Complementary iTRAQ-based proteomic and RNA sequencing-based transcriptomic analyses reveal a complex network regulating pomegranate (Punica granatum L.) fruit peel colour

Peel colour is an important factor affecting the marketability of pomegranate fruits. Therefore, elucidating the genetic mechanism of fruit peel colour development may be useful for breeding pomegranate cultivars with enhanced fruit peel colours. In this study, we combined an iTRAQ-based proteome-level analysis with an RNA sequencing-based transcriptome-level analysis to detect the proteins and genes related to fruit peel colour development in pomegranate. We analysed the ‘Tunisia’ (red fruit) and ‘White’ (white fruit) pomegranate cultivars at two stages of fruit development. A total of 27 differentially abundant proteins (increased abundance) and 54 differentially expressed genes (16 up-regulated and 38 down-regulated) were identified from our proteomics and transcriptomics data. The identified proteins and genes contribute to pomegranate fruit peel colour by participating in the biosynthesis of anthocyanins, stilbenoids, diarylheptanoids, gingerols, flavonoids, and phenylpropanoids. Several candidate proteins and genes corresponded to enzymes related to general reactions (PAL, 4CL, DFR, LDOX/ANS, CHS, and F3′5′H) and glycosylation (GT1 and UGAT) of compounds and pigments related to the colour of pomegranate fruit peel. Complementary proteome- and transcriptome-level analyses revealed a complex molecular network controlling fruit peel colour. The candidate genes identified in this study may be useful for the marker-based breeding of new pomegranate cultivars.

Transcriptional analysis of DEGs. To verify transcriptional-level changes, four cDNA libraries (i.e., SP1, SP2, TP1, and TP2) were constructed using total RNA extracted from the fruit peels of the two pomegranate cultivars. A total of 64.85, 61.99, 59.99, and 67.46 million raw sequence reads were generated from the SP1, SP2, TP1, and TP2 libraries, respectively (Supplementary Table S1). After removing low-quality reads and adaptor sequences, 37.43, 35.63, 34.68, and 38.76 million clean reads were obtained for SP1, SP2, TP1, and TP2, respectively, with 45.23%, 44.06%, 42.25%, and 41.89% of the reads mapped to the reference genome, respectively. The proportion of unique reads that could be aligned to the genome sequence ranged from 33.33% for TP2 to 37.34% for SP1. Finally, 18,918 and 20,545 unique genes were detected in SP1_TP1 and SP2_TP2, respectively. Compared with the SP group, the TP group had 4,073 (1,447 up-regulated and 2,626 down-regulated) significant DEGs (i.e., |log2(TP/SP)| > 1 and P ≤ 0.001) at the fruit colouring stage, and 7,223 (2,945 up-regulated and 4,278 down-regulated) significant DEGs at the ripening stage ( Fig. 1 and Table 1). These results suggested that many genes were differentially expressed between the two fruit development stages in two pomegranate cultivars, with more DEGs at the fruit ripening stage.
Comparative analysis between protein abundance and gene expression levels. To evaluate the relationship between transcript levels and protein abundance, we compared the DAPs and DEGs between the two analysed fruit development stages. A total of 552 shared DAPs and 1,684 shared DEGs were identified during the comparison between SP1_TP1 and SP2_TP2 ( Fig. 2A and Table 1). Among the shared DAPs, 311 were more abundant and 241 were less abundant in SP1_TP1 than in SP2_TP2, while 304 were more abundant and 248 were less abundant in SP2_TP2 than in SP1_TP1 (Fig. 2B). Of the common DEGs, 655 were up-regulated and 1,029 were down-regulated in SP1_TP1, whereas 636 were up-regulated and 1,048 were down-regulated in SP2_TP2 (Fig. 2B). Furthermore, 184 and 478 DAPs and their corresponding DEGs were identified in SP1_TP1 and SP2_TP2, respectively (Fig. 2C). Of these, only 60 DAPs (26 with increased abundance and 34 with decreased abundance) and 183 DAPs (40 with increased abundance and 143 with decreased abundance) were regulated in the same direction as their corresponding DEGs in SP1_TP1 and SP2_TP2, respectively (Fig. 2B,C). There were more DEGs than DAPs in both SP1_TP1 and SP2_TP2, with considerable differences between the trends in transcript levels and the trends in protein abundance. To analyse the consistency between transcriptomic and proteomic changes during the development of fruit peel colour, we conducted a correlation analysis using the quantitative data for DAPs and DEGs (Fig. 2D,E; Supplementary Table S2). Pearson's correlation tests indicated that the fold-changes in the DAPs were significantly (P < 0.001) negatively correlated with the fold-changes in the corresponding DEGs (r pearson = −0.29 and −0.23 in SP1_TP1 and SP2_TP2, respectively). Thus, there was a poor correlation between transcript levels and protein abundance.

KEGG pathway annotations for DAPs and DEGs.
To annotate the functions of genes and proteins, we conducted a pathway enrichment analysis of the DAPs and DEGs in SP1_TP1 and SP2_TP2 based on the KEGG database (Fig. 3). In SP1_TP1, 521 DAPs were significantly enriched in 11 pathways (corrected P value < 0.05; Fig. 3A), while 3,181 DEGs were significantly enriched in 30 pathways (corrected P value < 0.05; Fig. 3B). The following pathways were enriched with both DAPs and DEGs in SP1_TP1: anthocyanin biosynthesis; stilbenoid, diarylheptanoid, and gingerol biosynthesis; photosynthesis; phenylalanine metabolism; flavonoid biosynthesis; phenylpropanoid biosynthesis; biosynthesis of secondary metabolites; and metabolic pathways. In SP2_TP2, 630 DAPs were significantly enriched in 14 pathways, while 2,936 DEGs were significantly enriched in 22 pathways (corrected P value < 0.05; Fig. 3). The following pathways were common to both the DAPs and DEGs in SP2_ TP2: anthocyanin biosynthesis; stilbenoid, diarylheptanoid, and gingerol biosynthesis; photosynthesis; flavonoid biosynthesis; α-linolenic acid metabolism; and peroxisome and phenylpropanoid biosynthesis. An additional comparative analysis indicated that four pathways (i.e., anthocyanin biosynthesis; stilbenoid, diarylheptanoid, and gingerol biosynthesis; flavonoid biosynthesis; and phenylpropanoid biosynthesis) were common between SP1_TP1 and SP2_TP2. Thus, these four pathways were further investigated as candidate pathways related to the development of pomegranate fruit peel colour.

Identification of DAPs and DEGs associated with candidate pathways. A total of 51 and 89
DAPs detected in SP1_TP1 and SP2_TP2, respectively, were associated with the four candidate pathways, with 34 DAPs common to both sample groups (Supplementary Table S3). Additionally, 241 and 397 DEGs identified in SP1_TP1 and SP2_TP2, respectively, were related to the four candidate pathways, including 100 DEGs common to both sample groups (Supplementary Table S4). After filtering out the DAPs and DEGs that were differentially regulated between SP1_TP1 and SP2_TP2, 27 DAPs with increasing abundance and 54 DEGs (16 up-regulated DEGs and 38 down-regulated DEGs) were annotated as being involved in anthocyanin biosynthesis; stilbenoid, diarylheptanoid, and gingerol biosynthesis; flavonoid biosynthesis; and phenylpropanoid biosynthesis (  Tables 2 and 3). These DAPs and DEGs likely influence pomegranate fruit peel colour at the proteome and transcriptome levels. Except for Gglean022299.1, the DAPs represented 13 crucial enzymes (Fig. 4B). With the exception of Gglean025205.1, Gglean018889.1, and Gglean015246.1, the DEGs encoded 20 pivotal enzymes (Fig. 4D). Nine enzymes were affected by corresponding genes with differentially regulated trends at the transcriptome level. More DEGs than DAPs were involved in the formation of pomegranate fruit peel colour, and the DEGs showed complex differential regulation at the transcriptome level. Most of the genes encoding the DAPs were not included among the DEGs, consistent with the observed differences between the proteome and  Fig. S1), which is involved in phenylpropanoid biosynthesis.
Validation of gene expression levels. The expression levels of 12 genes, including Gglean009951.1, Gglean020650.1, Gglean015001.1, and Gglean015003.1, were determined by quantitative real-time polymerase chain reaction (qRT-PCR). The expression patterns were similar to those generated from high-throughput

Discussion
Peel colour is a key factor influencing the marketability of fruits. Thus, elucidating the genetic mechanism of the regulation of fruit peel colour may be useful for breeders interested in generating new pomegranate cultivars with enhanced fruit colours. Consequently, fruit peel development has been a topic of interest among fruit crop researchers and has been extensively studied. To date, however, no quantitative trait loci related to fruit colour have been identified, and none of the genes related to pomegranate fruit peel colour have been confirmed.
In this study, more DAPs and DEGs were detected between the 'Tunisia' and 'White' cultivars at the fruit ripening stage than at the fruit colouring stage, suggesting that greater changes in peel colour occurred at the ripening stage (Fig. 6). An integrated quantitative proteomics and transcriptomics analysis revealed that there were more DEGs than DAPs in both SP1_TP1 and SP2_TP2, with only a few of the DEGs encoding the DAPs. These results were similar to those reported for potato 17 and orchid 18 . There were inconsistencies between the trends in transcript levels and the trends in protein abundance. These results may indicate that protein abundance is affected by post-translational modifications and splicing events in cells, rather than changes in gene transcript  19 . A correlation analysis revealed a negative correlation between protein abundance and the expression levels of the corresponding genes (Fig. 2D,E). An earlier study also reported a relatively poor correlation between transcriptome and proteome data (r pearson = 0.27-0.40) 20 . A possible explanation for the low correlation between transcript levels and protein abundance is that the transcription level can fluctuate more quickly than protein translation and modification processes. Thus, changes in the abundance of a protein occur after the level of its corresponding transcript has stabilised 18 . Our results suggest that iTRAQ and transcriptomic analyses are complementary methods for profiling candidate proteins mediating specific physiological processes, including pomegranate fruit peel colour development.
A KEGG pathway enrichment analysis was completed to avoid false positive results, and the common pathways shared by DAPs and DEGs were selected for further study. Accordingly, we functionally annotated 27 proteins and 54 genes from among the thousands of detected DAPs and DEGs. These proteins and genes were associated with 13 and 20 critical enzymes, respectively, which contributed to pomegranate fruit peel colour mainly by catalysing reactions in pathways related to anthocyanin biosynthesis; stilbenoid, diarylheptanoid, and gingerol biosynthesis; flavonoid biosynthesis; and phenylpropanoid biosynthesis ( Fig. 4; Tables 2 and 3). A total of 13 DAPs and 17 DEGs were detected as core regulators of anthocyanin biosynthesis in pomegranate fruit peel (Fig. 5), implying that the colour differences between white and red peels are due to variable anthocyanin production 21 .
Anthocyanin biosynthesis is fairly complex, and is associated with diverse metabolites including phenylpropanoids and flavonoids 22 . To date, diverse genes (i.e., PAL, 4CL, DFR, LDOX/ANS, CHS, and F3′5′H) involved in the regulation of anthocyanin biosynthesis have been identified and their functions in the formation of pigments have been characterised in fruit crops including Rosaceae species 23 , apple 24 , peach 25 , and pear 8 . In the current study, the expression levels of genes encoding F3′5′H and LDOX/ANS were up-regulated and the abundance of their corresponding proteins also increased during fruit colour development ( Fig. 4; Tables 2 and 3). In contrast, although the abundance of PAL, 4CL, CHS, and DFR proteins increased, their corresponding genes were down-regulated during fruit colour development ( Fig. 4; Tables 2 and 3). Both PAL and 4CL are critical for the conversion of phenylalanine to anthocyanins 13 . A decrease in transcription but an increase in the abundance of the encoded proteins ensured a sufficient supply of anthocyanin precursors (e.g., p-coumaroyl-CoA) in 'Tunisia' fruit peels (Fig. 5). Similarly, CHS catalyses the conversion of p-coumaroyl-CoA to naringenin chalcone (Fig. 5). This represents a key regulatory step during the synthesis of flavonoids, which is a major pigment in many flowers, leaves, and fruits 26,27 . Naringenin is converted into several anthocyanin-related substances (e.g., dihydrokaempferol, leucopelargonidin, and pelargonidin) by the actions of F3′5′H, DFR, and LDOX/ANS (Fig. 5). These enzymatic reactions have been documented in sweet cherry 28 , apple 24 , mango 13 , and peach 25 . The results of a previous study indicated that a single nucleotide polymorphism in PgLDOX is responsible for the 'white' anthocyanin-less phenotype of pomegranate fruits 21 . Thus, we hypothesised that these genes may be conserved and play a crucial role in the anthocyanin biosynthesis related to pomegranate fruit peel colour development. Caffeoyl-CoA, CHS, and F3′5′H catalyse a chain of reactions to generate dihydromyricetin, a coloured chemical compound related to leucoanthocyanidins 29 . Leucoanthocyanidin reductase [EC:1.17.1.3] converts leucoanthocyanidin to gallocatechin as well as eucopelargonidin to afzelechin (Fig. 5). These two reactions ultimately produce anthocyanins. It is possible that these pathways also contribute to pomegranate fruit peel colour development.
Plant scientists have long been interested in flavonoid pigments because they are responsible for the diverse colours (e.g., yellow, red, purple, and blue) of various organs, including fruits and flowers 30,31 . In this study, changes in FS transcript levels and the abundance of FS protein tended to induce the biosynthesis of flavones and flavonols (Fig. 5). Down-and up-regulated expression of Gglean024784.1 and Gglean024783.1, respectively, may help regulate the UGAT-catalysed conversion of cyanidin 3-malonylglucoside to the stable compound cyanidin 3,5-O-diglucoside. Additionally, GT1 can catalyse the glycosylation of the 5-OH and the 3-OH groups on the anthocyanidin molecule. Although the GT1 transcript levels decreased during fruit colour development, the abundance of GT1 protein increased, which likely promoted the conversion of cyanidin to cyanidin 5-glucoside and then to cyanidin 3,5-O-diglucoside. These reactions result in the production of various anthocyanins (Fig. 5). This is consistent with the findings of a previous study on anthocyanin biosynthesis in rose 32 . Our results also confirmed that the glucosyltransferase-catalysed glycosylation at two different positions on the precursor molecule is not limited to rose species 32 . Thus, we believe that genes regulating anthocyanin biosynthesis via glycosylation play important roles in the stabilization of pigments in pomegranate fruit peels.
In addition to anthocyanins and flavonoids, other secondary metabolites are produced in the phenylpropanoid biosynthesis pathway by the activities of enzymes such as CAD [EC:1.1. 1.195]. We detected three CAD proteins with increased abundance and four CAD genes among the DEGs (one up-regulated and three down-regulated), including Gglean015001.1 and Gglean015003.1, during fruit colour development in pomegranate. An earlier study confirmed that CAD belongs to the polyphenol oxidase (PPO) family 33 , and catalyses the interconversion between aldehydes and alcohols ( Supplementary Fig. S1). Disrupting the expression of CAD genes will result in the atypical incorporation of hydroxycinnamaldehyde into lignin, thereby modifying the cell wall structure 34 . A previous study revealed that PPO protects red pear fruit or leaf cells against pathogens by catalysing the synthesis of lignin and quinines 35 . Thus, CAD may induce the synthesis of lignin and quinines to alter the cell wall structure to enhance pathogen resistance, which may explain the relatively strong disease resistance of red pomegranate fruits 36 .  The regulatory functions of the other identified enzymes in pathways related to anthocyanin biosynthesis, especially those in the stilbenoid, diarylheptanoid, and gingerol biosynthesis pathways, have not been characterised. Combined analyses of metabolomics data may further clarify their functions in relation to the regulation of pomegranate fruit peel development. In conclusion, the transcriptome and proteome data generated in this study revealed a complex transcriptional and translational network regulating pomegranate fruit peel colour development. These candidate proteins and genes may be useful for marker-based breeding of new pomegranate cultivars.

Methods
Plant materials. The 'Tunisia' and 'White' pomegranate cultivars analysed in this study were grown and managed according to local production practices in Xingyang, China. Both cultivars were obtained from the Zhengzhou Fruit Research Institute, Chinese Academy of Agricultural Sciences, Zhengzhou, China. The blooming stage was defined as the period during which 50% of the pomegranate flowers were open. According to our observations, the fruit development periods of the two cultivars were similar. The differences in the fruit peel colours between the two cultivars developed during the fruit colouring stage (60 days after blooming) and especially during the ripening stage (120 days after blooming). The peel of 'Tunisia' fruits reddened during the fruit colouring and ripening stages, in contrast to the white fruits of the 'White' cultivar (Fig. 6). During the fruit colouring and ripening periods, the peels of three normally growing fruits were removed and pooled. Three replicates were collected. The peels were immediately frozen in liquid nitrogen for 30 min and stored at −80 °C until use. For convenience, the 'Tunisia' and 'White' fruit peels were abbreviated as TP and SP, respectively.
Protein extraction. Proteins were extracted from two biological replicates of pomegranate fruit peels as previously described 37 . Briefly, Lysis Buffer 3 [8 M urea and 40 mM Tris-HCl containing 1 mM PMSF (phenylmethylsulfonyl fluoride), 2 mM EDTA (ethylenediaminetetraacetic acid), and 10 mM DTT (dithiothreitol), pH 8.5] was added to fruit peel samples, which were then ground. After centrifuging the ground material at 25,000 × g for 20 min at 4 °C, five volumes of 10% TCA/acetone with 10 mM DTT were added to the supernatant to precipitate proteins at −20 °C. The precipitation step was repeated with acetone alone until the supernatant became colourless. The precipitated proteins were air-dried and resuspended in Lysis Buffer 3. Samples were sonicated on ice for 5 min to resuspend proteins and then centrifuged as before. The resulting supernatants were incubated at 56 °C with 10 mM DTT for 1 h to reduce the proteins. The proteins were then alkylated with 55 mM iodoacetamide at room temperature for 45 min in darkness. Five volumes of acetone were added to samples to precipitate proteins at −20 °C. Proteins were resuspended in Lysis Buffer 3 and then sonicated on ice for 5 min. The protein concentration was determined by Bradford's method using bovine serum albumin (BSA) as the standard.
Protein digestion and iTRAQ labelling. Protein solutions (100 µg) were diluted 4-times with 100 mM tetraethylammonium bromide, after which proteins were digested overnight with Trypsin Gold (Promega, Madison, WI, USA) at 37 °C (40:1, protein:trypsin). The peptides were desalted with a Strata X C18 column (Phenomenex, Torrance, CA, USA) and then vacuum-dried according to the protocol recommended by the manufacturer. Peptide samples were labelled using iTRAQ 8-plex kits (AB Sciex Inc., MA, USA). The two 'Tunisia' samples (TP1 and TP2) were labelled with iTRAQ tags 113 and 115, while the two 'White' samples (SP1 and SP2) were labelled with tags 117 and 119.
Peptide fractionation. Peptides were separated using a Shimadzu LC-20AB HPLC Pump system coupled with a high-pH RP column. The peptides were first reconstituted in Buffer A (5% ACN and 95% H 2 O, with the pH adjusted to 9.8 with ammonia) to a final volume of 2 ml, which was then loaded onto a column containing 5-μm particles (Phenomenex). Peptides were separated with a gradient of 5% Buffer B (5% H 2 O and 95% ACN, with the pH adjusted to 9.8 with ammonia) for 10 min, 5-35% Buffer B for 40 min, and 35-95% Buffer B for 1 min at a flow rate of 1 ml/min. The system was maintained in 95% Buffer B for 3 min, followed by a decrease to 5% Buffer B within 1 min and equilibration with 5% Buffer B for 10 min. The eluants were monitored by measuring the absorbance at 214 nm, and fractions were collected every 1 min. The eluted peptides were pooled as 20 fractions and vacuum-dried.
Analysis by LC-MS/MS. Each fraction was resuspended in Buffer A (2% ACN and 0.1% FA in water) and centrifuged at 20,000 × g for 10 min. The supernatant was loaded onto a C18 trap column (5 μl/min for 8 min) on an LC-20AD nano-HPLC instrument equipped with an autosampler (Shimadzu, Kyoto, Japan). The peptides were eluted from the column and separated using an analytical C18 column (75-μm inner diameter) packed in-house. The 8%-35% Buffer B (2% H 2 O and 0.1% FA in ACN) gradient was applied at 300 nl/min over 35 minutes, and then increased to 60% in 5 min, maintained at 80% for 5 min, and then decreased to 5% over 0.1 min. The column was equilibrated with 5% Buffer B for 10 min. The eluted peptides underwent nanoelectrospray ionisation before being analysed by MS/MS (Q-Exactive mass spectrometer; Thermo Fisher Scientific, San Jose, CA, USA) coupled with the HPLC system.
Protein identification and quantification based on iTRAQ data. Proteins were identified and quantified using the Mascot 2.3.02 search engine (Matrix Science, Boston, MA, USA). Our genome database was used to identify proteins with the IQuant program 38 . To assess the confidence of the peptide identifications, the PSMs were pre-filtered at a PSM-level FDR of 1%. The identified peptide sequences were then assembled into a set of accurately identified proteins based on the "simple principle". To quantify proteins, peptides were automatically selected by calculating the reporter peak area using the default parameters of the Mascot software package. The resulting data set was auto-bias corrected, and the variations resulting from the unequal mixing of samples with different labels were eliminated. The DAPs between the TP and SP samples were defined as the proteins with a fold-change of >1.2 (mean value of all compared groups) or <0.85 and a P value (t-test of all comparison groups) of <0.05. To minimise the protein-level false-positive rates, a protein FDR of 1%, which was based on an established "picked" protein FDR strategy 39 , was estimated after proteins were tentatively identified (protein-level FDR ≤ 0.01).
Nuclear RNA extraction and sequencing. Total RNA was extracted from the fruit peels of the two pomegranate cultivars sampled at two fruit development stages for subsequent RNA sequencing analysis. The RNA was extracted from two biological replicates of frozen samples (100 mg) using the RNAprep Pure Plant Kit (Tiangen Biotech, Beijing, China). An ND 1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA) was used to evaluate the quality of the extracted RNA. Additionally, RNA with an RNA Integrity Number > 8 according to the 2100 Bioanalyzer (Agilent, USA) was used to prepare cDNA libraries with the RNA Library Prep Kit (Illumina, San Diego, CA, USA). The resulting libraries were sequenced on a HiSeq2000 platform (Illumina) to generate 100-bp paired-end reads.
Processing of sequence data and mapping reads to reference genome. The sequenced data were filtered by removing adaptor sequences, empty reads, reads with more than 5% unknown nucleotides, low-quality sequences (base quality ≤ 20), or sequences with >10% Ns using SOAPnuke (version 1.5.2) 40 . Clean reads were mapped to the reference genome sequence using HISAT (version 0.1.6-beta) 41 . The reads were assembled into transcripts and compared with reference gene models using Cufflinks 42 . Gene expression was quantified using RSEM (RNA-Seq by Expectation Maximization, version 1.2.12) 43 . The data were normalised as fragments per kilobase of transcript per million fragments mapped (FPKM) 44 . The differences in transcript abundance between two genotypes were calculated based on the ratio of FPKM values. The FDR control method was used to identify the threshold of the P value using Cuffdiff (included in the cufflinks package). Only transcripts with P ≤ 0.001 and |log2 (TP/SP)| > 1 were further analysed.
KEGG pathway enrichment analyses of DAPs and DEGs. The KEGG pathway enrichment analysis of the DAPs or DEGs was conducted using the KOBAS2.0 website (http://kobas.cbi.pku.edu.cn/) 45 . We identified significantly enriched metabolic pathways by using the hyper geometric test (http://en.wikipedia.org/wiki/ Hypergeometric_distribution). The metabolic pathways that were significantly enriched compared with the whole genome background were considered with corrected values (P < 0.05). Quantitative real-time PCR analysis. Total RNA was used as the template for cDNA synthesis with reverse transcriptase (Takara Bio, Kusatsu, Japan) following the manufacturer's instructions. The qRT-PCR analyses were conducted using the SYBR premix Ex Taq ™ kit (Takara, Dalian, China) and a LightCycler ® 480 instrument (Roche, IN, USA), with gene-specific primers designed using Primer3 software 46 . The reactions were conducted in a 20-µl volume containing 10 µl 2 × SYBR Green Master Mix (Takara), 300 nM each primer (Supplementary Table S5), and 2 µl 10-fold diluted cDNA template. The qRT-PCR program was as follows: 95 °C for 10 s; and 40 cycles of 95 °C for 15 s and 60 °C for 30 s. The qRT-PCR analyses involved three biological replicates, each with two technical replicates. Relative gene expression levels were calculated according to the 2 −ΔΔCt method 47 .
Data availability. The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository under the dataset identifier PXD009129.