Central Roles and Regulatory Mechanisms of Dual-Specificity MAPK Phosphatases in Developmental and Stress Signaling.

Mitogen-Activated Protein Kinase (MAPK) cascades are conserved signaling modules that integrate multiple signaling pathways. One level of control on the activity of MAPKs is through their negative regulators, MAPK phosphatases (MKPs). Therefore, MKPs also play an integrative role for plants responding to diverse environmental stimulus; but the mechanism(s) by which these phosphatases contribute to specific signals remains largely unknown. In this review, we summarize recent advances in characterizing the biological functions of a sub-class of MKPs, dual-specificity phosphatases (DSPs), ranging from controlling plant growth and development to modulating stress adaptation. We also discuss putative regulatory mechanisms of DSP-type MKPs, which plants may use to control the correct level of responses at the right place and time. We highlight insights into potential regulation of cross-talk between different signaling pathways, facilitating the development of strategies for targeting such cross-talk and to help improve plant resistance against adverse environmental conditions without affecting the growth and development.

Introduction

To rapidly adapt to various environmental challenges, plants need to balance diverse signal inputs which involves crosstalk between different signaling pathways. A common strategy for integrating these signals is through use of shared components, including mitogen-activated protein kinase (MAPK) cascades that play essential roles in signal transduction and amplification for many distinct cellular responses. MAPK cascade modules are conserved in all eukaryotes and consist of three kinase components: MAPK kinase kinases (MAPKKKs) phosphorylate dual-specificity MAPK kinases (MAPKKs), which then phosphorylate and activate the terminal MAPKs in a Thr-X-Tyr activation loop (Widmann et al., 1999; Bartels et al., 2010). The Arabidopsis genome encodes 20 MAPKs, 10 MAPKKs, and 60 MAPKKKs (Ichimura et al., 2002; Hamel et al., 2006); and several complete MAPK cascades in plants have been described (Colcombet and Hirt, 2008).

Because the same MAPK signaling modules can be activated by multiple extracellular stimuli, controlling the intensity and duration of MAPK activation is a critical determinant for organisms to generate correct biological outcomes for these different inputs. Therefore, an important point of regulating signaling is through dephosphorylation of MAPKs to attenuate their activity. Dephosphorylation of either the threonine and/or tyrosine residue within the activation motif inactivates MAPKs; and this dephosphorylation can be regulated by diverse types of protein phosphatases, including phosphoprotein phosphatases (PPPs) and metal-dependent protein phosphatases (PPMs), which are serine/threonine phosphatases, and tyrosine phosphatases (PTPs) (Shi, 2009; Bartels et al., 2010; Uhrig et al., 2013; Shankar et al., 2015). Representative members of the PPP family include protein phosphatase PP1, PP2A, PP2B, PP4, PP5, PP6, PP7; and the PPM family includes PP2Cs (Shi, 2009). These protein phosphatases likely have a variety of additional substrates, but some of PP2C-types have been shown to play important roles in regulating pathogen-associated signaling and defense responses at least partially through their control of MAPK activity (Meskiene et al., 2003; Schweighofer et al., 2007; Brock et al., 2010; Galletti et al., 2011; Sidonskaya et al., 2016; Mine et al., 2017). In support of potential integrative roles for MAPK-regulating phosphatases, the diverse functions of PP2Cs in plant hormone signaling, plant immunity, nutrition deficiency and development have been reviewed elsewhere (Fuchs et al., 2012; Singh et al., 2016).

PTPs are biochemically distinct protein phosphatases and include tyrosine specific phosphatases and dual-specificity (Ser/Thr and Tyr) phosphatases (DSPs) (Shankar et al., 2015). DSP-type MKPs are involved in diverse developmental processes and/or environmental stresses, ranging from salinity, drought, and UV-B radiation to pathogens (Gupta et al., 1998; Ulm et al., 2001, 2002; Lee and Ellis, 2007; Bartels et al., 2009; Lee et al., 2009; Walia et al., 2009; Anderson et al., 2011, 2014). In addition, most DSP-type MKPs in plants have several non-catalytic domains with the potential to interact with components of MAPK-independent signaling pathways (Bartels et al., 2010). These additional domains indicate that DSP-type MKPs are likely to coordinate different responses.

Because information on this small subset of protein phosphatases with diverse roles in plant biology has not been collated, the purpose of this review is to summarize recent progress in investigating and understanding the physiological roles of DSP-type MKPs in regulating multiple biological processes. We also discuss the putative regulatory mechanisms of DSP-type MKPs, which likely adds regulatory complexity for MKPs to orchestrate crosstalk between different signaling pathways.

Dual specificity MAPK phosphatases as negative regulators of MAPK signaling

MAPK signaling cascades are essential components for regulating multiple cellular responses in eukaryotes. Once signals are initiated, they also need to be attenuated to prevent over-activation and to reset the system to basal levels after the initial stimulation. Phosphatases are important negative regulators of MAPK signaling. Among these, dual-specificity (Ser/Thr and Tyr) phosphatases (DSPs) belong to a subfamily of the tyrosine phosphatases (PTPs) that can dephosphorylate both phosphoserine/phosphothreonine and phosphotyrosine within the activation loop of MAPKs (Keyse and Emslie, 1992; Alessi et al., 1993; Sun et al., 1993; Ward et al., 1994). Twenty-two DSPs have been identified in Arabidopsis genome (Kerk et al., 2008), five of which have been shown experimentally to interact with and dephosphorylate MAPKs and, therefore, form the group of functional DSP-type MKPs (hereafter referred to in this review as MKPs) in Arabidopsis (Gupta et al., 1998; Ulm et al., 2001, 2002; Lee and Ellis, 2007; Lee et al., 2009; Walia et al., 2009). These five MKPs include DUAL-SPECIFICTY PROTEIN TYROSINE PHOSPHATASE 1 (DsPTP1), MAP KINASE PHOSPHATASE 1 (MKP1), MAP KINASE PHOSPHATASE 2 (MKP2), INDOLE-3-BUTYRIC ACID RESPONSE 5 (IBR5), and PROPYZAMIDE HYPERSENSITIVE 1 (PHS1).

In vitro and/or in vivo studies have shown that these five MKPs physically interact with MAPKs and/or regulate their activation (Table 1). DsPTP1 was the first dual-specificity protein phosphatase from higher plants shown to inactivate a MAPK (MPK4) in vitro (Gupta et al., 1998). MKP1 physically interacts with MPK3, MPK4, and MPK6 both in vitro and in vivo; and it deactivates MPK6 in protoplast-based assays (Ulm et al., 2002; Bartels et al., 2009). MKP2, which interacts with MPK3 and MPK6 both in vitro and in vivo, is able to dephosphorylate phospho-MPK3 and phospho-MPK6 in vitro (Lee and Ellis, 2007). IBR5, a MPK12 interacting partner in vitro and in vivo, has been shown to dephosphorylate and thus deactivate MPK12 (Lee et al., 2009). PHS1 interacts with Arabidopsis MAPKs MPK12 and MPK18 in a yeast two-hybrid interaction assay, and recombinant PHS1 dephosphorylates the activated MPK18 in vitro (Walia et al., 2009).

Table 1

Functions of DSP-type MAPK phosphatases in plants.

	Regulatory mechanism	Interacting partners	Phosphatase substrates	Predominant subcellular localization	Biological roles	References
DsPTP1	Transcriptional induction by osmotic stress; Catalytic activation by CaM binding in vitro	MPK4 (in vitro); CaM (in vitro)	pNPP, pMBP, MPK4	N.A.	Osmotic stress (−); ABA responses (+)	Gupta et al., 1998 Yoo et al., 2004 Liu et al., 2015b
MKP2	Catalytic activation by MPK3 and MPK6 in vitro	MPK3 (in vitro, in vivo); MPK6 (in vitro, In vivo)	OMFP, MPK3, MPK6	Nucleus (Arabidopsis transgenic plants); Nucleus and cytoplasm (Transient expression in tobacco cells)	Oxidative stress (+); Pathogen resistance	Lee and Ellis, 2007 Lumbreras et al., 2010
IBR5	Alternative splicing	MPK12 (in vitro, in vivo)	OMFP, MPK12	Nucleus (Arabidopsis transgenic plants driven by CaMV 35S promoter); Nucleus and cytoplasm (Arabidopsis transgenic plants driven by native promoter)	Auxin responses (+); ABA responses (+) Resistance protein (CHS3, SNC1, RPS4, RPM1)	Monroe-Augustus et al., 2003 Strader et al., 2008a Strader et al., 2008b Lee et al., 2009 Strader and Bartel, 2009 Jayaweera et al., 2014 Johnson et al., 2015 Liu et al., 2015a
OsIBR5	Transcriptional induction by PEG6000, ABA and H2O2	SIPK (in vitro); WIPK (in vitro); NTF3 (in vitro); MEK1 (in vitro)	N.A.	Cytoplasm and nucleus (Transient expression in rice protoplasts)	Drought/osmotic stress (−)	Li et al., 2012
PHS1	Transcriptional induction by ABA	MPK12 (in vitro) MPK18 (in vitro, in vivo)	OMFP, MPK18	Cytoplasm (Arabidopsis transgenic plants)	Cortical microtubule organization (+); ABA responses (−); Flowering (+)	Naoi and Hashimoto, 2004 Quettier et al., 2006 Walia et al., 2009 Pytela et al., 2010; Fujita et al., 2013; Tang et al., 2016
MKP1	Catalytic activation by phosphorylation; Catalytic activation by CaM binding; Increased protein stability by phosphorylation	MPK3 (in vitro, in vivo); MPK4 (in vitro) MPK6 (in vitro, in vivo) CaM (in vitro)	OMFP, MPK6	Cytoplasm (Arabidopsis transgenic plants)	Genotoxic resistance (+); Pathogen resistance (−); Salt resistance (−); Stomata development (+)	Ulm et al., 2001; Ulm et al., 2002; Lee et al., 2008; Bartels et al., 2009; Anderson et al., 2011; Park et al., 2011; González Besteiro and Ulm, 2013; Anderson et al., 2014; Jiang et al., 2017b; Tamnanloo et al., 2018
NtMKP1	Transcriptional induction by wounding and TMV-induced cell death; Catalytic activation by SIPK	SIPK (in vitro); CaM (in vitro)	OMFP, SIPK	N.A.	Wounding (−); Cell death (−); Pathogen resistance (−)	Yamakawa et al., 2004; Katou et al., 2005; Oka et al., 2013
TMKP1	Transcriptional regulation by salt and osmotic stress; Catalytic activation by 14-3-3 protein; Catalytic activation by TMKP3	CaM (in vitro); TMPK3 (in vivo); TMPK6 (in vivo)	OMFP	Nucleus (Transient expression in tobacco cells)	Salt stress (+)	Zaïdi et al., 2010; Ghorbel et al., 2015; Zaidi et al., 2016; Ghorbel et al., 2017
OsMKP1	Transcriptional induction by wounding	CaM (in vitro)	N.A.	N.A.	Wounding (−)	Katou et al., 2007

NA, not available; −, negative regulator; +, positive regulator; OMFP, 3-O-methylfluorescein; pMBP, phosphorylated myelin basic protein; pNPP, para-nitrophenyl phosphate; TMV, tobacco mosaic virus.

Supporting a role for these proteins as negative regulators of MAPK activation, MKP genetic mutants often showed prolonged and/or hyper-activation of MAPKs following stimulation; and a secondary mutation in or knock down of MAPKs in the background of the cognate interacting MKP mutant partially or completely suppressed the phenotypes of MKP mutants. For instance, both genotoxic stress and pathogen challenge treatments result in hyper-activation of MPK3 and MPK6 in the mkp1 null mutant compared to wild type (Ulm et al., 2002; Anderson et al., 2011). Interestingly, loss of MPK6 alone reverted a subset of mkp1-dependent phenotypes in a mkp1 mpk6 double mutant, including the pathogen resistance, pathogen induced seedling growth inhibition and transcriptional variations (Anderson et al., 2011, 2014; Jiang et al., 2017b). A similar scenario has also been shown in the mkp2-RNAi mutant which is associated with a prolonged MPK3 and MPK6 activation during ozone treatment (Lee and Ellis, 2007). In addition, a knock down of MPK12 by RNAi in ibr5 mutants partially reverted the auxin-insensitivity phenotype of ibr5; and a phs1 mpk18 double mutant shows partial suppression of the phs1-1 phenotypes (Lee et al., 2009; Walia et al., 2009). Therefore, building upon the biochemical data, genetic interactions between MKPs and their interacting MAPKs also are clearly established.

Dual specificity MAPK phosphatases are regulators of plant growth and development

MAP kinase phosphatase IBR5 is a positive regulator of auxin responses, demonstrating a role for MKPs as coordinators of plant growth and development. The first evidence came from the observation that root growth of the ibr5-1 mutant was more resistant to inhibitory concentrations of endogenous auxins (i.e., indole-3-butyric acid and indole-3-acetic acid), synthetic auxins and auxin transport inhibitors (Monroe-Augustus et al., 2003). The double mutant combination of ibr5-1 with an auxin receptor mutant, tir1, displayed more extreme auxin resistance compared with either single mutant, suggesting that IBR5 regulates TIR1-mediated auxin signaling pathways (Strader et al., 2008a). To investigate potential mechanisms underlying the enhanced auxin resistance in the ibr5 mutant, the accumulation of DR5::GUS, the GUS reporter driven by an auxin-responsive promoter, were measured after auxin treatments; and the ibr5 mutant showed reduced induction of DR5::GUS in both roots and hypocotyls (Strader et al., 2008a). Many Aux/IAA repressor proteins directly prevent transcriptional activation induced by auxin treatments (Tiwari et al., 2003, 2004). Furthermore, stabilization of Aux/IAA repressor proteins were observed in numerous other auxin-resistant mutants, including tir1 (Gray et al., 2001). Therefore, the accumulation of the Aux/IAA repressor proteins AxR3/IAA17 and IAA28 was investigated in the ibr5 mutant. Interestingly, unlike other auxin-resistance mutants, both AxR3/IAA17 and IAA28 were not stabilized in ibr5, suggesting that IBR5 facilitates auxin responses independently and/or downstream of TIR1-mediated degradation of Aux/IAA repressor proteins (Strader et al., 2008a). Possible targets of IBR5-regulated pathways came from genetic screens for suppressors of ibr5-1. Suppressor mutations in PLEIOTROPIC DRUG RESISTANCE 8 (PDR8) and PDR9 genes were characterized, and these two genes encode ABC transporters implicated in the efflux of synthetic auxins (Strader et al., 2008b; Strader and Bartel, 2009).

The mutation of ibr5-1 causes a premature stop codon, resulting in a truncated protein lacking the conserved phosphatase domain (Monroe-Augustus et al., 2003). To examine the contribution of the phosphatase domain and/or phosphatase activity for the full function of IBR5, a mutant version of IBR5 lacking the active site cysteine was expressed in the background of ibr5-1; and the responses to auxin treatment were tested. Expression of the catalytically inactive version failed to fully complement the phenotypes of ibr5-1, suggesting that phosphatase activity is required for full IBR5 function (Strader et al., 2008a).

In addition to regulating root growth, IBR5 also controls the size of above ground organs. In ibr5-6 mutants affecting the active site of the dual-specificity phosphatases, plants have reduced petal size and a smaller stature compared to wild type (Johnson et al., 2015). Microarray studies identified a set of genes associated with auxin synthesis, transport, regulation and responses that were mis-regulated in ibr5-6 mutants compared to wild type (Johnson et al., 2015). These results support earlier studies that IBR5 regulates auxin signaling pathways and, in addition, also suggest that IBR5 may control the size and shape of petals through modulation of auxin signaling pathways.

Another area where MKPs have been shown to affect plant growth and development is in the control of the dynamics and organization of microtubules, in which PHS1 has been implicated to play an essential role. A semi-dominant phs1-1 allele in Arabidopsis thaliana exhibits less ordered and slightly more fragmented cortical microtubule arrays in the roots of seedlings, and the epidermal cells of phs1-1 roots are twisted in a left-handed helix under normal growth condition (Naoi and Hashimoto, 2004). When treated with low doses of microtubule-destabilizing drugs, the elongation of phs1-1 roots were more severely inhibited; and the epidermal cells swelled, suggesting that the phs1-1 mutants are hypersensitive to the microtubule-destabilizing drugs (Naoi and Hashimoto, 2004). Additionally, the phs1-1 mutation exaggerates the temperature-sensitive phenotypes of microtubule organization 1-1 (mor1-1) mutants, which display a defect in a microtubule-associated protein (Whittington et al., 2001; Naoi and Hashimoto, 2004). Together, these results indicate that cortical microtubules are destabilized in the semi-dominant mutant phs1-1. Interestingly, other null mutant alleles of PHS1 are indistinguishable from wild type under standard growth conditions (Pytela et al., 2010).

In the phs1-1 mutant, an Arg64 residue is replaced with Cys (R64C) in the putative kinase interaction motif (KIM) of MAPKs such that the mutation might interfere with interactions with the target MAPK(s). Therefore, it has been proposed that PHS1 may regulate multiple MAPKs; and a subset of its target kinases may be involved in the organization of cortical microtubules. To further investigate the mechanism underlying microtubule regulation, a screen for PHS1-interacting MAPKs was performed; and MPK12 and MPK18 were identified by yeast two-hybrid assays (Walia et al., 2009). Interestingly, mpk18 seedlings also display defects in microtubule related functions; and a secondary mutation resulting in the loss of MPK18 in phs1-1 partially complements the root growth phenotypes of phs1-1 (Walia et al., 2009). This study provides support for the idea that PHS1 regulates the organization of microtubules through controlling the activity of the interacting MAPKs. If this hypothesis is correct, the phosphatase activity of PHS1 should play an essential role in this process. To explore this possibility further, a GFP fusion of the phosphatase-dead Cys792-to-Ser mutant (PHS1C792S-GFP) was expressed in the background of phs1-5 to examine if the phosphatase-dead form of PHS1 functions as a dominant-negative microtubule destabilizer (Fujita et al., 2013). In transgenic seedlings, the organization of cortical microtubules was almost completely depolymerized. Additionally, a combination of the phosphatase-dead and R64C mutations results in substantially more depolymerization of cortical microtubules in the root epidermal cells than seen in the R64C mutation alone. These results indicate that the phosphatase inactive form of PHS1 triggers the destabilization of microtubule. One of the possible explanations for the destabilization caused by the phosphatase-dead form of PHS1 is that the PHS1 might have intrinsic microtubule destabilizing activity, which is normally suppressed by its phosphatase activity. To search for the putative region associated with potential microtubule destabilized activity, an examination of truncations of PHS1 has been performed, and an internal 69 kDa fragment lacking the phosphatase catalytic domain and KIM domain has been characterized (Fujita et al., 2013). Interestingly, this region has weak homology to the slime mold actin-fragmin kinase, which phosphorylates Thr349 of α-tubulin at the longitudinal inter-dimer interface, thereby generating a polymerization-incompetent isoform, and effectively depolymerizing microtubule arrays when expressed in plant and animal cells (Fujita et al., 2013). Such tubulin kinase activity may be suppressed by the phosphatase activity of PHS1 under normal growth condition, because α-tubulin is not normally phosphorylated in Arabidopsis plants grown in standard growth conditions; and transiently or stably expressed full-length PHS1 does not affect microtubule stability in Arabidopsis cells (Fujita et al., 2013). Also α-tubulin is not phosphorylated in the phs1 null mutants; and expression of putative kinase domain of PHS1 results in phosphorylation of α-tubulin in the mutants (Fujita et al., 2013). As PHS1 interacts with and dephosphorylates MAPK18, it is possible that MAPK18 and/or other MAPKs may activate the tubulin kinase domain of PHS1, but that these MAPKs are normally inactivated by the phosphatase domain of PHS1.

In addition to controlling the microtubule organization, PHS1 is also involved in flowering time in Arabidopsis. The knock-out mutant phs1-5 displayed a late flowering phenotype; and this alteration appears to result from altered expression of key genes in phs1-5 (Tang et al., 2016). CONSTAN (CO) functions as an activator of flowering whereas FLOWERING LOCUS C (FLC) is a repressor (Michaels and Amasino, 1999; Sheldon et al., 2000; Hayama and Coupland, 2004; Putterill et al., 2004). Both CO and FLC regulate the expression of the floral integrator FLOWERING LOCUS T (FT) which acts in the apical meristem to induce floral identity genes (Abe et al., 2005; Searle et al., 2006). Mutation of phs1-5 increased the expression of FLC and decreased the expression of CO, subsequently decreasing the expression of FT. These results suggest that PHS1 plays a positive role during floral transition by modulating the transcript levels of both CO and FLC (Tang et al., 2016).

MKP1 has also been shown to be involved in controlling the cell fate transition during stomata development (Tamnanloo et al., 2018). The mkp1 mutants display significantly reduced number of stomata compared to wild type, and this reduction can be reverted by expressing MKP1 in the mutant but not by crossing with other MKPs, suggesting the major and specific role of MKP1 in regulating stomatal development (Tamnanloo et al., 2018). Further biochemical analysis shows that MKP1 acts downstream of YODA (a MAPK kinase kinase) and upstream of MPK3/MPK6; and functions at the early stage of stomatal development by promoting the differentiation of stomatal precursor cells (Tamnanloo et al., 2018).

Dual specificity MAPK phosphatases are central hubs integrating biotic and abiotic stress

Plants are constantly exposed to diverse environmental stimuli and need to respond rapidly and effectively to these changes. MAPK phosphatases have been found biochemically and genetically to be important regulators of a broad range of stress responses, potentially functioning as central hubs for integrating multiple stress signaling pathways.

DSP-type MAPK phosphatases are regulators of plant immune responses

In Arabidopsis, several DSP-type phosphatases have been implicated in regulating pathogen associated responses and resistance (Figure 1). MAPK PHOSPHATASE 1 (MKP1) is an important negative regulator of plant immunity. Diverse defense responses are hyper-induced in the Arabidopsis mkp1 null mutant following pathogen-associated molecular pattern (PAMP) treatment, including activation of MPK6 and MPK3, production of reactive oxygen species (ROS), accumulation of a subset of PAMP-regulated transcripts, and inhibition of seedling growth (Anderson et al., 2011; Jiang et al., 2017b). Consistent with enhanced PAMP responses, the mkp1 mutant also displays enhanced resistance to the virulent pathogen Pseudomonas syringae pv. tomato (Pto) DC3000 (hereafter referred to as DC3000) (Anderson et al., 2011). Similar to the results from Arabidopsis, suppression of NtMKP1 in tobacco plants also resulted in elevated resistance against multiple pathogens including a necrotrophic pathogen, Botrytis cinerea, and lepidopteran herbivores, Mamestra brassica and Spodoptera litura (Oka et al., 2013). Interestingly, enhanced resistance against DC3000 in Arabidopsis mkp1 can be explained by decreased abundance of specific extracellular plant metabolites that DC3000 uses as signals to activate its virulence program (Anderson et al., 2014). Thus, MKP1 seems to regulate a novel layer of immunity against pathogen infection. However, the molecular mechanisms by which MKP1 regulates the secretion of extracellular plant metabolites need to be further explored; and how generally the regulatory roles of metabolites on pathogen resistance can be applied to other pathogen species and crop species should also be tested.

Figure 1

Roles of DSP-type MAPK phosphatases in modeling plant immunity. MKP1 is a negative regulator of PAMP responses (e.g., MPK3/6 activation, PAMP-induced gene expression and ROS production) and bacterial resistance. MKP1 also regulates SNC1-mediated signaling pathways. MKP2 positively regulates the resistance to necrotrophic fungal pathogen whereas negatively regulates the resistance to biotrophic bacterial pathogen. IBR5 is involved in regulating several resistance proteins, including CHS3, SNC1, RPM1, and RPS4. (−), negative regulator; (+), positive regulator. Dash lines represent the indirect regulation indicated from genetic data; and solid lines represent the direct regulation indicated from physical interactions.

MAPK PHOSPHATASE 2 (MKP2) dephosphorylates phospho-MPK3 and phospho-MPK6 in vitro, and has distinct functions in regulating different pathogen interactions (Lee and Ellis, 2007; Lumbreras et al., 2010). Plants lacking MKP2 have enhanced resistance against Ralstonia solanacearum, a biotrophic pathogen, whereas increased susceptibility to Botrytis cinerea, a necrotrophic pathogen (Lumbreras et al., 2010). In addition, bimolecular fluorescence complementation (BiFC) experiments have shown that MKP2 interacts with MPK3 and MPK6 in vivo; and fungal elicitors decreased the MKP2-MPK3 association but increased the MKP2-MPK6 interaction (Lumbreras et al., 2010). In agreement with enhanced MKP2-MPK6 interactions, co-infiltration of MKP2 and MPK6 into N. benthamiana leaves significantly reduced fungal elicitor-induced HR responses compared to infiltration with MPK6 alone. Interestingly, infiltration of MPK3 did not cause significant effects in these assays (Lumbreras et al., 2010). These results suggest that MKP2 exerts differential regulation on MPK3 and MPK6 during pathogen infection.

MKPs also contribute to regulation of several resistance (R) proteins. IBR5 plays a positive role in regulating R protein CHS3, as evidenced by that mutation of ibr5-7 suppresses the chilling-induced defense responses of chs3-1 (Liu et al., 2015a). Biochemical studies have shown that IBR5 interacts with CHS3 through the TIR domain of CHS3 in vivo, and IBR5 forms a complex with chaperone protein HSP90 and SGT1b (Suppressor of the G2 allele of skp1) to stabilize CHS3 protein, thus increasing the accumulation of CHS3 (Liu et al., 2015a). Similarly, an ibr5 mutant partially suppresses temperature-sensitive growth and autoimmune phenotypes resulting from constitutive activation of R protein SNC1 (Suppressor of npr1-1, Constitutive 1). IBR5 interacts with and promotes the accumulation of SNC1 (Liu et al., 2015a). Additionally, IBR5 is also involved in controlling disease resistance mediated by R proteins RPM1 and RPS4. The ibr5 mutants are more susceptible to avirulent bacterial pathogens DC3000 (avrRpm1) and DC3000 (avrRps4) (Liu et al., 2015a). MKP1 has also been shown to play important roles in regulating the plant growth homeostasis by repressing inappropriate stress signaling mediated by SNC1. When the Arabidopsis mkp1 mutation was introgressed into the Columbia ecotype from Wassilewskija, it showed weak dwarfism compared to wild type plants under standard growth conditions, and such dwarfing was caused by constitutive activation of SNC1-mediated responses (Bartels et al., 2009). These studies demonstrate the roles of MKPs in regulating plant immunity against pathogen infection through modulating multiple signaling layers in PTI and ETI.

DSP-type MAPK phosphatases are regulators of multiple abiotic stresses

In addition to regulating resistance against pathogen infection, MKPs also constitute important components regulating multiple abiotic stresses, including genotoxic stress, osmotic/drought stress and salinity stresses (Figure 2). For instance, the absence of MKP1 in the Arabidopsis mkp1 mutant results in hypersensitivity to various genotoxic stresses (e.g., UV-C and methyl methanesulphonate treatments), suggesting that MKP1 plays essential roles in genotoxic stress relief (Ulm et al., 2001); and this regulation appears to be primarily through inactivation of its strongest interacting partner, MPK6, in planta (Ulm et al., 2002). More recently, it was found that MKP1 negatively regulates the UV-B induced stomatal closure whereas MPK6 positively regulates this process. Both aspects of regulation involve modulating hydrogen peroxide (H2O2)-induced nitric oxide (NO) production in guard cells (Li et al., 2017).

Figure 2

Overview of DSP-type MAPK phosphatases for multiple abiotic signaling pathways and putative regulatory mechanisms. MAPK phosphatases participate in responses to UV light, wounding, osmotic stress, salt stress and reactive oxygen species (ROS) stress. The different pathways and putative regulatory mechanisms are described in text. Dash lines represent the indirect regulation indicated from genetic data; and solid lines represent the direct regulation indicated from physical interactions.

In contrast to the role of MKP1 as a positive regulator of genotoxic stress survival, MKP1 has been identified to be a negative regulator of salinity resistance as demonstrated by the fact that loss of MKP1 increased resistance to salt stress (Ulm et al., 2002). Interestingly, ectopic over-expression of the wheat ortholog TMKP1 in Arabidopsis mkp1 results in enhanced salt stress tolerance, indicating a positive role of TMKP1 in regulating salt stress responses and/or a possible dominant effect from ectopic overexpression. The elevated salinity resistance was accompanied by increased antioxidant enzyme activities and lower malondialdehyde (MDA), superoxide anion O2− and hydrogen peroxide levels in the TMKP1 transgenic seedlings (Zaidi et al., 2016). Despite of their significant homology (49% amino acid identity), MKP1 and TMKP1 seem to act in an antagonistic manner to regulate salt stress responses, which might be explained by distinct subcellular localization and differential catalytic regulation by Ca2+ (Lee et al., 2008; Bartels et al., 2009; Zaïdi et al., 2010; Ghorbel et al., 2015).

During tissue wounding, MKPs have been reported to be general negative regulators in several species. In rice, the transcriptional level of OsMKP1 was rapidly induced by wounding, and knocking out OsMKP1 confers hyper-activation of two stress responsive MAPKs, OsMPK3 and OsMPK6, before and after wounding treatments (Katou et al., 2007). In addition, transcriptome analyses in osmkp1 showed that five out of 13 genes upregulated in the mutant are clearly linked to wounding responses, suggesting that wounding responses are constitutively activated in osmkp1 mutant (Katou et al., 2007). Similarly, tobacco NtMKP1 also negatively regulated wounding responses as NtMKP1-suppressed plants exhibited hyper-activation of wound-induced MAPKs, WIPK and SIPK (Oka et al., 2013). Furthermore, suppression of NtMKP1 increased the production of JA and ET upon wounding, and the expression of JA- or ET-inducible genes basic PR-1 and PI-II were also significantly enhanced in response to wounding in the transgenic plants (Oka et al., 2013). These results suggest that NtMKP1 negatively regulates activation of MAPKs WIPK and SIPK, suppressing the accumulation of JA and ET as well as JA- or ET- inducible gene expression during wounding responses.

There is also increasing evidence highlighting the importance of MKPs in osmotic stress signaling pathways. DsPTP1 functions as a negative regulator in osmotic stress signaling in Arabidopsis seed germination and seedling establishment (Liu et al., 2015b). The null mutant dsptp1 displayed less sensitivity to osmotic stress as shown by a higher seed germination rate and longer root length in response to osmotic stress, along with increased proline accumulation, reduced MDA content and ion leakage, and enhanced antioxidant enzyme activity (Liu et al., 2015b). Interestingly, DsPTP1 positively regulates ABA accumulation and ABA signaling in response to osmotic stress (Liu et al., 2015b). Studies show that loss of DsPTP1 decreased ABA accumulation in dsptp1 mutants compared to wild type plants possibly by reducing the expression of ABA-biosynthesis gene NCED3 and increasing the expression of ABA-catabolism gene CYP707A4 under osmotic stress condition (Liu et al., 2015b). Consistently, down regulation of DsPTP1 also suppressed the expression of positive regulators of ABA signaling such as ABI3 and ABI5 while enhancing the expression of negative regulator ABI1 (Liu et al., 2015b). In contrast to DsPTP1, PHS1 was identified to be a negative regulator of ABA signaling. ABA treatment increased transcript levels of PHS1 gene, and phs1-3 mutants exhibited a hypersensitivity to ABA in seed germination, light-induced stomata opening and gene expression during early development. Furthermore, knock-down mutations of PHS1 also altered the basal expression of ABA-regulated genes, enhancing the upregulation of two ABA-induced genes (At5g06760, RAB18) and downregulation of two ABA-repressed genes (AtCLC-A, ACL) (Quettier et al., 2006). However, ABA accumulation is not significantly modified in seeds and seedlings of phs1-3 mutants, suggesting that PHS1 is involved in regulating the ABA signaling but not ABA metabolism (Quettier et al., 2006). In addition to altering ABA signaling, osmotic stress also triggers transient depolymerization of cortical microtubules in cells (Shoji et al., 2006; Wang et al., 2007; Ban et al., 2013), and PHS1 has been shown to be associated with salt/osmotic stress induced cortical microtubule depolymerization (Fujita et al., 2013). Tubulin kinase activity was suppressed by the phosphatase activity of PHS1 under normal growth conditions; but upon osmotic stress, such suppression was relieved, leading to the phosphorylation on Thr349 residue of α-tubulin, contributing to the formation of polymerization-inefficient tubulins (Fujita et al., 2013).

Studies in crops have also highlighted the importance of MKPs in osmotic stress. Rice OsIBR5 was shown to be a negative regulator of osmotic stress, because overexpression of rice OsIBR5 in tobacco plants resulted in hypersensitivity to drought and H2O2 treatments. These results might be explained by the fact that drought-induced stomatal closure was significantly reduced by overexpression of OsIBR5 in tobacco plants. In addition, OsIBR5 interacted with tobacco MAPKs SIPK and WIPK; and drought-induced activity of WIPK was compromised in OsIBR5-overexpressing tobacco plants, suggesting that OsIBR5 may regulate osmotic stress signaling through controlling drought-induced MAPKs activities (Li et al., 2012). The scenario is a bit more complicated in wheat with TMKP1 being induced in sensitive wheat varieties and repressed in tolerant ones under salt and osmotic stress, suggesting that TMKP1 may function as a negative regulator of salt and osmotic stress in the sensitive variety whereas suppression of its expression in the tolerant variety contributes to an improved stress tolerance (Zaïdi et al., 2010).

Reactive oxygen species (ROS) are generated from partial reduction of oxygen (O2), including hydrogen peroxide (H2O2), hydroxyl radical (HO.), singlet oxygen (1O2) and superoxide anion () (Foyer and Noctor, 2009). For plants, ROS is formed both internally and externally from cellular respiration and photosynthesis or by environmental challenges such as UV and ozone (Boldt and Scandalios, 1997; Pellinen et al., 1999; Mittler, 2002). To survive, plants need to balance redox homeostasis because high levels of ROS accumulation is detrimental to plant cells (Moller and Jensen, 2007). Several studies have suggested that MKPs are involved in ROS signaling and responses. Silencing of MKP2 in plants resulted in hypersensitivity to ozone treatments and prolonged activation of MPK3 and MPK6. The seedling growth of mkp2 mutants was more severely inhibited by the oxidative agent methyl-viologen (MV) compared to wild type plants (Lee and Ellis, 2007; Lumbreras et al., 2010). However, the accumulation of superoxide radical anions and hydrogen peroxide was not significantly altered in the mkp2 mutants (Lumbreras et al., 2010). These results suggest that loss of MKP2 disrupts oxidative stress responses, but not through changing the ROS levels and homeostasis but by enhancing the susceptibility of mkp2 plants to ROS accumulation. MKP1 is also implicated to play a role in ROS signaling. When treated with bacterial PAMP elf26 (26 conserved amino acids from bacterial elongation factor EF-Tu), mkp1 mutants produced more ROS than in wild type plants (Anderson et al., 2011). Furthermore, a sequence of peroxisomal targeting signal 1 (PTS1) was identified in the MKP1 protein; and the full-length MKP1 protein was observed to transport from cytoplasm to peroxisomes in response to different biotic and abiotic stresses when transiently expressed in mesophyll protoplasts (Kataya et al., 2015). However, a detailed mechanism of how MKP1 or MKP2 regulates the ROS signaling remains unclear.

Regulatory mechanisms of dual specificity MAPK phosphatases

Plants have multiple perception systems to sense distinct environmental signals. However, multiple signaling pathways appear to merge together downstream and share common modules for transducing and amplifying signals. Such mechanisms are very efficient and effective for plants to quickly respond to the environment. However, questions arise about how specificity of signaling outputs is achieved if different signaling networks all coalesce in shared hubs. One possibility is that MKPs, which participate in diverse signaling pathways, may play a key role in integrating these signaling pathways. Therefore, precise regulation of MKPs is likely critical for plants to generate the correct biological responses. Recent progress on the regulatory mechanisms of MKPs may facilitate our understanding of the role of MKPs in mediating crosstalk between different signaling pathways and ensuring the signal specificity.

Transcriptional and post-transcriptional regulation of MKPs

Transcriptional and post-transcriptional regulation provide potential layers of control, and the expression levels of MKPs have been found to respond differentially to various stress signals (Figure 2). For instance, transcript levels of PHS1 are induced by ABA treatment (Quettier et al., 2006). Similarly, rice OsIBR5's transcription is also enhanced by ABA treatment, other osmotic stresses including PEG6000, and hydrogen peroxide (H2O2) treatments (Li et al., 2012); and rice OsMKP1 and tobacco NtMKP1 transcripts increase after wounding (Yamakawa et al., 2004; Katou et al., 2007). Interestingly, different expression patterns of wheat TMKP1 were observed between different wheat cultivars with induced expression in sensitive cultivars and repressed in tolerant ones (Zaïdi et al., 2010). In contrast, the expression of Arabidopsis MKP1 does not appear to be significantly altered after exposure to either UV-B treatment or pathogen infection (González Besteiro and Ulm, 2013; Jiang et al., 2017a), suggesting that MKP1 is mainly under post-translational regulation. Although the regulation of the IBR5's transcription has not been reported, it has been shown that IBR5 is post-transcriptionally regulated, generating two transcripts, AT2G004550.1 and AT2G04550.3, by alternative splicing to produce two IBR5 isoforms IBR5.1 and IBR5.3 (Jayaweera et al., 2014). IBR5.1 and IBR5.3 isoforms have overlapping, but also distinct, functions as the mutant alleles share many phenotypes but also confer distinct morphological defects (Jayaweera et al., 2014). Part of these differences may be explained by the fact that IBR5 isoforms have displayed different localization patterns, with IBR5.1 localized in both the nucleus and cytoplasm whereas IBR5.3 is exclusively in nucleus (Jayaweera et al., 2014).

Post-translational protein modification alters phosphatase activity of MKPs

Modulating the activity of MKPs can change the activation profiles of their target kinases (e.g., MAPKs), contributing to differences in amplitude and duration of signaling. Many examples have shown that the phosphatase activity of MKPs can be regulated by post-translational modification. Mammalian MKP1s (not an orthologue of plant MKP1s) and yeast Msg5 are phosphorylated by their own substrates MAPKs, and phosphorylation regulates not only the activities but also the abundance of the phosphatases, establishing an efficient negative feedback loop (Brondello et al., 1999; Sohaskey and Ferrell, 2002; Li et al., 2007). For instance, in hamster fibroblasts, the active p42/44 MAPKs phosphorylate MKP1, leading to the reduction of proteasomal degradation, thereby, stabilizing the MKP1 protein (Brondello et al., 1999). Similar regulatory mechanisms have been demonstrated in plants. In Arabidopsis, MKP1 is phosphorylated by MPK6 in vitro; and phosphorylation increased its phosphatase activity (Park et al., 2011). Similarly, the phosphatase activity of MKP2 is elevated in the presence of either recombinant MPK3 or MPK6 in vitro (Lee and Ellis, 2007). This level of regulation has also been found in crop species. For instance, the phosphatase activity of tobacco NtMKP1 is also increased by co-incubation of its substrates such as SIPK (Katou et al., 2005), and the catalytic activity of wheat TMKP1 is significantly enhanced by co-incubation of TMPK3 (Zaïdi et al., 2010). In addition to in vitro studies, in vivo studies using Arabidopsis transgenic lines expressing MKP1 protein have also shown that MKP1 is phosphorylated in response to both UV-B treatment and pathogen challenges (González Besteiro and Ulm, 2013; Jiang et al., 2017a). The phosphorylation of MKP1 contributes to its stability and is required for its biological function during both UV-B stresses and pathogen infection (González Besteiro and Ulm, 2013; Jiang et al., 2017a).

Another important role of phosphorylation is serving as a docking site for recruiting interacting proteins. For wheat TMKP1, it was shown that TMKP1 associates with 14-3-3 proteins through a canonical model 14-3-3 binding motif (574KLPSLP579); and phosphorylation of TMKP1 is required for the interaction (Ghorbel et al., 2017). In addition, interaction with 14-3-3 proteins increased the phosphatase activity of TMKP1, and TMKP1 activation was further enhanced by Mn2+ (Ghorbel et al., 2017). Thus, MKPs phosphorylation can modify phosphatase activity, protein stability, and interaction with other proteins, all of which may facilitate roles of MKPs in regulating different responses and also possibly integrating distinct signals.

Differential localization of MKPs and interacting MAPKs may affect specific signaling regulation

Differential localization of MKPs could lead to regulation of subcellular pools of MAPKs with different positional information. More specifically, where the kinases are located when active may be important in conveying specific signals. For instance, expression of PHS1-GFP fusion protein in tobacco cells and epidermal cells of Arabidopsis showed that PHS1 was mainly localized in the cytoplasm (Walia et al., 2009; Pytela et al., 2010). Accordingly, the interaction between PHS1 and MKP18 also occurred in cytoplasm (Walia et al., 2009). The cytoplasmic localization of PHS1 may also explain the predominant role of PHS1 in regulating microtubule organization through controlling the phosphorylation status of tubulins. The localization of Arabidopsis IBR5 is less clear. Studies using transgenic plants expressing fluorescently tagged IBR5 and its interacting MAPK MPK12 under constitutive promoters indicated that both IBR5 and MPK12 were primarily localized in the nucleus (Lee et al., 2009). However, transgenic plants with IBR5 driven by its native promoter indicate that IBR5 is distributed in both the nucleus and cytoplasm (Jayaweera et al., 2014). Arabidopsis MKP1 was found to be predominantly in cytoplasm, and its interaction with MPK6 was also mainly cytoplasmic (Bartels et al., 2009). Later studies report that MKP1 harbors a non-canonical PTS1-like tripeptide which is conserved in MKP1 orthologs (Kataya et al., 2015). Experiments with transient expression of MKP1 in mesophyll protoplasts indicate that MKP1 can move from cytoplasm into peroxisomes under stressful conditions, suggesting a potential role for MKP1 in regulating peroxisomal functions by reversible phosphorylation (Kataya et al., 2015). Also interacting with MPK3/6, Arabidopsis MKP2 was found primarily localized in the nucleus of MKP2-YFP-expressing plants, the same subcellular compartment where ozone-activated MAPKs were translocated (Ahlfors et al., 2004; Lee and Ellis, 2007). However, transient expression of GFP-tagged MKP2 in tobacco cells showed MKP2 localized in both nucleus and cytoplasm, and BiFC studies demonstrated that the interaction between MKP2 and MPK3/6 occurred also in both the nucleus and the cytoplasm (Lumbreras et al., 2010). Therefore, even sharing the same target MAPKs, MKP1, and MKP2 likely play different roles in regulating pathogen infections and other responses, which may result from differential localization of MKP1 and MKP2 as well as differences in the compartments where they interact with MAPKs. In addition, expression of MKPs may also affect the shuttling of MAPKs between nucleus and the cytoplasm. As shown by expression in BY2 tobacco cells, a GFP-TMKP1 fusion protein accumulated in the nucleus with TMPK3-RFP or TMPK6-RFP also accumulating in the nucleus (Zaïdi et al., 2010). However, when expressing the truncated form GFP-TMKP1ΔN1−133 (truncating the N-terminal non-catalytic region), which was mainly localized in cytoplasm, the localization of both MAPKs also changed to the cytoplasm (Zaïdi et al., 2010). One of the possible explanations is that MKPs alter the phosphorylation status of MAPKs which plays essential roles in partitioning between the nucleus and cytoplasm, a mechanism that is well established in yeast and mammalian system (Lenormand et al., 1993; Ferrigno et al., 1998; Gatis et al., 1998; Khokhlatchev et al., 1998). Another possibility is that MKPs serve as a nuclear and/or cytoplasmic tether for these MAPKs as has been shown in yeast (Mattison and Ota, 2000). Together, MKPs localized in differential subcellular compartments may contribute to controlling different pools of active MAPKs as well as the shuttling of MAPKs between the nucleus and the cytoplasm, leading to proper responses to specific signal inputs.

MKPs may play a role in integrating Ca2+ signaling pathways

Phosphatases may also contribute to signal specificity through combinatorial integration with other kinases. MAPK phosphatases in multiple species have been reported to be calmodulin (CaM) binding proteins, where CaM is a Ca2+-sensor protein, indicating a potential link to calcium-mediated signaling pathways. For instance, tobacco NtMKP1 and rice OsMKP1 bind CaM through a single putative CaM binding domain (CaMBD) (Yamakawa et al., 2004; Katou et al., 2007), and Arabidopsis MKP1 and DsPTP1 bind CaM via two different CaMBDs (Yoo et al., 2004; Lee et al., 2008). Therefore, these interaction between CaM and MKPs may contribute to the specific regulation of MKPs. For instance, in vitro studies found that binding of CaM increases phosphatase activities on p-nitrophenyl phosphate (pNPP) substrates but decreases phosphatase activity on the phosphotyrosine of myelin basic protein (MBP), suggesting that calmodulin differentially regulates substrate specificity (Yoo et al., 2004). In addition, different CaMs have different binding affinities to MKPs. Bacterially expressed tobacco NtMKP1 physically interacts with three plant-specific types of CaMs, showing high affinity to NtCaM1 and NtCaM3 but lower affinity to NtCaM13 (Yamakawa et al., 2004). Even the same CaM has different binding affinities to different CaMBDs in MKPs. For instance, two CaMBDs (CaMBDI and CaMBDII) are present in the Arabidopsis MKP1, and CaM binds to both CaMBDs in a Ca2+-dependent manner (Lee et al., 2008). The binding affinity of CaMDBII was found to be higher than that of CaMBDI; and mutations on W453, L456 in CaMBDI and W678, I684 in CaMBDII disrupt the binding (Lee et al., 2008). Binding of CaMs to these two CaMBDs increased MKP1 phosphatase activity about 2-fold (Lee et al., 2008), indicating the possible regulation of MAPK phosphatases through Ca2+ signaling pathways. Interestingly, the CaMBDI mutant (W453R) but not CaMBDII mutant (W678R) can be activated by CaM, which indicates that CaMBDII plays a more important role than CaMBDI for the regulation of MKP1 (Lee et al., 2008). There may be additional variation between species, however, as wheat TMKP1 binds to CaM in a Ca2+-dependent manner as in Arabidopsis, but binding of CaM inhibits the phosphatase activity of TMKP1. Interestingly, the presence of Mn2+ can reverse the inhibitory effect of CaM binding, resulting in enhanced phosphatase activity of TMKP1 (Ghorbel et al., 2015). Together, these results indicate that regulation of MKPs may provide a connection between Ca2+- and MAPK signaling. Such regulation may contribute to the differential activation of MKPs, eventually leading to modulation of different pathways to produce biologically specific responses.

Conclusions and future prospects

This review summarizes current knowledge of the roles of MKPs in multiple signaling pathways. MKPs are involved in many aspects of a plant's life cycle, including growth and development as well as the adaption to various biotic and abiotic stresses. As different signaling pathways integrate through MKPs, it is critical for MKPs to undergo precise regulation to generate correct biological outcomes. These investigations of regulatory mechanisms have provided insights into putative mechanisms that might explain how the phosphatases assist in producing specific signals. The potential combinatorial complexity of different transcriptional/post-transcriptional regulations, differential localization affecting subcellular pools of MAPKs, and the possibility to integrate information from other pathways may have profound effects on organizing the amplitude and duration of targeted kinases.

As important as the MKPs appear to be, most of our knowledge regarding their functions is limited to their roles in negatively regulating MAPK signaling, and few other potential upstream and/or downstream targets have yet to be characterized. Genome-wide analyses will certainly facilitate a better understanding of MKPs-mediated signaling pathways by identification of both molecular players in the pathways as well as additional putative MKP targets. A better understanding of how plants coordinate and balance different signaling pathways in response to diverse environmental stimuli could lead to more rationally designed strategies for improving crop yield under changing environmental conditions. Promising results such as the deletion of MKP1 resulting in enhanced resistance to various biotic and abiotic stresses without compromising plant growth (Ulm et al., 2001, 2002; Anderson et al., 2011, 2014) suggest that it may be possible to produce crops with elevated resistance against adverse environmental stresses. As apparent integrators of diverse signaling pathways, MKPs are important targets for modulating cross-talk to help overcome barriers for the improvement of plant resistance.

Author contributions

LJ and SP conceived the main subject of this review and wrote the manuscript. YC and LL provided the suggestions and revisions.

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.