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Article

Increased ACS Enzyme Dosage Causes Initiation of Climacteric Ethylene Production in Tomato

1
Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba 305-8572, Ibaraki, Japan
2
Department of Horticulture, Zhejiang University, Hangzhou 310058, China
3
RIKEN Center for Sustainable Resource Science, Yokohama 230-0045, Kanagawa, Japan
4
Tsukuba Plant Innovation Research Center, University of Tsukuba, Tsukuba 305-8572, Ibaraki, Japan
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2022, 23(18), 10788; https://doi.org/10.3390/ijms231810788
Submission received: 15 August 2022 / Revised: 6 September 2022 / Accepted: 12 September 2022 / Published: 15 September 2022

Abstract

:
Fruits of wild tomato species show different ethylene-dependent ripening characteristics, such as variations in fruit color and whether they exhibit a climacteric or nonclimacteric ripening transition. 1-Aminocyclopropane-1-carboxylic acid (ACC) synthase (ACS) and ACC oxidase (ACO) are key enzymes in the ethylene biosynthetic pathway encoded by multigene families. Gene duplication is a primary driver of plant diversification and angiosperm evolution. Here, interspecific variations in the molecular regulation of ethylene biosynthesis and perception during fruit ripening in domesticated and wild tomatoes were investigated. Results showed that the activated ACS genes were increased in number in red-ripe tomato fruits than in green-ripe tomato fruits; therefore, elevated dosage of ACS enzyme promoted ripening ethylene production. Results showed that the expression of three ACS isogenes ACS1A, ACS2, and ACS4, which are involved in autocatalytic ethylene production, was higher in red-ripe tomato fruits than in green-ripe tomato fruits. Elevated ACS enzyme dosage promoted ethylene production, which corresponded to the climacteric response of red-ripe tomato fruits. The data suggest that autoinhibitory ethylene production is common to all tomato species, while autocatalytic ethylene production is specific to red-ripe species. The essential regulators Non-ripening (NOR) and Ripening-Inhibitor (RIN) have experienced gene activation and overlapped with increasing ACS enzyme dosage. These complex levels of transcript regulation link higher ethylene production with spatiotemporal modulation of gene expression in red-ripe tomato species. Taken together, this study shows that bursts in ethylene production that accompany fruit color changes in red-ripe tomatoes are likely to be an evolutionary adaptation for seed dispersal.

1. Introduction

Tomato (Solanum section Lycopersicon) includes all domesticated varieties and 12 wild relatives [1]. A great majority of wild tomato relatives are native to the Andes in the western side of South America from Ecuador to Northern Chile. The Andes region is characterized by a variety of climatic zones. These variable growth conditions gave rise to unique tomato phenotypes that are likely adaptive to the local habitat [2,3,4]. Fruits consumed by animals are carried over long distances to increase seed dispersal, which reduces parental competition and increases plant reproductive success [5]. Grumet and Herner [6] studied the ripening behavior of wild tomato relatives and grouped nine species into three categories. The first category includes the wild species S. lycopersicum var. cerasiforme, S. pimpinellifolium, and S. galapagense. Fruits of these species change color and show the typical climacteric ethylene production, which is a prominent feature of cultivated tomato fruits. The second category consists of S. pennellii, S. habrochaites, S. chmielewskii, and S. parviflorum. Species in this category have green fruits that ripen on the vine. Ethylene production is related to fruit softening in S. chmielewskii and S. parviflorum. However, there is no relationship between ethylene synthesis and fruit ripening in S. pennellii and S. habrochaites. S. peruvianum and S. chilense belong to the third category. Fruits of these species abscise prior to ripening and produce a trace amount of ethylene on the vine. The history of tomato domestication is considered as a “two-step” process in which modern cultivated tomato varieties were domesticated from S. pimpinellifolium that belong to the wild red-ripe species, after it gave rise to the intermediate species S. lycopersicum L. var. cerasiforme [7,8,9]. Red-ripe tomato species produce climacteric fruits that continue to ripen after harvest. Climacteric fruits show an increased respiratory rate and an ethylene production burst at the beginning of ripening and before the appearance of color [5,10].
The phytohormone ethylene is a key signaling molecule in the ripening of fruit [11]. 1-Aminocyclopropane-1-carboxylic acid (ACC) synthase (ACS) and ACC oxidase (ACO) are two key enzymes, and ACS is indicated as the rate-limiting enzyme in ethylene biosynthesis [12]. ACS and ACO are encoded by multigene families in higher plants. The tomato genome has at least nine ACS genes (LEACS1A, LEACS1B, and LEACS2 to 8) and five ACO genes (LEACO1 to 5) [13]. Multiple gene paralogs were created according to gene duplication events during the evolution of plants. Duplicated genes present a large potentiality for functional divergence and the new functions acquisition during plant evolution. Although most duplicated genes are lost over time [14], some are retained through neofunctionalization, subfunctionalization, or beneficial increases in gene dosage [15]. Duplicated genes create novel morphological, nutritional, and physiological phenotypes and exhibit changes in expression patterns from that of the original copy by altering the sequence of regulatory elements [16].
Two systems regulate ethylene production in climacteric fruits: autoinhibitory ethylene production called system 1 and autocatalytic ethylene production called system 2. System 1 is characterized by ethylene at basal levels in unripe fruits and vegetative tissues, which are regulated by LEACS1A and LEACS6. On the other hand, substantial increases in ethylene production during fruit ripening and flower senescence are regulated by LEACS2 and LEACS4 in system 2 [17]. Targeted inhibition of LEACS2 [18] and LEACS4 [19] gene expression reduced ethylene production and, thus, delayed fruit ripening. The transcription factors (TFs) Ripening-Inhibitor (RIN) and Non-Ripening (NOR) have been identified as essential regulator of tomato fruit ripening. [20,21]. ACS and ACO mRNA accumulation is inhibited in RIN and NOR knockout mutants, which delays fruit ripening [22,23]. In addition, RIN binding sites are identified in the NOR promoter region, and NOR promoter demethylation is required to activate gene expression during ripening [24].
In this study, interspecific variations in the molecular regulation of ethylene and carotenoids were investigated during fruit ripening of tomato in S. lycopersicum cv. Ailsa Craig, S. pimpinellifolium, S. pennellii, and S. peruvianum, which are species that exhibit the three ripening categories mentioned above. The expression levels of ethylene and carotenoid biosynthetic genes were correlated with ethylene production and coloration to identify ethylene-dependent divergence in fruits of red-ripe and green-ripe tomatoes. Promoter sequences were analyzed to identify regulatory elements responsible for modulating differential ethylene-related genes expression during ripening of fruit. Results of this study reveal that gene duplication events and modifications of upstream regulatory sequences in ethylene biosynthetic genes contributed to the diversification of domesticated tomato and their wild relatives. This research provides insights into the adaptive evolution of climacteric fruits and will facilitate the introgression of desirable traits from wild tomato relatives to cultivated varieties.

2. Results

2.1. Differences in Fruit Maturation and Ethylene Production during Ripening

The classic parameters of fruit skin color changes were documented to define the dynamics of fruit maturity stages in different tomato species. Fruit skin color was observed from 20 to 55 days after pollination (DAP) (Figure 1A). Fruits of the cultivated tomato, S. lycopersicum, var. M82 or Ailsa Craig, changed skin color from green (MG stage) to yellow (breaker, BR stage) at 40 ± 2 DAP. Fruits reached full maturity (red stage) at 50 ± 2 DAP. The BR stage of Moneymaker fruits was observed at 45 ± 2 DAP, and the red stage was observed at 50 ± 2 DAP. S. pimpinellifolium and S. lycopersicum var. cerasiforme fruits changed skin color from green to yellow (BR stage) at 38 ± 2 DAP and then reached the red stage at 48 ± 2 DAP. Fruits of S. pennellii and S. peruvianum remained green throughout the investigation period (Figure 1A).
Ethylene production rate was significantly different among fruits of red-ripe tomatoes and their green-ripe wild relatives (Figure 1B). In fruits of red-ripe tomatoes, ethylene production remained at baseline levels from 20 to 40 DAP. A rise in ethylene occurred at 40–50 DAP, and then declined thereafter. The peak ethylene production rates of M82, Ailsa Craig, and Moneymaker fruits were 0.004 ± 0.00107 μL/g/h, 0.0062 ± 0.00017 μL/g/h, and 0.0046 ± 0.00033 μL/g/h, respectively. Ethylene production of S. pimpinellifolium and S. lycopersicum var. cerasiforme fruits increased rapidly at 30 DAP. The peak ethylene production rate of S. pimpinellifolium fruits was 0.010 ± 0.00078 μL/g/h, which was recorded at 45 DAP, while that of S. lycopersicum var. cerasiforme fruits was 0.006 ± 0.00024 μL/g/h, which occurred at 40 DAP. S. pennellii and S. peruvianum, which have fruits that are green upon ripening, produced baseline levels of ethylene throughout fruit development and in over-ripe fruits (Supplementary Figure S1). Taken together, the results show a correlation between ethylene production and fruit skin color changes.

2.2. Expression Profiling of Ethylene and Carotenoid Biosynthetic Genes

Accumulation of mRNA at different fruit developmental stages was observed in four representative tomato species, namely, S. lycopersicum cv. Ailsa Craig (a red-ripe cultivated tomato), S. pimpinellifolium (a red-ripe wild relative), S. pennellii, and S. peruvianum (green-ripe wild relatives). Ripe fruits can be easily distinguished by skin color in red-ripe species, while time to fruit maturity is determined by observing changes in seed coat color in green-ripe species (Supplementary Figure S2). S. pennellii and S. peruvianum changed seed coat color at 70 and 45 DAP, respectively. Thus, fruits at these stages were considered to be at maturity levels equivalent to the red stage of red-ripe species. S. lycopersicum cv. Ailsa Craig is one of the most widely studied cultivars in studies on tomato, which was used as a benchmark. Real-time quantitative PCR (qRT-PCR) showed that the highly expressed ACS genes were increased in number in red-ripe tomato fruits than in green-ripe tomato fruits (Figure 2A,B). For example, in the red-ripe cultivar, Ailsa Craig, the levels of LEACS1A, LEACS2, LEACS4, LEACS6, LEACO1, and LEACO3 transcripts were relatively high at ripening. Furthermore, the expression level of LEACS2 and LEACS4 was upregulated in ripe fruits of S. pimpinellifolium. However, LEACS1A expression in S. pimpinellifolium fruits was 145-fold lower than that in Ailsa Craig fruits. In the green-ripe species, S. pennellii, LEACO3 was the only gene that increased expression during ripening. Although ACS genes were expressed in S. pennellii fruits at the ripening stage, their levels were lower than those in Ailsa Craig fruits. Specifically, the expression of LEACS2 in S. pennellii fruits was 2000-fold lower than that in Ailsa Craig fruits. The expression of ACS and ACO genes in S. peruvianum fruits was lower than that in Ailsa Craig fruits. Specifically, transcripts of LEACS2 and LEACS4 in S. peruvianum fruits were 970-fold and 32-fold lower, respectively, than those in Ailsa Craig fruits. On the other hand, LEACS6 mRNA accumulated in immature fruits of S. peruvianum. Phytoene synthase (PSY) has been identified as the rate-limiting enzyme in carotenoid biosynthesis, and PSY1 is transcriptionally regulated by ethylene in cultivated tomato. In, addition, z-carotene desaturase (ZDS) is a key enzyme for accumulation of lycopene, while lycopene ε-cyclase (LCYE) and lycopene β-cyclase (LCYB) produce cyclic carotenoids through lycopene breakdown [25]. Transcripts of PSY1 showed 197-fold lower expression in S. pennellii and 48-fold lower expression in S. peruvianum compared to that in Ailsa Craig, respectively, and ZDS showed 120-fold lower expression in S. peruvianum and fivefold lower expression compared to that in Ailsa Craig (Figure 2C). Transcripts of LCYE showed 158-fold higher expression in S. pennellii and 250-fold higher expression in S. peruvianum compared to that in Ailsa Craig. Transcripts of LCYE were 1.8-fold higher in S. pennellii and 2.5-fold higher in S. peruvianum fruit. Expression of RIN and NOR, which encode ripening-related transcription factors, was higher in fruits of red-ripe species than in those of green-ripe species (Figure 2D).

2.3. Statistical Motif Analysis in Regulatory Sequences

Conservation of upstream regulatory sequences was analyzed for selected ethylene biosynthesis-related genes in cultivated tomato, S. lycopersicum var. cerasiforme, S. pimpinellifolium, and S. pennellii. The genes analyzed included LEACS1A, LEACS2, LEACS4, LEACS6, LEACO1, LEACO3, RIN, and NOR (Figure 3A and Supplementary Figure S3A). Promoter sequences of LEACS6 and RIN were highly conserved among the four species. The regulatory sequence of LEACS1A had two more MYC-binding sites in cultivated tomato S. lycopersicum var. cerasiforme and S. pennellii than in S. pimpinellifolium (Figure 3A), and S. pimpinellifolium had one insertion located between −223 bp and −207 bp from LEACS1A transcription start site. Another insertion located between −168 bp and −123 bp was identified in the LEACS1A upstream sequence of red-ripe tomato species. The regulatory sequence of LEACS2 had one more MYB and two fewer ERE cis-acting elements in S. pennellii compared to red-ripe tomato species. There were two insertions in the LEACS2 upstream sequence of red-ripe tomato species and S. pennellii. The insertion located between motif 15 and motif 17 was identified in the LEACS4 upstream sequence of cultivated tomato which was shared among red-ripe tomatoes. The sequence showed high similarity with Gypsy-36_BiGl-I retrotransposons (the Gypsy group of LTR retrotransposon family) (Supplementary Table S2). Screening of regulatory DNA elements revealed an increase in the number of MYB-binding sites in the LEACS4 promoter of red-ripe tomatoes. The increased MYB-binding sites in the red-ripe tomatoes LEACS4 promoter occurred in sequences with insertions located between motif 15 and motif 17, which contained two MYB-binding sites and one MYC-binding site (Figure 3A). Motif analysis also revealed that the promoter sequence located at −500 bp from the LEACO1 transcription start site was highly conserved among red-ripe tomato species. Regulatory sequences of NOR were highly conserved among red-ripe tomatoes; however, the sequences located at −1100 to −2000 bp from S. pennellii were different (Supplementary Figure S3A). Conservation of upstream regulatory sequences was also analyzed for carotenoid biosynthesis-related genes. The ZDS upstream sequence showed two additional motifs (7 and 11) specific to the S. pennellii sequence and an additional motif-14 specific to red-ripe tomato species (Supplementary Figure S3B). The LCYE upstream sequence showed a large insertion (from motif 9 to 19) in S. pennellii, which revealed a number of MYB, MYC, W-box, and ERE cis-acting elements (Figure 3B). The insert sequence showed high similarity with MuDR-8_Stu transposons (the MuDR-type DNA transposon family) (Supplementary Table S3). The LCYB upstream sequence showed one more MYB-binding site in S. pennellii, but one fewer than in red-ripe species.

2.4. Exogenous Ethylene Response Assays

The triple response assay is used to evaluate how seedlings respond to exogenous ethylene. Seedlings typically exhibit short hypocotyls and roots, along with an exaggerated apical hook curvature, when exposed to ethylene. S. pimpinellifolium, S. pennellii, and S. peruvianum seedlings exposed to ethylene had hypocotyls and roots that were significantly shorter than those of controls and showed the formation of an exaggerated apical hook (Figure 4A,B).
Expression of LEACS2 was positively induced by exogenous ethylene treatment in tomato fruits, except in S. peruvianum. LEACS2 expression increased eight-, 20-, and twofold in Ailsa Craig, S. pimpinellifolium, and S. pennellii, respectively, when treated with exogenous ethylene. By contrast, exogenous ethylene inhibited LEACS2 accumulation in S. peruvianum fruits (Figure 4C). LEACS6 expression is negatively affected by exogenous ethylene treatment [17]. Here, LEACS6 expression was four-, two-, three-, and fivefold lower in Ailsa Craig, S. pimpinellifolium, S. pennellii, and S. peruvianum, respectively, compared to the control (Figure 4C). Expression of PSY1 was positively induced by exogenous ethylene treatment in tomato fruits, except in S. peruvianum. PSY1 expression increased three-, 12-, and eightfold in Ailsa Craig, S. pimpinellifolium, and S. pennellii, respectively, when treated with exogenous ethylene (Figure 4D). Expression of LCYE was fivefold higher in S. pennellii and 3.5-fold lower in Ailsa Craig, when treated with exogenous ethylene (Figure 4D). LCYB expression was four-, four-, 1.5-, and threefold lower in Ailsa Craig, S. pimpinellifolium, S. pennellii, and S. peruvianum, respectively, when treated with exogenous ethylene. ZDS expression showed no significant difference.

2.5. Quantification of DNA Methylation in the NOR Promoter

Highly conserved elements at −1814 to −1404 bp of the NOR promoter were hypermethylated before ripening (Supplementary Figure S4). Results of qAMP confirmed that the genome of cultivated tomato undergoes demethylation processes during ripening (Figure 5), which is consistent with the results of Zhong [24]. Cytosines of Ailsa Craig NOR promoter were hypermethylated at 20 DAP. Cytosine methylation levels then dropped rapidly at 30–45 DAP, while the NOR promoter remained in a demethylated state at 55 DAP. The S. pimpinellifolium NOR promoter showed a hypermethylated state at 20 DAP; however, it remained in a demethylated state at 30–55 DAP. The S. pennellii NOR promoter demethylated rapidly after 30 DAP, which was equivalent to the immature stage (i.e., turning stage at 70 DAP). The only species that was different with regard to NOR promoter methylation state was S. peruvianum. In this species, the NOR promoter remained in an unmethylated state at 20 DAP.

3. Discussion

Tomato includes thousands of varieties and 12 wild tomato species. Cultivated tomatoes are usually red when mature, which is the preferred color of consumers. Fruit color change is greatly involved in ethylene production. Autocatalytic ethylene production participates in ripening, which consists of mechanistic processes evolved for ground animal seed dispersal before red tomatoes were domesticated by humans. Although cultivated tomatoes can come in variety of colors, sizes, shapes, and flavor, there has been a sharp decline in genetic diversity due to domestication bottlenecks. Wild relatives reveal large genetic and phenotypic diversity which are desirable genetic resources for sustainable use of tomato breeding. Green-ripe wild relatives, such as S. pennellii and S. peruvianum, fail to show the typical climacteric ethylene production during fruit maturation. This research provides insights into the adaptive evolution of climacteric fruits and will facilitate the introgression of desirable traits from wild tomato relatives to cultivated varieties. The comparison between red-ripe and green-ripe tomatoes demonstrated a significant difference in the genetic regulation of ethylene and carotenoid biosynthesis. We found that increased ethylene production in red tomatoes is related to the enhanced dosage of ACS enzyme. Knowledge gained from the study of climacteric ethylene production will assist molecular manipulation, which is a rapid way to prevent adverse effects in wild relatives, including the non-climacteric feature.

3.1. Ethylene-Mediated Carotenoid Biosynthesis Is an Evolutionary Adaptation

Ripening in fleshy fruits is accompanied by changes in biochemistry, physiology, and structure, which attract seed-dispersing animals. Birds, in particular, are essential for plant reproductive success because they carry ingested seeds over long distances [4]. They tend to eat smaller fruits with bright colors, such as red or purple, as well as fruits without seed protection [26]. The gaseous plant hormone, ethylene, triggers physiological, biochemical, and molecular changes that lead to fruit ripening [27]. In this regard, inhibiting ethylene perception and signaling with 1-methylcyclopropene (1-MCP) or hydrogen sulfide (H2S) inhibits fruit coloration and softening [28,29]. This study showed that the green-ripe tomato species, S. pennellii and S. peruvianum, had low ethylene levels, which is a feature of non-climacteric fruits (Figure 1). By contrast, ethylene levels in red-ripe tomato species were significantly elevated at the onset of color change. The burst of ethylene production that accompanies fruit color change in S. pimpinellifolium is likely to be an evolutionary adaptation for seed dispersal. The bright color of red-ripe fruits is more attractive to tree dispersers, thus enabling increased opportunities for seeds to spread. Fruit color is specified by the type and balance of pigments in the pericarp. Tomato relatives produce fruits that are green, purple, yellow, or red [30]. Red and yellow colors in fruits are largely the result of carotenoids, while purple is caused by anthocyanin. Ethylene-driven activation of gene expression is a rate-limiting step in carotenoid biosynthesis. Ethylene-mediated ripening mechanisms of modern cultivated tomatoes are thought to be inherited from their wild ancestors. PSY1 and ZDS are key enzymes in the lycopene biosynthetic pathway, while LCYB and LCYE are required for the formation of α-carotene and β-carotene [25]. We demonstrated that red-ripe varieties triggered lycopene accumulation but lowered the formation of α-carotene and β-carotene. On the contrary, green-ripe wild relatives feature more accessible lycopene breakdown (Figure 2C). Interestingly, in S. pennellii, although the expression of PSY1 was induced with exogenous ethylene, it circumvented any lycopene accumulation induced by the expression of LCYE (Figure 4D). S. peruvianum showed a high level of LCYB and LCYE expression upon ripening (Figure 2C), allowing lycopene breakdown. Other wild tomato relatives, such as S. chilense and S. cheesmaniae, synthesize anthocyanins in fruit epidermal tissue, leading to anthocyanin-spotted green-ripe fruits or fully purple fruits. Tomato wild species with purple fruits are grown in the high altitude and radiation-enriched Andean regions of South America [31]. Anthocyanins are induced by abiotic stresses, such as drought, high salinity, excess light, and cold. The purple and red color in wild tomato fruits could represent alternative evolutionary adaptations for attracting seed dispersers which are different from those in fruits exhibiting ethylene-mediated carotenoid biosynthesis.

3.2. Increased Dosage of ACS Enzyme Is Favored by Selection

The tomato genome contains multiple copies of genes that are closely related in structure and function. Early ancestors of cultivated tomato were probably polyploids that arose through two consecutive triplication events [32]. Therefore, tomatoes have a significant number of duplicated genes. Polyploidization increases plant diversity and is, therefore, considered a primary driver of angiosperm evolution. In the tomato genome, there are 11 ACS genes and six ACO genes [32]. These genes are differentially expressed at various stages of development and ripening. Tomato paralogous gene predictions indicate that LEACS1A, LEACS2, LEACS4, and two silenced LEACS genes belong to the ORTHOMCL532 cluster [32]. Alternatively, the amino-acid sequence that belongs to the protein encoded by LEACS6 is not identical to that of the ORTHOMCL532 cluster. Previous studies on cultivated tomatoes revealed that LEACS6 functions in wounding and plays a major role in developing fruits [33,34]. qRT-PCR revealed that LEACS6 expression is highly conserved among red- and green-ripe tomato species, which indicated that LEACS6 has an ancestral and essential function (Figure 2 and Supplementary Table S4). The expression of other duplicated genes, such as LEACS1A, LEACS2, and LEACS4, is temporally restricted during ripening. Results of this study indicate that duplicated ancestral genes followed by sub-functionalization contributed to tomato diversification.
Although duplicated genes can be retained without acquiring new functions, increased enzyme dosage could be beneficial because of elevated metabolic activity [15]. In red-ripe tomatoes, S. pimpinellifolium revealed higher ethylene production compared with cultivated tomatoes (Figure 1B). Although three ACS genes (LEACS1A, LEACS2, and LEACS4) were activated in cultivated tomato, the gene expression levels of two activated ACS genes (LEACS2 and LEACS4) were significantly higher in S. pimpinellifolium (Figure 2A). Our survey indicates that ACS was the rate-limiting enzyme in ethylene biosynthesis. Clustering of ACS genes, such as LEACS1A, LEACS2, and LEACS4, which have similar functions in ethylene-mediated fruit ripening, is one example of metabolic benefits brought about by increased enzyme dosages. Transcript levels of LEACS1A, LEACS2, and LEACS4 remained relatively low in mature fruits of S. pennellii and S. peruvianum (Figure 2A and Figure 6), which correlated with lack burst of ethylene production and could explain the predominance of green coloration. In red-ripe tomatoes, the transient increase in LEACS1A transcripts was accompanied by elevated LEACS4 expression at the beginning of ripening. LEACS2 and LEACS4 are in charge of the maintaining system 2 ethylene production among cultivated tomatoes [13]. According to the results presented here, activation of LEACS2 and LEACS4 gene expression is probably accompanied by the recruitment of activators to several enhancer sites in the upstream promoter region (Figure 3). It is plausible that tomato breeding led to the evolution of a complex autocatalytic system, in which LEACS1A activation triggers ripening-mediated ethylene biosynthesis in modern cultivated tomato cultivars.

3.3. Divergence in Transcriptional Regulation

Transposable elements (TEs) are considered one of the major drivers of genome evolution. Duplicated genes can arise adjacent to upstream transcriptional regulatory sites that alter their expression. Furthermore, TEs and repeat sequences can disrupt promoters of duplicated genes. In this study, relatively long insertions were found in the regulatory region of ACS4 and LCYE (Figure 2). TEs represent a variable and high proportion of regulatory region; moreover, sequence motifs that potentially regulate the expression of ACS4 and LCYE were identified in this study (Figure 3 and Supplementary Figure S5). Additional MYB and MYC binding sites triggered by insertions in the LEACS4 promoter were found in red-ripe tomatoes. MYB and MYC encode transcription factors (TFs), which regulate plant defense responses via jasmonate (JA) signaling [35] and ABA-dependent or -independent pathways [36]. A recent study suggested that SlMYB70 overexpression delays fruit ripening via direct transcriptional repression of LEACS2 and LEACO3 [37]. Disruptive insertions within the promoter region of ethylene-related genes correlate with their function (Figure 2 and Figure 3), which could account for changes in ethylene but also carotenoid biosynthetic gene expression.
The TFs NOR and RIN are key regulators of ethylene biosynthesis during fruit ripening. Whole-genome bisulfite sequencing revealed that RIN binding sites are frequently localized in demethylated regions of numerous ripening gene promoters, including NOR. Moreover, RIN binding to promoters of ripening-related genes occurs simultaneously with demethylation [24]. The low levels of NOR expression in S. pennellii and S. peruvianum (Figure 2D) was accompanied by demethylated and unmethylated NOR promoter in S. pennellii and S. peruvianum, respectively (Figure 5). Therefore, a methylated promoter is not the cause of low NOR expression in green-ripe tomatoes. The involvement of NOR in ethylene biosynthesis appears to be an acquired mechanism to accelerate ethylene-dependent color changes during fruit ripening. In S. pennellii, the hypermethylated NOR promoter suggests that epigenetic regulation of NOR has been established. Although S. pennellii and S. peruvianum are green-ripe fruits, the genetic architecture of gene expression regulation is highly diversified among plants. Results presented here indicate that molecular pathways for RIN- and NOR-triggered ethylene production overlap with the increased ACS enzyme dosage (Figure 6). These complex levels of transcript regulation link higher ethylene production with spatiotemporal modulation of gene expression in red-ripe tomato species.

3.4. Ethylene Perception in Fruits

Although LEACS6 transcript accumulation was associated with autoinhibition of ethylene production, LEACS6 transcripts decreased rapidly at the onset of ripening [13]. Previous research demonstrated that LEACS6 gene expression decreased after exogenous ethylene treatment [38]. In this study, LEACS6 transcript abundance significantly declined after exogenous ethylene treatment in cultivated tomato and its three wild relatives (Figure 4C). Autocatalytic ethylene production participates in ripening and senescence, which are considered to be mechanistic processes that define climacteric fruits during evolution [5]. A major feature of autocatalytic ethylene synthesis in cultivated tomato is ethylene-inducible ACS2 expression [10]. The observation that exogenous ethylene treatment significantly promoted LEACS2 gene expression in Alisa Craig and S. pimpinellifolium was consistent with an autocatalytic ethylene biosynthetic pathway (Figure 4C). In the green-ripe wild tomato relative, S. peruvianum, LEACS2 expression in fruits was low and was not upregulated by the treatment of exogenous ethylene (Figure 2A and Figure 4C). However, the observation of inhibited hypocotyl and root growth in the seedling triple response assay suggests the presence of functional ethylene receptors in S. peruvianum (Figure 4A,B). Inactivation of LEACS2 coupled with low ethylene production could explain the lack of ethylene response in S. peruvianum fruits (Figure 6). By contrast, exogenous ethylene-inducible LEACS2 occurred in fruits of S. pennellii (Figure 4C), which is another green-ripe wild tomato relative. Therefore, autocatalytic ethylene synthesis and minimal ethylene production during fruit ripening in S. pennellii are likely the result of lower NOR and RIN expression and a reduction in ACS enzyme dosage (Figure 6).

4. Materials and Methods

4.1. Plant Materials and Growth Conditions

Cultivated tomatoes (S. lycopersicum cv. M82, Moneymaker, and cv. Ailsa Craig) and their wild relatives (S. pimpinellifolium, S. pennellii, S. peruvianum, and S. lycopersicum var. cerasiforme) were provided by National BioResource Project Tomato (NBRP-Tomato) (https://tomatoma.nbrp.jp/ (accessed on 20 July 2022)). The plants were grown in a glasshouse located at the Tsukuba-Plant Innovation Research Center (T-PIRC) Farm, University of Tsukuba from April 2020 to January 2021 in a randomized scheme. Plants were fertilized once a week using HYPONeX (Hyponex, Japan). Flowers were marked on the date of pollination. Then, the fruits were sampled at 20 DAP to 55 DAP. After harvest, seeds and the fruit columella were removed immediately, ground in liquid nitrogen, and stored at −80 °C until use.

4.2. Ethylene Production in Fruits

Measurements of ethylene production were conducted on fruits that were harvested every 5 days for the duration of fruit development, which spanned 20–55 DAP. Fruits of cultivated tomatoes and their wild relatives were placed in 270 mL and 50 mL glass bottles, respectively. Bottles were left open for 1 h after placing the fruit inside. The air was then blown off to remove the effect of wound-induced ethylene production. Bottle caps were tightened, and bottles containing the fruit were incubated for 4 h at room temperate. A sample of air (1 mL) was taken with a medical syringe and injected into a Shimadzu 5890 series gas chromatograph equipped with a flame ionization detector. Ethylene concentration was normalized to reagent-grade ethylene standards with respect to fruit weight, volume, and time for incubation using the following equation:
Ethylene concentration (μL/g fresh weight/h) = X × Y/Z × T × 1000, where X is the concentration (ppm), Y
is the volume of the bottle (mL), Z is the fruit weight (g), and T is the time (h).
Three biological replicates were analyzed for each species.

4.3. Exogenous Ethylene Treatment

The triple response assay was carried out to compare variations in ethylene responsiveness among seedlings of S. lycopersicum cv. Ailsa Craig, S. pimpinellifolium, S. pennellii, and S. peruvianum. Two day old seedlings were grown on Murashige and Skoog (MS) medium in 50 mL vials, and then treated with 100 ppm of ethylene at 24 °C in the dark for 7 days. Seedlings treated with air were used as the control. Root and shoot length were obtained from at least five measurements for each species. The ethylene responsiveness of fruits of Ailsa Craig at 40 DAP and S. pimpinellifolium at 38 DAP, which corresponded to the mature green (MG) stage, was examined. For the green-ripe species, S. pennellii at 60 DAP and S. peruvianum at 40 DAP were used because these times were equivalent to the MG stage of Ailsa Craig and S. pimpinellifolium. Fruits were harvested and then stored in a 270 mL or 50 mL open bottle for 2 h in order to remove wound-induced ethylene effects. Fruits were then incubated with 1000 ppm of ethylene at room temperature for 24 h. Fruits treated with air were used as controls.

4.4. DNA Extraction and Sequencing

Tomato fruits at different development stages were homogenized using a Multi-Bead Shocker (YASUI KIKAI). Then, 100 mg of fruit powder was used for genomic DNA extraction. Samples were mixed with 400 mL of DNA extraction buffer that consisted of 250 mM NaCl, 200 mM Tris-HCl, 25 mM EDTA (pH 8.0), and 60 μL of 10% SDS, followed by shaking. Mixed samples were incubated at 65 °C for 30 min. Next, 150 μL of 5 M KAC was put in the mixed samples and stored on ice for 30 min. Phenol/chloroform/isoamyl alcohol (300 μL) was added after incubation in ice and centrifuged at 13,000 rpm for 5 min. The supernatant was collected, before adding an equal amount of 2-propanol. The supernatant/2-propanol mixture was centrifuged for 10 min at 5000 rpm. After centrifugation, the resulting precipitate was washed with 70% ethanol and then resuspended in water. Genomic DNA concentration was measured using a Multiskan spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA).
The upstream sequence of S. peruvianum was amplified with gene-specific primers (Supplementary Table S1), and a QIAquick PCR purification kit (QIAGEN) was used for PCR product purification following the manufacturer’s protocol. TA cloning was carried out with the pGEM-T easy Vector System (Promega, Madison, WI, USA). Positive clones were screened through colony PCR with specific primers. QIAprep Spin Miniprep kit (QIAGEN) was used for plasmid DNA extraction following the manufacturer’s protocol. The product was used as the template for sequencing with the BigDyeKit (Applied Biosystems, Inc., Foster City, CA, USA).

4.5. Promoter Analysis

Promoter sequences of ethylene biosynthetic genes were downloaded from the National Center for Biotechnology Information (NCBI; https://www.ncbi.nlm.nih.gov/ (accessed on 1 June 2022)) and Sol Genomics Network (https://www.solgenomics.net/ (accessed on 1 June 2022)). Multiple sequences were aligned using the Geneious software. Conserved motifs were determined using MEME 5.3.3 (https://meme-suite.org/meme/tools/meme (accessed on 1 June 2022)) and plotted using TBtools [39]. Regulatory sequence elements were determined using Plant CARE (http://bioinformatics.psb.ugent.be/webtools/plantcare/html/ (accessed on 1 June 2022)). Transposable elements were determined using Repbase (https://www.girinst.org/repbase/update/index.html (accessed on 1 June 2022)).

4.6. RNA Extraction and Quantitative RT-PCR Analysis

Firstly, 100 mg of fruit powder was used for total RNA extraction using TRIzol (Invitrogen, Waltham, MA, USA) following the manufacturer’s instructions. At least three biological replications were used. The quality of total RNA was checked through agarose gel electrophoresis using 2× RNA loading buffer (FUJIFILM). Concentrations of total RNA were measured using a Multiskan spectrophotometer (Thermo Fisher Scientific). Complementary DNA (cDNA) was synthesized using ReverTra Ace qPCR RT Master Mix and then used as the template for qRT-PCR. qRT-PCR was performed using a StepOne Plus (Applied Biosystems, Foster City, CA, USA) real-time PCR system. Each reaction contained 5 μL of Fast SYBR Green Master Mix, 10 nM of forward and reverse primers, 2.4 μL of MilliQ water, and 2 μL of template. The qRT-PCR program consisted of the following steps: 95 °C/20 s incubation, 40 cycles of 95 °C/10 s, and 60 °C/30 s. Transcript quantification was dependent on the 2−ΔΔCt analysis method [40]. Sl-Ubiquitin was used as the internal reference gene. Student’s t-tests were used to detect statistical significances using Microsoft Excel (version 2016).

4.7. DNA Methylation Using Real-Time PCR (qAMP)

The DNA methylation level of cultivated tomato was obtained from the tomato epigenome database (http://ted.bti.cornell.edu/epigenome/ (accessed on 5 February 2022)). DNA products were digested using the methylation-sensitive restriction enzyme (MSREs), HhaI (TAKARA), for 2 h. Replacement of the enzyme with water was used as the control. Each PCR reaction contained 5 μL of GoTaq Green Master Mix, 10 nM of forward and reverse primers (Supplementary Table S1), 0.8 μL of 25 nM MgCl2, 1.8 μL of MilliQ water, and 2 μL of digested DNA. For control samples, the PCR program consisted of the following steps: 95 °C/3 min incubation, 35 cycles of 95 °C/30 s, 52 °C/30 s, and 72 °C/30 s. For digested DNA, the PCR program consisted of the following steps: 95 °C/3 min incubation, 40 cycles of 95 °C/30 s, 52 °C/30 s, and 72 °C/30 s. Data were collected from three biological replicates.

5. Conclusions

In conclusion, the transcription regulation of ethylene and carotenoid biosynthesis revealed interspecific variations in tomato and related wild species. Activation of ACS genes expression in red-ripe tomatoes resulted in increased involvement of a number of ACS genes in ripening. The involvement of NOR and RIN in ethylene biosynthesis appears to be an acquired mechanism when the red-ripe tomatoes developed special features to improve its chance of survival. The upregulated gene expression is probably accompanied by the recruitment of activators to several enhancer sites in the upstream regulatory region. Cultivated tomato inherited these features from red-ripe tomato wild relatives in which the enhanced dosage of ACS enzyme caused a burst of ethylene production. In addition to carotenoid biosynthesis, lycopene accumulation is induced by ethylene-mediated regulations, and lycopene breakdown is decreased during ripening in red-ripe tomatoes. By contrast, green-ripe wild relatives lack ethylene production and lycopene accumulation; however, they have a higher lycopene breakdown capacity, which keeps fruits green during maturation.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms231810788/s1. References [41,42,43,44,45] are cited in the supplementary materials.

Author Contributions

N.W. designed the research; H.C. and N.W. performed the research; H.C., N.W., M.K., H.E. and S.B. analyzed the data; H.C. and N.W. wrote the paper. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Lotte Research Promotion Grant (grant number LF000665).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors thank the laboratory members at the University of Tsukuba for valuable discussions about this project. We are also grateful to Hiroshi Shiba (University of Tsukuba, Japan) and Sumiko Sugaya (University of Tsukuba, Japan) for productive discussions about this work. This work was supported by the Lotte Research Promotion Grant (grant number LF000665). Seeds of cultivated tomatoes (S. lycopersicum cv. M82, S. lycopersicum cv. Moneymaker, and S. lycopersicum cv. Ailsa Craig) and wild relatives (S. pimpinellifolium, S. pennellii, S. peruvianum, and S. lycopersicum var. cerasiforme) were provided by National BioResource Project (NBRP) Tomato.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Bai, Y.; Lindhout, P. Domestication and Breeding of Tomatoes: What Have We Gained and What Can We Gain in the Future? Ann. Bot. 2007, 100, 1085–1094. [Google Scholar] [CrossRef] [PubMed]
  2. Nakazato, T.; Bogonovich, M.; Moyle, L.C. Environmental Factors Predict Adaptive Phenotypic Differentiation within and between Two Wild Andean Tomatoes. Evol. Int. J. Org. Evol. 2008, 62, 774–792. [Google Scholar] [CrossRef] [PubMed]
  3. Nakazato, T.; Franklin, R.A.; Kirk, B.C.; Housworth, E.A. Population Structure, Demographic History, and Evolutionary Patterns of a Green-Fruited Tomato, Solanum Peruvianum (Solanaceae), Revealed by Spatial Genetics Analyses. Am. J. Bot. 2012, 99, 1207–1216. [Google Scholar] [CrossRef] [PubMed]
  4. Nakazato, T.; Warren, D.L.; Moyle, L.C. Ecological and Geographic Modes of Species Divergence in Wild Tomatoes. Am. J. Bot. 2010, 97, 680–693. [Google Scholar] [CrossRef]
  5. Lü, P.; Yu, S.; Zhu, N.; Chen, Y.-R.; Zhou, B.; Pan, Y.; Tzeng, D.; Fabi, J.P.; Argyris, J.; Garcia-Mas, J.; et al. Genome Encode Analyses Reveal the Basis of Convergent Evolution of Fleshy Fruit Ripening. Nat. Plants 2018, 4, 784–791. [Google Scholar] [CrossRef]
  6. Grumet, R.; Fobes, J.F.; Herner, R.C. Ripening Behavior of Wild Tomato Species. Plant Physiol. 1981, 68, 1428–1432. [Google Scholar] [CrossRef]
  7. Blanca, J.; Cañizares, J.; Cordero, L.; Pascual, L.; Diez, M.J.; Nuez, F. Variation Revealed by SNP Genotyping and Morphology Provides Insight into the Origin of the Tomato. PLoS ONE 2012, 7, e48198. [Google Scholar] [CrossRef]
  8. Blanca, J.; Montero-Pau, J.; Sauvage, C.; Bauchet, G.; Illa, E.; Díez, M.J.; Francis, D.; Causse, M.; van der Knaap, E.; Cañizares, J. Genomic Variation in Tomato, from Wild Ancestors to Contemporary Breeding Accessions. BMC Genom. 2015, 16, 1–19. [Google Scholar] [CrossRef]
  9. Lin, T.; Zhu, G.; Zhang, J.; Xu, X.; Yu, Q.; Zheng, Z.; Zhang, Z.; Lun, Y.; Li, S.; Wang, X.; et al. Genomic Analyses Provide Insights into the History of Tomato Breeding. Nat. Genet. 2014, 46, 1220–1226. [Google Scholar] [CrossRef]
  10. Klee, H.J.; Giovannoni, J.J. Genetics and Control of Tomato Fruit Ripening and Quality Attributes. Annu. Rev. Genet. 2011, 45, 41–59. [Google Scholar] [CrossRef]
  11. Giovannoni, J.J. Genetic Regulation of Fruit Development and Ripening. Plant Cell 2004, 16, S170–S180. [Google Scholar] [CrossRef]
  12. Sharma, K.; Gupta, S.; Sarma, S.; Rai, M.; Sreelakshmi, Y.; Sharma, R. Mutations in Tomato 1-Aminocyclopropane Carboxylic Acid Synthase2 Uncover Its Role in Development beside Fruit Ripening. Plant J. 2021, 106, 95–112. [Google Scholar] [CrossRef]
  13. Barry, C.S.; Giovannoni, J.J. Ethylene and Fruit Ripening. J. Plant Growth Regul. 2007, 26, 143–159. [Google Scholar] [CrossRef]
  14. Innan, H.; Kondrashov, F. The Evolution of Gene Duplications: Classifying and Distinguishing between Models. Nat. Rev. Genet. 2010, 11, 97–108. [Google Scholar] [CrossRef]
  15. Panchy, N.; Lehti-Shiu, M.; Shiu, S.-H. Evolution of Gene Duplication in Plants. Plant Physiol. 2016, 171, 2294–2316. [Google Scholar] [CrossRef]
  16. Arsovski, A.A.; Pradinuk, J.; Guo, X.Q.; Wang, S.; Adams, K.L. Evolution of Cis-Regulatory Elements and Regulatory Networks in Duplicated Genes of Arabidopsis. Plant Physiol. 2015, 169, 2982–2991. [Google Scholar] [CrossRef]
  17. Yokotani, N.; Nakano, R.; Imanishi, S.; Nagata, M.; Inaba, A.; Kubo, Y. Ripening-Associated Ethylene Biosynthesis in Tomato Fruit Is Autocatalytically and Developmentally Regulated. J. Exp. Bot. 2009, 60, 3433–3442. [Google Scholar] [CrossRef]
  18. Oeller, P.W.; Lu, M.-W.; Taylor, L.P.; Pike, D.A.; Theologis, A.A. Reversible Inhibition of Tomato Fruit Senescence by Antisense RNA. Science 1991, 254, 437–439. [Google Scholar] [CrossRef]
  19. Hoogstrate, S.W.; van Bussel, L.J.; Cristescu, S.M.; Cator, E.; Mariani, C.; Vriezen, W.H.; Rieu, I. Tomato ACS4 Is Necessary for Timely Start of and Progression through the Climacteric Phase of Fruit Ripening. Front. Plant Sci. 2014, 5, 466. [Google Scholar] [CrossRef]
  20. Gao, Y.; Zhu, N.; Zhu, X.; Wu, M.; Jiang, C.-Z.; Grierson, D.; Luo, Y.; Shen, W.; Zhong, S.; Fu, D.-Q.; et al. Diversity and Redundancy of the Ripening Regulatory Networks Revealed by the FruitENCODE and the New CRISPR/Cas9 CNR and NOR Mutants. Hortic. Res. 2019, 6, 39. [Google Scholar] [CrossRef] [Green Version]
  21. Robinson, R. Ripening Inhibitor: A Gene with Multiple Effects on Ripening. Rep Tomato Genet Coop 1968, 18, 36–37. [Google Scholar]
  22. Ito, Y.; Nishizawa-Yokoi, A.; Endo, M.; Mikami, M.; Shima, Y.; Nakamura, N.; Kotake-Nara, E.; Kawasaki, S.; Toki, S. Re-Evaluation of the Rin Mutation and the Role of RIN in the Induction of Tomato Ripening. Nat. Plants 2017, 3, 866–874. [Google Scholar] [CrossRef]
  23. Gao, Y.; Wei, W.; Fan, Z.; Zhao, X.; Zhang, Y.; Jing, Y.; Zhu, B.; Zhu, H.; Shan, W.; Chen, J.; et al. Re-Evaluation of the nor Mutation and the Role of the NAC-NOR Transcription Factor in Tomato Fruit Ripening. J. Exp. Bot. 2020, 71, 3560–3574. [Google Scholar] [CrossRef]
  24. Zhong, S.; Fei, Z.; Chen, Y.-R.; Zheng, Y.; Huang, M.; Vrebalov, J.; McQuinn, R.; Gapper, N.; Liu, B.; Xiang, J.; et al. Single-Base Resolution Methylomes of Tomato Fruit Development Reveal Epigenome Modifications Associated with Ripening. Nat. Biotechnol. 2013, 31, 154–159. [Google Scholar] [CrossRef]
  25. Gapper, N.E.; McQuinn, R.P.; Giovannoni, J.J. Molecular and Genetic Regulation of Fruit Ripening. Plant Mol. Biol. 2013, 82, 575–591. [Google Scholar] [CrossRef]
  26. Janson, C.H. Adaptation of Fruit Morphology to Dispersal Agents in a Neotropical Forest. Science 1983, 219, 187–189. [Google Scholar] [CrossRef]
  27. Liu, M.; Pirrello, J.; Chervin, C.; Roustan, J.-P.; Bouzayen, M. Ethylene Control of Fruit Ripening: Revisiting the Complex Network of Transcriptional Regulation. Plant Physiol. 2015, 169, 2380–2390. [Google Scholar] [CrossRef]
  28. Hurr, B.M.; Huber, D.J.; Lee, J.H. Differential Responses in Color Changes and Softening OfFlorida 47’Tomato Fruit Treated at Green and Advanced Ripening Stages with the Ethylene Antagonist 1-Methylcyclopropene. HortTechnology 2005, 15, 617–622. [Google Scholar] [CrossRef]
  29. Hu, K.-D.; Zhang, X.-Y.; Wang, S.-S.; Tang, J.; Yang, F.; Huang, Z.-Q.; Deng, J.-Y.; Liu, S.-Y.; Zhao, S.-J.; Hu, L.-Y.; et al. Hydrogen Sulfide Inhibits Fruit Softening by Regulating Ethylene Synthesis and Signaling Pathway in Tomato (Solanum lycopersicum). HortScience 2019, 54, 1824–1830. [Google Scholar] [CrossRef]
  30. Peralta, I.E.; Knapp, S.; Spooner, D.M. Nomenclature for Wild and Cultivated Tomatoes. Tomato Genet. Coop. Rep. 2006, 56, 6–12. [Google Scholar]
  31. Colanero, S.; Tagliani, A.; Perata, P.; Gonzali, S. Alternative Splicing in the Anthocyanin Fruit Gene Encoding an R2R3 MYB Transcription Factor Affects Anthocyanin Biosynthesis in Tomato Fruits. Plant Commun. 2020, 1, 100006. [Google Scholar] [CrossRef] [PubMed]
  32. Tomato Genome Consortium. The Tomato Genome Sequence Provides Insights into Fleshy Fruit Evolution. Nature 2012, 485, 635–641. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Cara, B.; Giovannoni, J.J. Molecular Biology of Ethylene during Tomato Fruit Development and Maturation. Plant Sci. 2008, 175, 106–113. [Google Scholar] [CrossRef]
  34. Tatsuki, M. Ethylene Biosynthesis and Perception in Fruit. J. Jpn. Soc. Hortic. Sci. 2010, 79, 315–326. [Google Scholar] [CrossRef]
  35. Boter, M.; Ruíz-Rivero, O.; Abdeen, A.; Prat, S. Conserved MYC Transcription Factors Play a Key Role in Jasmonate Signaling Both in Tomato and Arabidopsis. Genes Dev. 2004, 18, 1577–1591. [Google Scholar] [CrossRef]
  36. Tuteja, N. Abscisic Acid and Abiotic Stress Signaling. Plant Signal. Behav. 2007, 2, 135–138. [Google Scholar] [CrossRef]
  37. Cao, H.; Chen, J.; Yue, M.; Xu, C.; Jian, W.; Liu, Y.; Song, B.; Gao, Y.; Cheng, Y.; Li, Z. Tomato Transcriptional Repressor MYB70 Directly Regulates Ethylene-Dependent Fruit Ripening. Plant J. 2020, 104, 1568–1581. [Google Scholar] [CrossRef]
  38. Barry, C.S.; Llop-Tous, M.I.; Grierson, D. The Regulation of 1-Aminocyclopropane-1-Carboxylic Acid Synthase Gene Expression during the Transition from System-1 to System-2 Ethylene Synthesis in Tomato. Plant Physiol. 2000, 123, 979–986. [Google Scholar] [CrossRef]
  39. Chen, C.; Chen, H.; Zhang, Y.; Thomas, H.R.; Frank, M.H.; He, Y.; Xia, R. TBtools: An Integrative Toolkit Developed for Interactive Analyses of Big Biological Data. Mol. Plant 2020, 13, 1194–1202. [Google Scholar] [CrossRef]
  40. Livak, K.J.; Schmittgen, T.D. Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2ΔΔCT Method. Methods 2001, 25, 402–408. [Google Scholar] [CrossRef]
  41. Takayama, M.; Koike, S.; Kusano, M.; Matsukura, C.; Saito, K.; Ariizumi, T.; Ezura, H. Tomato Glutamate Decarboxylase Genes SlGAD2 and SlGAD3 Play Key Roles in Regulating γ-Aminobutyric Acid Levels in Tomato (Solanum Lycopersicum). Plant Cell Physiol. 2015, 56, 1533–1545. [Google Scholar] [CrossRef]
  42. Shinozaki, Y.; Hao, S.; Kojima, M.; Sakakibara, H.; Ozeki-Iida, Y.; Zheng, Y.; Fei, Z.; Zhong, S.; Giovannoni, J.J.; Rose, J.K.; et al. Ethylene Suppresses Tomato (Solanum Lycopersicum) Fruit Set through Modification of Gibberellin Metabolism. Plant J. 2015, 83, 237–251. [Google Scholar] [CrossRef]
  43. Mantelin, S.; Bhattarai, K.K.; Jhaveri, T.Z.; Kaloshian, I. Mi-1-Mediated Resistance to Meloidogyne Incognita in Tomato May Not Rely on Ethylene but Hormone Perception through ETR3 Participates in Limiting Nematode Infection in a Susceptible Host. PLoS ONE 2013, 8, e63281. [Google Scholar] [CrossRef]
  44. Wang, N.; Chen, H.; Nonaka, S.; Sato-Izawa, K.; Kusano, M.; Ezura, H. Ethylene Biosynthesis Controlled by NON-RIPENING: A Regulatory Conflict between Wounding and Ripening. Plant Physiol. Biochem. 2018, 132, 720–726. [Google Scholar] [CrossRef]
  45. Efremov, G.I.; Slugina, M.A.; Shchennikova, A.V.; Kochieva, E.Z. Differential Regulation of Phytoene Synthase Psy1 during Fruit Carotenogenesis in Cultivated and Wild Tomato Species (Solanum Section Lycopersicon). Plants 2020, 9, 1169. [Google Scholar] [CrossRef]
Figure 1. Comparison of fruit ripening and ethylene production among tomato species and cultivars. Changes in skin color (A) and quantification of ethylene production during fruit development (B). Scale bar = 1 cm. DAP: days after pollination. Fruits were observed from 20 to 55 DAP for each species and cultivar. Error bars in (B) represent the standard deviation (SD) of five biological replicates.
Figure 1. Comparison of fruit ripening and ethylene production among tomato species and cultivars. Changes in skin color (A) and quantification of ethylene production during fruit development (B). Scale bar = 1 cm. DAP: days after pollination. Fruits were observed from 20 to 55 DAP for each species and cultivar. Error bars in (B) represent the standard deviation (SD) of five biological replicates.
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Figure 2. Quantitative RT-PCR analysis of ethylene biosynthetic genes and carotenoid biosynthetic genes. Relative quantification revealing dynamic change in gene expression of LEACS genes (A), LEACO genes (B), carotenoid biosynthetic genes (C), and the key ripening transcription factors (D). The white bars indicate the relative expression levels of genes at the immature stage. Gray bars indicate relative gene expression levels at the start of fruit ripening, and black bars correspond to relative gene expression levels at the over-ripening stage. The gene expression level of S. lycopersicum cv. Ailsa Craig at the ripening stage was selected as a reference sample. Significant differences (p < 0.05) are indicated by lowercase letters. ACS, 1-aminocyclopropane-1-carboxylic acid (ACC) synthase gene; ACO, ACC oxidase genes; PSY1, Phytoene synthase 1; ZDS, z-carotene desaturase; LCYE, lycopene ε-cyclase; LCYB, lycopene β-cyclase; RIN, Ripening-Inhibitor; NOR, Non-Ripening.
Figure 2. Quantitative RT-PCR analysis of ethylene biosynthetic genes and carotenoid biosynthetic genes. Relative quantification revealing dynamic change in gene expression of LEACS genes (A), LEACO genes (B), carotenoid biosynthetic genes (C), and the key ripening transcription factors (D). The white bars indicate the relative expression levels of genes at the immature stage. Gray bars indicate relative gene expression levels at the start of fruit ripening, and black bars correspond to relative gene expression levels at the over-ripening stage. The gene expression level of S. lycopersicum cv. Ailsa Craig at the ripening stage was selected as a reference sample. Significant differences (p < 0.05) are indicated by lowercase letters. ACS, 1-aminocyclopropane-1-carboxylic acid (ACC) synthase gene; ACO, ACC oxidase genes; PSY1, Phytoene synthase 1; ZDS, z-carotene desaturase; LCYE, lycopene ε-cyclase; LCYB, lycopene β-cyclase; RIN, Ripening-Inhibitor; NOR, Non-Ripening.
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Figure 3. In silico analysis of cis-regulatory elements. Regulatory elements are found at upstream sequences of ethylene biosynthetic genes (A) and carotenoid biosynthetic genes (B). Insertions and deletions at the regulatory sequences are connected by black lines. Yellow bars, ABA-responsive element (ABRE); green bars, ethylene-responsive element (ERE); blue bars, MYB protein-binding domain (MYB); red bars, MYC family protein-binding domain (MYC); gray bars, WRKY TF-binding domain (W-box). LY, S. lycopersicum; CER, S. lycopersicum var. cerasiforme; PIM, S. pimpinellifolium; PEN, S. pennellii.
Figure 3. In silico analysis of cis-regulatory elements. Regulatory elements are found at upstream sequences of ethylene biosynthetic genes (A) and carotenoid biosynthetic genes (B). Insertions and deletions at the regulatory sequences are connected by black lines. Yellow bars, ABA-responsive element (ABRE); green bars, ethylene-responsive element (ERE); blue bars, MYB protein-binding domain (MYB); red bars, MYC family protein-binding domain (MYC); gray bars, WRKY TF-binding domain (W-box). LY, S. lycopersicum; CER, S. lycopersicum var. cerasiforme; PIM, S. pimpinellifolium; PEN, S. pennellii.
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Figure 4. Responsiveness of tomato species to exogenous ethylene. Triple response assay of seedlings (A,B) and gene expression in fruits exposed to exogenous ethylene (C,D). Gray bars represent controls, while black bars indicate ethylene-treated samples. Ailsa Craig, S. lycopersicum cv. Ailsa Craig; PIM, S. pimpinellifolium; PEN, S. pennellii; PER, S. peruvianum. Asterisks indicate significant differences as determined by the t-test (* p < 0.05, ** p < 0.01).
Figure 4. Responsiveness of tomato species to exogenous ethylene. Triple response assay of seedlings (A,B) and gene expression in fruits exposed to exogenous ethylene (C,D). Gray bars represent controls, while black bars indicate ethylene-treated samples. Ailsa Craig, S. lycopersicum cv. Ailsa Craig; PIM, S. pimpinellifolium; PEN, S. pennellii; PER, S. peruvianum. Asterisks indicate significant differences as determined by the t-test (* p < 0.05, ** p < 0.01).
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Figure 5. Analysis of DNA methylation by qAMP in upstream regions of NOR. Levels of methylation change over time. DAP: days after pollination.
Figure 5. Analysis of DNA methylation by qAMP in upstream regions of NOR. Levels of methylation change over time. DAP: days after pollination.
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Figure 6. Current understanding of genetic control of ethylene biosynthesis and ethylene-mediated coloration in tomato. Bold lines and thin lines indicate the strength in corresponding activity. Characters in black indicate highly accumulated intermediates or enzymes, and characters in gray indicate relatively lowly accumulated intermediates or enzymes. * Significant response in S. lycopersicum cv. Ailsa Craig; ※ significant response in S. pennellii; # significant response in S. peruvianum.
Figure 6. Current understanding of genetic control of ethylene biosynthesis and ethylene-mediated coloration in tomato. Bold lines and thin lines indicate the strength in corresponding activity. Characters in black indicate highly accumulated intermediates or enzymes, and characters in gray indicate relatively lowly accumulated intermediates or enzymes. * Significant response in S. lycopersicum cv. Ailsa Craig; ※ significant response in S. pennellii; # significant response in S. peruvianum.
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Chen, H.; Bai, S.; Kusano, M.; Ezura, H.; Wang, N. Increased ACS Enzyme Dosage Causes Initiation of Climacteric Ethylene Production in Tomato. Int. J. Mol. Sci. 2022, 23, 10788. https://doi.org/10.3390/ijms231810788

AMA Style

Chen H, Bai S, Kusano M, Ezura H, Wang N. Increased ACS Enzyme Dosage Causes Initiation of Climacteric Ethylene Production in Tomato. International Journal of Molecular Sciences. 2022; 23(18):10788. https://doi.org/10.3390/ijms231810788

Chicago/Turabian Style

Chen, Haoting, Songling Bai, Miyako Kusano, Hiroshi Ezura, and Ning Wang. 2022. "Increased ACS Enzyme Dosage Causes Initiation of Climacteric Ethylene Production in Tomato" International Journal of Molecular Sciences 23, no. 18: 10788. https://doi.org/10.3390/ijms231810788

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Chen, H., Bai, S., Kusano, M., Ezura, H., & Wang, N. (2022). Increased ACS Enzyme Dosage Causes Initiation of Climacteric Ethylene Production in Tomato. International Journal of Molecular Sciences, 23(18), 10788. https://doi.org/10.3390/ijms231810788

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