Transcriptional and Post-transcriptional Regulation of Organellar Gene Expression (OGE) and Its Roles in Plant Salt Tolerance

Given their endosymbiotic origin, chloroplasts and mitochondria genomes harbor only between 100 and 200 genes that encode the proteins involved in organellar gene expression (OGE), photosynthesis, and the electron transport chain. However, as the activity of these organelles also needs a few thousand proteins encoded by the nuclear genome, a close coordination of the gene expression between the nucleus and organelles must exist. In line with this, OGE regulation is crucial for plant growth and development, and is achieved mainly through post-transcriptional mechanisms performed by nuclear genes. In this way, the nucleus controls the activity of organelles and these, in turn, transmit information about their functional state to the nucleus by modulating nuclear expression according to the organelles’ physiological requirements. This adjusts organelle function to plant physiological, developmental, or growth demands. Therefore, OGE must appropriately respond to both the endogenous signals and exogenous environmental cues that can jeopardize plant survival. As sessile organisms, plants have to respond to adverse conditions to acclimate and adapt to them. Salinity is a major abiotic stress that negatively affects plant development and growth, disrupts chloroplast and mitochondria function, and leads to reduced yields. Information on the effects that the disturbance of the OGE function has on plant tolerance to salinity is still quite fragmented. Nonetheless, many plant mutants which display altered responses to salinity have been characterized in recent years, and interestingly, several are affected in nuclear genes encoding organelle-localized proteins that regulate the expression of organelle genes. These results strongly support a link between OGE and plant salt tolerance, likely through retrograde signaling. Our review analyzes recent findings on the OGE functions required by plants to respond and tolerate salinity, and highlights the fundamental role that chloroplast and mitochondrion homeostasis plays in plant adaptation to salt stress.


Introduction
Soil salinity severely affects plant development and growth and leads to yield losses. The high concentration of salts causes ionic imbalance and osmotic stress. Accordingly, salinity alters the ionic homeostasis of plant cells by causing toxic excess of sodium (Na + ) and a deficiency of ions, such as potassium (K + ) and Ca +2 because Na + in excess disturbs the uptake of these cationic nutrients [1]. High Na + content in the cytosol can also inhibit enzymatic activity, and can even interfere with protein regulation is crucial for plant growth and development. In chloroplasts, this is achieved mainly at the post-transcriptional level through the control of RNA translation, processing, splicing, decay, or editing [19]. Therefore, OGE must appropriately respond to changes that occur via development and environmental cues, including abiotic stresses, such as salinity. However, information about the effects that OGE disturbance has on plant tolerance to salinity is still limited. Notwithstanding, several works have recently reported thorough phenotypic and molecular characterizations of plant mutants, and to a lesser extent, of transgenic overexpression (OE) lines affected in nuclear genes involved in OGE in plastids or mitochondria, which exhibit altered sensitivity to salt stress. These genes regulate the expression of organellar genes at both the transcriptional and (mainly) post-transcriptional levels. Our review focuses on the results taken from analyzing these mutants and OE lines, and consequently, on OGE functions required for plant salt tolerance and response. Together, they highlight the important role of chloroplast and mitochondrion homeostasis in plant adaptation to salinity.

Effects of Perturbed OGE on Plant Tolerance to Salinity
As many of the genes involved in OGE reside in the nuclear genome, their mRNAs must be translated into the cytoplasm, and the proteins they code must be imported to chloroplasts or mitochondria. In this way, the nucleus can control the activity of these organelles, while the latter transmit information about their functional state to the nucleus by modulating nuclear activity according to these organelles' physiological requirements [20]. Accordingly, perturbed plastid gene expression is signaled to the nucleus, and affects the expression of photosynthesis-associated genes. In line with this, OGE is one of the several plant retrograde signaling routes proposed [21][22][23].
In the last few years, dozens of salt-responsive nuclear genes encoding chloroplast-or mitochondrialtargeted proteins from different plant species have been reported, some of which are involved in gene expression in these organelles (reviewed in [24,25]). The analysis of several plant mutants, mainly in Arabidopsis thaliana (hereafter Arabidopsis) and rice, has revealed a connection between chloroplast and mitochondrial functions and the response to salt stress. Some of these mutants are affected in nuclear genes involved in OGE and display altered responses to different abiotic stress conditions, including salinity (reviewed in [20]). Examples of such are genes that encode: (a) mitochondrial transcription termination factors (mTERFs), pentatricopeptide repeat (PPR), and other RNA-binding proteins that post-transcriptionally regulate OGE through RNA metabolism (e.g., DEAD-box RNA helicases (RHs) and RNA-recognition motifs (RRMs)-containing proteins); (b) the SIGMA FACTOR 5 (SIG5) required for plastid gene transcription; and (c) PLASTID-SPECIFIC RIBOSOMAL PROTEIN 2 (PSRP2).

Defective mTERF Mutants Show Altered Responses to Salinity
One of the gene families involved in OGE regulation is mTERF, for which several Arabidopsis mutants showing altered sensitivity to salt have been reported [26,27]. The mTERF proteins are targeted to chloroplasts or mitochondria, and contain a variable number of repeats of a motif dubbed "mTERF", which is about 30 amino acids long. Plant genomes, mainly those of higher plants, contain larger numbers of mTERF genes than animals. Accordingly, 35 and 45 mTERFs have been reported in Arabidopsis and rice, respectively [28,29], and larger numbers have been proposed for other plants (e.g., 55, 56, and 62 for Populous trichocarpa, Glycine max, and Malus domestica, respectively [29]). This contrasts with the four mTERF (MTERF1 to 4) genes present in the nuclear genomes of metazoans. Both the expansion and diversification of plant mTERFs have been related to the tolerance and acclimation of plants to abiotic stress [27]. In vertebrates, mTERFs participate in mitochondria transcription termination, initiation, translation, and likely in mtDNA replication [30,31]. In plants, information about mTERF functions is rather limited. To date, very few mTERFs have been molecularly characterized; they all post-transcriptionally regulate the expression of chloroplast or mitochondria genes, and can bind DNA or RNA. Accordingly, Arabidopsis BELAYA SMERT/RUGOSA2 (BSM/RUG2) [28,32], mTERF15 [33], and Zea mays ZmTERF4 [34] are involved in organellar intron II splicing; mTERF6 has been proposed to participate in the maturation of the chloroplast isoleucine tRNA (trnI.2) gene [35] and the transcription termination of the plastid rpoA polycistron, which is important for transcription and translation in this organelle [36]. Along these lines, the first mTERF characterized in a photosynthetic organism, the MOC1 gene of the unicellular green alga Chlamydomonas reinhardtii, is also involved in transcription termination in mitochondria [37,38]. Recently, Sun et al. [39] reported that mTERF4/COE1 (also known as BSM/RUG2) cooperates with the PPR protein GUN1 (GENOMES UNCOUPLED1) in plastid gene expression and retrograde signaling. Taken together, these results strongly support a role for plant mTERFs in regulating OGE.
As far as we know, a phenotype of altered sensitivity to salinity has been reported for mda1 (mTERF defective in Arabidopsis1), mterf6, mterf9, mterf10, and mterf11 mutants. Indeed, mutants mda1, affected in the mTERF5 gene [40], and mterf9 [41] are less sensitive to NaCl than the wild type, whereas mterf6-2, mterf6-5 [42], mterf10, and mterf11 [43] are salt-hypersensitive (Table 1). This suggests that mTERF5 and mTERF9 would negatively regulate Arabidopsis salt tolerance, whereas mTERF6, mTERF10, and mTERF11 would function as positive regulators of such tolerance [42]. Consistent with all this, the mTERF10 and mTER11 overexpression lines are more insensitive to NaCl than the wild type [43]. Interestingly, some of these mutants also exhibit an altered response to the abscisic acid (ABA) hormone, which plays a central role in the response and adaptation of plants to different abiotic stress conditions [44]. Accordingly, mutants mda1 and mterf9 are less sensitive to ABA than the wild type, whereas mutants mterf6 and mterf11 are ABA hypersensitive (Table 1) [40][41][42][43]. These results suggest that the enhanced or reduced tolerance of these mutants to salinity might be due, at least in part, to altered ABA signaling. The phenotype of an altered ABA response has also been reported for other mutants that exhibit enhanced or reduced sensitivity to abiotic stresses, besides salinity, which reinforces the fundamental role of this hormone in plant tolerance to adverse environmental conditions [20]. All the mterf mutants reported to show a salt stress phenotype are affected in mTERFs targeted to chloroplasts, and belong to either the "chloroplast cluster" (mTERF5, mTERF6, and mTERF9) or the "chloroplast associated-cluster" (mTERF10 and mTERF11) of proteins, which reveals the importance of chloroplast homeostasis for plant response to salinity [29]. In short, the analysis of the mterf mutants clearly indicates the involvement of mTERFs in the tolerance and acclimation of plants to adverse environmental conditions, especially to salt stress.
Apart from the above-reported results, Zhao et al. [59] made a systematic characterization of maize mTERF genes by bioinformatics and molecular biological approaches. By quantitative RT-PCR (qRT-PCR), these authors analyzed the expression profile of several maize mTERF genes under light and dark, and with salt and phytohormone treatments. Interestingly, the transcript levels of the maize mTERF12 gene, the ortholog of Arabidopsis mTERF6, as well as those of maize mTERF13 and mTERF28, changed after exposure to NaCl, AlCl 3 , or ABA compared to those of the untreated plants. This scenario supports the proposed function of mTERF genes in response to salinity [59].

PPRs and Tolerance to Salt Stress
Like mTERFs, the PPR family of proteins participates in plant OGE, as PPRs regulate the processing of chloroplast and mitochondria RNAs, including splicing, stability, editing, and even translation [60]. As for mTERFs, the plant PPR family has also expanded, but to a higher level. Indeed, PPR is one of the largest families in land plants [61]. Accordingly, lycophyte Selaginella, rice, and Arabidopsis genomes, respectively, harbor more than 800, 650, and 450 PPR genes [62]. In contrast, metazoan genomes typically encode fewer than 10 PPR proteins [60]. PPRs are grouped into two subfamilies, namely P and PLS, according to the pattern of tandem repeats of a degenerate 35-amino acid repeat [63]. The PPR proteins of the P subfamily contain the canonical P motif, whereas those of the PLS subfamily contain, apart from the P motif, two variants that derive from the P motif: the large (L) and short (S) motifs [63]. The vast majority of PPR proteins are predicted to be targeted to mitochondria or chloroplasts. They can specifically bind RNA or DNA, and control different biological processes, such as embryogenesis, chloroplast, and seed development, as well as plastid retrograde signaling [47].
Despite the many PPR identified proteins in higher plants, very few have been reported to be involved in stress response: GENOMES UNCOUPLED 1 (GUN1) [64], PPR40 [45,46], ABA OVERLY-SENSITIVE 5 (ABO5) [65], LOVASTATIN INSENSITIVE 1 (LOI1) [66], PENTATRICOPEPTIDE REPEAT PROTEIN FOR GERMINATION ON NaCl (PGN) [47], SLOW GROWTH 1 (SLG1) [49], ABA HYPERSENSITIVE GERMINATION 11 (AHG11) [48], SLOW GROWTH 2 (SLO2) [50] and PPR96 [53] in Arabidopsis, and WHITE STRIPE LEAF (WSL) in rice [52]. All these PPR proteins are located in mitochondria, except for GUN1 and WSL, which are targeted to chloroplasts. Among these proteins, a role in salinity tolerance has been described for Arabidopsis PPR40, PGN, SLO2, PPR96, AHG11, and SLG1, and for rice WSL. Mitochondrial mutants ppr40, pgn, ahg11, slg1, and slo2 and chloroplast mutant wsl display a similar response to ABA, salt, and osmotic stresses. They are all hypersensitive to these adverse environmental conditions during germination and early seedling growth. Most of these mutants exhibit changes in the endogenous levels of ROS, probably due to a perturbed mitochondrial function, which is the consequence of defects in the regulation of different mitochondrial RNA editing events in some cases.
The first PPR protein reported to be involved in salt tolerance was Arabidopsis PPR40. As mentioned above, the ppr40-1 mutant is hypersensitive to ABA, salinity, and osmotic stress, accumulates high ROS levels, and shows an altered expression of stress-responsive genes and semidwarf growth (Table 1). No defects have been found in mitochondria RNA editing in the ppr40-1 mutant [45]. A second mutant allele, ppr40-2, displays less severe alterations of developmental and stress responses, which suggests that is a weak loss-of-function allele of the PPR40 gene [45]. The overexpression of the PPR40 gene improves salt tolerance, likely because of the mitochondrial electron transport's enhanced stability and reduced oxidative damage when faced with this adverse condition [46].
The Arabidopsis PGN protein is also targeted to mitochondria, and similarly to ppr40 mutant seedlings, pgn mutants exhibit high ROS levels in response to salinity, as well as the down-regulation of different stress responsive genes (Table 1) [47]. Loss of PGN function results in altered responses to biotic and abiotic stresses. Thus, pgn mutants display susceptibility to necrotrophic fungal pathogens, as well as enhanced sensitivity to salinity, ABA, and glucose. These results suggest a role for PGN in the mitochondria homeostasis of ROS in response to biotic or abiotic stresses, including salinity [47].
The mutant ahg11 was identified in a genetic screening, conducted to isolate Arabidopsis mutants with an altered response to ABA. To avoid the isolation of mutants affected in ABA synthesis or catabolism, EMS mutagenesis was performed in an aba2-1 genetic background, which displayed low ABA levels. Mutants ahg11 showed enhanced sensitivity to ABA, NaCl, and mannitol during seed germination, but not later during development, which indicates that AHG11 functions in the stress response in both seeds and young seedlings [48]. RNA editing of the mitochondrial nad4 transcript is lacking in mutant ahg11, which results in an amino acid change in the NAD4 protein of complex I (Table 1). Murayama et al. [48] suggest that this editing defect might presumably affect the activity of complex I and lead to a redox imbalance in mutant ahg11 by causing altered responses to stress.
Like ahg11, the Arabidopsis slg1 mutant shows similar ABA, salt, and osmotic stress phenotypes during germination and in early growth stages (Table 1). Unlike the AHG11 protein, SLG1 is also involved in stress tolerance after germination [49]. In this way, slg1 adult plants are more tolerant to drought stress than the wild type, likely due to a more rapid stomata response in the mutant, which is consistent with greater sensitivity to ABA, as this hormone plays a key role in the response to drought stress by controlling stomata closure. Similarly to ahg11, the slg1 mutant also shows defects in mitochondrial RNA editing, specifically in the nad3 transcript, by bringing about a change from serine to proline in the NAD3 protein that strongly affects the structure of the protein, and concomitantly, the activity of complex I (Table 1) [49].
The slo2 mutants are defective in an RNA editing factor that plays a key role in Arabidopsis growth through energy metabolism regulation [51]. Loss of SLO2 function causes several RNA editing defects, and affects different mitochondrial transcripts and results in amino acid changes in four proteins belonging to complex I of the electron transport chain (Table 1). Interestingly, the levels of complexes I, III, and IV are substantially lower in slo2 mutants. These results led Zhu et al. [51] to propose that RNA editing defects result in the dysfunction of mitochondrial electron transfer chain complexes, and contribute to the slo2 mutant phenotype. In a later work, Zhu et al. [50] investigated the involvement of SLO2 in tolerance to stress. They found that slo2 mutants display hypersensitivity to ABA, salt, and osmotic stress, and insensitivity to ethylene during germination and in early seedling stages (Table 1). On the contrary, adult slo2 plants proved more drought-and salinity-tolerant. The slo2 mutants also accumulate high H 2 O 2 levels and are more susceptible to infection by the pathogenic fungus Botrytis cinerea (Table 1). Taken together, these results indicate that SLO2 is required for proper sensitivity to ABA, ethylene, biotic, and abiotic stress [50].
Recently, Liu and colleagues [53] characterized the Arabidopsis PPR96 gene encoding a mitochondrialocated protein, which is involved in the response to salt, ABA, and oxidative stress. The ppr96 knockout mutants are more tolerant than the wild type to NaCl, ABA, and the oxidative stress caused by hydrogen peroxide (Table 1). PPR96 expression was up-regulated in response to salt and oxidative stress treatments, according to a microarray in silico analysis, and was experimentally confirmed by qRT-PCR [53]. Nevertheless, Liu et al. [53] did not test whether the mutant displayed defects in the editing of mitochondrial transcripts.
Altogether, the phenotypic and molecular characterizations of mutants ahg11, slg1, and slo2 strongly support a connection between OGE regulation in mitochondria at the level of RNA editing and plant tolerance to ABA and abiotic stresses, such as salinity.
A function performed by a chloroplast PPR protein in the abiotic stress response has been reported in rice [52]. The wsl mutant displays enhanced sensitivity to NaCl and ABA during germination, and accumulates higher ROS levels than the wild type (Table 1). Interestingly, plastid rRNAs and proteins accumulate in wsl plants at lower levels than in the wild type. This is likely the result of the defective plastid translation caused by the inefficient splicing of the chloroplast rpl2 gene, which encodes the ribosomal protein RPL2 of this organelle [52]. Unlike the mitochondrial cases discussed above, Tan et al. [52] were unable to detect defects in chloroplast RNA editing in the wsl mutant, which indicates a role for this PPR protein in RNA regulation at the splicing rather than the editing level.
Very recently, the importance of PPR proteins in abiotic stresses tolerance has been further supported by a genome-wide transcriptomic analysis of the PPR family in poplar, which identified 154 PtrPPR genes induced by biotic and abiotic treatments, including salinity [67].

Roles of Plant Organellar DEAD-Box RHs in Salinity Response
Another group of proteins involved in the control of OGE, which are hence experimentally related to the stress responses mediated by chloroplasts and plant mitochondria, is that of DEAD-box RNA helicases (DEAD-box RHs), the largest known RNA helicase subfamily. The helicase core of DEAD-box RHs is composed of the N and C terminal domains, which are structurally similar to recombination protein RecA, in which nine conserved motifs can be identified. Motif II of the N-terminal domain contains the amino acid sequence Asp-Glu-Ala-Asp (D-E-A-D), which gave a name to the subfamily. Variations in motif II determine three related RNA helicase subgroups, namely DEAD, DEAH, and Ski2, whose members are referred to as DExD/H-box proteins [68,69].
DEAD-box RHs are present in some viruses, many prokaryotes, and all eukaryotes, and they usually possess ATP-dependent RNA helicase activity, which allows them the localized unwinding of RNAs, and hence, to participate in different RNA metabolism processes, such as ribosome biogenesis, translation initiation, RNA splicing, turnover, and decay [70]. DEAD-box RHs are also involved in OGE in both chloroplasts and mitochondria. In fact, one of the first RH family members to be identified was Mss116, which is required for mitochondrial splicing in yeast [71].
Like mTERFs and PPRs, this family also extends in plants. Accordingly, Arabidopsis and rice show a similar number of presumed DEAD-box RHs, 58 and 60 [24], respectively, while Drosophila melanogaster and Caenorhabditis elegans show nearly half these numbers with 30 and 34 [72], respectively. By an in silico analysis, Nawaz and Kang [24] found that the numbers of chloroplastic DEAD-box RHs ranged from 7 to 12, and the mitochondrial ones from 4 to 7, in four different plant species.
Nowadays, growing evidence reveals the implication of DEAD-box RHs in plant responses to different kinds of stresses [24]. Regarding chloroplasts and mitochondria, it is known that some nuclear genes that encode organellar-localized DEAD-box RHs are induced by different stresses, including salinity. HVD1 (Hordeum vulgare DEAD box protein1) was the first salt-responsive DEAD-box RH gene to be described encoding a chloroplast protein [73]. The expression of the HVD1 gene is highly induced under salt and cold stresses, with subsequent recovery after exposure to salinity stress. In a genome-wide in silico study performed later, Umate et al. [74] found that several Arabidopsis DEAD-box RHs located in chloroplasts or mitochondria regulate transcription in response to various abiotic stresses (reviewed in [24]). In addition, the overexpression of some organellar-localized nuclear-encoded DEAD-box RHs has been described to confer resistance to salinity. Accordingly, the overexpression of OsSUV3 (Oryza sativa SUPPRESSOR OF VAR3), a mitochondrially-localized DExH/D-box-related DNA/RNA helicase, confers salt tolerance in rice by maintaining photosynthesis and antioxidant machinery [69]. Under salt stress, the levels of the plant hormones GA 3 (gibberellic acid 3), zeatin, and IAA (indole-3-acetic acid) increase in the SUV3 overexpressing lines, which, in turn, may induce the expression of genes to help cope with stress [75]. Recently, the chloroplast-targeted DEAD-box RH BrRH22 of Brassica rapa has been described to be induced by several abiotic stresses, including salinity and ABA treatment. Likewise, the chloroplast-localized DEAD-box RH OsRH58 of rice is up-regulated by salinity, dehydration, and heat, but not ABA, unlike BrRH22 [76]. Transgenic Arabidopsis OsRH58-expressing plants show increased growth and yield seeds under no stress conditions. The heterologous expression of BrRH22 or OsRH58 in Arabidopsis improves germination and plant growth under salinity conditions. Both proteins may possess RNA chaperone activity, which may, in turn, influence plastid translation under stress conditions, as the Arabidopsis transgenic plants expressing BrRH22 or OsRH58 show larger amounts of some chloroplast genome-encoded proteins when treated with either NaCl or mannitol [76,77].
To our knowledge, Arabidopsis AtRH3 is the only gene to encode an organellar-localized DEAD-box RH, whose involvement in the response to salinity has been reported by the isolation and characterization of loss-of-function mutant alleles. The impaired function of chloroplast targeted AtRH3 causes a range of effects, from embryonic lethality to delayed growth, as well as reduced greening of vegetative tissues, depending on the mutant allele's strength [54]. Lee and colleagues [55] showed that young viable atrh3-4 mutant seedlings were impaired in chloroplast biogenesis as these are smaller, and include fewer and smaller chlororibosomes than the wild type. The defective chloroplast development noted in atrh3-4 seedlings gives rise to ABA-deficient and salt-and cold-sensitive phenotypes (Table 1) [55,56]. The function of AtRH3 is needed for the splicing of most intron-containing chloroplast genes [54,56] and the spliced/unspliced transcript ratio is lower in atrh3 mutants (Table 1) [56]. Stress conditions do not affect this RNA processing defect, except for genes ndhA and ndhB, as the spliced/unspliced transcript ratio in atrh3 mutants is significantly lower, especially under salt or cold stress, but not after dehydration stress [56]. The correct splicing of chloroplast transcripts is probably mediated by the RNA chaperone activity of AtRH3 [56]. More recently, loss of function mutations of AtRH50, another Arabidopsis gene that codes for a chloroplast-localized DEAD-box RH, has been shown to increase cold sensitivity as a result of the defective processing of chloroplastic rRNA, and hence inefficient plastid translation [78]. The response of ath50 mutants to other abiotic stress, such as salinity, remains to be tested.

Mutations in Plastid Ribosomal Protein PSRP2 Alter Salinity Tolerance
The previous sections noticeably illustrate the relationship between changes in the activity of nuclear genes involved in the post-transcriptional regulation of OGE at the RNA level and salt stress phenotypes. The involvement of plastidial translational machinery in plant salt responses has also been investigated. Accordingly, salt stress causes a transient suppression of the de novo synthesis of proteins in Arabidopsis suspension cell cultures [79]. Furthermore, Omidbakhshfard and colleagues [80] tested the expression by qRT-PCR of 170 genes related to protein synthesis in Arabidopsis leaves after NaCl exposure at different time points. Some genes showed up-regulation under salinity stress, and coded for chloroplast-located translation-related proteins, such as ribosomal proteins L11 (PRPL11) and L9-1 (also known as PIGGYBACK 2), ATAB2, an A/U-rich RNA-binding protein, which likely functions as an activator of translation, and PDF1B, a peptide deformylase required to remove the N-formyl group from nascent peptides. Interestingly, these genes have been previously described as being important for chloroplast development, and have been proposed to represent potential biotechnological targets for plant salt tolerance optimization [80].
As far as we know, only a salt-stress related phenotype has been described for a mutant affected in a plastid translational protein. Accordingly, the Arabidopsis psrp2 mutant defective in PLASTID-SPECIFIC RIBOSOMAL PROTEIN 2 (PSRP2) of the 30S ribosomal subunit, one of the six Arabidopsis PSRP proteins, shows enhanced seedling growth under salinity stress (Table 1) [57]. On the contrary, the transgenic plants overexpressing PSRP2 display delayed germination and reduced seedling growth in response to salinity compared to the wild type (Table 1). These results suggest that PSRP2 functions as a negative regulator of germination and seedling growth under salinity conditions. Interestingly, PSRP2 contains two RNA recognition motifs (RRM), it can bind RNA and ssDNA, and it possesses RNA chaperone activity. All this suggests a connection between plastid translation and regulation of RNA metabolism [57].

Arabidopsis SIG5 Protects Chloroplasts from Abiotic Stress Damage
Transcriptional regulation is also fundamental for OGE in plants, and mutations in the genes involved in this process can lead to a salt stress phenotype. Along these lines, a small family of nuclear genes, called RpoT (RNA polymerase T7 phage-type), encoding monomeric RNA polymerases, is responsible for the transcription of chloroplast or mitochondria genes [81]. Furthermore, the transcription of plastid genes requires a second type of DNA-dependent RNA polymerase, similar to those of prokaryotes, which is encoded by the organellar genome and dubbed PEP (plastid-encoded RNA polymerase). PEP comprises four catalytic core subunits (α, β, β', and β", respectively, encoded by plastid genes rpoA, rpoB, rpoC1, and rpoC2) and requires nucleus-encoded sigma factors (SIG) to recognize specific promoter sequences to initiate plastid gene transcription [82].
One of the six SIG Arabidopsis genes, SIG5, is up-regulated in response to different stress conditions, including salinity [58]. SIG5 is required for the transcriptional activation of the blue light-responsive promoter of the psbD gene that encodes photosystem II (PSII) reaction center protein D2, which binds the essential redox co-factors needed for photosynthetic electron transfer [58]. Besides, seed germination and recovery from damage of PSII after salt stress are delayed in loss-of-function mutant sig5-2 compared to the wild type (Table 1). This led Nagashima et al. [58] to propose that SIG5 enhances the repair of the PSII reaction center under stress by protecting chloroplasts, and hence, the plants exposed to adverse environmental stress conditions. Interestingly, the expression of the orthologous gene from the liverwort Marchantia polymorpha (MpSIG5) is induced by blue-light irradiation under several stress conditions, which suggests the conservation of the responsible mechanism [83]. Nevertheless, the expression of the psbD gene of Marchantia did not occur in conjunction with MpSIG5 induction, which indicates that SIG5 might play a divergent physiological role in different plant phyla [83].
Recently, Zhao et al. [84] obtained Arabidopsis SIG5 overexpression lines, which are more tolerant to salt stress than the wild type. These results are in agreement with those from Nagashima et al. [58] mentioned above. Furthermore, Zhao and colleagues [84] also identified an upstream regulator of SIG5, ATHB17 (ARABIDOPSIS THALIANA HOMEOBOX 17), an Arabidopsis HD-Zip transcription factor that binds to the cis-elements present in the SIG5 promoter. Similarly to SIG5, ATHB17 loss-of-function reduced plant salt tolerance, whereas ATHB17 overexpression enhanced it. Interestingly, these phenotypes were at least partially dependent on SIG5. Accordingly, ATHB17 overexpression in a sig5-1 mutant background showed tolerance to a salinity intermediate between that of the ATHB17 overexpression lines and the sig5-1 mutant [84]. Under salt stress conditions, various plastid genes regulated by SIG5 were down-regulated in the ATHB17 overexpression lines, but were up-regulated in the ATHB17 knockout lines, which suggests the positive regulation of these genes through SIG5 [84].

Conclusions and Future Perspectives
The results compiled in this review reveal that accurate OGE regulation in chloroplasts and mitochondria is fundamental for plants to tolerate and adapt to adverse environmental conditions, such as salt stress ( Figure 1). Consequently, perturbed OGE homeostasis affects plant responses to salinity, which can be detrimental for their survival. However, we are still far from fully understanding the role that OGE regulation plays in adapting plants to salinity. To make progress, it is necessary to know more details of the molecular functions of several genes involved in the control of OGE, whose disturbance results in stress phenotypes. This is especially relevant for the mTERF genes related to stress tolerance, because the mechanistic insight for most of them is lacking. Furthermore, unraveling why particular stressors specifically affect the expression of some OGE-related genes would shed light on their functional roles in plant tolerance to abiotic stresses. If we consider that a stress mutant phenotype has been reported for only a few PPR, mTERF, or DEAD-box RH genes, it is fundamental to identify and characterize mutants in plant model systems and crops affected in novel genes that transcriptionally or post-transcriptionally regulate OGE in plastids and mitochondria. This information is expected to contribute to the comprehensive understanding of the mechanisms regulating OGE in plants, and to provide insights to improve stress tolerance by identifying potential biotechnological targets for better plant growth and crop yields under salinity conditions. In turn, this would activate the expression of OGE regulators (e.g., mTERFs, PPRs or DEAD-box RHs proteins), which would result in anterograde signalling responses to adjust organellar function to salinity. In the figure, inside a mitochondrion (purple) and chloroplast (green), only those molecularly-characterized OGE regulators whose mutations lead to altered responses to salinity are depicted. The OGE processes affected in these mutants, as well as their enhanced (↑) or reduced (↓) sensitivity to salt stress, are shown (see also Table 1 for further information).

Funding:
The research conducted in the laboratory of V.Q. has been supported by a grant from the Conselleria d' Educació of the Generalitat Valenciana (Spain) (AICO/2015).

Conflicts of Interest:
The authors declare no conflict of interest.