- Citado por SciELO
versão impressa ISSN 1415-4757
versão On-line ISSN 1678-4685
Genet. Mol. Biol. v.30 n.3 supl.0 São Paulo 2007
Tercilio Calsa Jr.*; Antonio Figueira
Laboratório de Melhoramento de Plantas, Centro de Energia Nuclear na Agricultura, Universidade de São Paulo, Piracicaba, SP, Brazil
Plastid-related sequences, derived from putative nuclear or plastome genes, were searched in a large collection of expressed sequence tags (ESTs) and genomic sequences from the Citrus Biotechnology initiative in Brazil. The identified putative Citrus chloroplast gene sequences were compared to those from Arabidopsis, Eucalyptus and Pinus. Differential expression profiling for plastid-directed nuclear-encoded proteins and photosynthesis-related gene expression variation between Citrus sinensis and Citrus reticulata, when inoculated or not with Xylella fastidiosa, were also analyzed. Presumed Citrus plastome regions were more similar to Eucalyptus. Some putative genes appeared to be preferentially expressed in vegetative tissues (leaves and bark) or in reproductive organs (flowers and fruits). Genes preferentially expressed in fruit and flower may be associated with hypothetical physiological functions. Expression pattern clustering analysis suggested that photosynthesis- and carbon fixation-related genes appeared to be up- or down-regulated in a resistant or susceptible Citrus species after Xylella inoculation in comparison to non-infected controls, generating novel information which may be helpful to develop novel genetic manipulation strategies to control Citrus variegated chlorosis (CVC).
Key words: Citrus variegated chlorosis; in silico; sweet orange, tangerine.
Citrus species, such as sweet orange, mandarin, lime and lemon, have a large economic and social importance in Brazil, the world largest exporter of concentrated orange juice and producer of fresh fruit. Due to its industrial importance, considerable investment in genomic research in Brazil has been directed toward Citrus, including sequencing the complete genome of the first plant pathogen Xylella fastidiosa (Simpson et al., 2000), and the recent achievement of 182,529 expressed sequence tags (ESTs), derived from several Citrus tissues under various biotic or abiotic stresses, and from random genomic sequences (CitEST Database).
Crop yield potential is ultimately derived from photosynthesis, the process of converting solar energy into carbon backbones performed at thylakoid membranes of leaf chloroplasts (Taiz and Zeiger, 1998). Plastid is the generic name given to a group of specific plant cell organelles, which contain their own genome (plastome), ranging in size from 110 to 180 kbp depending on plant species. Plastids are maternally inherited in most crop species (Pyke, 1999), including Citrus (Moreira et al., 2002). The double-stranded chloroplast DNA exhibits complex structural dynamics in vivo (Lilly et al., 2001; Bendich, 2004), in contrast to the classic model of a closed circular genome. To date, more than 40 plants and algae plastomes have had their complete sequence complement determined (http://www.ncbi.nlm.nih.gov/Genomes). Plastome sequences have revealed a conserved structure even among distantly related taxa (Ogihara et al., 2002; Calsa et al., 2004), despite the occurrence of evolutionary events, such as plastid gene transfer to nucleus and/or mitochondria and functionally redundant gene loss (Sugiura, 2003).
Plastome sequences have been determined for a few tree species, including Pinus (Wakasugi et al., 1994), Eucalyptus (Steane, 2005) and Citrus (Bausher et al., 2006), opening new approaches for tree crop breeding, since plastids have been recognized as an interesting target for genetic engineering (Ruf et al., 2001; Maliga, 2003; Bock and Khan, 2004). In Citrus, plastid DNA regions have usually been used as cytoplasm inheritance markers in somatic hybridization and cybrid development (Guo et al., 2004; Takami et al., 2004). Nuclear-encoded proteins with plastid activity have been investigated in Citrus, especially associated with oxidative stress response (Mullineaux et al., 1998) and carotenoid biosynthesis (Tao et al., 2005).
A plastid transcript termination signal consists of secondary structures containing short poly-A sequences (Rott et al., 1998), which allow their eventual capture with oligo-dT primers, mainly from photosynthetic tissues, given the high ploidy and copy number of plastid genome in leaves. Plastid mRNAs may also be isolated under post-transcriptional control, because poly-adenylation is a degradation signaling mechanism (Hayes et al., 1999). As already verified in EST, SAGE and MPSS plant databases from Arabidopsis and sugarcane (Meyers et al., 2004; Robinson et al., 2004; Calsa and Figueira, 2007), tens or even hundreds of sequences displayed identity or high similarity to plastome genes or regions. These sequences may be actual plastid transcripts, or derived from nuclear genes resulting from DNA transfer events to the nucleus, a proven and quantified process (Stegemann et al., 2003). Potential Citrus plastome-encoded and plastid-directed nuclear-encoded expressed sequences in various organs were analyzed in this work. In addition, differential gene expression linked to photosynthesis from leaves infected or not with Xylella fastidiosa, the causal agent of Citrus variegated chlorosis (CVC) was analyzed.
Material and Methods
The Citrus sequence database (CitEST) was searched using the software GeneProject. Because the Citrus chloroplast genome sequence was not yet publicly available at the time of analysis, sequences potentially derived from the Citrus plastome were searched using the complete chloroplast genome sequences from Arabidopsis thaliana, Eucalyptus globulus, Pinus thunbergii, and Pinus koraiensis (GenBank AP000423; AY780259; D17510; and AY228468, respectively) through BlastN of the CitEST, accepting matches with E-value < 10-5. Positive matching reads were clustered using an internal CAP3 within GeneProject and annotated by BlastX against public protein databases. Sequences related to nuclear genes encoding plastid-targeted products were recovered by keyword search "(chloroplast OR plastid) AND precursor."
Retrieved sequences were assessed considering the standard CitEST nomenclature for reads and cDNA libraries, derived from leaves, bark, fruits or flowers of Citrus sinensis (CS libraries). The analyzed leaf expressed sequences included libraries of non-infected Citrus sinensis Pera IAC (CS-100) or 30 days after inoculation with Xylella fastidiosa (CS-102); and non-infected Citrus reticulata Ponkan (CR-100) or 30 days after inoculation with Xylella fastidiosa (CR-102). Leaf (C1) reads putatively associated to thylakoid membrane photosynthetic systems and primary carbon fixation were manually selected.
ESTs with identical or extremely similar putative annotations were counted, and their frequency was normalized for the total number of ESTs in each corresponding library, and expressed on a per thousand basis. The normalized frequencies of distinct libraries were statistically tested for differences based on Audic and Claverie (1997), considering significant p-value < 0.05. The normalized frequencies of contrasting libraries were also analyzed for expression pattern by hierarchical clustering and PlotCorr analyses using the Gene Expression Pattern Analysis (GEPAS; Herrero et al., 2003; 2004) online tools. The putative transcripts were arbitrarily categorized into high expression (above 5 reads per thousand); medium expression (between 2 and 5 reads per thousand); and low expression (below 2 reads per thousand) before hierarchical clustering.
Citrus plastome reads and partial shot-gun assembly
BlastN search of Citrus ESTs and random genomic sequences using the plastomes from E. globulus, P. thunbergii, P. koraiensi and Arabidopsis returned 362 significantly matched reads. From those, 155 (42.8%) were genomic sequences, while 207 were derived from ESTs from various organs, likely representing sequences transcribed from Citrus plastome of distinct plastid types (Table 1).
Plastome-matched Citrus sequences presented distinct similarity to the four queried species (Table 2). About one-fifth (19.3%) from all Citrus plastome-related sequences presented counterparts in Angiosperm dicotyledonous species (A. thaliana and E. globulus), while none was exclusively found to be similar with the analyzed Gymnosperm plastomes (Pinus). Conversely, the number of exclusive matches between Citrus and Eucalyptus was ten times higher than between Citrus and Arabidopsis (Table 2). Noteworthy, no Citrus sequence presented a simultaneous match to P. koraiensis and P. thunbergii, or a joint match to Pinus and Arabidopsis. Additionally, only one Citrus EST presented an exclusive match to the Arabidopsis plastome.
The categorization of plastome-related Citrus sequences based on putative annotation (Table 3) revealed that the exclusive Citrus - Arabidopsis sequence had an unknown putative function (yet to be identified in any other plant transcriptome), and derived from a fruit cDNA library. Most exclusive Eucalyptus-matched sequences were associated to no hit transcripts, although a few were categorized as hypothetical or ribosomal proteins. The highest proportion of the Citrus sequences with specific matches harbored simultaneous and exclusive similarity to Arabidopsis and Eucalyptus, both dicotyledonous Angiosperms, with lower resemblance to the Gymnosperm plastomes.
In an attempt to achieve a primary draft of the Citrus plastid DNA regions, the plastome-matched EST and genomic reads were assembled into clusters. This approach resulted in 65 contigs and 73 non-grouped sequences or singlets (Table 4). The sum of non-overlapping contigs reached 68,095 bp in size, while singlets altogether covered 55,695 bp. Since the reference Citrus chloroplast genome available to date comprises 160,129 bp (Bausher et al., 2006), the in silico assembly covered around 77.3% of the plastome in a transcriptionally informative manner.
Citrus chloroplast-related nuclear genes
Through keyword search, a total of 19,246 Citrus expressed sequences were found to match known nuclear genes coding for precursor proteins targeted to plastid. Based on organ of origin and treatment, it was possible to define a general transcriptional profile for nuclear-encoded plastid-targeted gene products for the various plastid types, such as chloroplast, chromoplast or proplastid in sweet orange (C. sinensis Pera IAC). There was no cDNA library prepared from sweet orange root tissues, but the identification of 104 expressed sequences derived from C. limonia Cravo roots exposed or not to water deficit, perfectly aligning several putative functionally plastid-related genes (data not shown), indicated that plastome-related sequences might also occur in roots of sweet oranges.
Considering only C. sinensis transcripts, it was possible to analyze putative differential gene expression between organs/tissues and, consequently different plastid types, as well as to identify genes with an apparent preferential transcription in sweet orange flowers or fruits. Genes showing the lowest expression differences among leaf, bark, fruit and flower were putatively annotated as coding for alpha-1,4 glucan phosphorylase; ribulose 1,5-bisphosphate carboxylase/oxygenase (RuBisCO) binding-protein; enolpyruvylshikimate-3-phosphate synthase (EPSPS); and cystathionine gamma-synthase (Figure 1A). The normalized frequencies for these genes presented the lowest standard errors among analyzed organs (not shown). On the other hand, the genes displaying the most variable expression were chlorophyll a/b binding proteins; photosystem I subunits; early light-induced protein; and chloroplast terpene synthase (Figure 1B). A sequence annotated as coding for photosystem subunit and another for the hypothetical chloroplast reading frame 19 displayed significantly higher preferential expression in vegetative organs (leaves and bark) than in reproductive organs (Figure 1C). On the other hand, the transcripts with the highest significant preferential expression in reproductive organs (flowers and fruits) were associated to inorganic pyrophosphatase; plastid terpene synthase; thiazole biosynthetic enzyme; and GcpE protein (Figure 1D). Additionally, significant preferential expression in fruits was observed for transcripts putatively encoding lipoxygenase C and isocitrate dehydrogenase (Figure 2A), while a significant preferential transcription in flowers was detected for a chloroplast translocon component, anthranilate synthase and alpha-glucan water dikinase (Figure 2B).
Chloroplast photosynthesis gene expression potentially affected by Citrus variegated chlorosis (CVC)
To detect potential relevant transcriptional variations associated with CVC occurrence, cDNA libraries from two Citrus species contrasting in their response to Xylella fastidiosa (susceptible sweet orange or resistant tangerine), after inoculation or not, were compared for differential expression of photosystem- and carbon fixation-associated genes based on normalized frequencies. From putative annotation, 37 reads associated with thylakoid photosynthesis complex subunits, and 30 reads related with the carbon fixation cycle were identified (not shown). The putative transcripts were arbitrarily categorized into high expression (above 5 reads per thousand); medium expression (between 2 and 5 reads per thousand); and low expression (below 2 reads per thousand). This enabled a more sensitive analysis of hierarchical clustering according to normalized frequency expression (also known as virtual northern). Clustering expression patterns suggested transcriptional variations between C. sinensis and C. reticulata, infected or not by Xylella fastidiosa. Considering that sweet oranges are highly susceptible to CVC, while tangerines are considered to be standard tolerant, gene differential expression might indicate specific reaction to CVC. For example, chlorophyll a/b binding protein 1 (LHC-II type I CAB-1) appeared to be strongly induced after Xylella infection in tangerine, whereas the expression level did not appear to change in sweet orange following infection (Figure 3A). Ferredoxin NADP-reductase (leaf isozyme) and Thioredoxin M appeared to be induced in tangerine within the first 30 days after infection (Figure 3B). Among low-expression genes, it was noticed that transcript levels of ATP synthase beta, gamma and delta chains increased with infection in tangerine, while the opposite occurred in sweet orange (Figure 3C). Additionally, chlorophyllase I appeared to be slightly down-regulated in tangerine (Figure 3C).
Regarding transcripts associated with the carbon fixation cycle, minor differential expression was observed for carbonic anhydrase and glyceraldehyde 3-phosphate dehydrogenase (GAPDH) in sweet orange and tangerine, with slight transcript accumulation after infection (Figure 4A). Ribulose 1,5-bisphosphate carboxylase (RuBisCO)-binding protein alpha subunit and pyruvate phosphate dikinase exhibited opposite expression profiles in both Citrus species, with an increase in transcripts in C. sinensis after infection with Xylella and a corresponding decrease in C. reticulata (Figure 4B). Divergent patterns between both species were also observed for several low-expressed genes, such as ribulose-phosphate 3-epimerase; ribulose 1,5-bisphosphate carboxylase (RuBisCO) small chain 3; ribulose 1,5-bisphosphate carboxylase N-methyltransferase; fructose-1,6-bisphosphatase and sedoheptulose-1,7-bisphosphatase (Figure 4C).
Correlation analyses using PlotCorr indicated the most variable expression between Xylella-infected tangerine and sweet orange (Figure 5). Among the photosystem components, the oxygen-evolving complex 25.6 kD protein and chlorophyll a/b binding protein 151 type II showed a more genotype-specific expression, with both transcripts accumulating in infected C. reticulata (Figure 5A). Conversely, three genes related to the carbon fixation cycle were detected as presenting a more genotype-specific transcription (Figure 5B). Two (RuBisCO activase and transketolase) displayed a tangerine-preferential expression, while a RuBisCO small chain subunit was significantly more expressed in sweet orange (Figure 5B).
In silico mining of plastid-related sequences in the CitEST database identified the presence of organelle-derived reads, with highly significant matches to plastome-specific regions. As expected, the plastome-specific transcripts were present at a low frequency, ranging from ca. 0.1% in ESTs to 4.4% in genomic libraries (Table 1). The data also suggested a stronger transcription of genes from chloroplast and chromoplast, respectively from shoots and fruits, associated with photosynthesis and fruit ripening (Table 1). From the plastome-matched Citrus sequences, almost half derived from a genomic library made from leaves, likely reflecting the high copy number of chloroplast DNA in that organ.
The level of matching similarity between Citrus sequences and the other species plastid genome (Table 2) corroborated taxonomic classification, with more resemblance between Citrus and the other dicots (Eucalyptus and Arabidopsis), all from the same taxon (subclass Rosids). However, surprisingly, Citrus sequences were less similar to the Arabidopsis genome, despite the fact that both share closer ancestry between the level of order and subclass (Sapindales and Brassicales, respectively, both Eurosids II or Malvids), while Eucalyptus belong to the Myrtales order and is not part of the Eurosids I (Savolainen et al., 2000). Citrus plastid sequences annotated as mRNA processing, ribosomal protein or others were more specifically related to Eucalyptus, suggesting that common life history traits might be important for similarity between these putative genes (Table 3). Genes putatively coding for plastid NADH-dehydrogenase, and those annotated as no hit or hypothetical protein comprised most of the Angiosperm specific-matches (Table 3), suggesting that these genes are more conserved between Citrus and the other dicotyledonous plastomes.
Clustering the plastome-matched genomic and EST reads resulted in a draft of Citrus plastid genome, theoretically covering around 77% of the reference chloroplast genome available (Bausher et al., 2006). However, the contigs formed were unevenly distributed along the genome, since no cluster longer than 3 kbp was formed, and more than 90% of the contigs were smaller than 1.5 kbp (Table 4). This is likely due to the fact that large amounts of expressed sequences were used for assembly, with a significant lack of plastome intergenic regions in the libraries.
Transcriptional profiling of nuclear-encoded plastid-targeted proteins from various plastid types (chloroplasts, chromoplasts or proplastids) was achieved for leaf, bark, flower and fruit-expressed genes from C. sinensis Pera IAC, to presumably identify transcripts with minimum or maximum variation among organs and tissues, and consequently from distinct plastid types (Figure 1A-B). The least variable expressed sequences among sampled organs included putative genes involved in starch and amino acids biosynthesis (Figure 1A). Alpha-1,4-glucan phosphorylase has an essential role in plastid starch formation, and mobilization for sucrose and other polysaccharide precursors (Buchner et al., 1996). RuBisCO-binding protein activity was unexpected in reproductive organs, but was apparently found expressed in flower proplastids and fruit chromoplasts, possibly involved in regulation of RuBisCO oxygenase activity, and the subsequent photorespiratory decarboxylating-like pathway required in reproductive or maturing organs. Enolpyruvylshikimate-3-phosphate synthase (EPSPS) and cystathionine gamma-synthase are vital to essential amino acids biosynthetic routes. An EPSPS gene has already been genetically inserted and expressed in transplastomic tobacco, which displayed increased resistance to glyphosate (Ye et al., 2001). Together with cystathionine gamma-synthase, the first enzyme on the methionine biosynthesis pathway (Hacham et al., 2006), EPSPS expression in several organs suggested a relatively constant metabolic requirement for amino acids in Citrus.
Based on normalized frequencies, the most variable expressed sequences among leaf, bark, fruit and flower samples included chlorophyll a/b binding proteins and photosystem I subunits associated genes, generally performing photosynthesis maintenance (Figure 1B). The expression levels of an early light-induced regulatory protein and terpene synthase were also highly variable among organs. The former is associated with phytochrome-mediated light perception, and it has been already correlated with acclimatization to low temperatures in Poncirus (Zhang et al., 2005). Terpene synthase catalyzes a key step on sesquiterpene metabolism, and it has been described in Citrus due to its importance to typical citric flavor (Sharon-Asa et al., 2003).
The most significantly induced genes in vegetative organs, in comparison to reproductive ones, were related to photosystem subunits, especially in leaves (Figure 1C). A transcript, annotated as plastid hypothetical frame ORF19, previously detected in other species but still without any associated function, also exhibited a vegetative-specific expression pattern, suggesting an apparent photosynthetic role for this gene. Conversely, significant differential expression in reproductive organs was detected for genes usually associated with secondary metabolic pathways (Figure 1D): transcripts encoding an inorganic pyrophosphatase, a vacuolar enzyme associated with fruit acidity, sugar accumulation and ripening (Marsh et al., 2001); terpene synthase, a key enzyme for citric taste and flavor; thiazole biosynthesis enzyme, part of thiamine (B1 vitamin) metabolism and fruit ripening (Jacob-Wilk et al., 1997); and GcpE protein, involved in isoprenoid biosynthesis, known to participate in fruit maturation (Seemann et al., 2006).
All genes with a reproductive organ-specific expression pattern were associated with fruit ripening (Figure 2A). A fruit-specific preference in expression for lipoxygenase C and isocitrate dehydrogenase was detected in the survey for organ-specific sequences. Both enzymes corroborate a fruit-specific function, since lipoxygenase C is linked with the development of volatile compounds, carotenoids and jasmonate responses in fruit (Rangel et al., 2002), and plastid isocitrate dehydrogenase activity has been demonstrated to be associated with inorganic pyrophosphatase and accumulation of organic acids in fruit (Etienne et al., 2002).
A translocon component from protein importing complexes from outer membranes of chloroplast and chromoplast (Summer and Cline, 1999) was identified as presenting flower-specific expression (Figure 2B), suggesting a potential extended activity to leucoplasts. The same was observed for sequences associated to anthranilate synthase and alpha-glucan water dikinase, respectively involved in indol-alkaloid and terpenoid biosynthesis (Hong et al., 2006) and in starch degradation (Baunsgaard et al., 2005). The presence of these sequences suggested an intense leucoplastidic activity in Citrus flowers, especially concerning secondary products synthesis and reserve mobilization in non-photosynthetic tissues.
Clustering expression-patterns visually disclosed quantitative leaf transcriptional variation between C. sinensis (sweet orange) and C. reticulata (tangerine), whether infected or not with Xylella fastidiosa (Figure 3). Regarding the photosystems, it was observed that tangerine leaves, 30-days after inoculation, displayed an apparent accumulation of mRNAs related to ATP synthase subunits; chlorophyll a/b-binding proteins; ferredoxin NADP-reductase; and M-type thioredoxin, while a decrease in ATP synthase transcripts was detected in sweet orange. Maintenance of photosynthesis, suggested by differences in amounts of associated transcripts, might be a consequence of the lack of pathogen in the resistant species. Alternatively, these changes might be due to a metabolic distinction between CVC tolerant and susceptible species, with photosynthesis maintenance despite an occasional effect from toxins and/or catabolites released by Xylella, or from xylem clogging. Several genes associated with primary carbon fixation pathway in plastids also exhibited contrasting expression profiles (Figure 4). Transcripts encoding key enzymes responsible for a proper photosynthesis carbon assimilation, and subsequent synthesis of trioses and hexoses, transport or synthesis of more complex carbohydrates, as well as coding for regulatory proteins of these enzymes, appear to accumulate in tangerine infected leaves in comparison to an observed relative decrease in sweet orange leaves under the same conditions. Visually, chlorophyll a/b binding protein 151 type II, oxygen-evolving complex 25.6 kD protein, ribulose 1,5-bisphosphate carboxylase activase and transketolase appeared to be the most induced on infected C. reticulata leaves, while a ribulose 1,5-bisphosphate carboxylase small chain subunit transcript was abundant in C. sinensis.
The clarification of the role of the photosynthesis and carbon assimilation sequences on Xylella fastidiosa resistance in Citrus may open novel research opportunities. But, clearly further investigation is required to validate these findings and to distinguish between cause and effect of the detected differences in photosynthesis-related transcript accumulation in tangerine. In addition, plastome sequences may be helpful for developing plastid genetic engineering strategies in Citrus, promising for yield increase by photoassimilate enhancement or in fruit nutraceutical enrichment or development through secondary chromoplast metabolite manipulation.
The authors would like to thank the Citrus Biotechnology Laboratory, from the Centro de Citricultura "Sylvio Moreira" of the Instituto Agronômico de Campinas, for providing access to the CitEST database and necessary bioinformatic assistance. Support from CNPq and FAPESP was greatly appreciated.
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Laboratório de Melhoramento de Plantas
Centro de Energia Nuclear na Agricultura
Universidade de São Paulo
Av. Centenário 303
Caixa Postal 96, 13400-970 Piracicaba, SP, Brazil
Received: July 21, 2006; Accepted: February 14, 2007.
Associate Editor: Alessandra Alves de Souza
*Current address: Laboratório de Genética Molecular, Departamento de Genética, Centro de Ciências Biológicas, Universidade Federal de Pernambuco, Recife, PE, Brazil.