Journal of Botany

Journal of Botany / 2011 / Article

Review Article | Open Access

Volume 2011 |Article ID 289859 | 13 pages | https://doi.org/10.1155/2011/289859

Metabolic and Molecular Events Occurring during Chromoplast Biogenesis

Academic Editor: William K. Smith
Received13 Jan 2011
Accepted03 Jun 2011
Published15 Sep 2011

Abstract

Chromoplasts are nonphotosynthetic plastids that accumulate carotenoids. They derive from other plastid forms, mostly chloroplasts. The biochemical events responsible for the interconversion of one plastid form into another are poorly documented. However, thanks to transcriptomics and proteomics approaches, novel information is now available. Data of proteomic and biochemical analysis revealed the importance of lipid metabolism and carotenoids biosynthetic activities. The loss of photosynthetic activity was associated with the absence of the chlorophyll biosynthesis branch and the presence of proteins involved in chlorophyll degradation. Surprisingly, the entire set of Calvin cycle and of the oxidative pentose phosphate pathway persisted after the transition from chloroplast to chromoplast. The role of plastoglobules in the formation and organisation of carotenoid-containing structures and that of the Or gene in the control of chromoplastogenesis are reviewed. Finally, using transcriptomic data, an overview is given the expression pattern of a number of genes encoding plastid-located proteins during tomato fruit ripening.

1. Introduction

Chromoplasts are nonphotosynthetic plastids that accumulate carotenoids and give a bright colour to plant organs such as fruit, flowers, roots, and tubers. They derive from chloroplasts such as in ripening fruit [1], but they may also arise from proplastids such as in carrot roots [2] or from amyloplasts such as in saffron flowers [3] or tobacco floral nectaries [4]. Chromoplasts are variable in terms of morphology of the carotenoid-accumulating structures and the type of carotenoids [5, 6]. For instance, in tomato, lycopene is the major carotenoid, and it accumulates in membrane-shaped structures [7] while in red pepper beta-carotene is prominent and accumulates mostly in large globules [8]. Reviews specifically dedicated to the biogenesis of chromoplasts have been published [911]. Some information can also be found in papers dedicated to plastid differentiation in general [12, 13]. Thanks to transcriptomics and proteomics approaches, novel information is now available on the biochemical and molecular aspects of chromoplasts differentiation [1416]. The present paper will review these novel data and provide a recent view of the metabolic and molecular events occurring during the biogenesis of chromoplasts and conferring specificities to the organelle. Focus will be made on the chloroplast to chromoplast transition.

2. Chromoplast Differentiation Is Associated with Important Structural, Metabolic, and Molecular Reorientations

Important structural changes occur during the chloroplast to chromoplast transition, thylakoid disintegration being the most significant (Figure 1). Early microscopic observations have shown that plastoglobuli increase in size and number during the chloroplast-chromoplast transition [7] and that the internal membrane system is profoundly affected at the level of the grana and intergrana thylakoids [17]. Stromules (stroma-filled tubules) that are dynamic extensions of the plastid envelope allowing communication between plastids and other cell compartments like the nucleus [18] are also affected during chromoplastogenesis. A large number of long stromules can be found in mature chromoplasts contrasting with the few small stromules of the chloroplasts in green fruit [19]. It can therefore be assumed that the exchange of metabolites between the network of plastids and between the plastids and the cytosol is increased in the chromoplast as compared to the chloroplast. However, the most visible structural change is the disruption of the thylakoid grana, the disappearance of chlorophyll, and the biogenesis of carotenoid-containing bodies. Associated with the structural changes, the toc/tic transmembrane transport machinery is disintegrated [16, 20]. The noncanonical signal peptide transport [21] and intracellular vesicular transport [22, 23] may represent the most active form of trans-membrane transport into the chromoplast as compared to the chloroplast. Proteins involved in vesicular transport were detected in the tomato chromoplastic proteome [16].

One of the most visible metabolic changes occurring during the chloroplast to chromoplast transition is the loss of chlorophyll and the accumulation of carotenoids [24]. A spectral confocal microscopy analysis of carotenoids and chlorophylls has been carried out during the chloroplast to chromoplast transition in tomato fruit, including a time-lapse recording on intact live tissue [25]. Details of the early steps of tomato chromoplast biogenesis from chloroplasts are provided at the cellular level that show the formation of intermediate plastids containing both carotenoids and chlorophylls. This study also demonstrated that the chloroplast to chromoplast transition was synchronous for all plastids of a single cell and that all chromoplasts derived from preexisting chloroplasts.

The photosynthetic machinery is strongly disrupted and a reduction in the levels of proteins and mRNAs associated with photosynthesis was observed [26]. Also the decrease in photosynthetic capacity during the later stages of tomato fruit development was confirmed by transcriptomic data [27]. However, part of the machinery persist in the chromoplast. It has been suggested that it participates in the production of C4 acids, in particular malate a key substrate for respiration during fruit ripening [28]. In the tomato chromoplast proteome, all proteins of the chlorophyll biosynthesis branch are lacking [16]. In the early stages of tomato fruit ripening, the fruits are green and the plastids contain low levels of carotenoids that are essentially the same as in green leaves, that is, mainly β-carotene, lutein, and violaxanthin. At the “breaker” stage of ripening, lycopene begins to accumulate and its concentration increases 500-fold in ripe fruits, reaching ca. 70 mg/g fresh weight [24]. During the ripening of tomato fruit, an upregulation of the transcription of Psy and Pds, which encode phytoene synthase and phytoene desaturase, respectively, was reported [29]. One of the main components of the carotenoid-protein complex, a chromoplast-specific 35-kD protein (chrC), has been purified and characterized in Cucumis sativus corollas. It showed increasing steady-state level in parallel with flower development and carotenoid accumulation, with a maximum in mature flowers [30]. In tomato, concomitantly with increased biosynthesis of lycopene, the processes for splitting into β and γ carotene were absent [16]. The mRNAs of CrtL-b and CrtL-e were strongly downregulated during fruit ripening [29]. They encode lycopene β-cyclase and ε-cyclase, enzymes involved in the cyclization of lycopene leading to the formation of β and δ carotene, respectively. In these conditions, the low rate of cyclization and splitting contributes to the accumulation of lycopene in ripe tomato fruit.

In terms of reactive oxygen species, antioxidant enzymes are upregulated during chromoplast development, and lipids, rather than proteins, seem to be a target for oxidation. In the chromoplasts, an upregulation in the activity of superoxide dismutase and of components of the ascorbate-glutathione cycle was observed [31].

The plastid-to-nucleus signaling also undergoes important changes. In the chromoplast, the main proteins involved in the synthesis of Mg-protoporphyrin IX, a molecule supposed to play an important role in retrograde signaling [32] is absent, but other mechanisms such as hexokinase 1 or calcium signaling were present [16]. The plastid-nucleus communication is still an open subject with many still unanswered questions.

3. A Number of Metabolic Pathways Are Conserved during Chromoplast Differentiation

The comparison of data arising from proteomics of the chloroplast [33] and of the chromoplast [16] as well as biochemical analysis of enzyme activities suggest that several pathways are conserved during the transition from chloroplast to chromoplast. Such is the case for (i) the Calvin cycle which generates sugars from CO2, (ii) the oxidative pentose phosphate pathway (OxPPP) which utilizes the 6 carbons of glucose to generate 5 carbon sugars and reducing equivalents, and (iii) many aspects of lipid metabolism (Figure 2). Activities of enzymes of the Calvin cycle have been measured in plastids isolated from sweet pepper. They may even be higher in chromoplasts than in chloroplasts [34] In ripening tomato fruits, several enzymes of the Calvin cycle (hexokinase, fructokinase, phosphoglucoisomerase, pyrophosphate-dependent phosphofructokinase, triose phosphate isomerase, glyceraldehyde 3-phosphate dehydrogenase, phosphoglycerate kinase, and glucose 6-phosphate dehydrogenase) are active [35]. The activity of glucose 6-phosphate dehydrogenase (G6PDH), a key component of the OxPPP, was higher in fully ripe tomato fruit chromoplasts than in leaves or green fruits [36]. Also, a functional oxidative OxPPP has been encountered in isolated buttercup chromoplasts [37]. Proteomic analysis have demonstrated that an almost complete set of proteins involved in the OxPPP are present in isolated tomato fruit chromoplasts (Figure 2). The persistence of the Calvin cycle and the OxPPP cannot be related to photosynthesis since the photosynthetic system is disrupted. In nonphotosynthetic plastids, the Calvin cycle could provide reductants and also precursors of nucleotides and aromatic aminoacids to allow the OxPPP cycle to function optimally [16].

Starch transiently accumulates in young tomato fruit and undergoes almost complete degradation by maturity. In fact, starch accumulation results from an unbalance between synthesis and degradation. Enzymes capable of degrading starch have been detected in the plastids of tomato fruit. In addition, tomato fruit can synthesize starch during the period of net starch breakdown, illustrating that these two mechanisms can coexist [38]. As indicated in Figure 3, proteins for starch synthesis have been encountered in the tomato chromoplast (ADP-glucose pyrophosphorylase, starch synthase, and starch branching enzyme). In addition, the system for providing neutral sugars to the starch biosynthesis pathway is complete including the glucose-6P-translocator which imports sugars from the cytosol. The presence of active import of glucose-6P, but not glucose-1P, had been demonstrated in buttercup chromoplasts [37]. Although some starch granules may be present in ripe tomatoes, the amount of starch is strongly reduced [39]. The most probable explanation is that starch undergoes rapid turnover with intense degradation. This assumption is supported by the presence in the tomato chromoplast of most of the proteins involved in starch degradation (Figure 3). Particularly interesting is the presence of one glucan-water dikinase (GWD), one phospho-glucan-dikinase (PWD), and one phospho-glucan-phosphatase (PGP) that facilitate the action of β-amylases [40]. Mutants of these proteins, named starch excess (SEX1 corresponding to GWD and SEX4 to PGP), accumulate large amounts of starch [40]. In agreement with the above-mentioned hypothesis, high activity of β-amylase has been found during apple and pear fruit ripening at a time where starch has disappeared [41]. The presence of a glucose translocator for the export of sugars generated by starch degradation represents another support to the functionality of the starch metabolism pathways in chromoplasts. In olive fruit, a high expression of a glucose transporter gene was observed at full maturity when the chromoplasts were devoid of starch [42]. Nevertheless, the enzymatic activity of all of the proteins remains to be demonstrated inasmuch as posttranslational regulation of enzymes of starch metabolism has been reported [43] including protein phosphorylation [44]. Interestingly, orthologs of the 14-3-3 proteins of the μ family of Arabidopsis involved in the regulation of starch accumulation [45] are present in the tomato chromoplastic proteome (Figure 3). The 14-3-3 proteins participate in the phosphorylation-mediated regulatory functions in plants.

In chloroplasts, thylakoid membranes, as well as envelope membranes, are rich in galactolipids and sulfolipids [46]. Lipid metabolism is also highly active in the chromoplasts. Despite thylakoid disassembly, new membranes are synthesized such as those participating in the formation of carotenoid storage structures. These newly synthesized membranes are not derived from the thylakoids but rather from vesicles generated from the inner membrane of the plastid [47]. Key proteins for the synthesis of phospholipids, glycolipids, and sterols were identified [16] along with some proteins involved in the lipoxygenase (LOX) pathway. They have been described in the chloroplast, and they lead to the formation oxylipins, which are important compounds for plant defense responses [48]. In the tomato chromoplast, all proteins potentially involved in the LOX pathway leading to the generation of aroma volatiles were found [16].

The shikimate pathway, which is present in microorganisms and plants and never in animals, is a branch point between the metabolism of carbohydrates and aromatic compounds. It leads to the biosynthetic of the aromatic amino acids tyrosine, tryptophan, and phenylalanine [49]. The presence of an active shikimate pathway has been demonstrated in chromoplasts isolated from wild buttercup petals by measuring the activity of the shikimate oxidoreductase [50], and a number of proteins involved in the shikimate pathway have been encountered in the tomato chromoplast proteome [16]. The aromatic amino acids derived from the shikimate pathway are the precursors of a number of important secondary metabolites. Tyrosine is the precursor of tocopherols and tocotrienols. Tryptophane is involved in the synthesis of indole alkaloids which are essential for the generation of some glucosinolates, terpenoids, and tryptamine derivatives [50]. Phenylalanine is the precursor of several classes of flavonoids, including anthocyanins. It is also a precursor for the biosynthesis of volatile compounds which are important for fruit flavor and flower scent, eugenol, 2-phenylacetaldehyde and, 2-phenylethanol [51, 52]. In tomato fruit, for instance, 2-phenylacetaldehyde and 2-phenylethanol are generated from phenylalanine by an aromatic amino acid decarboxylase and a phenylacetaldehyde reductase, respectively [53, 54]. Nevertheless, there is no indication that the synthesis of the secondary metabolites derived from the shikimate pathway takes place in the chromoplast.

During fruit ripening, an increased synthesis of α-tocopherol was observed [55]. The biosynthesis of α-tocopherol was localized in the envelope membranes of the Capsicum annum [56], and the almost complete set of proteins of the pathway were present in the tomato chromoplast [16]. The accumulation of α-tocopherol, by protecting membrane lipids against oxidation, may contribute to delaying senescence [57].

4. Plastoglobuli, Plastoglobules, and the Chloroplast-to-Chromoplast Transition

Plastoglobules are lipoprotein particles present in chloroplasts (Figure 1) and other plastids. They have been recently recognized as participating in some metabolic pathways [58]. For instance, plastoglobules accumulate tocopherols and harbor a tocopherol cyclase, an enzyme catalyzing the conversion of 2,3-dimethyl-5-phytyl-1,4-hydroquinol to γ-tocopherol [59]. Plastoglobuli also accumulate carotenoids as crystals or as long tubules named fibrils [60, 61]. Part of the enzymes involved in the carotenoid biosynthesis pathway (ζ-carotene desaturase, lycopene β cyclase, and two β-carotene β hydroxylases) were found in the plastoglobuli [62].

Plastoglobules arise from a blistering of the stroma-side leaflet of the thylakoid membrane [63], and they are physically attached to it [45]. During the chloroplast-to-chromoplast transition, a change in the size and number of plastoglobuli was observed (Figure 1). They are larger and more numerous than in the chloroplast [7]. Plastoglobules are the predominant proteins of plastoglobules. Several types of plastoglobules have been described: fibrillin, plastid lipid-associated proteins (PAP) and carotenoid-associated protein (CHRC). All plastoglobules participate in the accumulation of carotenoids in the plastoglobule structure. Carotenoids accumulate as fibrils to form supramolecular lipoprotein structures. A model for fibril assembly has been proposed in which the core is occupied by carotenoids that interact with polar galacto- and phospho-lipids. Fibrillin molecules are located at the periphery in contact with the plastid stroma [64]. In tomato, the overexpression of a pepper fibrillin caused an increase in carotenoid and carotenoid-derived flavour volatiles [47] along with a delayed loss of thylakoids during the chloroplast-to-chromoplast transition. In fibrillin overexpressing tomato, the plastids displayed a typical chromoplastic zone contiguous with a preserved chloroplastic zone. PAP is another major protein of plastoglobules that also participates in the sequestration of carotenoids [64, 65]. As for CHRC, its downregulation resulted in a 30% reduction of carotenoids in tomato flowers [66]. Plastoglobuli are, therefore, complex assemblies that play a key role in carotenoid metabolism and greatly influence the evolution of the internal structure of the plastid during the chloroplast to chromoplast transition.

5. A key Player in Chromoplast Differentiation: The Or Gene

The Or gene was discovered in cauliflower where the dominant mutation Or conferred an orange pigmentation with the accumulation of β-carotene mostly in the inflorescence [67]. The Or gene was isolated by positional cloning [68]. It is localized in the nuclear genome and is highly conserved among divergent plant species [69]. The Or protein corresponds to plastid-targeted a DnaJ-like co-chaperone with a cysteine-rich domain lacking the J-domain [68]. DnaJ proteins are known for interacting with Hsp70 chaperones to perform protein folding, assembly, disassembly, and translocation. The Or mutation is not a loss of function mutation as indicated by the absence of phenotype upon RNAi silencing. It is probably a dominant-negative mutation affecting the interaction with Hsp70 chaperones [70]. The OR mutants displayed an arrest in plastid division so that a limited number of chromoplasts (one or two) were present in the affected cells [71]. Potato tubers over-expressing the Or gene accumulate carotenoids [69]. In the OR mutant, the expression of carotenoid biosynthetic genes was unaffected and chromoplasts differentiated normally with membranous inclusions of carotenoids similar to those of carrot roots. It is concluded that the Or gene is not involved in carotenoid biosynthesis but rather creates a metabolic sink for carotenoid accumulation through inducing the formation of chromoplasts [72].

6. Transcriptional and Translational Activity in the Plastid Undergo Subtle Changes during Chromoplast Biogenesis

Most proteins present in the plastid are encoded by nuclear genes. The plastid genome encodes around 84 proteins [60]. Restriction enzyme analysis between chloroplasts of leaves and chromoplasts of tomato fruit indicates the absence of rearrangements, losses, or gains in the chromoplastic DNA [61]. During chromoplast differentiation, the global transcriptional activity is stable, except for a limited number of genes such as accD, encoding a subunit of the acetyl-CoA carboxylase involved in fatty acid biosynthesis, trnA (tRNA-ALA), and rpoC2 (RNA polymerase subunit) [15]. Polysome formation within the plastids declined during ripening suggesting that, while the overall RNA levels remain largely constant, plastid translation is gradually downregulated during chloroplast-to-chromoplast differentiation. This trend was particularly pronounced for the photosynthesis gene group. A single exception was observed; the translation of accD stayed high and even increased at the onset of ripening [15].

Specific studies of few plastid-localized genes have been carried out. Genes involved in photosynthesis were, as expected, downregulated during chromoplast formation [25]. However, an upregulation of the large subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase and the 32 kD photosystem II quinone binding protein genes has been observed in the chromoplasts of squash fruits (Cucurbitae pepo) [62]. A possible explanation would be that these genes could be regulated independently from the plastid differentiation processes. Genes involved in carotenoid biosynthesis such as the lycopene β-cyclase (CYCB) were upregulated during chromoplast formation in many plants including the wild species of tomato Solanum habrochaites [63].

7. Changes in Gene Expression during Chromoplast Differentiation in Ripening Tomato

The availability of proteomic data of tomato chromoplasts [16] and expression data of a wide range of tomato genes (The Tomato Expression Database: http://ted.bti.cornell.edu) [73] allowed classifying genes encoding chromoplastic proteins according to their expression pattern (Table 1). Among the 87 unigenes whose encoded proteins are located in the chromoplast, the biggest functional class corresponds to genes involved in photosynthesis. Most of them (18 out of 24) are either permanently (Table 1(c)) or transiently (Table 1(e)) downregulated at the breaker stage. This is in agreement with the dramatic decrease in the photosynthetic activity of the chromoplast. Three of them show constant expression (Table 1(a): U313693 ATP synthase delta chain; U312985 glycine cleavage system H protein; U312532 oxygen-evolving enhancer protein) and three upregulation (Table 1(b): U312690 plastocyanin; U312593 chlorophyll A-B binding protein 4; U314994 phosphoglycolate phosphatase). In the case of Calvin cycle, 5 out of 12 genes (U312344 fructose-bisphosphate aldolase; U312608 fructose-bisphosphate aldolase; U312609 fructose-bisphosphate aldolase; U314254 ribulose bisphosphate carboxylase small chain 1A; U314701 ribulose bisphosphate carboxylase small chain 3B) had a constant decrease during chromoplast differentiation (Table 1(c)). In tomato fruit, the activity of the ribulose-1,5-bisphosphate carboxylase/oxygenase had a constant decrease during fruit ripening [74], which is in line with the transcriptomic and proteomic data. The genes encoding fructose-bisphosphate aldolase isoforms presented different expression profiles being either up- (U314788) or down- (U312344) regulated during tomato fruit ripening. An increase in overall transcript levels for the fructose-1,6-bisphosphate aldolase has been described during ripening [75]. The importance of transcripts and enzyme activity of the various isoforms are unknown. The remaining genes involved in the Calvin cycle showed either increased (Table 1(b); U312802 glyceraldehyde-3-phosphate dehydrogenase B; U312538 RuBisCO subunit binding-protein) or unchanged expression (Table 1(a); U316424 fructose-1,6-bisphosphatase; U312544 ribulose bisphosphate carboxylase/-oxygenase activase). Three genes coding for the OxPPP were found: two of them exhibited a transient increase in expression at the breaker stage (Table 1(d): U315528 ribose 5-phosphate isomerase-related; U332994 6-phosphogluconate dehydrogenase family protein) and one a transient decrease (Table 1(e): U315064 transaldolase). The 3 genes involved in tetrapyrrole biosynthesis are not part of the chlorophyll synthesis branch and all of them had an increased expression (Table 1(b): U315993 coproporphyrinogen III oxidase; U315267 uroporphyrinogen decarboxylase; U315567 hydroxymethylbilane synthase), suggesting that the synthesis of tetrapyrroles continues during the transition from chloroplast to chromoplast. As expected, most of the genes (5 out of 6) coding for enzymes involved in carotenoid synthesis showed continuous (Table 1(b): U314429 phytoene synthase; U315069 isopentenyl-diphosphate delta-isomerase II; U316915 geranylgeranyl pyrophosphate synthase; U318137 phytoene dehydrogenase) or transient (Table 1(d): U313450 geranylgeranyl reductase) upregulation. The precursors for carotenoid production are synthesized through the methylerythritol phosphate (MEP) pathway. The gene encoding hydroxymethylbutenyl 4-diphosphate synthase (HDS) (U314139) downstream in the pathway has stable expression (Table 1(a)). This is consistent with previous studies that showed that there were no significant changes in HDS gene expression during tomato fruit ripening [76].


289859.table.001aPhotosystem: U313693 ATP synthase delta chain; U312985 glycine cleavage system H protein; U312532 oxygen-evolving enhancer protein.
Calvin cycle: U316424 fructose-1, 6-bisphosphatase; U312544 ribulose bisphosphate carboxylase/-oxygenase activase.
Secondary metabolism: U314139 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate synthase.

289859.table.001bPhotosystem: U312690 plastocyanin; U312593 chlorophyll A-B binding protein 4; U314994 phosphoglycolate phosphatase.
Calvin cycle: U314788 fructose-bisphosphate aldolase; U312802 glyceraldehyde-3-phosphate dehydrogenase B; U312538 RuBisCO subunit binding-protein.
Redox: U314092 L-ascorbate peroxidase; U319145 thioredoxin family protein; U320487 monodehydroascorbate reductase.
Amino acid metabolism: U321505 anthranilate synthase; U317466 3-phosphoshikimate 1-Carboxyvinyltransferase; U317564 tryptophan synthase.
Lipid metabolism: U315474 3-oxoacyl-(acyl-carrier-protein) synthase I; U315475 3-oxoacyl-(acyl-carrier-protein) synthase I; U313753 pyruvate dehydrogenase E1 component. Major CHO metabolism: U315116 starch excess protein (SEX1); U333011 isoamylase, putative; U312423 1, 4-alpha-glucan branching enzyme; U312427 1, 4-alpha-glucan branching enzyme.
Secondary metabolism: U314429 phytoene synthase; U315069 isopentenyl-diphosphate delta-isomerase II; U316915 geranylgeranyl pyrophosphate synthase; U318137 phytoene dehydrogenase.
Tetrapyrrole synthesis: U315993 coproporphyrinogen III oxidase; U315267 uroporphyrinogen decarboxylase; U315567 hydroxymethylbilane synthase.
Mitochondrial electron transport: U316255 NADH-ubiquinone oxidoreductase.
Fermentation, ADH: U314358 alcohol dehydrogenase (ADH).
Miscellaneous, cytochrome P450: U313813 NADPH-cytochrome p450 reductase.
S-assimilation. APS: U313496 sulfate adenylyltransferase 1.
Development unspecified: U316277 senescence-associated protein (SEN1).
Cell organisation: U313480 plastid lipid-associated protein PAP, putative.
Hormone metabolism: U315633 lipoxygenase.
N-metabolism ammonia metabolism: U323261 glutamate synthase (GLU1).
Stress abiotic heat: U315717 HS protein 70.
Not assigned, No ontology: U317890 hydrolase, alpha/beta fold family protein.

289859.table.001cPhotosystem: U312531 oxygen-evolving enhancer protein; U313447 photosystem I reaction center subunit IV; U313204 chlorophyll A-B binding protein 2; U313245 ATP synthase gamma chain 1; U312436 chlorophyll A-B binding protein; U313211 chlorophyll A-B binding protein 2; U313212 chlorophyll A-B binding protein 2; U313213 chlorophyll A-B binding protein 2; U312572 photosystem II oxygen-evolving complex 23 (OEC23); U314260 photosystem I reaction center subunit III family protein.
Calvin cycle: U312344 fructose-bisphosphate aldolase; U312608 fructose-bisphosphate aldolase; U312609 fructose-bisphosphate aldolase; U314254 ribulose bisphosphate carboxylase small chain 1A; U314701 ribulose bisphosphate carboxylase small chain 3B.
Lipid metabolism: U319207 phosphatidylglycerol phosphate synthase (PGS1).
Redox: U313537 dehydroascorbate reductase.
Major CHO metabolism: U316416 glucan phosphorylase, putative.
N-metabolism: U314517 glutamine synthetase (GS2).
Amino acid metabolism: U317344 bifunctional aspartate kinase/homoserine dehydrogenase; U320667 cystathionine beta-lyase.

289859.table.001dRedox: U314061 peroxiredoxin Q; U314093 L-ascorbate peroxidase, thylakoid-bound (tAPX); U314923 2-cys peroxiredoxin.
OPP, Nonreductive PP: U315528 ribose 5-phosphate isomerase related; U332994 6-phosphogluconate dehydrogenase family protein; U316131 6-phosphogluconate dehydrogenase NAD-binding domain-containing protein.
Secondary metabolism: U317741 acetyl coenzyme A carboxylase carboxyl transferase alpha subunit family; U313450 geranylgeranyl reductase.
Amino acid metabolism: U317245 tryptophan synthase related.
N-metabolism ammonia metabolism: U317524 ferredoxin-nitrite reductase.
Lipid metabolism: U315697 enoyl-(acyl-carrier protein) reductase (NADH) U321151 lipoxygenase.
Transport metabolite: U312460 triose phosphate/phosphate translocator, putative.
Signalling calcium: U315961 calnexin 1 (CNX1).

289859.table.001ePhotosystem: U312843 chlorophyll A-B binding protein; U312858 cytochrome B6-F complex iron-sulfur subunit; U313214 chlorophyll A-B binding protein 2; U312791 phosphoribulokinase (PRK); U317040 photosystem II reaction center PsbP family protein; U312449 chlorophyll A-B binding protein CP26; U312661 chlorophyll A-B binding protein CP29 (LHCB4); U313789 ATP synthase family.
Calvin cycle: U312461 glyceraldehyde 3-phosphate dehydrogenase A; U312871 oxygen-evolving enhancer protein 3.
Redox: U315728 glutathione peroxidase.
OPP nonreductive PP transaldolase: U315064 transaldolase.
Signaling calcium: U318939 calcium-binding EF hand family protein.
Major CHO metabolism: U313315 beta amylase.

(*) Genes represented in this table are filtered from TED database [64] crossing with the proteins described by Barsan et al. [16]. The expression profiles were clustered with the Bioinformatics tools of the Matlab (MathWorks) software package and further reduced to five representative expression profiles according to their general tendencies represented in the first column. The expression values used in this analysis were taken from experiment E011 from TED database. Relative expression refers to the ratio between the expression values of each ripening point and MG. All data were normalized by the mean and log2 transformed. (a) Genes that remain stable during the ripening, (b) genes that have an increase or (c) a decrease until breaker stage and then reaches a plateau, (d) genes that have a positive or (e) negative transient expression around the breaker stage. (MG, mature green; B-1, 1 d before breaker; B, breaker stage; B + 1, 1 d after breaker; B + 5, 5 d after breaker; B + 10, 10 d after breaker.)

In the case of lipid metabolism, three genes showed increased expression (Table 1(b): U315474 3-oxoacyl-(acyl-carrier-protein) synthase I; U315475 3-oxoacyl-(acyl-carrier-protein) synthase I; U313753 pyruvate dehydrogenase E1 component), and two genes had transient increase (Table 1(d): U315697 enoyl-(acyl-carrier protein) reductase (NADH); U321151 lipoxygenase). Phosphatidylglycerol phosphate synthase showed decreased expression (Table 1(c)). This enzyme is involved in the biosynthesis of phosphatidylglycerol and is considered as playing an important role in the ordered assembly and structural maintenance of the photosynthetic apparatus in thylakoid membranes and in the functioning of the photosystem II [77]. The downregulation of this gene during chromoplast differentiation is consistent with thylakoid disintegration and photosynthesis disappearance.

Four genes of the starch metabolism present upregulation (Table 1(b)). Two of them are part of the starch biosynthesis (U312423 1,4-alpha-glucan branching enzyme; U312427 1, 4-alpha-glucan branching enzyme), and one of them is involved starch degradation U315116 starch excess protein (SEX1). The fourth one, an isoamylase (U333011) can participate either in starch degradation or in starch synthesis, depending on the isoform [78]. The expression of the gene that codes a starch degrading glucan phosphorylase (U316416) decreases, and the expression of another starch degrading gene, beta-amylase (U313315), has a negative transient expression (Table 1(b)). In addition, proteomic studies have shown the presence of two starch excess proteins (SEX1 and 4) that probably contribute to the absence of starch accumulation [16]. Starch is degraded during the chloroplast to chromoplast transition to provide carbon and energy necessary to sustain the metabolic activity during fruit ripening. Several enzymes are responsible for the processes, each one possessing several isoforms with different regulatory mechanisms [78].

Interestingly genes involved in aroma production such as ADH (U314358) or LOXC (U315633) had a constant increase in gene expression (Table 1(b)). This could be related to the increase in aroma production via the LOX pathway.

The microarray data discussed in this section cover a wide range of the tomato transcriptome. However, several isoforms of several genes are not represented in the database, which could explain some contradictory patterns of expression encountered in our analysis. Nevertheless, although not providing a full picture of the molecular events occuring during the chloroplast to chromoplast transition, these data confirm the regulation at the transcriptional level of the most salient events.

8. Conclusions and Perspectives

With the advent of high throughput technologies, great progress has been made in the recent years in the elucidation of the structure and function of plastids. The most important data obtained in the area have been generated for the chloroplast of Arabidopsis. Much less information is available for the chromoplast. However, recent studies with bell pepper [14] and tomato fruit [16] have allowed assigning to chromoplasts a number of proteins around 1000, which is in the same order of magnitude as Arabidopsis chloroplasts [33]. This number is, however, much lower than the number of proteins predicted to be located in the plastid which has been estimated at up to 2700 [79] or even 3800 [80]. The increased sensitivity of the mass spectrometry technologies associated with efficient methods of purification of plastids, particularly chromoplasts, will allow in the future identifying more proteins. So far, changes in the proteome have not been described during the differentiation of chromoplast. Such studies imply the development of efficient protocols for isolating plastids at different stages of differentiation during chromoplastogenesis. The combination of proteomics and transcriptomics may also give novel information on the process in a near future. The discovery of the Or gene has been a great step forward to the understanding of the molecular determinism of chromoplast differentiation. There is a need to better understand the regulatory mechanism controlling the expression of the Or gene. Many genes encoding for plastidial proteins are regulated by the plant hormone ethylene and, therefore, participate in the transcriptional regulation of the fruit ripening process in general [81, 82]. Other hormones such as ABA and auxin may also be involved. Interactions between hormones and other signals (light, for instance) during chromoplast differentiation represent another field of investigation to be explored. Because most of the proteins present in the chromoplast are encoded by nuclear genes, it will be important in future to better understand the changes occurring in the processes of transport of proteins to the chromoplast. It is suspected that vesicular transport is gaining importance, but more experimental evidence is required. Finally the dialog between the nucleus and the chromoplast and the signals involved needs to be explored. So far most of the studies in this area have been carried out with chloroplasts [83].

In conclusion, important steps forward have been made into a better understanding of chromoplast differentiation. Metabolic reorientations and specific biochemical and molecular events have been clearly identified. It is predictable that more information will arise from the indepth description of the molecular events occurring during the chloroplast to chromoplast transition using genomic tools.

Acknowledgments

Wanping Bian has received a bursary from the University of Chongqing (China) for a Ph. D. and Cristina Barsan from the French Embassy in Bucharest (Romania) for a joint “co-supervision” Ph. D. The “Fundación Séneca” (Murcia, Spain)” provided a postdoctoral fellowship to Isabel Egea and the government of Brazil (CNPq) a sabbatical fellowship to Eduardo Purgatto. The authors acknowledge the Midi-Pyrénées Regional Council for financial support. W. Bian and C. Barsan are participated equally to the work.

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