- Research article
- Open Access
Arabidopsis ETO1 specifically interacts with and negatively regulates type 2 1-aminocyclopropane-1-carboxylate synthases
© Yoshida et al; licensee BioMed Central Ltd. 2005
Received: 26 April 2005
Accepted: 10 August 2005
Published: 10 August 2005
In Arabidopsis, ETO1 (ETHYLENE-OVERPRODUCER1) is a negative regulator of ethylene evolution by interacting with AtACS5, an isoform of the rate-limiting enzyme, 1-aminocyclopropane-1-carboxylate synthases (ACC synthase or ACS), in ethylene biosynthetic pathway. ETO1 directly inhibits the enzymatic activity of AtACS5. In addition, a specific interaction between ETO1 and AtCUL3, a constituent of a new type of E3 ubiquitin ligase complex, suggests the molecular mechanism in promoting AtACS5 degradation by the proteasome-dependent pathway. Because orthologous sequences to ETO1 are found in many plant species including tomato, we transformed tomato with Arabidopsis ETO1 to evaluate its ability to suppress ethylene production in tomato fruits.
Transgenic tomato lines that overexpress Arabidopsis ETO1 (ETO1-OE) did not show a significant delay of fruit ripening. So, we performed yeast two-hybrid assays to investigate potential heterologous interaction between ETO1 and three isozymes of ACC synthases from tomato. In the yeast two-hybrid system, ETO1 interacts with LE-ACS3 as well as AtACS5 but not with LE-ACS2 or LE-ACS4, two major isozymes whose gene expression is induced markedly in ripening fruits. According to the classification of ACC synthases, which is based on the C-terminal amino acid sequences, both LE-ACS3 and AtACS5 are categorized as type 2 isozymes and possess a consensus C-terminal sequence. In contrast, LE-ACS2 and LE-ACS4 are type 1 and type 3 isozymes, respectively, both of which do not possess this specific C-terminal sequence. Yeast two-hybrid analysis using chimeric constructs between LE-ACS2 and LE-ACS3 revealed that the type-2-ACS-specific C-terminal tail is required for interaction with ETO1. When treated with auxin to induce LE-ACS3, seedlings of ETO1-OE produced less ethylene than the wild type, despite comparable expression of the LE-ACS3 gene in the wild type.
These results suggest that ETO1 family proteins specifically interact with and negatively regulate type 2 ACC synthases. Our data also show that Arabidopsis ETO1 can regulate type 2 ACS in a heterologous plant, tomato.
Ethylene is a simple gas that acts as a plant hormone; it controls various processes in the plant life cycle, including seed germination, root hair development, root nodulation, flower senescence, abscission, and fruit ripening . Ethylene also is synthesized in response to stresses such as pathogen attack, wounding, hypoxia, ozone, chilling, and freezing . These responses are controlled through integration of the pathways for ethylene biosynthesis, perception, and signal transduction. The ethylene biosynthesis and signalling pathways have been well characterized with regard to physiology, biochemistry, molecular biology, and genetics. Studies of Arabidopsis thaliana revealed a universally conserved set of components in the ethylene signaling pathway for all plants. Ethylene is perceived by ethylene receptor family ETR1, ETR2, EIN4, ERS1, ERS2 [3–6] and their assembly requires the RAN1 copper transporter . The signal is further transduced by the signaling pathway components CTR1, a Raf-like MAPKKK [8, 9], EIN2, an Nramp-related integral membrane protein , and a cascade of transcriptional regulators EIN3/EILs , ERF1 , EDF1-4 . The proteolysis of EIN3/EIL proteins by ethylene-regulated EBF1/2 F-box proteins plays a key role in regulation of all known responses to the hormone [14, 15]. A MAPK (including AtMPK6) cascade was proposed to be involved in ethylene signaling , however, a recent study showed that AtMPK6 is not involved in ethylene signaling but instead involved in the regulation of ethylene biosynthesis through AtACS6 [17, 18]. Other yet unidentified components are thought to be involved as well [19, 20].
The biosynthetic pathway of ethylene has been studied in detail, and genes encoding the two key enzymes have been cloned and characterized [21–25]. 1-aminocyclopropane-1-carboxylate (ACC) synthase (ACS) converts S-adenosyl-L-methionine (SAM) to ACC and then, ACC oxidase (ACO) produces ethylene through oxidization of ACC. Generally, the reaction catalyzed by ACS is a rate-limiting step .
Both ACS and ACO are encoded by gene families in many plant species. In the case of tomato (Lycopersicon esculentum Mill.), there are at least 10 ACS  and four ACO genes . The members of ACS and ACO gene families are differentially expressed in development or in response to stimuli such as germination, leaf senescence and flower abscission, fruit ripening, wounding, flooding, exposure to ozone, touch, hormone treatment, and pathogen attack [28–33]. Recent findings suggest that posttranscriptional regulation is an important aspect of the control of ACS expression [22, 34–38]. Pharmacological and molecular biological studies have suggested that phosphorylation is involved in the regulation of ACS activity [34, 39]. A tomato ACS, LE-ACS2, is phosphorylated in the C-terminal region and this modification appears to be involved in the posttranslational regulation of the enzyme . However, the molecular mechanisms by which plants regulate ethylene biosynthesis at the posttranscriptional or posttranslational levels remain unclear.
Recent studies of the Arabidopsis et hylene- o verproducer mutants (eto1,eto2-1,eto3) [36–38, 41] revealed mechanisms underlying the posttranslational regulation of ethylene biosynthesis. The eto mutants constitutively display the ethylene-evoked triple response phenotypes in the absence of exogenously applied hormone; they can be distinguished from ctr1 mutants, which also displays the triple response in the absence of ethylene, because the phenotypes of eto mutants are suppressed by inhibitors of ethylene biosynthesis and action [8, 42]. Therefore, the eto mutants are likely impaired in either the regulators or the structural enzymes of ethylene biosynthesis. eto1 is a recessive mutation that results in an approximately 10-fold ethylene overproduction in etiolated seedlings compared to wild-type plants , whereas eto2-1 and eto3 are dominant mutations that cause 20- and 100-fold increases of ethylene biosynthesis, respectively, in etiolated seedlings . The eto2-1 and eto3 were identified as mutations within the closely related AtACS5 and AtACS9 genes, respectively. These mutations cause alterations of the C-terminal amino acid sequences of each protein [36, 38]. Furthermore, both eto1 and eto2-1 mutations increase the stability of the AtACS5 protein , suggesting that the C-termini of some ACC synthases are involved in posttranslational regulation/processing or stability of the ACS proteins mediated by ETO1. Also another study showed that AtMPK6 phosphorylates the C-terminus of AtACS6 to stabilize the isozyme by a yet unknown mechanism .
The molecular mechanism(s) regulating the activity and stability of AtACS5 was revealed by identification of the ETO1 protein . ETO1 is a member of a novel plant-specific protein family with three distinct protein-protein interaction motifs, namely the BTB domain in its N-terminus and the TPR motifs together with a coiled-coil motif in its C-terminus. The C-terminal TPR domain interacts with AtACS5 and the N-terminal BTB domain interacts with AtCUL3, a constituent of E3 ubiquitin ligase complexes in which ETO1 is proposed to serve as a substrate-specific adaptor protein. ETO1 inhibits the enzyme activity of AtACS5 and targets this protein for degradation in a proteasome-dependent manner. Other studies also suggest that proteolysis is involved in regulation of ethylene biosynthesis [43, 44].
ETO1 has two paralogs in Arabidopsis, EOL1 and EOL2 (ETO1-LIKE), both of which also interact with and inhibit the activity of AtACS5. Although ETO1-related sequences are found in many other plant species including tomato, no studies have examined whether members of the ETO1 protein family can interact with and regulate ACC synthases other than AtACS5. In this study, using a heterologous system in tomato, we demonstrate that ETO1 specifically interacts with a subfamily of ACC synthases, namely type 2 ACC synthases including AtACS5, AtACS9 and LE-ACS3, but not with other types of ACC synthases including AtACS6, LE-ACS2 and LE-ACS4. We also show that constitutive expression of ETO1 results in posttranscriptional suppression of a type 2 ACC synthase, LE-ACS3, in transgenic tomato. These results suggest that members of the ETO1 protein family are components in the negative regulation of type 2 ACC synthases in the plant kingdom.
Fruit ripening is not altered in transgenic tomato plants that overexpress ETO1
ETO1 specifically interacts with LE-ACS3, but not with LE-ACS2 or LE-ACS4, in yeast cells
Although the lengths of the C-terminal tails of AtACS11, LE-ACS4, and LE-ACS5 are comparable to those of type 2 isozymes, they lack the RLSF motif and the R/D/E-rich region. Therefore, we classified these three isozymes as type 3 isozymes along with AtACS7, which has a much shorter C-terminal tail. Both AtACS5 and LE-ACS3, which interact strongly with ETO1, belong to type 2, whereas LE-ACS2 belongs to type 1 and LE-ACS4 to type 3. Because we previously showed that the C-terminus of AtACS5 is a target of ETO1, this raises the possibility that the C-termini of type 2 ACC synthases contain some specific features necessary for the interaction with ETO1 that may also be conserved in other plants.
ETO1 does not interact with a series of C-terminal deletion mutants of LE-ACS2 in yeast
As described above, one notable feature of type 2 ACC synthases is the length of the C-terminal tail after the RLSF motif. Type 1 ACC synthases possess longer C-terminal tails after the RLSF than type 2, whereas type 3 isozymes lack the RLSF. Furthermore, the C-terminus of ACS appears to be proteolyzed in vivo . Although another study showed that C-terminal truncation of a type 1 enzyme, LE-ACS2, does not occur in vivo , other type 1 ACC synthases may have their C-termini truncated to an "optimal length" (i.e., length comparable to type 2) and may then become capable of interacting with ETO1 family proteins. Therefore, we examined the effect of altering the length of ACS protein C-terminal tails on their interaction with ETO1.
The C-terminal sequence specific to type 2 ACC synthases is required for the interaction with ETO1
Next we examined the effect of type-2-specific amino acid sequence around the RLSF on the interaction with ETO1. As mentioned above, type 2 ACC synthases have a specific C-terminal consensus sequence (i.e., the WVFRLSF motif followed by the R/D/E-rich region). The RLSF is conserved in both type 1 and type 2 ACC synthases, whereas the WVF motif and R/D/E-rich region are conserved only in type 2 ACC synthases in tomato and Arabidopsis (Fig. 3). In the eto3 mutant, the valine residue in this WVF motif is mutated to aspartic acid in AtACS9 , suggesting an important role of this small motif (Fig. 3). We replaced the C-terminal 31 amino acids of LE-ACS2 with amino acids 456–469 of LE-ACS3 (LE-ACS2ΔC31::LE-ACS3456–469). This chimeric ACS protein was sufficient to recover the strong interaction with ETO1 to a level comparable to LE-ACS3 (Fig. 4). These results strongly suggest that the C-terminal tail specific to type 2 ACS, comprising the WVFRLSF motif and the R/D/E-rich region, is necessary and sufficient for the interaction with ETO1.
Overexpression of ETO1 suppresses auxin-induced ethylene biosynthesis in tomato seedlings
To investigate the interaction between ETO1 and LE-ACS3 in planta, we examined the induction of ethylene biosynthesis in etiolated tomato seedlings by a synthetic auxin, 2,4-D. Using T2 seedlings of a homozygous line of ETO1-OE (14-1-H2; not included in Fig. 1A), we measured ethylene evolution from auxin-treated wild-type and ETO1 transgenic tomato seedlings.
ETO1 interacts with and inhibits type 2 ACC synthases
In a previous study, we demonstrated that ETO1, a novel plant-specific BTB/TPR protein, negatively regulates an ethylene biosynthetic enzyme of Arabidopsis seedlings, AtACS5, via direct interaction . However, whether the interaction and the regulatory effect are limited to AtACS5 and its paralogs/orthologs – or are common to the entire plant ACC synthase family – has not been clarified. In this study, we showed the interaction between ETO1 and ACS is restricted to type 2 ACS isozymes. We classified ACC synthases into three types based on their C-terminal amino acid sequences. All members of 'class I' ACC synthases of tomato (LE-ACS1A, LE-ACS1B, LE-ACS6) in the classification of Oetiker et al.  correspond to our type 1 ACC synthases, while both of their 'class II' (LE-ACS2 and LE-ACS4) and 'class III' (LE-ACS3 and LE-ACS5) contains members of our type 1 and type 3. This discrepancy may result from the different methods of the phylogenetic anlysis (i.e. partial DNA sequences  and C-terminal amino acid sequences [this paper]). On the other hand, our type 2 isozymes of Arabidopsis are grouped into two closely related phylogenetic branches in the group B ACC synthases , and the type 3 isozymes belong to the branches in the group B other than the 'type 2' branches. Also our type 1 isozymes correspond to the group A isozymes . These coincidences may reflect the functional relevance of each type of the isozymes, and, indeed, functional heterodimerizations between closely related ACS isozymes have been demonstrated .
Another question is whether any other members of the ETO1 family interact with other types of ACC synthases. In the yeast two-hybrid system, both of the two paralogs of ETO1, EOL1 and EOL2, showed an interaction with ACC synthases from tomato similar to that of ETO1 (i.e., they interacted only with type 2 ACS but not with type 1 or type 3; data not shown). This suggests that type-2-specific regulation may be common to other members of the ETO1 family at least in yeast cells. However, a possibility that any EOL proteins may interact with and inhibit ACC synthases other than type 2 isozymes modified in planta is still not excluded.
C-Terminal sequence specific to type 2 ACS is a target of ETO1
The C-terminal amino acid sequence specific to type 2 ACS (i.e., the WVFRLSF followed by the R/D/E-rich region), is a target of ETO1. In addition, mutations found within the RLSF to the R/D/E-rich region of AtACS5 of eto2-1 and the WVF motif of AtACS9 of the eto3 mutant [36, 38] strongly implicate the importance of this amino acid sequence. Among molecular lesions of Arabidopsis eto1 mutations identified so far, eto1-1, which lacks only the last TPR motif, has a phenotype similar to the other alleles, and a C-terminal deletion mutant of ETO1 (tETO1) impaired in its last TPR motif failed to interact with AtACS5 in the yeast two-hybrid assay . These results indicate that TPR motifs of ETO1 are essential for interaction with AtACS5.
TPR motifs are involved in various protein-protein interactions. Generally, the interaction between TPR domains and their target peptide are strictly limited by both electrostatic and hydrophobic interactions . In this regard, type-2-specific C-termini of ACC synthases have some features required for the strict interaction with the TPR of ETO1. The crystal structure of LE-ACS2 has been determined, and the C-terminal tail of LE-ACS2 seems to protrude from the surface of the ACS monomer and dimer . In the dimeric form (head-to-tail orientation) of LE-ACS2, N-terminal residues 11–19 make contact with the C-terminal helix H14 just before the C-terminal tail. The significance of the interaction between the N- and the C-termini is not clear but may be important for conformation stabilization and catalysis, as suggested by biochemical studies . The WVF motif is likely located outside this N- and C-terminal interaction region and may be important for formation of the interacting surface with ETO1. Crystal structure analysis of the ETO1-ACS complex would reveal the significance of the WVF motif. Also, an isozyme of type 2 ACS, LE-ACS8, does not possess the precise WVF sequence. Instead, it contains WGF, which is very closely related to WVF (Fig. 3). In contrast to the eto3 version of AtACS9, in which the valine residue of the WVF motif was altered to the charged aspartic acid residue, the glycine residue in the C-terminus of LE-ACS8 is a neutral amino acid. Therefore, it is likely that LE-ACS8 may also interact with ETO1 as do other type 2 isozymes.
Posttranslational regulation of ethylene biosynthesis
We have identified many orthologous sequences of ETO1 from other plant species including tomato, suggesting that the ETO1-based regulatory system is common among the plant kingdom. In the present study, we showed that Arabidopsis ETO1 interacts with and posttranscriptionally regulates LE-ACS3, a type 2 ACS, in a heterologous plant, tomato. This indicates that the ETO1 protein family is a common component in the negative regulation of ethylene biosynthesis in plants. Given that ETO1-homologous sequences are found in all plants but not in animals or prokaryotes, this system of regulation of ethylene may have developed early in plant evolution. ACC synthases are similar to the subgroup I family of pyridoxal 5-phosphate (PLP)-dependent aminotransferases . Most of the similarity between these two families is found around the active sites, while the target of ETO1 lies in the C-terminus of ACS, which is outside the conserved region. It is an intriguing question as to how early plants acquired this unique mechanism to regulate ethylene biosynthesis.
Finally, one may ask why only type 2 ACC synthases are regulated by ETO1. It is imperative for plants to have ethylene synthesized in a timely manner. For instance, a remarkable phenotype of all eto mutants was observed in the etiolated seedling stage, suggesting that production of ethylene is regulated by ETO1 during germination. Although ethylene evolution is important for germination, seedlings with excessive level of ethylene for an extended time would continue to exhibit phenotype similar to that of the triple response, which is normally disappeared after germination. Also ethylene is important to respond to various stresses. To avoid unnecessary overproduction of ethylene in physiological and developmental processes, a tightly regulated system consisted of the type 2 ACC synthases and ETO1 protein family together with yet unknown system (for instance, AtMPK6-AtACS6 system) must have been evolved in plants to timely control ethylene biosynthesis until this important growth regulator and stress phytohormone is needed.
In this study, we elucidated the substrate specificity of ETO1 protein. We showed the interaction between ETO1 and ACS protein family is restricted to type 2 ACS isozymes which possess specific C-terminal amino acid sequences. Our data that ETO1 suppress auxin-induced ethylene evolution through induction of LE-ACS3 also show that Arabidopsis ETO1 can regulate type 2 ACS in a heterologous plant.
Plants of wild type and transformed tomato (L. esculentum cv. Shu-gyoku) were grown in greenhouses under standard conditions. For transformation, seedlings were grown on medium supplemented with 1/2 × Murashige and Skoog (MS) minimal salts.
Transformation of tomato
Tomato hypocotyls or cotyledons precultured on MS medium containing 1 mg/l NAA, 0.5 mg/l BA, and 3% sucrose were transformed by an Agrobacterium-mediated procedure . Full-length ETO1 cDNA was introduced in the sense orientation between the CaMV 35S promoter and Nos terminator of the pROK2 vector harbouring NPT2 gene as a selectable marker . Transformed plants were confirmed by PCR amplification using specific primers for the 35S promoter and the ETO1 cDNA.
Nucleic acid analysis
Genomic DNA was isolated using Isoplant II (Nippon Gene). Total RNA was extracted using RNeasy Plant Mini Kit (Qiagen). Transcription levels of ETO1 were analyzed by reverse RT-PCR analysis of total RNA. RNA (1 μg) was used in each RT-PCR following the manufacturer's protocol (Titan One Tube RT-PCR System, Roche Diagnostics). Gene-specific primers for ETO1 were used, and GAPDH was used as an internal control. Both of the primer sets were added to the same tube. PCR amplification was performed for a first round of 10 cycles as follows: denaturation at 94°C for 30 sec, annealing at 55°C for 30 sec, and extension at 68°C for 45 sec. Then the second round of cycles was performed as follows: denaturation at 94°C for 30 sec, annealing at 55°C for 30 sec, and extension at 68°C for 45 sec + 5/cycle sec. The final extension was carried out at 68°C for 7 min, and the reaction was then stopped at 4°C. For Northern blot analysis, total RNA (10 μg) was used for each lanes and blotted onto positively charged nylon membranes (Roche Diagnostics). DIG-labeled RNA probe for LE-ACS3 was synthesized following the manufacturer's protocol (Roche Diagnostics) and detected by CDP-Star (Roche Diagnostics).
Yeast two-hybrid assay
Yeast two-hybrid assays were performed as described previously . ETO1 cDNA was cloned into the pAS2 vector. cDNAs for LE-ACS2, LE-ACS3, and LE-ACS4 were synthesized by RT-PCR using SuperScriptII (Invitrogen) reverse transcriptase and PfuTurbo DNA polymerase (Stratagene) and cloned into pACT2. Deletion or chimeric mutants of LE-ACS2 and LE-ACS3 were constructed by PCR using PfuTurbo DNA polymerase. A quantitative liquid assay for β-galactosidase activity was performed according to the manufacturer's instructions (BD Biosciences). Each experiment was repeated at least three times using independent clones.
Measurement of ethylene biosynthesis
Etiolated seedlings (1 per vial) of T2 homozygous lines 14-1-H2 (ETO1/ETO1) and 14-1-H4 (wt/wt) were grown in vials (10-mm diameter, 75-mm length with a rubber septum) containing 1 g of sea sand (20–35 mesh, Wako Chemicals) and 0.5 ml of water at 28°C in the dark. After 6 d, 2,4-D (in 1% ethanol) was added to the final concentration of 100 μM and seedlings were incubated under the same conditions. On the next day, the accumulated ethylene was measured using a gas chromatograph (Model GC-7A, Shimadzu) equipped with an active alumina column (60/80 mesh, 3 mm × 1.5 m) and FID. A 0.5-ml volume of each sample from the headspace was injected onto the column. Eight individuals were used for each treatment. Ethylene production was calculated as pL· seedling-1· hr-1.
The authors thank E. Kadowaki-Fujii and T. Watase for their skilful assistance. We also acknowledge support from members of the Plant Biotechnology Laboratory, National Agricultural Research Center for Hokkaido Region, and members of the Laboratory of Rice Applied Genetics, National Agricultural Research Center. This work was partly supported by the Ministry of Agriculture, Forestry and Fishery of Japan (to HY).
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