Novel candidate genes influencing natural variation in potato tuber cold sweetening identified by comparative proteomics and association mapping
© Fischer et al.; licensee BioMed Central Ltd. 2013
Received: 22 March 2013
Accepted: 2 August 2013
Published: 7 August 2013
Higher plants evolved various strategies to adapt to chilling conditions. Among other transcriptional and metabolic responses to cold temperatures plants accumulate a range of solutes including sugars. The accumulation of the reducing sugars glucose and fructose in mature potato tubers during exposure to cold temperatures is referred to as cold induced sweetening (CIS). The molecular basis of CIS in potato tubers is of interest not only in basic research on plant adaptation to environmental stress but also in applied research, since high amounts of reducing sugars affect negatively the quality of processed food products such as potato chips. CIS-tolerance varies considerably among potato cultivars. Our objective was to identify by an unbiased approach genes and cellular processes influencing natural variation of tuber sugar content before and during cold storage in potato cultivars used in breeding programs. We compared by two-dimensional polyacrylamide gel electrophoresis the tuber proteomes of cultivars highly diverse for CIS. DNA polymorphisms in genomic sequences encoding differentially expressed proteins were tested for association with tuber starch content, starch yield and processing quality.
Pronounced natural variation of CIS was detected in tubers of a population of 40 tetraploid potato cultivars. Significant differences in protein expression were detected between CIS-tolerant and CIS-sensitive cultivars before the onset as well as during cold storage. Identifiable differential proteins corresponded to protease inhibitors, patatins, heat shock proteins, lipoxygenase, phospholipase A1 and leucine aminopeptidase (Lap). Association mapping based on single nucleotide polymorphisms supported a role of Lap in the natural variation of the quantitative traits tuber starch and sugar content.
The combination of comparative proteomics and association genetics led to the discovery of novel candidate genes for influencing the natural variation of quantitative traits in potato tubers. One such gene was a leucine aminopeptidase not considered so far to play a role in starch sugar interconversion. Novel SNP’s diagnostic for increased tuber starch content, starch yield and chip quality were identified, which are useful for selecting improved potato processing cultivars.
Sessile higher plants evolved various strategies to adapt to chilling conditions. Among other transcriptional and metabolic responses to cold temperatures plants accumulate a range of solutes including amino acids, glucosides or sugars. Although the precise function of sugars remains to be elucidated, their accumulation suggests roles as osmoregulators, cryoprotectants or signaling molecules. In mature potato tubers, the accumulation of soluble sugars during cold adaptation is referred to as cold induced sweetening (CIS) [1–3]. The sugars sucrose, glucose and fructose accumulating in photosynthetic inactive tissues like potato tubers are recruited from starch degradation [3, 4]. Enzymes involved in starch and sugar metabolism have been identified and studied intensively in potato and other plants at the biochemical and molecular level [5–7]. However, the regulation of this process is not entirely understood. Various enzymes, such as amylase, UDP glucose pyrophosphorylase or invertase, have been suggested to control the level of CIS in tubers either by increased or suppressed expression or activity [8–10]. The activity of invertase, which converts sucrose into glucose and fructose, is apparently subject to post-translational regulation by proteinaceous inhibitors [11–15].
Beside functions in plant adaption to cold temperatures CIS is an important issue for the potato processing industry. Long term storage of potato tubers at low temperatures is advantageous to reduce sprouting, thereby extending marketability. However, high concentrations of the reducing sugars glucose and fructose, either inherently or caused by CIS, negatively affect the quality of processed food products such as potato chips and French fries .
Potato cultivars show extensive natural variation in CIS capacity [17, 18]. Diversity in tuber sugar content might be explained by the variation of abundance and/or activity of carbohydrate metabolizing enzymes in source (photosynthetic leaves) and sink tissues (tubers), and by variable flux of sucrose from source to sink. Knowledge of the molecular basis of the diversity will contribute to the deciphering of plant cold adaptation and the development of diagnostic markers that can be used to select cultivars with low capacity of sugar accumulation and therefore improved processing quality.
Tuber starch and sugar content are quantitative traits controlled by multiple genetic and environmental factors. Molecular linkage mapping of quantitative trait loci (QTL) and candidate genes revealed co-localization of some QTL for tuber starch and sugar content with genes functional in carbohydrate metabolism or transport [17, 19–21]. More recently, association genetics demonstrated that DNA polymorphisms in genes encoding invertases and starch phosphorylases were associated with potato chip color, starch content and starch yield [22–24]. The genetic analyses support the working model that natural variation in tuber starch and sugar content is controlled by allelic variants of enzymes that function in starch and sugar metabolism. However, this model explains only part of the observed genetic variation.
To identify novel factors influencing sugar accumulation in tubers, unbiased and comprehensive approaches such as transcriptome and proteome profiling are required. Microarray hybridization experiments using a tomato gene chip hybridized with potato RNA allowed the identification of known as well as novel genes that were differentially expressed during tuber cold storage in a single potato genotype. Transcript levels of known candidate genes, such as invertase, were correlated with sugar accumulation . Analyzing the proteome captures both the variation of transcript abundance and the variation of post-transcriptional processes in biological samples, and differential expression of proteins reflects the translated genome in any environment or stress . Comparative proteome analysis has previously proven successful in identifying new candidate genes for controlling tuber quality traits [27–29].
The objective of this study was to decipher the molecular basis of natural variation in tuber reducing sugar content (RSC) and cold induced sweetening (CIS) ability in elite breeding materials of Solanum tuberosum. Using 2D-PAGE (two-dimensional polyacrylamide gel electrophoresis) we compared the tuber proteome of forty potato cultivars showing high diversity in tuber reducing sugar content and detected correlations between the expression level of distinct proteins and RSC. In addition a cold storage experiment was performed to tackle proteins differentially expressed in response to cold treatment as well as between CIS-tolerant (CIS-t) and CIS-sensitive (CIS-s) cultivars. Comparative 2D-PAGE protein profiling of pools of CIS-tolerant and CIS-sensitive genotypes at certain time points during cold storage identified at least fifty differentially expressed proteins. SNPs at two selected candidate loci encoding proteins either correlated with RSC or differentially expressed between CIS-tolerant and CIS-sensitive cultivars throughout cold storage were tested for association with tuber starch and chip quality in order to validate their potential role in controlling natural variation of these traits. Our approach led to the discovery of novel, potential regulatory genes that have not been connected so far to plant carbohydrate metabolism.
Tuber reducing sugar content (RSC) before and after cold treatment
Correlation between RSC and protein spot intensity without cold treatment
Proteins showing significant (ρ < 0.05) correlation between mean spot intensity and tuber sugar content in 40 cultivars
Granule-bound starch synthase
Granule-bound starch synthase
Putative Kunitz-type tuber invertase inhibitor precursor
400010146, 40001043, 400010139
Proteinase inhibitor II
Comparative protein profiling during cold treatment
Tuber proteins differentially expressed in genotype pool CIS-t versus pool CIS-s during 12 weeks storage at 4°C
Ratio of mean spot volume1
Serine protease inhibitor 7
Serine protease inhibitor 7
Kunitz-type enzyme inhibitor S9C11
Aspartic protease inhibitor 5
Kunitz-type proteinase inhibitor
Kunitz-type proteinase inhibitor
Kunitz-type proteinase inhibitor
Cysteine protease inhibitor 1
Proteinase inhibitor II
Proteinase inhibitor II
Proteinase inhibitor II
Patatin Group M-3
Heat shock proteins
Chloroplast small heat shock protein class I
Heat shock protein (HSP70)
101 kDa heat shock protein
Leucine aminopeptidase, chloroplastic
Leucine aminopeptidase, chloroplastic
Leucine aminopeptidase, chloroplastic
Leucine aminopeptidase, chloroplastic
Pathogenesis related proteins
Putative PR-10 type pathogenesis-related protein
Thirty six of fifty differential protein spots were assigned to various protease inhibitors (PI’s), isoforms of the storage protein patatin, a lipoxygenase (Lox), a phospholipase A1 (PLA1), phosphoglycerate kinase (PGK), several heat shock proteins (HSP), a leucine aminopeptidase (Lap), pathogenesis related protein 10 (PR10) and an actin (Data on protein identification provided in Additional file 5: Table S5). The largest group corresponded to protease inhibitors.
Twenty eight protein spots were differentially expressed before the onset of cold treatment, seventeen at higher level in genotype pool CIS-t and eleven in pool CIS-s. For example, three series of spots identified as Lox (spots 31–35, Figure 3A), PLA1 (spots 36, 39 and 40) and Lap (spots 47–50) showed higher expression in pool CIS-t compared to pool CIS-s. In contrast, Kunitz-type protease inhibitors (spots 2, 3, 4 and 6) and HSP’s (spot 5) were more abundant in pool CIS-s versus CIS-t.
Significant differential expression of eighteen proteins was maintained at all time-points during cold treatment. Of major interest are spots 6 and 19, which migrated at different pI and molecular weight but were assigned to the same miraculin accession when searching the NCBI protein database. The tryptic peptides matched to different loci on chromosomes III and XII in the potato genome sequence . The miraculin gene on chromosome III was consistently higher expressed in pool CIS-t and the miraculin gene on chromosome XII in pool CIS-s (Additional file 4: Table S4).
Additional expression patterns observed were: induction by cold treatment either in genotype pool CIS-t (e.g. spot 20) or CIS-s (e.g. spots 11, 14) or in both pools (e.g. spots 3, 7, 16), either transiently (e.g. spots 10, 11, 50) or continuously (e.g. spots 7, 20), or repression by cold treatment, either in pool CIS-t (e.g. spots 24, 38) or CIS-s (e.g. spot 17) or in both pools (e.g. spot 25).
Genomic organization of candidate genes and association with tuber quality traits
Single nucleotide polymorphisms (SNP’s) at two loci encoding the differentially expressed proteins ‘putative Kunitz-type tuber invertase inhibitor’ (AAL60242) and ‘chloroplastic leucine aminopeptidase’ (P31427) were tested for association with tuber quality traits in the CHIPS-ALL association mapping population .
a) Putative Kunitz-type tuber invertase inhibitor (KT-InvInh)
SNPs/Indels associated with tuber starch content (TSC), starch yield (TSY), chip quality after harvest (without cold storage, CQA) and 3 months cold storage (CQS) in the CHIPS-ALL population
Minor allele frequency
CQA 2R 2 [%]
CQS R 2 [%]
TSC R 2 [%]
TSY R 2 [%]
Putative Kunitz-type tuber invertase inhibitor (KT-InvInh)
A/G261 (±GATGAT114, G/T334)
C/G206 (C/G352, C/G362, A/T391, A/G/C430)
Leucine aminopeptidase, neutral (LapN)
b) Chloroplastic leucine aminopeptidase (Lap)
Comparative proteomics in combination with association genetics was used to decipher the molecular basis of natural variation in reducing sugar accumulation and CIS-tolerance in potato tubers. We identified proteins, the abundance of which correlated with tuber sugar content. Moreover, we identified proteins showing differential expression between groups of cultivars with high and low CIS-tolerance before and during cold storage.
Differential protein levels may be the cause or the consequence of the process leading to a phenotype such as tuber sugar content. The genes controlling phenotypic variation are a subset of all genes that have a metabolic, structural or regulatory function in phenotypic expression. Accordingly, DNA polymorphisms should be present in coding or regulatory regions of causal genes that are associated with the phenotypic variation. Comparative protein profiling and association genetics are therefore complementary approaches for zooming in on genes controlling complex traits. DNA polymorphisms at two loci encoding the differential proteins KT-InvInh and StLapA were associated with tuber quality traits like tuber starch content, tuber starch yield or chip quality. Consequently, they represent good candidate genes for contributing to the natural variation in tuber RSC and CIS tolerance. To be useful for breeding applications, the genetic material used for association analysis should originate from state of the art breeding programs. Our association panel, which consisted of varieties and advanced clones of commercial breeding programs in central Europe fulfilled this criterion . The newly discovered SNPs associated with chip quality, tuber starch content and starch yield in this genetic material can be used for marker assisted selection of superior processing cultivars.
For the identification of proteins up or down regulated in response to cold treatment and influencing natural variation in CIS tolerance we compared tuber protein profiles of CIS-s and CIS-t genotype pools during cold storage. The majority of the differential protein spots (28 out of 50) showed significant differences between genotype pools CIS-t and CIS-s before the onset of cold treatment (Table 2, Additional file 4: Table S4). These differences were generally maintained throughout cold storage. Consequently, our results suggest that these constitutive differences in protein expression are involved in that part of RSC, which is independent from cold treatment.
Among the differential spots were novel proteins such as leucine aminopeptidase that has not been considered so far to play a role in starch-sugar interconversion. Others like differential heat shock proteins corroborated previous findings [25, 28]. In contrast, several genes known to be associated with tuber sugar and starch content  were not detected as differentially expressed proteins, most likely due to limited resolution and sensitivity of 2D-PAGE. Nevertheless, this study demonstrates that comparative proteomics is suitable to identify novel candidate genes and yields results complementary to association mapping based on functional and positional candidate genes.
Proteins correlated with tuber sugar content
The most significant correlation was found for a putative Kunitz-type invertase inhibitor (KT-InvInh). This protein was previously purified from the soluble tuber protein fraction and was shown to inhibit soluble tuber invertase in vitro. The role of invertase in cold sweetening of potato tubers has been characterized previously [33–36]. Invertase enzymatic activity increased during cold storage, whereas an invertase inhibitory activity decreased, suggesting that invertase activity and thereby reducing sugar accumulation are regulated by a specific invertase inhibitor [14, 33, 37]. The negative correlation of KT-InvInh protein abundance with tuber sugar content is consistent with this model. KT-InvInh has no sequence similarity with other cloned invertase inhibitors of tobacco and potato [11–13, 38, 39].
Association analysis of KT-InvInh identified highly significant associations of nine SNPs and one indel with tuber starch content and starch yield but not with chip quality (Table 3). Interestingly, SNP307 (Additional file 6: Figure S1) was not associated with any trait. SNP307 causes the change from Valine (G307) to Methionine (A307), which was characteristic for the KT-InvInh protein . The allele A 307 had a frequency of 93% in the CHIPS-ALL population and was therefore nearly fixed. This might explain the lack of association with chip quality. The associations observed at the KT-InvInh locus might also result from linkage disequilibrium with other differentially expressed Kunitz-type inhibitors that are physically linked to KT-InvInh (see Additional file 4: Table S4 and below). Alternatively, KT-InvInh may target in vivo a protein, which regulates starch degradation. In this case KT-InvInh allelic variants could have a causal effect on tuber starch content and starch yield.
The two additional inhibitors negatively correlated with RSC were a miraculin and a potato inhibitor 2 (PIN2). Similarly to miraculins, PIN2s have not been considered as candidate genes in the context of starch-sugar interconversion. As correlations between two variables do not provide conclusive evidence for a causal relationship between them, the effect of protease inhibitors on sugar accumulation may be direct or indirect.
Proteins differentially expressed between genotype pools CIS-t and CIS-s
Fifty protein spots differed qualitatively or quantitatively between ten genotypes accumulating either low (CIS-t) or high reducing sugar levels (CIS-s) before and during cold treatment. Due to high sequence similarity between the members of some gene families, an unambiguous locus could not be assigned to all protein spots. Different spots matching to the same protein accession can be allelic variants of the same gene. Alternatively, spots derived from different genes can match to the same protein accession due to limited resolution of the protein databases. Among the annotated spots were isoforms of the most abundant tuber proteins patatin and protease inhibitors (PI) [27, 40–42]. Thirteen differentially expressed proteins were Kunitz-type protease inhibitors (KPI) or potato inhibitors 2 (PIN2). KPIs and PIN2s are encoded by multi-gene families organized in mixed clusters at the StKI locus on potato chromosome III [31, 43]. Several studies have demonstrated high sequence variability and genotype specific variants among potato protease inhibitors [29, 41–45]. The structural variation may indicate functional variation. Apart from proteases, enzymes like invertase and amylase were inhibited by PIs [15, 42, 46–48]. The genotype dependent, and in some cases cold induced or repressed expression suggests a regulatory role of several PIs in starch-sugar interconversion.
Remarkable differences between CIS-t and CIS-s genotypes were detected for patatin and phospholipase A1 (PLA1) isoforms. The role of patatin in potato tubers has been described as storage proteins that serve as nitrogen source for sprouting and early plant growth. The in vitro lipid acyl hydrolase (LAH) and phospholipase activity of patatin and related proteins of other plants suggest additional functions [49–51]. Phospholipases are involved in phospholipid and galactolipid degradation leading to changes in membrane composition and properties during cold acclimation [52, 53]. Increased membrane fluidity will lower the threshold temperature for membrane damage and will maintain activity of membrane associated proteins. Such a role of patatins and phospholipase A1 in altering membrane lipid composition could explain differences between genotypes with strong (CIS-s) and weak (CIS-t) cold acclimation responses.
Lipoxygenase (Lox) is a dioxygenase which catalyses the hydroperoxidation of polyunsaturated fatty acids. The Lox that was differentially expressed between genotype pools CIS-t and CIS-s corresponded to a 9-Lox. 9-Lox oxidizes preferentially linoleic acid to 9(S)-hydroperoxy linoleic acid, which is the predominant hydroperoxide isoform in potato tubers [54, 55]. Metabolites generated by 9-Lox were involved in tuber development. Suppression of 9-Lox activity in tubers correlated with reduced tuber yield, decreased tuber size and a disruption of tuber formation . The role of 9-Lox in dormant potato tubers is unclear. Several studies investigated Lox activity in potato tubers during cold sweetening [54, 57]. Lox was supposed to contribute to peroxidative damage occurring during cold storage. However, there was no clear correlation between cold sweetening and membrane permeability or lipid saturation level . Furthermore, cold sweetening is a reversible process since sugar levels decrease when tubers are transferred back to higher temperatures, which is not in agreement with the irreversible peroxidation of membranes . Although speculative at this point, we propose that patatin, PLA1 and Lox isoforms modulate in a cultivar specific manner the properties of membranes, which leads to genotypic differences in cold acclimation and sweetening by yet unknown mechanisms.
The adaptation of tubers to low temperature might include other pathways besides starch-sugar interconversion and membrane composition. Interesting candidates in this respect are the isoforms of a chloroplastic (plastidic) leucine aminopeptidase (LapA) which were more abundant in CIS-t than in CIS-s genotypes. The corresponding locus on chromosome XII consists of duplicated, physically closely linked Lap genes and is linked to QTL for tuber starch and sugar content. Plant leucine aminopeptidases are involved in a wide range of physiological processes . LapA was first identified in potato in response to wounding and is assumed to be unique for Solanaceous plants . LapA was induced by water deficit, salinity, pathogen attack and in response to jasmonic and abscisic acid [58, 60, 61]. The neutral Lap (LapN) was constitutively expressed in various plant species and is assumed to play a role in general cell maintenance, whereas expression of acidic Lap (LapA) was more specific . Our findings suggest a novel regulatory function of LapA in starch-sugar interconversion. StLapA, presumably located in amyloplasts, may inhibit starch degradation by proteolysis of active enzymes, thereby indirectly repressing sugar accumulation.
Association analysis identified SNP2746 in the StLapN gene that was strongly associated with chip quality with and without cold storage, tuber starch content and starch yield. Attempts to score SNPs directly in the differentially expressed StLapA gene failed due to the presence of insertion-deletion polymorphisms in the amplicons derived from highly heterozygous tetraploid individuals. Since StLapN is separated from StLapA only by few kilobase pairs and since linkage disequilibrium (LD) in potato can extend over several hundred kilobase pairs , the association of SNP2746 with the tuber traits may be due to LD with StLapA. The average RSC of cultivars possessing the SNP allele A 2746 was clearly lower than the average of cultivars lacking this allele throughout cold storage (Figure 4), which makes this SNP an attractive marker for breeding applications.
Differential spots were also assigned to proteins involved in metabolic processes like glycolysis or stress response. Heat shock proteins involved in stress responses were more abundant exclusively in the CIS-s genotypes. HSPs are ubiquitous molecular chaperones which protect other proteins from missfolding after temperature stresses. Accumulation of HSPs in response to cold stress has been reported [25, 64, 65]. Genotypic variation of HSPs can therefore have consequences for several metabolic processes in potato tubers including cold sweetening.
Reducing sugar levels and tuber bruising
Intriguing overlaps were observed between the types of proteins that were differentially expressed in genotypes with high and low reducing sugar levels (this study) and genotypes with high and low susceptibility to tuber bruising . Bruising describes the enzymatic discoloration of internal tuber tissue upon mechanical damage and seems biochemically unrelated with starch-sugar interconversion. In both studies however, protease inhibitors, patatins, lipoxygenase and phospholipase A1 (identical to lipase class III) were independently identified as genotype dependent differential proteins. In the case of Kunitz-type enzyme inhibitor S9C11, Lox and PLA1, the tryptic peptides matched unambiguously to the same loci (PGSC0003DMG400010147, PGSC0003DMG400020999 and PGSC0003DMG401031759), indicating that the differential proteins were products of the same genes, though the alleles associated with RSC and bruising susceptibility might not be the same. Susceptibility to bruising is strongly correlated with higher tuber starch content, and membrane stability may also play a role . This suggests tuber starch content and/or membrane structure as common denominators of sugar levels and bruising, which influence both RSC and bruising susceptibility. PIs together with components of lipid metabolism and/or signaling might regulate both traits either directly or indirectly via regulation of tuber starch content or membrane composition.
The combination of proteomics and association genetics described in this paper provides an innovative route to better understand complex plant traits at the molecular level, particularly in non model plants such as the potato. Comparative proteomics across a diversity panel enabled the identification of unapparent candidate genes not noticed in classical functional approaches, where protein abundance or activity in response to environmental changes is studied in a single genotype. Association of DNA polymorphisms in loci encoding differentially expressed proteins validated a role of leucine aminopeptidase in tuber starch content, starch yield and chip quality. Lap has not been considered so far as acting in carbohydrate metabolism or cold induced sweetening. The SNP’s associated with tuber quality can be used for marker-assisted selection of CIS resistant cultivars.
Plant material and tissue sampling
Field grown tubers of 39 cultivars and one breeding clone (Additional file 1: Table S1) were provided by Böhm-Nordkartoffel Agrarproduktion OHG (BNA, Ebstorf, Germany). Twenty cultivars had been selected for having good processing quality compared with twenty others having bad processing quality. After delivery, tubers were stored for twelve weeks at 4°C in the dark. Prior to and after one, two, four and twelve weeks of cold storage, tissue of three peeled tubers per cultivar and time point were individually snap frozen in liquid nitrogen. For protein extraction, frozen tuber tissue was ground to fine powder in a bead mill (Retsch, Haan, Germany) and stored at -80°C until use. Tissue aliquots were freeze-dried, for sugar extraction. For correlation analysis, total tuber proteins of all 40 cultivars without cold storage were separated by 2D-SDS-PAGE. For comparative proteome analysis during cold storage, tuber protein extracts from cultivars ‘Verdi’, ‘Lady Claire’, ‘Omega’, ‘Eurobeta’ and breeding clone 18 (pool “CIS-tolerant”, “CIS-t”), and ‘Elfe’, ‘Marabel’, ‘Solara’, ‘Melba’ and ‘Allians’ (pool “CIS-sensitive”, “CIS-s”) were pooled and analyzed. The population ‘CHIPS-ALL’ comprising 207 tetraploid genotypes was used for association mapping, which consisted of 33 standard varieties and 76, 91 and 7 breeding clones from Böhm-Nordkartoffel Agrarproduktion OHG (BNA, Ebstorf, Germany), Saka Pflanzenzucht GbR (Windeby, Germany) and Nordring-Kartoffelzucht-und Vermehrungs-GmbH (NORIKA, Groß Lüsewitz, Germany), respectively. This population has been evaluated in replicated field trials for chip color after harvest in autumn (without cold storage, CQA) and after three months storage at 4°C (CQS), for tuber yield (TY), starch content (TSC) and starch yield (TSY) .
Glucose, fructose and sucrose measurement
Glucose, fructose and sucrose were estimated as described  with minor modifications. 100 mg dry powder were extracted with 1 ml ice cold 80% Ethanol and incubated at 80°C for 1 h. Extracts were concentrated to 100 μl using a vacuum concentrator (SpeedVac®, Thermo Fisher Scientific, MA, USA). 900 μl dH2O were added and samples were mixed until precipitates were dissolved. Saccharose, glucose and fructose were measured by a coupled enzymatic assay (“D-Glucose, D-Fructose, Saccharose”, R-Biopharm, Darmstadt, Germany) following the suppliers instructions. Sugar content was obtained as percent tuber dry weight (μg*100 μg-1 dry weight). Tuber reducing sugar content (RSC) resulted from the sum of glucose and fructose content. RSC was measured in three tubers per cultivar (biological replicates) and means and standard errors were estimated.
Total protein was extracted from 300 mg ground frozen tuber-tissue as described . Protein pellets were re-suspended in urea-buffer (8 M urea, 2 M Thiourea). Protein abundance was estimated using the Qubit® protein assay kit (Invitrogen, CA, USA). The resulting protein extracts were frozen in liquid N2 and stored at -80°C until use.
2D-PAGE, image acquisition and data analysis
For correlation analysis between RSC and protein expression levels in 40 cultivars, protein of three individual tubers per cultivar was separated by analytical 2D-PAGE. 150 μg total tuber protein were subjected to isoelectric focusing (IEF) (Zoom® strips pH3-7NL, Invitrogen, CA, USA) using the Protean IEF system (BIORAD, CA, USA) according to the manufactures instructions. IPG (isoelectric focusing gel) strips were rehydrated for 12 h in 7 M urea, 2 M thiourea, 2% CHAPS (3-[(3-Cholamidopropyl) dimethylammonio]-1-propanesulfonate), 0.5% IPG-buffer pH 3–10 (Invitrogen, CA, USA), 25 mM DTT (Dithiothreitol) and trace amounts of bromphenol blue. Prior to SDS-PAGE IPG-strips were equilibrated at room temperature in 6 M urea, 0.375 M Tris–HCl pH 8.8, 2% SDS, 20% glycerol, 2% DTT for 10 min followed by a second equilibration in the same buffer except that DTT was replaced by 2.5% iodoacetamide. SDS-PAGE was run using 12% NuPAGE®Novex Bis-Tris gels (Invitrogen, CA, USA) in MES-SDS buffer system at 200 V. Gels were fixed for 1 h in 50% methanol, 10% acetic acid at room temperature followed by three washes with H2O. Gels were stained with PageBlue™ staining solution (Fermentas, St. Leon-Rot, Germany) according to the instructions of the manufacturer. Protein gels were digitalized using a daylight scanner integrated within the Proteineer spII spotting system (Bruker Daltonics, Bremen, Germany). Gels of three biological replicates per cultivar were analyzed. Protein spots were detected on scanned gels using the default spot detection settings in Proteome Weaver 2-DE analysis software package (BIORAD, CA, USA). Spot intensities were calculated subsequent to normalization of the spots using the pair-match-based normalization algorithm implemented in the software. Mean spot intensities and standard errors were calculated for 26 selected spots that were detectable in more than 70% of all gels of the cultivars and replicates. For correlation analysis, residuals of mean spot intensity and RSC were checked graphical for normal distribution and transformed into logarithmic values. Multiple R2 were calculated by regression analysis of logarithmic RSC values, respectively spot intensities and the genotype. Pearson’s product–moment correlation coefficient and significance were calculated using the SPSS software package (IBM, NY, USA). Spots showing significant correlations (p < 0.05) were isolated from 2D-gels and digested with trypsin. Tryptic peptides were identified by mass spectrometry (MS) and protein sequence database comparisons (see below). For comparative proteome analysis during cold storage, tuber protein extracts from cultivars ‘Verdi’, ‘Lady Claire’, ‘Omega’, ‘Eurobeta’ and breeding clone 18 (CIS-tolarant, CIS-t), and ‘Elfe’, ‘Marabel’, ‘Solara’, ‘Melba’ and ‘Allians’ (CIS-sensitive, CIS-s) were used. Total protein was extracted from three tubers per cultivar and time point prior to and after two, four and twelve weeks of storage at 4°C. Equimolar amounts of protein from a single tuber of CIS-t and CIS-s genotypes were combined, resulting in three pooled samples (biological replicates) per time point. 300 μg pooled protein was separated by 2D-PAGE using two different conditions for IEF and SDS-PAGE. IEF was performed using 24 cm IPG strips with immobilized pH gradients ranging from pH4-7 and pH 3–10 according to the manufacturer’s guidelines (GE Healthcare, WI, USA). IPG-strips were equilibrated (see above) and subjected to 16% SDS-PAGE (24 x 20 cm, 1 mm thickness) using the Tris-tricine buffer system  or 10% SDS-PAGE (24 × 20 cm, 1.5 mm thickness) using Tris-glycine buffer system . Electrophoresis was carried out in the Ettan™DALTsix electrophoresis unit (GE Healthcare, WI, USA) at 30 V for 1 h followed by a constant current at 270 mA or using the PROTEAN Plus Dodeca Cell (BIORAD, CA, USA) at 30 V for 1 h, followed by a constant current at 200 mA. Electrophoresis was run for 16 h until the bromphenol-blue dye reached the bottom of the gel. Gels were fixed in 50% methanol/10% acetic acid for 2 h at room temperature and stained with PageBlue™ staining solution. Gel images were acquired as described above. Spots were detected using the default spot detection settings in the Delta2D analysis software (DECODON GmbH, Greifswald, Germany). Twenty four gel pictures (three biological replicates of pooled CIS-t and CIS-s genotypes at four time-points) were included in the analysis. Four analysis sets were composed of the gels generated before (T0) and after two, four and twelve weeks of cold storage. Delta2D analysis software was used to produce a fused image of the gels of one analysis set to identify qualitative and quantitative differences between CIS-t and CIS-s genotypes. Within one analysis set spot intensities were normalized by the vertical normalization algorithm implemented in the Delta2D software. The algorithm is based on the division of the spot intensity by the sum of all spot intensities on the respective gel. Significant differences in spot intensities between CIS-t and CIS-s were evaluated by statistical analysis implemented in the Delta2D software using the “between samples” T-Test assuming different group variances (Welch approximation) and without correction for multiple testing. Differentially expressed proteins were identified as described below.
MS Analysis, MALDI Data Acquisition, Database Searching
Spots were selected from Coomassie-stained gels, excised and digested with trypsin using the Proteineer spII and dp systems (Bruker Daltonics, Bremen, Germany). Sample digests were spotted onto Anchorchip steel targets (Bruker Daltonics, Bremen, Germany) prepared with a thin layer of α-cyano-4-hydroxycinnamic acid (HCCA) matrix . Peptide mass fingerprint (PMF) data were collected on an UltraflexIII MALDI ToF/ToF mass spectrometer (Bruker Daltonics, Bremen, Germany) and used for a first round of database searching using MASCOT 2.3 (http://www.matrixscience.com) against NCBI nr core collection and the potato genome sequencing consortium (PGSC) Solanum tuberosum group Phureja DM protein database. PMF searches were initially performed with a mass tolerance set to 50 ppm and re-performed with a tolerance of 150 ppm when post-calibration based on tryptic self-digest peptides failed.
Following sample recrystallization, LIFT MS/MS spectra were collected on up to five precursors selected from the PMF on the basis of peak intensity and relative isolation . MS/MS data were used to search both databases with a mass tolerance of 0.4 Da for both parent and fragment masses of MS/MS searches. For both MS and MS/MS, MASCOT scores falling below the 95% certainty criterion for the respective database were not considered significant.
Genomic positions of genes corresponding to the identified proteins were identified based on blastn and tblastn searches of the potato  and tomato  genome sequences (http://solanaceae.plantbiology.msu.edu/integrated_searches.shtml, http://solgenomics.net/tools/blast/index.pl).
Generation of SNP markers
Locus specific amplicons were generated by PCR (polymerase chain reaction) using genomic DNA of the individuals of the CHIPS-ALL population as template. A 1150 bp DNA fragment comprising the ‘putative Kunitz-type tuber invertase inhibitor’ (KT-InvInh, PGSC0003DMG400010146) was amplified with the forward (5´-TCAATAGAATTCCTTACCCG-3´) and reverse (5´-CAATAACGATATCTAGACCTGATTAAC-3´) primers at 55°C annealing temperature. An 850 bp DNA fragment from ‘neutral leucine aminopeptidase’ (LapN, superscaffold PGSC0003DMB000000116-chr12:910581..2552409) was amplified using the forward (5´-GCTTCCTGGTCTTGGCTCA-3´) and reverse (5´-GCAGCCAGGTCAGAAATCAA-3´) primers at 60°C annealing temperature. Standard PCR conditions were: 25 μL reaction mixture containing 50 ng genomic DNA in 1× Ammonium PCR buffer (Ampliqon, Scovlunde, Denmark), 2.5 mM MgCl2, 0.2 mM of each dNTP, 5 μM each forward and reverse primer and 1 U Taq polymerase (Ampliqon, Scovlunde, Denmark); 4 min initial denaturation at 94°C; 34 cycles of 45 sec denaturation at 94°C, 30 sec annealing at 55°C, 75 sec elongation at 72°C; final elongation at 72°C for 6 min. Amplicons were custom sequenced at the Max-Planck Genome Center Cologne using the dideoxy chain-termination sequencing method, an ABI PRISM Dye Terminator Cycle Sequencing Ready Reaction Kit and an ABI PRISM 3730 automated DNA Sequencer (Applied Biosystems, Weiterstadt, Germany). KT-InvInh amplicons were sequenced with the internal reverse primer 5´-CTACGCCTTGATGAACACAAATG-3′ and LapN amplicons were sequenced with the forward primer. Single nucleotide polymorphisms (SNP) in amplicon sequences were detected and scored as described .
y* represent the adjusted trait means. ‘Origin’ is a fixed factor with four classes, which corresponds to the origin of each cultivar from one of three breeding programs or standards. ‘Marker’ is a fixed factor with five levels corresponding to the five marker genotypic classes of a bi-allelic SNP (A 1 A 1 A 1 A 1 , A 1 A 1 A 1 A 2 , A 1 A 1 A 2 A 2 , A 1 A 2 A 2 A 2 and A 2 A 2 A 2 A 2 ).
Analysis of variance (ANOVA) was used to detect significant differences between RSC means of the genotype groups with the SNP allele StLapN-SNP 2746 present or absent in the 40 cultivars.
Cold induced sweetening
Reducing sugar content
Quantitative trait loci
Chip quality after harvest
Chip quality after cold storage
Polymerase chain reaction
Tuber starch content
Single nucleotide polymorphism.
This work was carried out in the department of Plant Breeding and Genetics headed by Maarten Koornneef. Funding was provided by the Max-Planck Society within the BIOSOL project (molecular analysis and sustainable utilization of BIOdiversity of SOLanum tuberosum), in cooperation with the Fraunhofer Society.
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