200 mM of NaCl for four weeks ( Figure 7E,F).
To investigate the difference in biomass accumulation between WT and OxPdPTP1 poplars under normal and 200 mM NaCl condition, shoot fresh weight, root fresh weight, and total fresh biomass was measured after four weeks. The results showed less total biomass accumulation and shoot weight in OxPdPTP1 under salt conditions, compared to WT plants. However, compared with WT poplars, more total biomass accumulation and shoot weight Figure 6. Na + and K + contents in WT and OxPdPTP1 lines. (A) Na + contents and (B) K + contents in leaf, stem, and root under 0 mM NaCl treatment for five days. (C) Na + contents and (D) K + contents in leaf, stem, and root under 350 mM of NaCl for five days. Each column is a mean of three replicates ± SD. Asterisks indicate significant differences: ** p < 0.01.

Overexpression of PdPTP1 Reduced Salt-Stress Tolerance in Transgenic Poplar under Long-Term Salt Stress
To further explore the effects of OxPdPTP1 on poplar during salt stress, Greenhouse experiment was applied to WT and OxPdPTP1 plants under 0 and 200 mM NaCl condition for a four-week period. As shown in Figure 7, compared with WT plants, OxPdPTP1 plants' growth was severely limited under 200 mM NaCl treatment ( Figure 7A). OxPdPTP1 poplars showed a significantly lower plant height and stem height growth rate during the period of salt treatment. Interestingly, under nonstress growing conditions, OxPdPTP1 poplars had a slightly greater plant height and stem height growth rate than WT plants ( Figure 7B,C). Consistent with the growth phenotype under 200 mM NaCl treatment, OxPdPTP1 poplars had a significantly lower photosynthetic rate than WT plants during salt stress ( Figure 7D). Furthermore, the REL and leaf RWC of OxPdPTP1 plants were similar to that of WT plants under normal growth conditions, while the OxPdPTP1 poplars showed higher REL and lower leaf RWC than WT poplars after exposure to 200 mM of NaCl for four weeks ( Figure 7E,F).
condition. The results showed that OxPdPTP1 poplars had a higher photosynthetic rate than the WT poplars ( Figure S4A). Both stomatal conductance (Gs) and leaf transpiration in WT and OxPdPTP1 poplars increased with elevated light intensity, with OxPdPTP1 poplars showing a higher Gs and transpiration ( Figure S4B,C). Conversely, the instantaneous WUE value of OxPdPTP1 poplars was lower than that of WT plants ( Figure S4D). In summary, those results suggested that OxPdPTP1 poplars showed worse growth status than WT poplars under 200 mM NaCl treatment, while they performed better under optimal condition.  To investigate the difference in biomass accumulation between WT and OxPdPTP1 poplars under normal and 200 mM NaCl condition, shoot fresh weight, root fresh weight, and total fresh biomass was measured after four weeks. The results showed less total biomass accumulation and shoot weight in OxPdPTP1 under salt conditions, compared to WT plants. However, compared with WT poplars, more total biomass accumulation and shoot weight were found in OxPdPTP1 poplars under normal conditions ( Figure 8A,B). However, the root weight showed no obvious difference between WT and transgenic poplars under either normal or salt-stress irrigation ( Figure 8C).
Under normal growth conditions, no significant difference in chlorophyll contents of WT and OxPdPTP1 poplars was observed, but there was a significant difference when exposed to 200 mM of NaCl for four weeks ( Figure 8D-F). Chlorophyll a content in OxPdPTP1-1 and OxPdPTP1-2 plants showed 52.42% and 49.08% reduction, but 31.97% in WT plants under salinity ( Figure 8E). Similarly, salinity reduced chlorophyll b content of WT plants by 4.82%, whereas it reduced that of OxPdPTP1-1 and OxPdPTP1-2 plants by about 17.84% and 11.78% ( Figure 8F). Consistently, the total chlorophyll content of WT plants decreased by 26.76%, but that of OxPdPTP1-1 and OxPdPTP1-2 substantially decreased by 45.81% and 42.02%, respectively, after four weeks ( Figure 8D), indicating that chlorophyll of OxPdPTP1 poplar is prone to be degraded under salinity stress.

PdPTP1 Interacts with PdMPK3, PdMAPK6 In Vivo and In Vitro
To understand the mechanism through which PdPTP1 regulates poplar salt-stress response, we performed a yeast two-hybrid assay to identify PdPTP1-interacting proteins, including PdMAPK1, PdMAPK3, PdMAPK4, PdMAPK6, PdMAPK7, and PdMAPK9. Among the six candidates we identified, PdMAPK3/4/6 interacted strongly with PdPTP1 ( Figure 9A). We used a BiFC assay to further address the spatial specificity of PdPTP1-PdMAPKs complex formation. However, we cannot detect a sign of interaction between PdPTP1 and PdMAPK4. Additionally, the BiFC assay also showed that no sign of interaction could be detected between PdPTP1 and PdMAPK1, PdMAPK7, and PdMAPK9, or any of the negative controls ( Figure 9B). To investigate the impact of PdPTP1 on plant photosynthetic rate, we conducted a photosynthesis-light curves experiment on OxPdPTP1 and WT poplars under normal condition. The results showed that OxPdPTP1 poplars had a higher photosynthetic rate than the WT poplars ( Figure S4A). Both stomatal conductance (Gs) and leaf transpiration in WT and OxPdPTP1 poplars increased with elevated light intensity, with OxPdPTP1 poplars showing a higher Gs and transpiration ( Figure S4B,C). Conversely, the instantaneous WUE value of OxPdPTP1 poplars was lower than that of WT plants ( Figure S4D). In summary, those results suggested that OxPdPTP1 poplars showed worse growth status than WT poplars under 200 mM NaCl treatment, while they performed better under optimal condition.

PdPTP1 Interacts with PdMPK3, PdMAPK6 In Vivo and In Vitro
To understand the mechanism through which PdPTP1 regulates poplar salt-stress response, we performed a yeast two-hybrid assay to identify PdPTP1-interacting proteins, including PdMAPK1, PdMAPK3, PdMAPK4, PdMAPK6, PdMAPK7, and PdMAPK9. Among the six candidates we identified, PdMAPK3/4/6 interacted strongly with PdPTP1 ( Figure 9A). We used a BiFC assay to further address the spatial specificity of PdPTP1-PdMAPKs complex formation. However, we cannot detect a sign of interaction between PdPTP1 and PdMAPK4. Additionally, the BiFC assay also showed that no sign of interaction could be detected between PdPTP1 and PdMAPK1, PdMAPK7, and PdMAPK9, or any of the negative controls ( Figure 9B).

Discussion
Poplar is widely distributed throughout the world and serves as a model organism for tree molecular biology and forest biotechnology because of its relatively small genome, rapid growth rate, ease of vegetative propagation, and genetic transformation [29,30]. Apart from scientific importance, poplar is used for the construction industry, paper making, and biofuel production and thus has significant economic value [31]. As a perennial tree species, poplar trees are routinely exposed to complex environmental stresses, such as salt, drought, and low temperature during their long life span, and these stresses adversely affect their growth and survival [32,33]. To meet the increasing demand of poplar productivity, it is important for us to understand molecular responses to stress in poplar and further improve stress tolerance through genetic engineering. In this work, we show that PdPTP1 is a negative component in the salt signaling pathway. PdPTP1 overexpression poplars displayed hypersensitivity to salt stress.

Discussion
Poplar is widely distributed throughout the world and serves as a model organism for tree molecular biology and forest biotechnology because of its relatively small genome, rapid growth rate, ease of vegetative propagation, and genetic transformation [29,30]. Apart from scientific importance, poplar is used for the construction industry, paper making, and biofuel production and thus has significant economic value [31]. As a perennial tree species, poplar trees are routinely exposed to complex environmental stresses, such as salt, drought, and low temperature during their long life span, and these stresses adversely affect their growth and survival [32,33]. To meet the increasing demand of poplar productivity, it is important for us to understand molecular responses to stress in poplar and further improve stress tolerance through genetic engineering. In this work, we show that PdPTP1 is a negative component in the salt signaling pathway. PdPTP1 overexpression poplars displayed hypersensitivity to salt stress.

PdPTP1 is a Tyr-Specific PTP in Poplar
The conserved catalytic signature (I/V)HCXAGXXR(S/T)G defined the large PTP superfamily, which now, in addition to DsPTPs, includes Tyr-specific PTPs that only dephosphorylate tyrosine [34]. In the present study, PdPTP1 contains the (I/V)HCXAGXXR(S/T)G motif in the catalytic domain characteristic of PTPs superfamily ( Figure S1). Moreover, the PdPTP1 harbors two conserved motifs which are present in all members of Tyr-specific PTPs but was not detectable in the sequence of any other DsPTPs family: KNRY motif necessary to permit the access of phosphotyrosine residues to the active site and WPD motif essential for the phosphotyrosine activity in all eukaryotes ( Figure S1) [35]. Another unique sequence signature for Tyr-specific PTPs in plants, IHNT motif, also appears in the amino acid sequence of PdPTP1 ( Figure 1B) [36]. Taken together, the presence of these motifs clearly places the PdPTP1 within the Tyr-specific PTPs family.

PdPTP1 Overexpression Reduced Tolerance to Salt Stress in Poplar due to the Impaired Ion and ROS Homeostasis
In plants, PTP1 is involved in various stresses, such as salt, oxidative, osmotic, pathogen response, wounding, and ABA signaling [14,19,24,36,37]. Our results found that the transcript of PdPTP1 was induced by NaCl and oxidative treatment ( Figure 3B,C), and this finding is consistent with previous studies that the transcript of AtPTP1 was upregulated by high salinity and H 2 O 2 [14,38]. These results indicate that PdPTP1 protein may play an important role in response to salt stress. For further understanding of PdPTP1 function under salt stress, we treated OxPdPTP1 poplar with salt stress and found that OxPdPTP1 poplar displayed hypersensitivity to salt ( Figure 4); similar results were obtained in cotton (Gossypium spp.), in which GhDsPTP3a, a member of PTPs, reversely regulated salt tolerance in cotton [39], indicating a conserved function of PTPs in regulating salt response.

PdPTP1 Overexpression Reduced Salt Tolerance in Poplar due to the Impaired ROS Homeostasis
Salt stress leads to the accumulation of high levels of ROS. ROS is highly reactive and can lead to impaired physiological function through cellular damage of phospholipids [7,40]. The data obtained in the present study showed that the OxPdPTP1 plant suffered remarkable ROS toxicity under salt stress ( Figure 5), resulting in higher REL and more accumulation of MDA than WT plant ( Figure 4E,F), which cause more serious membrane damage and thus accelerated the OxPdPTP1 plant's aging and death. In order to avoid destruction of ROS, plants have developed enzymatic components such as SOD and CAT [2]. In the present study, the CAT and SOD activities in OxPdPTP1 plants were lower than in the WT plant ( Figure 5D,E), which suggested that obvious lower activity of antioxidant enzymes rendered the OxPdPTP1 poplar to suffer more serious ROS toxicity and thus reduced salt tolerance in OxPdPTP1 poplar.

PdPTP1 Overexpression Reduced Salt Tolerance in Poplar due to the Impaired Ion Homeostasis
Maintaining cellular ion homeostasis is an important adaptive trait of salt-tolerant plants during salt stress. A suitable K + /Na + in the cytoplasm prevents cellular damage and nutrient deficiency [2]. In this present study, on one hand, more Na + accumulates in leaves and stems, but less in roots of OxPdPTP1 poplars than WT poplars under salinity condition ( Figure 6C). On the other hand, lower K + was observed in leave, stems, and roots of OxPdPTP1 poplars ( Figure 6D), which suggested that salt sensitive phenotype of OxPdPTP1 plants result from impaired ion homeostasis. This result is consistent with the previous report that GhDsPTP3a reduces Na + efflux and thus causes plant hypersensitivity to salt stress [39].
Salt stress poses a serious threat to photosynthesis and the electron transport system [41]. Excessive cytoplasmic Na + gives rise to imbalanced cellular ion contents, causing reduced maximum photochemistry efficiency of PSII and substantial reduction in photosynthesis [42,43]. In this study, we observed that overexpression of PdPTP1 poplars significantly decreased the maximal photochemical yield of PSII (Fv/Fm) in OxPdPTP1 poplars compared with WT poplars after salt treatment ( Figure 4C). The ratio Fv/Fm was used as parameters to evaluate the maximum photochemical efficiency of PSII in the dark-adapted state and decline of Fv/Fm value reflects the occurrence of photoinhibition of photosynthesis [44]. Lower Fv/Fm indicated that light-use efficiency of the OxPdPTP1 plant decreased under salt-stress conditions and explains why the OxPdPTP1 plant has a lower photosynthetic rate than the WT plant ( Figure 4B). Taken together, these results suggested that the photosynthetic machinery is damaged by deleterious salt effects, probably due to the excessive Na + accumulation in OxPdPTP1 poplars.
3.5. The Hypersensitivity of OxPdPTP1 Poplar to Salt Is Associated with PdMPK3/6 In plants, MAPK cascades are universal signal transduction modules, which can sense stress signals and transduce them into suitable responses [45]. Many data suggested that MAPKs is rapidly activated in plants exposed to a variety of abiotic and biotic stresses, including salt, cold, drought, UV-irradiation, wounding, and pathogen [46,47]. Among them, MPK3/6 has been well studied in salt stress [48][49][50]. For example, MPK3/6 phosphorylate and activate HSFA4A, thereby controlling ROS homeostasis and positively regulating salt-stress responses [13]. AtMPK6 activated by PLD1-derived phosphatidic acid (PA) phosphorylates and activates the SOS1 Na + /H + antiporter activity and thus enhances salt tolerance [11]. These reports indicated that MPK3/6 improve salt tolerance by re-establishing cellular ROS and ion homeostasis. MAPKs can be activated by phosphorylating Thr and Tyr residues in an activation loop of MAPK by dual-specificity MAPKKs. On the contrary, dephosphorylation of Thr or/and Tyr bring the enzymes back to the inactive state. This can be achieved by PTPs and DsPTPs [24]. In Arabidopsis, AtPTP1 had been shown to be able to dephosphorylate and deactivate AtMPK3/6 either in vitro or in vivo [19,26]. The tight regulation of MAPKs by MAPKKs and PTPs is a prerequisite to the fine-tune physiological outcome of signaling produce specific and adequate physiological responses [26]. In the present study, we found that PdPTP1 interacted with PdMPK3/6 in vitro and in vivo ( Figure 7A,B), and transgenic poplar of overexpressing PdPTP1 showed sensitivity to salt due to the toxicity of ion and ROS. Therefore, we suppose that the overexpression of PdPTP1 may be associated with decreased levels of active MAPK3/6 in response to salinity, which result in disrupted ion and ROS balance of poplars under salt stress and therefore exhibited a salt-hypersensitive phenotype. In particular, PdPTP1 mRNA was induced by salt, indicating PdPTP1 may act in a feedback loop to avoiding hyperactivation of PdMAPK3/6 and thus guarantee a fine-tune physiological response. Similarly, in fission yeast, Pyp2, which encodes a tyrosine-specific phosphatase, functions in a feedback loop to inactivate Styl MAPK kinase, following exposure to osmotic stress [51]. However, the precise role of PdPTP1 in MAPK3/6 dephosphorylation is under further investigation.
Taken together, we propose a model for the putative pathway of regulation of salt stress by PdPTP1 ( Figure 10). Under salt stress, the MAPKKK-MAPKK-PdMAPK3/6 cascades are activated. Activated PdMAPK3/6 may be directly dephosphorylated by PdPTP1. PdPTP1 may cooperate with PdMAPK3/6 to regulate ion homeostasis and, on the other hand, scavenge ROS, to avoid oxidative damage in response to salt.

Plant Materials and Stress Treatments
Populus alba × P. glandulosa (84K) seedlings were cultured in half-concentrated Murashige and Skoog (MS) medium supplemented with 0.05 mg/L of IBA and 0.05 mg/L of NAA (Sigma, St. Louis, MO, USA) [52], and NE19 plantlets were cultured in MS medium in a controlled environment growth room (temperature: 25 °C:20 °C, dark:light; relative humidity: 45%; photoperiod: 16 h:8 h, light:dark). Various abiotic stress was conducted on 60-day-old NE19 seedlings, to verify the expression patterns of PdPTP1 in different tissues, salinity stress, and oxidative stress. For oxidative stress, 100 µM of Methylviologen (MV) (Sigma, 856177) was sprayed once on the leaves of NE19. The leaves of treated poplars were harvested at 0, 1, 4, 6, 12, and 24 h, after MV treatment. For salinity stress, NE19 plants were subjected to 350 mM of NaCl. The leaves of treated poplars were harvested at 0, 1, 4, 6, 12, and 24 h, after salinity treatment. The harvested samples were immediately frozen in liquid nitrogen and stored at −80 degrees.

RNA Extraction and Quantitative Real-Time Polymerase Chain Reaction
The leaves of control and treated poplars, as described above, were collected to extract total RNA by using the CTAB reagent, a method described previously [53]. Then, cDNA was created by 1 µg of RNA, using the Prime Script™ RT reagent Kit with gDNA Eraser (Perfect Real Time, Takara, RR047Q, Dalian, China), according to manufacturer's instructions. The quantitative real-time polymerase chain reaction (qRT-PCR) was performed, as previously

Plant Materials and Stress Treatments
Populus alba × P. glandulosa (84K) seedlings were cultured in half-concentrated Murashige and Skoog (MS) medium supplemented with 0.05 mg/L of IBA and 0.05 mg/L of NAA (Sigma, St. Louis, MO, USA) [52], and NE19 plantlets were cultured in MS medium in a controlled environment growth room (temperature: 25 • C:20 • C, dark:light; relative humidity: 45%; photoperiod: 16 h:8 h, light:dark). Various abiotic stress was conducted on 60-day-old NE19 seedlings, to verify the expression patterns of PdPTP1 in different tissues, salinity stress, and oxidative stress. For oxidative stress, 100 µM of Methylviologen (MV) (Sigma, 856177) was sprayed once on the leaves of NE19. The leaves of treated poplars were harvested at 0, 1, 4, 6, 12, and 24 h, after MV treatment. For salinity stress, NE19 plants were subjected to 350 mM of NaCl. The leaves of treated poplars were harvested at 0, 1, 4, 6, 12, and 24 h, after salinity treatment. The harvested samples were immediately frozen in liquid nitrogen and stored at −80 degrees.

RNA Extraction and Quantitative Real-Time Polymerase Chain Reaction
The leaves of control and treated poplars, as described above, were collected to extract total RNA by using the CTAB reagent, a method described previously [53]. Then, cDNA was created by 1 µg of RNA, using the Prime Script™ RT reagent Kit with gDNA Eraser (Perfect Real Time, Takara, RR047Q, Dalian, China), according to manufacturer's instructions. The quantitative real-time polymerase chain reaction (qRT-PCR) was performed, as previously with methods [54], using the TB Green ® Premix Ex Taq™ GC (Perfect Real Time, Takara, RR071Q, Dalian, China) with gene-specific primers and the internal control gene (ACTIN). The relative value for the expression level of each gene was calculated by the 2 −∆∆Ct method [55]. Primers were designed by using Primer 5.0 (Sigma-Aldrich Corp, St. Louis, MO, USA) and the list in Table S1.

Salt-Stress Tolerance Evaluation of Transgenic Poplars
All of the plants (height 20-30 cm) were grown in suitably sized pots (10 cm long, 10 cm wide, and 10 cm high) of the same soil (nutrient soil, peat, and vermiculite 1:1:1), and each pot had a tray. In order to investigate the functional role of PdPTP1 in response to salt stress, potted WT lines and OxPdPTP1 lines were treated with short-term salt treatment and long-term salt treatment. To short-term salt treatment, WT lines and OxPdPTP1 lines with similar size and growth status were chosen and subjected to 0 or 350 mM of NaCl for 5 days. Net photosynthetic rate, transpiration, stomatal conductance and intercellular CO 2 concentration in the 9th to 11th leaves of OxPdPTP1 and WT poplars were measured by the Li-6400 Photosynthesis System (Li-Cor, Lincoln, NE, USA) at day 0, day 3, and day 5. Five days after exposure to 350 mM of NaCl, photosynthetic activity in the 10th to 13th leaves of WT lines and OxPdPTP1 lines was monitored by Maximal PSII quantum yield (Fv/Fm) values, using a PAM chlorophyll fluorometer (PAM100) after 20 min of dark adaptation. Relative electrolyte leakage (REL), leaf relative water content (RWC), Malondialdehyde (MDA) content, and root reduction activity of WT lines and OxPdPTP1 lines were determined as described through previous protocol [54]. Root reduction activity was analyzed by the triphenyl tetrazolium chloride (TTC) method [56]. For the long-term salt treatment, WT lines and OxPdPTP1 lines with similar size and growth status were chosen and subjected to 1/8 MS solution supplemented with or without 200 mM of NaCl, every 4 days for 4 weeks. The height of WT lines and OxPdPTP1 lines was measured weekly. Net photosynthetic rate, transpiration, stomatal conductance and intercellular CO 2 concentration in the 9th to 11th leaves of WT plants and transgenic lines were measured by the Li-6400 Photosynthesis System (Li-Cor, Lincoln, NE, USA) weekly. After 4 weeks, leaf RWC, REL, shoot biomass, root biomass, and chlorophyll content of each poplar were measured.

Measurement of Na + and K + Contents
At the end of 350 mM of NaCl treatment for 5 days, the leaves, stems, and roots were harvested for Na + and K + assay, as described previously [57,58]. Briefly, the samples were dried at 80 • C, for 2 day, milled to fine powder, weighed, and digested with concentrated sulfuric acid. The Na + and K + contents were determined by using an atomic absorption spectrometer (TAS-986; Purkinje General Instrument Co., Beijing, China).

Subcellular Localization Analysis
For subcellular localization of PdPTP1, pSuper:PdPTP1:GFP, and pSuper:GFP fusion constructs were transformed into tobacco epidermal cells by the previously published protocol [59] and tobacco and poplar protoplasts by means of polyethylene glycol (PEG) treatment [60]. The transformed protoplasts, tobacco, and transgenic poplar leaves were observed by laser confocal fluorescence microscopy (Leica TCS SP8; Leica, Wetzlar, Germany). The LAS-AF software was used to record the images.

Yeast Two-Hybrid
Yeast two-hybrid analysis was performed, using the protocol described by the previously published protocol [61]. The full lengths of PdMAPK1, PdMAPK3, PdMAPK4, PdMAPK6, PdMAPK7, and PdMAPK9 cDNA fragments were introduced to pGADT7 vectors (Clontech, Mountain View, CA, USA) and used as the prey, and the full length of PdPTP1 coding sequences cDNA fragment was introduced to pGBKT7 vectors (Clontech) and used as the bait, to identify the interacting proteins. Yeast strain AH109 was co-transformed with bait and prey constructs. Yeast cells with the two constructs were selected on minimal medium without leucine (Leu) and tryptophan (Trp) medium. Positive clones were confirmed by growing on minimal medium containing 6 mM of 3-amino-1,2,4-triazole without Leu, Trp, and histidine (His), and minimal medium without Leu, Trp, His, and adenine (Ade).

Phylogenetic and Domain Analysis of PdPTP1
The MtPTP1, NtPTP1, and LePTP1 protein sequences were obtained from NCBI (National Coalition Building Institute, https://www.ncbi.nlm.nih.gov/), and sequences data of the other proteins shown in the diagram can be found in the GenBank database, under the accession numbers (Table S2) The phylogenetic tree of PTPs was established with MEGA X by the Maximum Likelihood method, and the maize calcium-dependent protein kinase (ZmCDPK2; AAA69507) was used as an outgroup [63]. The alignments were generated by the multiple sequence alignment by the Florence Corpet website (http://multalin.toulouse.inra.fr/multalin/multalin.html) [64].

Statistical Analyses
The experiment was repeated at least three times, independently. The results are presented as the means ± SDs. Data were analyzed through LSD multiple range tests in the one or two way ANOVA program of SPSS (IBM SPSS17.0). Significance was defined as p < 0.05 (*) and p < 0.01 (**).