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Comparative genomics provides a tool to utilize the exponentially increasing sequence information from model plants to clone agronomically important genes from less studied crop species. Plant disease resistance (R) loci frequently lack synteny between related species of cereals and crucifers but appear to be positionally well conserved in the Solanaceae. In this report, we adopted a local RGA approach using genomic information from the model Solanaceous plant tomato to isolateR3a, a potato gene that confers race-specific resistance to the late blight pathogenPhytophthora infestans.R3ais a member of theR3complex locus on chromosome 11. Comparative analyses of theR3complex locus with the correspondingI2complex locus in tomato suggest that this is an ancient locus involved in plant innate immunity against oomycete and fungal pathogens. However, theR3complex locus has evolved after divergence from tomato and the locus has experienced a significant expansion in potato without disruption of the flanking colinearity. This expansion has resulted in an increase in the number ofRgenes and in functional diversification, which has probably been driven by the co-evolutionary history betweenP. infestansand its host potato. Constitutive expression was observed for theR3agene, as well as some of its paralogues whose functions remain unknown. [ABSTRACT FROM AUTHOR]

Plants have evolved complex defence mechanisms to avoid invasion of potential pathogens. Despite this, adapted pathogens deploy effector proteins to manipulate host susceptibility (S) genes, rendering plant defences ineffective. The identification and mutation of plant S genes exploited by bacterial pathogens are important for the generation of crops with durable and broad-spectrum resistance. Application of mutant S genes in the breeding of resistant crops is limited because of potential pleiotropy. New genome editing techniques open up new possibilities for the modification of S genes. In this review, we focus on S genes manipulated by bacteria and propose ways for their identification and precise modification. Finally, we propose that genes coding for transporter proteins represent a new group of S genes. Plant pathogenic bacteria use host susceptibility (S) genes to promote disease development. Many bacterial species use effector proteins to target S genes, resulting in effector-triggered susceptibility. S genes are evolutionarily retained across plant species. S genes can be identified and precisely mutated through new genome engineering tools. Impairment of S genes can lead to recessively inherited broad-spectrum resistance to bacteria. [ABSTRACT FROM AUTHOR]

Summary: Kiwifruit (Actinidia spp) is a woody, perennial and deciduous vine. In this genus, there are multiple ploidy levels but the main cultivated cultivars are polyploid. Despite the availability of many genomic resources in kiwifruit, SNP genotyping is still a challenge given these different levels of polyploidy. Recent advances in SNP array technologies have offered a high‐throughput genotyping platform for genome‐wide DNA polymorphisms. In this study, we developed a high‐density SNP genotyping array to facilitate genetic studies and breeding applications in kiwifruit. SNP discovery was performed by genome‐wide DNA sequencing of 40 kiwifruit genotypes. The identified SNPs were stringently filtered for sequence quality, predicted conversion performance and distribution over the available Actinidia chinensis genome. A total of 134 729 unique SNPs were put on the array. The array was evaluated by genotyping 400 kiwifruit individuals. We performed a multidimensional scaling analysis to assess the diversity of kiwifruit germplasm, showing that the array was effective to distinguish kiwifruit accessions. Using a tetraploid F1 population, we constructed an integrated linkage map covering 3060.9 cM across 29 linkage groups and performed QTL analysis for the sex locus that has been identified on Linkage Group 3 (LG3) in Actinidia arguta. Finally, our dataset presented evidence of tetrasomic inheritance with partial preferential pairing in A. arguta. In conclusion, we developed and evaluated a 135K SNP genotyping array for kiwifruit. It has the advantage of a comprehensive design that can be an effective tool in genetic studies and breeding applications in this high‐value crop. [ABSTRACT FROM AUTHOR]

SUMMARY: Phytophthora infestans is a pathogenic oomycete that causes the infamous potato late blight disease. Resistance (R) genes from diverse Solanum species encode intracellular receptors that trigger effective defense responses upon the recognition of cognate RXLR avirulence (Avr) effector proteins. To deploy these R genes in a durable fashion in agriculture, we need to understand the mechanism of effector recognition and the way the pathogen evades recognition. In this study, we cloned 16 allelic variants of the Rpi‐chc1 gene from Solanum chacoense and other Solanum species, and identified the cognate P. infestans RXLR effectors. These tools were used to study effector recognition and co‐evolution. Functional and non‐functional alleles of Rpi‐chc1 encode coiled‐coil nucleotide‐binding leucine‐rich repeat (CNL) proteins, being the first described representatives of the CNL16 family. These alleles have distinct patterns of RXLR effector recognition. While Rpi‐chc1.1 recognized multiple PexRD12 (Avrchc1.1) proteins, Rpi‐chc1.2 recognized multiple PexRD31 (Avrchc1.2) proteins, both belonging to the PexRD12/31 effector superfamily. Domain swaps between Rpi‐chc1.1 and Rpi‐chc1.2 revealed that overlapping subdomains in the leucine‐rich repeat (LRR) domain are responsible for the difference in effector recognition. This study showed that Rpi‐chc1.1 and Rpi‐chc1.2 evolved to recognize distinct members of the same PexRD12/31 effector family via the LRR domain. The biased distribution of polymorphisms suggests that exchange of LRRs during host–pathogen co‐evolution can lead to novel recognition specificities. These insights will guide future strategies to breed durable resistant varieties. Significance statement: In this manuscript the cloning of novel late blight resistance genes and their cognate effectors is described. The mechanism of recognition, host pathogen co‐evolution, and implications for deployment of the knowledge in agriculture are discussed. [ABSTRACT FROM AUTHOR]

The European Commission's Farm to Fork (F2F) strategy, under the European Green Deal, acknowledges that innovative techniques, including biotechnology, may play a role in increasing sustainability. At the same time, organic farming will be promoted, and at least 25% of the EU's agricultural land shall be under organic farming by 2030. How can both biotechnology and organic farming be developed and promoted simultaneously to contribute to achieving the Sustainable Development Goals (SDGs)? We illustrate that achieving the SDGs benefits from the inclusion of recent innovations in biotechnology in organic farming. This requires a change in the law. Otherwise, the planned increase of organic production in the F2F strategy may result in less sustainable, not more sustainable, food systems. Sustainable food systems will require profound changes in people's consumption patterns and lifestyles, which is true regardless of the farming methods used and does not change the fact that organic farming often requires more land than conventional farming for the same quantity of food output. Some features of organic farming in the EU contribute to the Sustainable Development Goals (SDGs); other features may jeopardize the achievement of SDGs 2, 13, and 15. The negative indirect effects of additional land-use change may outweigh the positive direct effects on global climate and biodiversity, so that a large-scale switch to organic farming in the EU could possibly turn out to be a disservice to global sustainability. Achieving the SDGs would benefit from the inclusion of biotech innovations in organic farming. The implementation of required changes in the EU law is unlikely under current political realities but is nevertheless recommended from a scientific perspective. [ABSTRACT FROM AUTHOR]

Background: Scientific literature carries a wealth of information crucial for research, but only a fraction of it is present as structured information in databases and therefore can be analyzed using traditional data analysis tools. Natural language processing (NLP) is often and successfully employed to support humans by distilling relevant information from large corpora of free text and structuring it in a way that lends itself to further computational analyses. For this pilot, we developed a pipeline that uses NLP on biological literature to produce knowledge networks. We focused on the flesh color of potato, a well-studied trait with known associations, and we investigated whether these knowledge networks can assist us in formulating new hypotheses on the underlying biological processes. Results: We trained an NLP model based on a manually annotated corpus of 34 full-text potato articles, to recognize relevant biological entities and relationships between them in text (genes, proteins, metabolites and traits). This model detected the number of biological entities with a precision of 97.65% and a recall of 88.91% on the training set. We conducted a time series analysis on 4023 PubMed abstract of plant genetics-based articles which focus on 4 major Solanaceous crops (tomato, potato, eggplant and capsicum), to determine that the networks contained both previously known and contemporaneously unknown leads to subsequently discovered biological phenomena relating to flesh color. A novel time-based analysis of these networks indicates a connection between our trait and a candidate gene (zeaxanthin epoxidase) already two years prior to explicit statements of that connection in the literature. Conclusions: Our time-based analysis indicates that network-assisted hypothesis generation shows promise for knowledge discovery, data integration and hypothesis generation in scientific research. [ABSTRACT FROM AUTHOR]

We discuss options to reform the EU genetically modified organisms (GMO) regulatory framework, make risk assessment and decision-making more consistent with scientific principles, and lay the groundwork for international coherence. The first in a three-part series, this article focuses on reform options related to the scope of the legislation and the GMO definition. [ABSTRACT FROM AUTHOR]

Potato (Solanum tuberosum) is an important food crop consumed all over the world, but it is generally sensitive to drought conditions. One of the major physiological processes affected by drought stress is carbon partitioning: the plant's choice of where to allocate its photoassimilates. Our aim was to investigate the molecular factors and possible bottlenecks affecting carbon partitioning during drought. We studied potato cultivars with contrasting drought responses in the greenhouse in the years 2013–2015, and further investigated the expression of genes involved in carbon partitioning and metabolite levels. Our results indicate that one of the most severe effects of drought stress on potato is the arrest of stolon differentiation and formation of tubers. We also identified some physiological traits like stomatal conductance and chlorophyll content as affecting carbon assimilation, partitioning and eventual tuber yield. The gene expressions and biochemical analyses highlight the various tissues prioritized by the plant for assimilate transport during drought stress, and give indications of what distinguishes drought tolerance and sensitivity of cultivated potato. Some of the key genes studied (like Sucrose synthase and Sucrose transporters) may be inclusive breeding targets for drought tolerance in potato. • Sugar export from source leaves, not its availability, is key in drought tolerance. • Tuber initiation arrest can alter carbon transport to underground tissues. • Starch storage in leaves is a limitation to potato tuber yield under drought. [ABSTRACT FROM AUTHOR]

We discuss options to reform the EU genetically modified organism (GMO) regulatory framework, make risk assessment and decision-making more consistent with scientific principles, and lay the groundwork for international coherence. In this third of three articles, we focus on labeling and coexistence as well as discuss the political reality and potential ways forward. [ABSTRACT FROM AUTHOR]

Here, we discuss options to reform the EU genetically modified organism (GMO) regulatory framework, to make risk assessment and decision-making more consistent with scientific principles, and to lay the groundwork for international coherence. We discussed the scope and definitions in a previous article and, thus, here we focus on the procedures for risk assessment and risk management. [ABSTRACT FROM AUTHOR]

Is the European Union (EU) regulatory framework for genetically modified organisms (GMOs) adequate for emerging techniques, such as genome editing? This has been discussed extensively for more than 10 years. A recent proposal from The Netherlands offers a way to break the deadlock. Here, we discuss how the proposal would affect examples from public plant research. [ABSTRACT FROM AUTHOR]

The CALCINEURIN B-LIKE PROTEIN family genes (CBLs) encode a group of plant-specific calcium sensor proteins that play critical roles in plant development and stress response. Although genome-wide analysis of CBL family genes has been conducted in several diploid plant species, less is known about their functions in allopolyploid plant species. This study conducted a detailed analysis of tobacco CBL family genes. Of the 24 NtCBL genes identified, 14 were derived from the maternal genome donor N. sylvestris , and 10 were from the paternal genome donor N. tomentosiformis. Phylogenetic analysis revealed that NtCBLs could be clustered into three different groups with distinct N-terminal characteristics. All NtCBLs contain EF-hand motifs, but amino acid substitutions and configuration changes may be responsible for variations in their Ca2+-binding abilities. Alternative splicing is common for NtCBL gene transcripts, which may contribute to variations in translation efficiency or protein interaction preferences. Several NtCBL genes exhibited shoot- or root-predominant expression patterns, and some were responsive to salt and/or drought stress. NtCBL4A-1 , an ortholog of Arabidopsis thaliana AtCBL4 (SOS3), was predominantly expressed in roots and exhibited a lower gene expression level under salt stress. Further functional analysis showed that overexpression of NtCBL4A-1 increased the sensitivity of transgenic tobacco to Na+-induced salt stress, which is inconsistent with the role of AtCBL4 in contributing to salt tolerance. This study provides data for identifying CBL gene functions and selecting candidate stress-tolerant genes in N. tabacum. Additionally, the results may aid gene function studies in other allopolyploid plant species. • Twenty-four CBL s were genome-wide characterized in allotetraploid Nicotiana tabacum. • NtCBL homoeologs exhibit different expression dominance in specific tissues or developmental stages, which may offer an additional level of finetuning CBL functions. • The expression of NtCBL4A-1 decreases under salt stress in tobacco roots, which contradicts its known function in salt tolerance in other species. • Overexpression of NtCBL4A-1 interferes with the salt tolerance of tobacco, resulting in Na+-induced necrotic lesions on leaves. [ABSTRACT FROM AUTHOR]

In purple-fruited Capsicum genotypes, fruit anthocyanin content first increases, and later decreases upon ripening. In this study, the response of this transient anthocyanin accumulation as a function of light intensity and light spectrum was investigated. Harvested fruit at the mature purple stage were illuminated by white-red LED lights at a photosynthetic photon flux density of 0 (darkness), 80, 160 and 320 μmol m-2 s-1 or illuminated by 24 (white light), 57%, 72% and 99% blue light (400–500 nm) at a photosynthetic photon flux density of 80 μmol m-2 s-1 for 28 d. Total anthocyanin, chlorophyll, capsanthin and soluble sugar contents, and their related gene expression, were measured. Anthocyanin content was hardly affected by white-red light intensity. Increasing the blue light fraction increased anthocyanin levels, via enhancing anthocyanin biosynthesis. This is supported by kinetic modelling and higher expression levels of the anthocyanin biosynthetic genes CaMYB , CaCHS , CaDFR , CaANS and CaUFGT. A higher blue light fraction delayed fruit ripening. This is supported by delayed sugar accumulation as indicated by kinetic modelling and transcriptome analysis. Transcriptome analysis indicated that 91% of the differentially expressed genes down-regulated during ripening had a higher expression in the 72% compared to 24% blue light treatment. In addition, PCA analysis of transcriptomic data indicated fruit ripening and senescence related genes NCED1 , NCED2 , NOR and RIN were expressed less in fruit illuminated by 72% blue light. Pathways upstream of ethylene production were downregulated in fruits illuminated with higher blue light fractions that might result in suppressed ethylene production. Higher fractions of blue light during postharvest storage might be applied to improve fruit anthocyanin levels but are not suited to create ripe anthocyanin rich pepper fruit. • Transient anthocyanin accumulation in purple pepper was investigated. • Light intensity did hardly affect anthocyanin levels in purple pepper fruit. • Illumination by higher blue light fractions resulted in higher anthocyanin synthesis. • Higher blue light fractions delayed ripening-related processes. • Most ripening related genes were downregulated with higher blue light fractions. [ABSTRACT FROM AUTHOR]

In all fruit and vegetable crops, reduction in quality during postharvest storage leads to substantial losses of primary production with enormous economic consequences. Also in tomato, fruit shelf-life is an important quality trait. In this study a collection of tomato accessions, consisting of 92 S. lycopersicum landraces and old cultivars and several S. pimpinellifolium accessions, was phenotyped for several shelf-life parameters and biochemical characterization was performed during the postharvest shelf-life of fruit from selected accessions. This collection was selected based on available genotypic data and represents the genetic diversity present in the EU–SOL tomato core collection (Roohanitaziani, 2020). The core collection was grown in a greenhouse, and fruit were harvested at the breaker-turning stage and stored in a controlled climate chamber for 42 d at 18 ⁰C. The shelf-life attributes firmness loss, weight loss, as well as color pigments, were measured once a week and evaluated over time. All three shelf-life-related parameters varied markedly among accessions, resulting in fruit with different shelf-life. The most promising accessions of the first screen were re-grown and analyzed to validate the initial results and six accessions with contrasting shelf-life were selected for metabolite analysis. Fruit were harvested at the breaker stage and stored for 35 d at 18 ⁰C. Samples were taken at weekly intervals and analyzed for volatile compounds, primary metabolites and cell wall polysaccharide monomers. During storage long and short shelf-life accessions showed considerable differences in their content of sugars, such as galactose and polyamines, such as putrescine in their pericarp. The content of three cell wall sugars, galactose, arabinose and galacturonic acid, underwent considerable changes during postharvest storage. The short shelf-life accessions contained a higher amount of arabinose and galactose in their cell wall than other accessions which is indicative of highly branched pectin. This knowledge provides a better understanding of the difference in pectin structure between short and long shelf-life fruit during the ripening process. • 92 tomato accessions were phenotyped for postharvest shelf-life attributes. • The short shelf-life accession contained a higher amount of arabinose and galactose in its cell wall. • In short shelf-life accession free galactose level increased dramatically upon postharvest storage. • Fruit of long shelf-life accessions contain high amount of putrescine in their pericarp. [ABSTRACT FROM AUTHOR]

Four potato cellulose synthase (CesA) homologs (StCesA1, 2, 3 and 4) were isolated by screening a cDNA library made from developing tubers. Based on sequence comparisons and the fact that all four potato cDNAs were isolated from this single cDNA-library, all four StCesA clones are likely to play a role in primary cell wall biosynthesis. Several constructs were generated to modulate cellulose levels in potato plants in which the granule-bound starch synthase promoter was used to target the modification to the tubers. The StCesA3 was used for up- and down-regulation of the cellulose levels by sense (SE-StCesA3) and antisense (AS-StCesA3) expression of the complete cDNA. Additionally, the class-specific regions (CSR) of all four potato cellulose synthase genes were used for specific down-regulation (antisense) of the corresponding CesA genes (csr1, 2, 3 and 4). None of the transformants showed an overt developmental phenotype. Sections of tubers were screened for altered cell wall structure by Fourier Transform Infrared microspectroscopy (FTIR) and exploratory Principal Component Analysis (PCA), and those plants discriminating from WT plants were analysed for cellulose content and monosaccharide composition. Several transgenic lines were obtained with mainly decreased levels of cellulose. These results show that the cellulose content in potato tubers can be reduced down to 40% of the WT level without affecting normal plant development, and that constructs based on the CSR alone are specific and sufficient to down-regulate cellulose biosynthesis. [Copyright &y& Elsevier]

Abstract: Two transgenic potato lines, csr2–1 and csr4–8 that contained two different antisense cellulose synthase (CesA) genes, csr2 and csr4, respectively were crossed. The aim, amongst others, was to investigate the possibility of generating double transformants to validate a hypothetical presence of the proteins of the two CesA genes in the same cellulose synthase enzyme complex. SYBR-Green quantitative real-time reverse transcription polymerase chain reaction (RT-PCR) assays were carried out on four CesA gene transcripts (CesA1, 2, 3, and 4) in the wild type genetic background, and on the two antisense CesA gene transcripts (CesA2 and 4) in the progeny resulting from the cross between the two transgenic potato lines. The quantitative RT-PCR analyses revealed different expression patterns of the two CesA genes. The CesA2 mRNA was shown to be relatively more abundant than CesA4 mRNA, regardless of the genetic background, suggesting that the two proteins are not present in the same enzyme complex. [Copyright &y& Elsevier]

• European sweet quinoa cultivars are extremely tolerant to salinity. • Quinoa varieties have a high capacity for ion exclusion under salinity. • Quinoa can adapt to increasing salinity stress by changing salinity response mechanisms. • Genotypic variation was found for salinity tolerance traits. • Epidermal bladder cells did not contribute substantially to ion exclusion. Quinoa is a nutritious seed crop with a great potential to grow in saline soils. Here, we studied ion concentrations in quinoa tissues throughout the life cycle of the plant, and linked ion dynamics to responses in growth parameters, seed yield and efficiency of photosynthesis under salinity (0–400 mM NaCl). Ion dynamics changed from high ion exclusion (>99 %, root contents lower than root medium and low accumulation of ions in the leaves) before flowering, to a build-up of ions during seed filling. This indicates a change in strategy in maintaining the necessary gradient of water potential from the root medium to the leaves. K+ concentrations in leaves also increased by more than 100 % in response to prolonged severe salt stress, which may point to a role of this ion in leaf osmotic adjustment. Accumulation of ions in epidermal bladder cells did not contribute substantially to Na+-exclusion as it was less than 6 % of the total Na+ taken up in leaves. Growth under salt stress was mostly impaired by anatomical adaptations (reduced SLA), while initial light use efficiency (Fv/Fm) and NAR were not affected. The variety Pasto showed a "survival strategy" to high salinity with higher ion exclusion and a higher reduction in transpiration than the other varieties, at the expense of lower biomass and seed yield. [ABSTRACT FROM AUTHOR]

Targeted and random mutagenesis of gene families require accurate quantification. Droplet digital PCR (ddPCR) enables high-throughput screening of copy number variation (CNV). We tested the accuracy of ddPCR for CNV analysis in the large α-gliadin gene family, using degenerate primers. First, duplex ddPCR assays measured α-gliadins in diploid (15–17 copies) and tetraploid (70–76 copies) wheat accessions and a corresponding number in resulting Synthetic Hexaploid Wheat, demonstrating linear amplification up to 86–95 genes. Second, we amplified 61 α-gliadin genes in Chinese Spring. Most α-gliadins of the homoeologous chromosomes 6A and 6D were correctly amplified, as corroborated using deletion and nullisomic-tetrasomic lines, but one group of genes from 6B were not amplified with these primers. Third, in Paragon we amplified 61 α-gliadin genes while selected γ-irradiated mutant lines revealed reductions of 25–50%. Finally, using two duplex ddPCR assays, we showed that CRISPR/Cas9-targeting of α-gliadins in Fielder produced indels (1–50 bp) in up to 10 α-gliadin genes plus large deletions (>300 bp) in 20 of 87 amplified α-gliadin genes. ddPCR is suitable for high-throughput screening of CNV and gene-editing-induced mutations in large gene families, in polyploids. In wheat, ddPCR enables screening of gliadins in breeding programs towards hypoimmunogenic gluten for coeliac patients. Image 1 • ddPCR enables high-throughput screening of copy number variation (CNV). • We demonstrate linear detection up to 95 alpha-gliadin genes in single a bread wheat variety. • Our dual-assay ddPCR approach distinguished CRISPR/Cas-induced small indels in alpha-gliadins from large deletions. [ABSTRACT FROM AUTHOR]

• Far-red radiation increased tomato fruit production. • Far-red significantly affected dry mass partitioning pattern in tomato. • Higher fruit dry mass fraction explained far-red increased fruit production. • Far-red reduced resistance against Botrytis cinerea in tomato leaves. The addition of far-red (FR, 700–800 nm) radiation to standard growth light triggers a set of photomorphogenic responses collectively termed shade avoidance syndrome. Recent research showed that additional FR increased fruit yield in greenhouse tomato production. However, the mechanism behind this increase is not clear; nor is it known whether there is a trade-off between growth and defense against plant diseases in tomato under additional FR. The aims of this study were 1) to quantify the effect of additional FR on tomato fruit growth, 2) to explain this effect based on underlying growth components and 3) to examine the FR effect on resistance against the necrotrophic fungus Botrytis cinerea. Tomato (Solanum lycopersicum 'Moneymaker') plants were grown for four months with 30 or 50 μmol m−2 s−1 of FR added to 150 μmol m−2 s−1 red + blue or white background LED lighting. Growth and development parameters were recorded, and a growth component analysis was conducted. Bioassays for resistance against B. cinerea were conducted on leaf samples collected from each light treatment. Additional FR increased total fruit dry mass per plant by 26–45%. FR affected multiple growth components, among which the fraction of dry mass partitioned to fruits was the most prominent with a 15–35% increase. Truss appearance rate was increased 11–14% by FR while instantaneous net photosynthesis rate was not affected. FR also resulted in more severe disease symptoms upon infection with B. cinerea. In conclusion, additional FR increases tomato fruit production mainly by increasing dry mass partitioning to fruits, rather than improving photosynthesis or increasing total plant biomass. However, FR also reduces resistance of tomato leaves against B. cinerea. [ABSTRACT FROM AUTHOR]

Summary Potato plants form tuberous storage organs on underground modified stems called stolons. Tubers are rich in starch, proteins, and other important nutrients, making potato one of the most important staple food crops. The timing of tuber development in wild potato is regulated by day length through a mechanism that is closely related to floral transition [ 1, 2 ]. Tuberization is also known to be regulated by the availability of assimilates, in particular sucrose, the transported form of sugar, required for starch synthesis. During the onset of tuber development, the mode of sucrose unloading switches from apoplastic to symplastic [ 3 ]. Here, we show that this switch may be mediated by the interaction between the tuberization-specific FT homolog StSP6A and the sucrose efflux transporter StSWEET11 [ 4 ]. The binding of StSP6A to StSWEET11 blocked the leakage of sucrose to the apoplast, and is therefore likely to promote symplastic sucrose transport. The direct physical interaction between StSWEET11 and StSP6A proteins represents a link between the sugar and photoperiodic pathways for the regulation of potato tuber formation. Our data suggest that a previously undiscovered function for the FT family of proteins extends their role as mobile signals to mediators of source-sink partitioning, opening the possibility for modifying source-sink interactions. Graphical Abstract Highlights • Tuber formation is dependent on the link between photoperiod and sugar transport • Potato FT-like tuberigen interacts with a sugar transporter to block sucrose leakage • StSWEET11-StSP6A interaction promotes symplastic transport of sucrose Abelenda et al. show that a tuber-specific, FT-like protein interacts with a SWEET sugar efflux transporter to block sucrose leakage into the apoplast. This work helps to explain the redirection of assimilate flow to developing sink organs and opens the possibility of engineering source-sink relationships. [ABSTRACT FROM AUTHOR]