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bioRxiv2019

Two Y chromosome-encoded genes determine sex in kiwifruit

Dioecy, the presence of male and female individuals, has evolved independently in multiple flowering plant lineages. Although theoretical models for the evolution of dioecy, such as the \"two-mutation\" model, are well established, little is known about the specific genes determining sex and their evolutionary history. Kiwifruit, a major tree crop consumed worldwide, is a dioecious species. In kiwifruit, we had previously identified a Y-encoded sex-determinant candidate gene acting as the suppressor of feminization (SuF), named Shy Girl (SyGI). Here, we identified a second Y-encoded sex-determinant that we named Friendly boy (FrBy), which exhibits strong expression in tapetal cells. Gene-editing and complementation analyses in Arabidopsis thaliana and Nicotiana tabacum indicated that FrBy acts for the maintenance of male (M) functions, independently of SyGI, and that these functions are conserved across angiosperm species. We further characterized the genomic architecture of the small (< 1 Mb) male specific region of the Y-chromosome (MSY), which harbors only two genes significantly expressed in developing gynoecia and androecia, respectively: SyGI and FrBy. Resequencing of the genome of a natural hermaphrodite kiwifruit revealed that this individual is genetically male but carries deletion(s) of parts of the Y-chromosome, including SyGI. Additionally, expression of FrBy in female kiwifruit resulted in hermaphrodite plants. These results clearly indicate that Y-encoded SyGI and FrBy act independently as the SuF and M factors in kiwifruit, respectively, and provide insight into the evolutionary path leading to a two-factor sex determination system but also a new breeding approach for dioecious species.

plant biology↗

bioRxiv2019

The PPR-related splicing cofactor MSP1/EMB1025 protein, encoded by At4g20090, encode an essential protein that is required for the splicing of nad1 intron 1 and for the biogenesis of complex I in Arabidopsis mitochondria

Group II introns are particularly plentiful within plant mitochondrial genomes (mtDNAs), where they interrupt the coding-regions of many organellar genes, especialy within complex I (CI) subunits. Their splicing is essential for the biogenesis of the respiratory system and is facilitated by various protein-cofactors that belong to a diverse set of RNA-binding cofactors. These including maturases, which co-evolved with their host-introns, and various trans-acting factors, such as members of the pentatricopeptide-repeat (PPR) protein family. The genomes of angiosperms contain hundreds of PPR-related genes that are postulated to reside within the organelles and affect diverse posttranscriptional steps, such as editing, RNA-stability and processing or translation. Here, we report the characterization of MSP1 (Mitochondria Splicing PPR-factor 1; also denoted as EMB1025), which plays a key role in the processing of nad1 pre-RNAs in Arabidopsis mitochondria. Mutations in MSP1 gene-locus (At4g20090) result in early embryonic arrest. To analyze the putative roles of MSP1 in organellar RNA-metabolism we used a modified embryo-rescue method, which allowed us to obtain sufficient plant tissue for the analysis of the RNA and protein profiles associated with msp1 mutants. Our data indicate that MSP1 is essential for the trans-splicing of nad1 intron 1 in Arabidopsis mitochondria. Accordingly, msp1 mutants show CI biogenesis defects and reduced respiratory-mediated functions. These results provide with important insights into the roles of nuclear-encoded factors during early plant development, and contribute to our limited understanding of the importance of RNA-maturation and splicing in plant mitochondria during early embryogenesis.

plant biology↗

bioRxiv2019

Reconstructing the transcriptional ontogeny of maize and sorghum supports an inverse hourglass model of inflorescence development

Assembling meaningful comparisons between species is a major limitation in studying the evolution of organismal form. To understand development in maize and sorghum, closely-related species with architecturally distinct inflorescences, we collected RNAseq profiles encompassing inflorescence body plan specification in both species. We reconstructed molecular ontogenies from 40 B73 maize tassels and 47 BTx623 sorghum panicles and separated them into transcriptional stages. To discover new markers of inflorescence development, we used random forest machine learning to determine stage by RNAseq. We used two descriptions of transcriptional conservation to identify hourglass-like developmental stages. Despite short evolutionary ancestry of 12 million years, we found maize and sorghum inflorescences are most different during their hourglass-like stages of development, following an inverse-hourglass model of development. We discuss if agricultural selection may account for the rapid divergence signatures in these species and the observed separation of evolutionary pressure and developmental reprogramming.\n\nHighlightsO_LITranscript dynamics identify maize tassel and sorghum panicle developmental stages\nC_LIO_LIRandom forest predicts developmental age by gene expression, providing molecular markers and an in silico staging application\nC_LIO_LIMaize and sorghum inflorescences are most similar when committing stem cells to a determinant fate\nC_LIO_LIExpression conservation identifies hourglass-like stage, but transcriptomes diverge, similar to inverse hourglass observations in cross-phyla animal embryo comparisons\nC_LI

plant biology↗

bioRxiv2019

ELIMAKI locus is required for mechanosensing and proprioception in birch trees

The remarkable vertical and radial growth observed in tree species, encompasses a major physical challenge for wood forming tissues. To compensate with increasing size and weight, cambium-derived radial growth increases the stem width, thereby supporting the aerial body of trees. This feedback appears to be part of a so-called \"proprioception\" (1, 2) mechanism that controls plant size and biomass allocation. Yet, how trees experience or respond to mechanical stress derived from their own vertical loading, remains unknown. Here, we combined two strategies to dissect the proprioceptive response in birch. First, we show that in response to physical loading, trees promote radial growth with different magnitudes along the stem. Next, we identified a mutant cultivar (B. pubescens cv. Elimaki) in which the main stem shows normal vertical development, but collapses after three months. By inducing precocious flowering, we generated a backcrossed population (BC1) by producing two generations in 4 years. In his scheme, we uncovered a recessive trait (eki) that segregates and genetically maps with a Mendelian monogenic pattern. Unlike WT, eki is resistant to vertical mechanical stimulation. However, eki responds normally to the gravitropic stimulus by making tension wood. Before the collapse, cell size in eki is compromised resulting in radial growth defects, depending on stem height. Cell walls of developing xylem and phloem tissues have delayed differentiation in eki, and its tissues are softer compared to WT as indicated by atomic force microscopy (AFM). The transcriptomic profile of eki highlighted the overlap with that of the Arabidopsis response to touch. Taken together, our results suggest that the mechanical environment and cell wall properties of developing woody tissues, can significantly affect the growth responses to vertical loading thereby compromising their proprioceptive capacity. Additionally, we introduce a fast forward genetics strategy to dissect complex phenotypes in trees.

plant biology↗

bioRxiv2019

The MADS-box transcription factor PHERES1 controls imprinting in the endosperm by binding to domesticated transposons

MADS-box transcription factors are ubiquitous in eukaryotic organisms and play major roles during plant development. Nevertheless, their function in seed development remains largely unknown. Here we show that the imprinted Arabidopsis thaliana MADS-box TF PHERES1 (PHE1) is a master regulator of paternally expressed imprinted genes, as well as of non-imprinted key regulators of endosperm development. PHE1 binding sites show distinct epigenetic modifications on maternal and paternal alleles, correlating with parental-specific transcriptional activity. Importantly, we show that the CArG-box-like DNA-binding motifs bound by PHE1 have been distributed by RC/Helitron transposable elements. Our data provide an example of molecular domestication of these elements, which by distributing PHE1 binding sites throughout the genome, have facilitated the recruitment of crucial endosperm regulators into a single transcriptional network.

plant biology↗

bioRxiv2019

Maize Kernel Development Stage the Primary Factor in Differential Gene Expression in Response to Two Methods of Field Inoculation with Aspergillus flavus

BackgroundAflatoxins, produced by the fungus Aspergillus flavus, often contaminate preharvest maize (Zea mays L.) grain under heat and drought stresses, posing serious health hazards to humans and livestock, and resulting in significant costs to identify and dispose of contaminated grain. This study was designed to investigate the changes in differential gene expression during seed morphogenesis and maturation in the \"aflatoxin resistant\" Argentinian inbred line Tx772 when challenged by the introduction of A. flavus through two different methods of ear inoculation; non-wounding (silk channel, used to select Tx772), wounding (side needle) and a non-inoculated control.\n\nMethod and FindingsGrain maturity had the largest effect on overall RNA-Seq differential gene expression (DGE) as measured by edgeR of the Bioconductor platform. However, within each stage of development, ranging from blister to dent, similar up-regulation in expression of many maize genes following inoculation with either method was observed; a total of 16 genes previously associated with resistance to pathogens were identified among the transcripts differentially expressed (DE) at p [≤] .05, FDR [≤] .10, and fold change [≥] 2.0 over all stages. The side needle technique produced a larger effect of infection as evidenced by 6,324 fungal reads versus 518 in silk channel and a higher level of aflatoxin. Correlations between approximately 7,000 fungal reads and the number of maize DE genes for each of the eight treatment groups was 0.56 (p = .152) and was 0.65 (p < .001) with levels of aflatoxin ranging from 0 to 137 ng g-1.\n\nConclusionThese correlations provided an internal measure of effectiveness of inoculation methods that were associated with the mostly up-regulation of defense-related genes in response to the presence of Aspergillus flavus in a unique maize genetic background.

plant biology↗

bioRxiv2019

Coordinated circadian timing through the integration of local inputs in Arabidopsis thaliana

Every plant cell has a genetic circuit, the circadian clock, that times key processes to the day-night cycle. These clocks are aligned to the day-night cycle by multiple environmental signals that vary across the plant. How does the plant integrate clock rhythms, both within and between organs, to ensure coordinated timing? To address this question, we examined the clock at the sub-tissue level across Arabidopsis thaliana seedlings under multiple environmental conditions and genetic backgrounds. Our results show that the clock runs at different speeds (periods) in each organ, which causes the clock to peak at different times across the plant in both constant environmental conditions and light-dark cycles. Closer examination reveals that spatial waves of clock gene expression propagate both within and between organs. Using a combination of modeling and experiment, we reveal that these spatial waves are the result of the period differences between organs and local coupling, rather than long distance signaling. With further experiments we show that the endogenous period differences, and thus the spatial waves, are caused by the organ specificity of inputs into the clock. We demonstrate this by modulating periods using light and metabolic signals, as well as with genetic perturbations. Our results reveal that plant clocks are set locally by organ specific inputs, but coordinated globally via spatial waves of clock gene expression.

plant biology↗

bioRxiv2019

Differences of endogenous polyamines and putative genes associated with paraquat resistance in goosegrass (Eleusine indica L.)

BackgroundParaquat is one of the most effective herbicides used to control weeds in agricultural management, while the pernicious weed goosegrass (Eleusine indica) has evolved resistance to herbicides, including paraquat. Polyamines provide high-level paraquat resistance in many plants. In the present study, we selected three polyamines, namely, putrescine, spermidine, and spermine, as putative genes to investigate their correlation with paraquat resistance by using paraquat-resistant (R) and paraquat-susceptible (S) goosegrass populations.\n\nResultsThere was no significant difference in the putrescine nor spermine content between the R and S biotypes. However, 30 and 90 min after paraquat treatment, the spermidine concentration was 346.14-fold and 421.04-fold (P < 0.001) higher in the R biotype than in the S biotype, but the spermidine concentration was drastically reduced to a marginal level after 90 min. Since the transcript level of PqE was low while the spermidine concentration showed a transient increase, the PqE gene was likely involved in the synthesis of the paraquat resistance mechanism, regulation of polyamine content, and synthesis of spermidine and spermine. PqTS1, PqTS2, and PqTS3 encode transporter proteins involved in the regulation of paraquat concentration but showed different transcription patterns with synchronous changes in polyamine content.\n\nConclusionEndogenous polyamines (especially spermidine) play a vital role in paraquat resistance in goosegrass. PqE, PqTS1, PqTS2, and PqTS3 were speculated on the relationship between polyamine metabolism and paraquat resistance. To validate the roles of PqE, PqTS1, PqTS2, and PqTS3 in polyamine transport systems, further research is needed.

plant biology↗

bioRxiv2019

Natural Amelioration of Mn-induced Chlorosis Facilitated by Mn Down-regulation, Ammonium and Rainwater in Sugarcane Seedlings

We had previously reported that manganese (Mn)-induced chlorosis is a serious problem in ratoon sugarcane seedlings grown in acidic soils. To further monitor the progression of chlorosis and elucidate the corresponding mechanism, both plant growth and nutrient status of sugarcane plants and soils were investigated in the growth seasons of ratoon cane seedlings in 2016 and 2018. The impacts of rainfall and ammonium on chlorosis were also investigated hydroponically. The results showed that the chlorotic seedlings could green in mid-summer; Mn content in the first expanded leaf decreased significantly, whereas iron (Fe) content increased significantly during the progression of greening. The leaf Mn content in the greened seedlings decreased by up to 78.1% when compared with that in the initial chlorotic seedlings. The seedlings also showed a significant increase in seedling height and weight of the expanded leaves, accompanied by a decrease in plant Mn content during the progression of greening. Moreover, young seedlings with less Mn content showed earlier greening than older seedlings with more Mn content. The exchangeable ammonium content in the soils increased significantly during the progression of greening, and the addition of 1 mM ammonium to the chlorotic seedlings resulted in a decrease in leaf Mn content by up to 80%. Furthermore, leaf SPAD value and Fe content increased by 2.0-fold and 1.4-fold, respectively, after rainwater was applied to the chlorotic seedling. These results indicate Mn-induced chlorotic seedlings can turn naturally green, and downregulation of plant Mn content, rainfall in summer, and soil ammonium contribute to the greening of chlorotic seedlings.

plant biology↗

bioRxiv2019

O-glycosylation of SPL transcription factors regulates plant developmental transitions downstream of miR156

The timing of plant developmental transitions is decisive for reproductive success and thus tightly regulated. The transition from juvenile to adult vegetative and later to the reproductive phase is controlled by an endogenous pathway regulated by miR156, targeting the SQUAMOSA PROMOTER BINDING PROTEIN (SBP/SPL) family of transcription factors. SPLs regulate a number of developmental processes, such as trichome formation, leaf shape and floral transition. Such complex regulatory pathways often involve post-translational modifications (PTMs), integrating a range of internal and external signals. One of these PTMs is O-glycosylation, the attachment of a single monosaccharide to serine or threonine of nuclear and cytoplasmic proteins, which is found on a number of very diverse proteins. O-GlcNAcylation is the most common type of cytosolic O-glycosylation, but in plants also O-fucose modification occurs. Here we show that mutants defective in the O-fucosyltransferase SPINDLY (SPY) show accelerated developmental transitions. Genetic analysis shows that this effect is independent of miR156 levels, but partly dependent on functional SPLs. In a phenotyping analysis, we found that SPY and SPLs also control leaf growth, as loss of function mutants showed defects in cell expansion, while SPL9 also regulates cell division in rosette leaves. Moreover, SPLs interact directly with SPY and are O-glycosylated. Our results show that O-glycosylation is involved at several steps in the regulation of developmental transitions and organ growth in Arabidopsis thaliana.

plant biology↗

bioRxiv2019

CRK2-mediated control of ROS production by phosphorylation of the RBOHD C-terminus in Arabidopsis

Reactive oxygen species (ROS) are important messengers in eukaryotic organisms and their production is tightly controlled. Active extracellular ROS production by NADPH oxidases in plants is triggered by receptor-like protein kinase (RLK)-dependent signaling networks. Here we show that the cysteine-rich RLK CRK2 kinase activity is required for plant growth and CRK2 exists in a preformed complex with the NADPH oxidase RBOHD in Arabidopsis. Functional CRK2 is required for the full elicitor-induced ROS burst and consequently the crk2 mutant is impaired in defense against the bacterial pathogen Pseudomonas syringae pv. tomato DC3000. Our work demonstrates that CRK2 regulates plant innate immunity. We identified in vitro CRK2-dependent phosphorylation sites in the C-terminal region of RBOHD. Phosphorylation of S703 RBOHD is enhanced upon flg22 treatment and substitution of S703 with alanine reduced ROS production in Arabidopsis. Phylogenetic analysis suggests that phospho-sites in C-terminal region of RBOHD are conserved throughout the plant lineage and between animals and plants. We propose that regulation of NADPH oxidase activity by phosphorylation of the C-terminal region might be an ancient mechanism and that CRK2 is an important element in regulating MAMP-triggered ROS production. One-sentence summaryCRK2 associates with and activates RBOHD to trigger MAMP-induced ROS production and reveals a novel regulatory mechanism for plant NADPH oxidases through phosphorylation of the C-terminus.

plant biology↗

bioRxiv2019

Correlative evidence for co-regulation of phosphorus and carbon exchanges with symbiotic fungus in the arbuscular mycorrhizal Medicago truncatula

In the research of arbuscular mycorrhizal (AM) symbiosis a considerable progress was made. But despite that, key questions still remain unanswered - for example it is well known that biotrophic fungus release phosphate (P) to- and recieves carbon (C) from the plant symbiont, but the particular genes, and their products, responsible for this exchange are still not fully understood. Here, we made a de novo quest for such genes involved in C transfer. Using physiological intervention of 90% shading and the correlation of expression levels of MtPT4, the AM-specific marker, and our candidate genes we demonstrate that several novel genes may be involved in AM symbiosis in Medicago truncatula. Also, we examined the expression of phosphate transporters (MtPT1-6) and we discuss the balance of \"direct\" and \"mycorrhizal\" P uptake pathways upon symbiotic fungus infection and C deprivation.

plant biology↗

bioRxiv2019

Exogenous Melatonin accelerates seed germination in cotton(Gossypium hirsutum L.)

Seed germination is considered as the beginning of the spermatophyte lifecycle, as it is a crucial stage in determining subsequent plant growth and development. Although many previous studies have found that melatonin can promote seed germination, the role of melatonin in cotton germination remains unexamined. The main objective of this study is the characterization of potential promotional effects of melatonin (at doses of 0, 10, 20, 50, 100 and 200 M) on cotton seed germination. This experiment demonstrated that low concentrations of melatonin can promote germination, while high concentrations failed to promote germination and even inhibited germination. Together, these results indicate that a 20 M melatonin treatment optimally promotes cotton seed germination. Compared with the control, germination potential (GP), germination rate (GR) and final fresh weight (FW) increased by 16.67%, 12.30% and 4.81% respectively. Although low concentrations of melatonin showed some improvement in vigor index (VI), germination index (GI) and mean germination time (MGT), these effects did not reach significant levels. Antioxidant enzyme activity during seed germination was most prominent under the 20 M melatonin treatment. Superoxide dismutase (SOD) and peroxidase (POD) activities were significantly increased by 10.37-59.73% and 17.79-47.68% compared to the melatonin-free control. Malondialdehyde (MDA) content was reduced by 16.73-40.33%. Two important plant hormones in seed germination were also studied. As melatonin concentration increased, ABA content in seeds decreased first and then increased, and GA3 content showed a diametrically opposite trend, in which the 20 M melatonin treatment was optimal. The 20 M melatonin treatment reduced ABA content in seeds by 42.13-51.68%, while the 20 M melatonin treatment increased GA3 content in seeds to about 1.7-2.5 times that of seeds germinated without melatonin. This study provides new evidence suggesting that low concentrations of melatonin can promote cotton seed germination by increasing the activity of antioxidant enzymes, thereby reducing the accumulation of MDA and regulating plant hormones. This has clear applications for improving the germination rate of cotton seeds using melatonin.

plant biology↗

bioRxiv2019

Unveiling two new trichome-specific promoters of interest for metabolic engineering in Nicotiana tabacum

Main conclusion pRbcS-T1 and pMALD1, two new trichome-specific promoters of Nicotiana tabacum, were identified and their strength and specificity were compared to those of previously described promoters in this species. Nicotiana tabacum has emerged as a suitable host for metabolic engineering of terpenoids and derivatives in tall glandular trichomes, which actively synthesize and secrete specialized metabolites. However, implementation of an entire biosynthetic pathway in glandular trichomes requires the identification of trichome-specific promoters to appropriately drive the expression of the transgenes needed to set up the desired pathway. In this context, RT-qPCR analysis was carried out on wild-type N. tabacum plants to compare the expression pattern and gene expression level of NtRbcS-T1 and NtMALD1, two newly identified genes expressed in glandular trichomes, with those of NtCYP71D16, NtCBTS2, NtCPS2, and NtLTP1, which were reported in the literature to be specifically expressed in glandular trichomes. We show that NtRbcS-T1 and NtMALD1 are specifically expressed in glandular trichomes like NtCYP71D16, NtCBTS2, and NtCPS2, while NtLTP1 is also expressed in other leaf tissues as well as in the stem. Transcriptional fusions of each of the six promoters to the GUS-VENUS reporter gene were introduced in N. tabacum by Agrobacterium-mediated transformation. Almost all transgenic lines displayed GUS activity in tall glandular trichomes, indicating that the appropriate cis regulatory elements were included in the selected promoter regions. However, unlike for the other promoters, no trichome-specific line was obtained for pNtLTP1:GUS-VENUS, thus in agreement with the RT-qPCR data. These data thus provide two new transcription promoters that could be used in metabolic engineering of glandular trichomes.

plant biology↗

bioRxiv2019

Effect of Septoria brown spot on soybean yield in Illinois

Brown spot caused by Septoria glycines is a prevalent foliar disease in all soybean production areas. Application of foliar fungicides after bloom reduces the disease severity, yet yield responses are not consistent among locations and years. Our research goal was to determine the effect of different levels of Septoria brown spot on yield. Different levels of disease severity were effectively obtained in the field by weekly application of chlorothalonil for three, six, and nine times after disease inoculation at V3/V4 stage. Fungicide treatments had a significant effect on vertical progress and chlorotic area with no statistically significant effect on yield. Soybean yield was negatively correlated with vertical progress of the disease (r = -0.36). The vertical progress was the best linear predictor of yield. Based on this model, when the vertical progress of brown spot at R6 increased by 10%, the yield decreased by 142.13 kg/ha (3.4%). A variance component analyses of our data showed that location was the most critical factor, illustrating the significant effect of local environmental conditions on the disease. Power analyses indicated that at least eight locations are needed to detect an effect of 269 kg/ha. Our results provide useful information to improve the experimental design for future experiments addressing the yield constrain by late season diseases of soybean.

plant biology↗

bioRxiv2019

Plant uses in a traditional fisherman community in northeastern Brazil

BackgroundKnowledge of traditional plant use in rural communities is under threat from urbanization and also land use change. Hence, elucidating region-specific patterns traditional knowledge of habitat resource use is crucial for assisting policy making with regard to nature conservation, human nutrition, and human health. Using original data from northeast Bahia, Brazil, we aim to document the collective knowledge of plant use possessed by artisanal fishermen and women in fishing communities, related to medicinal, construction, technology and ritualistic/religious uses.\n\nMethodsData were collected through interviews with and opportunistic guided tours by local specialists to record the local knowledge of plant use and methods of use.\n\nResultsThrough interviews, 116 species of plants from 104 genera and 47 botanical families were identified along with their local names, plant parts utilized, habitats, and preparation methods, and an additional 26 spp. for which only local names were available. Of these, 72 spp. are used as medicine, 48 spp. as non-conventional edibles, 31 spp. for construction and 11 for religious/mystical purposes. Female informants generally cited more food and medicinal plants than male informants. All interviewees unanimously expressed that the use of plants for medicines and fishing technology has significantly reduced or been superseded by modern materials.\n\nConclusionThe present study demonstrates that the rich collective plant use knowledge of an artisanal fishing community in northeast Brazil. The results of this study serves as a framework for to extend ethnobotanical investigations to other traditional fishing communities in the vicinity, and also to examine more social and demographic factors influencing traditional knowledge related to uses of plants. Finally, the rich tradition of plant use in the region underpins the need to encourage measures to preserve this cultural knowledge and conserve the natural environments that are a source of these plants.

plant biology↗

bioRxiv2019

Redistribution of NORTIA in response to pollen tube arrival facilitates fertilization in Arabidopsis thaliana

During gamete delivery in Arabidopsis thaliana, intercellular communication between the attracted pollen tube and the receptive synergid cell leads to subcellular events in both cells culminating in the rupture of the tip-growing pollen tube and release of the sperm cells to achieve double fertilization. Live imaging of pollen tube reception revealed dynamic subcellular changes that occur in the female synergid cells. Pollen tube arrival triggers the trafficking of NORTIA (NTA) MLO protein from Golgi-associated compartments and the accumulation of endosomes at or near the synergid filiform apparatus, a membrane-rich region that acts as the site of communication between the pollen tube and synergids. Domain swaps and site-directed mutagenesis reveal that NTAs C-terminal cytoplasmic tail with its calmodulin-binding domain influences the subcellular localization and function of NTA in pollen tube reception and that accumulation of NTA at the filiform apparatus is necessary and sufficient for MLO function in pollen tube reception.

plant biology↗

bioRxiv2019

Overexpression of the Arabidopsis thaumatin-like protein 1 in transgenic potato plants enhances resistance against early and late blights

The Arabidopsis thaumatin-like protein 1 (ATLP1), which belongs to the PR5 family of pathogenesis-related proteins, is induced by pathogen attacks and by systemic acquired resistance (SAR)-inducing compounds. To test whether the overexpression of ATLP1 will enhance fungal resistance in transgenic plants, the cDNA of this gene under the control of a constitutive promoter was transferred into Solanum tuberosum Cv. Desiree. The expression of the introduced gene was confirmed by Northern and Western blot analyses. Western blot analysis performed with intercellular fluid (ICF) showed that ATLP1 is secreted to apoplast. Several independent transgenic lines with high-level expression of the ATLP1 were assayed for resistance against early blight (Alternaria solani) and late blight (Phytophthora infestans). The rate of Alternaria lesions development was significantly reduced in the ATLP1 transgenic lines as compared to a control line. Percent reductions in area under the disease progress curve (AUDPC) values for the ATLP1 transgenic lines as compared to control line ranged between 52 and 82%. In response to P. infestans, infection efficiency (IE), lesion size (LS) and sporulation capacity (SC) were significantly reduced in ATLP1 transgenic lines as compared to a control line. On the average, IE, LS and SC were reduced by 18, 22 and 20%, respectively, for all transgenic lines with a maximum reduction of 25% in IE, 25% in LS and 32% in SC. Resistance assays against P. infestans using whole plants showed 40-70% reduction in symptoms as compared to control. These results suggest that constitutive expression of a heterologous ATLP in potato confers enhanced resistance against early and late blights.

plant biology↗