Conference Schedule

Day1: June 20, 2018

Keynote Forum

Biography

Bernard E Bihain created GENCLIS in 2004. After receiving his Doctorate in Medicine from the Free University of Brussels in 1984, he began a surgery internship followed by a Postdoctoral fellow at Columbia University in 1988.Thereafter, he took a position in 1990 as Assistant Professor of Physiology at the University of Louisiana. He was awarded the position of INSERM Research Director in 1992 and became Professor and Chairman of the Department of  Biochemistry, University of Rennes, where INSERM Unit 391was created in 1994. He then undertook the Direction of the Department of Functional Genomics of the genomic company Genset. He has actively contributed to the emergence of genomic technologies. His pragmatism, stemming from his experience as a surgeon, powers the translational activities of GENCLIS. He has authored over 50 publications in peer-reviewed journals, and his studies are cited in more than 5000 scientific articles.


Abstract

Background: In all cells, a significant percentage of RNA sequences may diverge from the DNA template. Unlike editing, RNA-DNA Divergences (RDD) caused by transcription infidelity lead to base substitutions within and across base families and this RNA are translated. Here we report on a novel Trait Identification event causing single-base omission (RDD gap) in three different legumes with different allergenicity.

 

Methodology: Because of the degeneracy of the genetic code, RNA with frameshifts translates into protein variants with cationic peptide at the carboxy-terminal end that may thereby modify their immunogenicity. RNA sequences from peanut, soybean and green bean were aligned to their respective DNA templates and gap rates were calculated as the proportion of gap per RNA read.

Findings: RDD gap rate was highest in peanut, intermediate in soybean and lowest in green bean. Allergens from peanut and soybean differ from non-allergenic proteins of the same species by a greater diversity of gap in allergens. The same increased gap density was also observed in sesame allergens. Three recombinants Ara h 2 translated from frameshifted RNA but not the protein translated from RNA with canonical sequence induced specific IgE production without adjuvant and clinical allergy in mice. Analysis of RDD gap pattern of peanut proteins that were not described as peanut allergens led to identification of two novel peanut proteins with a gap profile consistent with

allergenicity. The recombinant form of these two novel peanut allergens candidate show specific reactivity toward IgE present in sera of peanut allergic patients but not of subjects without peanut allergy.

Conclusion & Significance: Specific DNA sequences in legumes and at least one grain allows transcriptional slippage. Translation of frameshifted RNA produce low abundance diversified variants causing IgE production. Genomic editing and production conditions minimizing RDD gap occurrence may significantly reduce the allergenicity of these important protein sources.

 

Biography

Lihong Xiao is senior most scientist at Zhejiang A & F University, China, her expertise in the improvement of tree nut quality and nutritional content based on Genome-Wide Association analysis (GWAS) and gene editing (CRISPR/Cas9). Her research interests are also focused on understanding fundamental mechanisms of plant abiotic stress responses to adverse en­vironments and to explore the mechanisms and its evolution of stem cell maintenance by integrating extensive approaches, including “omics” (small RNA and mRNA transcriptome, proteomics and phosphate-protein, meth­ylome) and Whole Genome Sequencing (WGS) as well as data analysis, genetics, cytology (including light, electron and confocal microscopy imag­ing), histochemistry, molecular biology, etc.

 


Abstract

Pecan and Chinese hickory are the only two commercially cultivated tree nuts in the genus Carya. Their nutritional value and health benefits are superior to many other tree nuts contribute to growing consumption with potential to become major crops and suggest ability to improve world food security. Unfortunately, few resources are available to facilitate their genetic improvement. Here we report reference genome sequences for two highly heterozygous individuals – pecan cultivar (Pawnee) and a domesticated Chinese hickory. Both experienced two genome duplication events before divergence from walnut. The genomes encode 31,075 (pecan) and 32,907 (Chinese hickory) protein-coding genes.Gene family expansion highlighted the key genes and pathways involved in biotic (Chinese hickory) and abiotic (pecan) tolerance, accumulation on unsaturated fatty acid, non-structural polyphenol metabolism, nonessential amino acid and B vitamins. We also report the reduced-coverage genomes for 15 other hickories and two Juglans species, which, together with the two reference genome sequences, reveal the  

evolutionary history and the disjunctive distribution of Carya species. We believe these genomic resources should be an important first step towards the genetic improvement of hickory nuts.

 

Biography

Patrizia Galeffi is a Senior Scientist at ENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development. Her main scientific activities are focused on Biotechnology, Plant Genetics and Molecular Biology area: molecular study of genes in durum wheat responding to abiotic stresses; functional genomics, transcriptomics and gene expression profiling in plants; plant biodiversity, in particular cereal diversity; plant transformation and transgenic plants; bioinformatics and statistics applied to agronomical and molecular data; triticale as biomass for bioenergy and bioethanol; antibody molecular biology; antibody engineering; antibodies for plant pathogen resistance; plants as a bio-factory to produce antibodies for pharmacological use; molecular design of stable engineered antibodies; nanomaterials. She is an author of around 40 publications in peer-reviewed journals, Active Reviewer of several international scientific journals and member of the Panel Editors of Journal of Food, Agriculture and Environment. She is an author of five patents, certified agent for technology transfer and member of ENEA Patent Commission.

 


Abstract

Introduction of ENEA

Tracks

  • Plant Proteins | Plant Genomics | Landscape Plant Physiology | Plant Genome Transcription | Plant Science | Plant Molecular Genetics | Plant Metabolism
Location: Olimpica 3+4

Bernard E Bihain

Genclis, France

Chair

Aung Htay Naing

Kyungpook National University, South Korea

Co Chair

Biography

Annamaria Bevivino has her expertise in soil microbial diversity. She is Se­nior Scientist at ENEA, Italian National Agency for New Technologies, Energy and Sustainable Development, and Professor in Agro-Food Microbiology at University Campus Bio-Medico, Rome, Italy. Actually, she is a Management Committee Substitute for Italy of FPS COST Action FP1305: Linking below­ground biodiversity and ecosystem function in European forests (BioLink), actively participating in the activities of WG3: Belowground biodiversity in plantations and tree crops. She is Academic Editor for PlosOne and Fron­tiers in Microbiology and Member of Italian Society of General Microbiology and Microbial Biotechnology, Federation of European Microbiological soci­eties, Italian Society of Agro-Food and Environmental Microbiology, Interna­tional Union of Microbiological Societies. She is author of 43 peer-reviewed published papers in international journals, and more than 150 communica­tions to national and international congresses.

 


Abstract

Soil is a complex and dynamic ecosystem whose functionality is related to the equilibrium existing among chemical, physical and biological parameters and the resident microbial communities. Soil microorganisms play a central role in decomposing organic matter, in determining the release of mineral nutrients, and in nutrient cycling, and have direct and indirect effects on both crop growth and quality, as well as on the sustainability of soil productivity. In addition, soil microorganisms substantially contribute to the resistance and resilience of agro-ecosystems to biotic and abiotic disturbance and stress. Therefore, changes in microbial communities may directly affect soil ecosystem function since microbes can respond rapidly to environmental changes because of the vastness of microbial biomass and diversity. Given the role of soil microbes in soil safeness and function, there is the need to improve our knowledge about the ecology of microbial populations for proper agriculture management, at both levels of whole population structure and defined taxonomic/ functional groups, such as those involved in inorganic nitrogen turnover and biogeochemical cycles. Different approaches can be followed for studying diversity and community structure and evaluating dynamics processes at a global level or at the level of distinct taxonomic groups, for identification and typing, and for functional characterization. Here, author summarise the methodological approaches to unravel the composition and function of belowground microbiota, ranging from classical and culture-based methods to molecular and high-throughput sequencing-based metagenomic analyses.

A holistic approach taking into consideration all of potential factors and drivers is necessary when examining the structure–function relationships of soil microbial communities for providing insight into the long-standing questions of which species of microorganisms are present?, what are they doing? who is active out there? and how do the activities of these microorganisms relate to ecosystem functions? An in-depth analysis of these interactions could be of crucial importance in designing new and effective microbial consortia for optimizing plant production and developing new strategies for disease control.

 

Biography

Maciej Majka is working in the Cereal Genomics Team in the Institute of Plant Genetics in Poznan, Poland. He has completed his MSc in Molecular Cytogenetics at the University of Silesia in Katowice, Poland. He is a Princi­pal Investigator of his three years long scientific project financed by the Na­tional Science Centre (Poland): Genetic improvement of triticale by distant crosses with Aegilops tauschii × Secale cereale amphiploid forms in order to transfer the leaf rust resistance genes. He is an Executor in four other sci­entific projects. He is an author/co-author of 14 papers in reputed journals from the JCR list.

 


Abstract

Leaf rust caused by the Puccinia triticina Eriks is one of the most dangerous diseases of cereals. Genetic manipulation of host resistance is both cost-effective and safe for environment method of controlling leaf rust. Wild Aegilops species, characterized by a high genetic variability, constitute the rich source of genetic resources especially resistance to fungal diseases. The main goal of this work was to examine the resistance of (Ae. tauschii × S. cereale) × Triticosecale hybrids to leaf rust in inoculation tests with isolates of P. triticina with different virulence patterns. Hybrid plants were selected for the presence of 2D chromosomes in triticale background using fluorescent and genomic in situ hybridization. Presence of Leaf rust (Lr) resistance genes was confirmed with associated molecular markers. Resistance was determined at macroscopic and microscopic level at two stages of development: seedlings and adult plants (flag leaf). Our results revealed the decreased reaction of hybrid plants at the seedling stage followed by the increasement of resistance in further stages of development, what indicates that obtained hybrid plants may especially exhibit Adult Plant Resistance

(APR) resistance conferred by Lr22a introgressed from Ae. tauschii. On the basis of the macroscopic and microscopic analysis, this resistance can be determined as additive and race-specific. We selected Monosomic 2D Addition (M2DA) triticale genotypes highly resistant to P. triticina infection from which, we obtained double haploid lines that can be used for further breeding work to increase the agronomic value of cultivated triticale.

 

Biography

Akiko Kozaki has studied the function of indeterminate domain family pro­teins, which are plant specific group of transcription factors. She is also interested in the TOR signaling pathway in plants and the regulation of oil synthesis in plants.

 


Abstract

Seed germination is a crucial process in the life cycle of plants and the control of the timing of germination is important not only for plants but also for agriculture. Plant growth depends on several environmental conditions, such as light, moisture, nutrients, temperature, and so on. Therefore, seeds have to monitor the environmental condition to germinate at proper timing. Previous studies have shown that germination is regulated by these environmental conditions and many components, including plant hormones, such as Gibberellins (GA) and Abscisic Acid (ABA) and have identified several genes involved in the regulation of seed germination. We found that several INDETERMINATE DOMAIN (IDD) family transcription factors in Arabidopsis expressed in seeds are involved in the regulation of seed germination. The IDD family transcription factor was first identified as a regulator of maize flowering and recent studies show that some IDD transcription factors play important roles in GA signaling pathway, root patterning and gravitropism. Here, we present the results about IDD4 gene. The T-DNA tag line of IDD4 gene (idd4) showed delayed germination compared to Wild Type (WT) and the addition of 1 M ABA further delayed the germination of idd4. These results indicated that IDD4 gene promotes germination and suppress the sensitivity to ABA. In contrast, 50% of idd4 seeds germinated in the dark while WT seeds did not germinate. The result indicated that IDD4 gene inhibits germination in the dark. We analyzed the expression of gene involved in the synthesis, catabolism and signaling of GA and ABA, and germination regulation. In this presentation.

 

Biography

Chongling Yan has his expertise on the biogeochemical Process of heavy metals and Organic Pollutants (POPs) in wetland ecosystem (water/sedi­ment/plant). He has made some progress in distribution of heavy metals and the relationship between them and plants, environmental conditions and chemical-physical properties in estuary sediments, speciation distribu­tion of heavy metal in the mangrove sediment and the influence of man­grove roots on bio-availability of heavy metals.

 


Abstract

Mangrove ecosystem, a bushy woody plant community in the intertidal shores, mainly distributes in tropic and subtropic estuaries and plays an important role in estuarine ecosystems. Meanwhile, mangrove is severely polluted by heavy metals in consequence of human activities, notably cadmium. In this study, transcriptome sequencing was performed and the complex regulatory networks of cadmium tolerance in K. obovata were revealed. K. obovata was selected as research materials and treated with 5 mg/L cadmium for five days, then the total RNA of six samples (namely Ctrl-root, Ctrl-stem, Ctrl-leaf, Cd-root, Cd- stem, Cd-leaf) was extracted and prepared for RNA-seq and sRNA-seq base on Illumina HiSeq 2500 sequencing platform. Clean data obtained from sequencing was used for de novo assembly, differential expression analysis, function annotation, pathway enrichment analysis and other personalized analysis. Comprehensive dissection of molecular regulatory network of Cd tolerance involving Cd transport, chelation, plant hormone signaling, transcriptional regulation, phenylpropanoid metabolism, lignification and miRNA regulation was achieved in K. obovata. Notably this research is great important and may help in elucidating the gene networks involved in plant responses to various kinds of stress.

 

Biography

Danielle Keidar Friedman is a PhD Candidate at Ben Gurion University, Isra­el. Her study focuses on transposable elements dynamics in allopolyploid wheat species. She is studying SINE (Short Interspersed Nuclear Elements) and MITE (Miniature Inverted-repeat Transposable Elements) proliferation following polyploidization events, their possible impact on gene expression and regulation and their mode of transposition.

 


Abstract

The impact of Transposable Elements (TEs) on genome structure and function is intensively studied in eukaryotes, especially in plants where TEs can reach up to 90% of the genome in some cases, such as in wheat. We have performed a genome-wide in silico analysis using the updated publicly available genome draft of bread wheat (T. aestivum), in addition to the updated genome drafts of the diploid donor species, T. urartu and Ae. tauschii, to retrieve and analyze a non-LTR retrotransposon family, termed Au SINE (Short Interspersed Nuclear Elements), which was found to be widespread in plant species. Then, we have performed site-specific PCR and realtime RT-PCR analyses to assess the possible impact of Au SINE on gene structure and function. To this end, we retrieved 133, 180 and 1886 intact Au SINE insertions from T. urartu, Ae. tauschii and T. aestivum genome drafts, respectively. The 1886 Au SINE insertions were distributed in the seven homoeologous chromosomes of T. aestivum, while ~67% of the insertions were associated with genes. Detailed analysis of 40 genes harboring Au SINE revealed allelic variation of those genes in the Triticum-Aegilops genus. In addition, expression analysis revealed that both regular transcripts and alternative Au SINE-containing transcripts were simultaneously amplified in the same tissue, indicating retention of Au SINE-containing introns. Analysis of the wheat transcriptome revealed that hundreds of protein-coding genes that harbor Au SINE in at least one of their mature splice variants. Au SINE might play a prominent role in speciation by creating transcriptome variation.

 

Day2: June 21, 2018

Keynote Forum

Biography

Patrizia Galeffi is a Senior Scientist at ENEA, Italian National Agency for New Technologies, Energy and Sustainable Economic Development. Her main scientific activities are focused on Biotechnology, Plant Genetics and Molecular Biology area: molecular study of genes in durum wheat responding to abiotic stresses; functional genomics, transcriptomics and gene expression profiling in plants; plant biodiversity, in particular cereal diversity; plant transformation and transgenic plants; bioinformatics and statistics applied to agronomical and molecular data; triticale as biomass for bioenergy and bioethanol; antibody molecular biology; antibody engineering; antibodies for plant pathogen resistance; plants as a bio-factory to produce antibodies for pharmacological use; molecular design of stable engineered antibodies; nanomaterials. She is an author of around 40 publications in peer-reviewed journals, Active Reviewer of several international scientific journals and member of the Panel Editors of Journal of Food, Agriculture and Environment. She is an author of five patents, certified agent for technology transfer and member of ENEA Patent Commission.

 


Abstract

Introduction: Drought tolerance is one of the main components of yield and its stability, and its improvement is a major challenge to breeders. Transcription factors are considered among the best candidate genes for developing functional markers, since they are components of the signal transduction pathways that coordinate the expression of several downstream genes. In the present study, we report preliminary results concerning the ability of various SNPs of TdDRF1 gene to cluster 288 lines of durum wheat selected from the Durum Wheat Reference Collection (DWRC). The TdDRF1 gene was isolated, cloned and sequenced in a large number of durum varieties in greenhouse experiments. The sequences were aligned and analyzed in order to highlight SNPs. Among all, 26 polymorphisms were used to design specific KASP markers and some of them were able to cluster the 288 different lines. These results are preliminary, but promising, in view of association studies with interesting agronomical traits.

Keywords: Tolerance, Stability, Transcription factors, Greenhouse, Agronomical traits.

Methodology & Theoretical Orientation: Durum Wheat Reference Collection (DWRC) resulted from an initiative by Durum Wheat Genomics and Breeding Expert Working Group, in the frame of the activities of the wheat initiative, aimed to optimize the utilization of the durum wheat genetic resources. The DWRC panel consists of a stratified collection of 960 accessions extensively genotyped and organized in four main subpanels (elite, landraces, durum relatives and INRA evolution population). In this study, 288 lines were selected, including the whole elite subpanel and some landraces. The KASP (Kompetitive Allele Specific PCR) genotyping technology (patented by LGC Ltd) represents a new high-throughput and low cost genotyping platform, lacking limitations of low throughput, labor intensiveness and high costs characterizing common SNP genotyping, as allele-specific PCR (AS-PCR), cleaved amplified polymorphic sequences (CAPS) and Temperature-Switch PCR (TSPCR). 26 markers designed on TdDRF1 gene polymorphisms were used to genotyping 288 lines that represented a large spectrum of varieties already analyzed in field trials around the world.

Conclusion & Significance: In our study, the variability inside a functional gene was used as a tool for genotyping. Association studies with agronomic data will be carried out in order to exploit these alleles as new molecular markers. We thank DWGB-EWG for giving us the possibility of using the DWRC.

 

Biography

Aung Htay Naing obtained his PhD degree majoring in Horticultural Biotechnol­ogy from Kyungpook National University where he is now working as Research Professor. He has been serving as Editorial Members and Peer Reviewers in international journals scoping for Horticulture, Plant Sciences, and Plant Bio­technology.

 


Abstract

Co-expression of Rosea1 (Ros1) and Delila (Del) control regulation of anthocyanin in snapdragon flowers, while their overexpression in tomato, petunia, and tobacco also exhibited the similar functions. However, little data exist on how Ros1 expression alone controls the anthocyanin regulation and on whether it is involved in the mechanism that leads to abiotic stress tolerance. Overexpression of Ros1 promoted accumulation of anthocyanin in leaf and flower of tobacco (Nicotiana tabacum ‘Xanthi’) by elevating all key biosynthesis genes, particularly through more regulating NtDFR and NtANS in the former, while through more elevating NtDFR transcript levels in the latter. Under normal conditions, T2-Ros1 and Wild-Type (WT) were able to well survive by producing well-developed broad leaves and regular roots, while a reduction in plant growth was observed under the cold and drought stresses. However, the T2-Ros1 was able to more tolerate the stresses than WT by induction of higher Reactive Oxygen Species (ROS) scavenging activities (DPPH, ABTS), antioxidant-related gene expression (SOD, CAT and POX), and stress-responsive gene expression (CBF1, Osmotin, and ABA). In addition, Ros1 is phylogenetically clustered with other MYB TFs that confer different abiotic stresses. These results suggest that overexpression of Ros1 elevates expression of anthocyanin biosynthetic gene, antioxidant-related genes, and stress-responsive genes. The resultant increase in the genes expression improves anthocyanin accumulation and abiotic stresses tolerance.

 

Tracks

  • Plant Immunology | Plant Breeding | Transgenic Plants | Plant Extracts | Plant Biotechnology | Plant Fungi And Diseases
Location: Olimpica 3+4

Patrizia Galeffi

Italian National Agency, Italy

Chair

Lihong Xiao

Zhejiang A & F University, China

Co Chair

Biography

Vincenzo Lionetti is expertise in plant science field and he work as a profes­sor at Sapienza University di Roma, Italy.

 


Abstract

The intensification of agricultural practices and climatic changes lead to an increased need for crop protection against pathogens. The identification of new plant genetic resources for resistance to pests becomes imperative to assure yields and food security. Fungi are the most important plant pathogens since they cause both yield reduction and food contamination by mycotoxins. Botrytis cinerea, the causal agent of grey mold disease, is a broad-spectrum fungal necrotrophic that causes serious pre- and post-harvest rot in more than 200 species worldwide, including important fruit crops. Cell Wall (CW) is the foremost interface at which interactions between plants and fungi take place. Pectin, one of the main components of CW, is methyl esterified in the Golgi and secreted in the CW in a high methyl esterified form. The activity of Pectin Methyl Esterase (PMEs) and methyl esterification status of pectin are critical for the outcome of plant-fungus interaction. The higher methyl esterification makes pectin less susceptible to the hydrolysis by microbial cell wall degrading enzymes and consequently, microbial growth is reduced. PME activity was associated to the production of de-methyl esterified and active oligogalacturonides, the best characterized Damage- Associated Molecular Patterns (DAMPs) in plants. Moreover, PME is responsible for the release of methanol, which may function as DAMP alerting adjacent non-infected tissues or neighboring plants. Despite this evidence, the current knowledge about the molecular mechanisms regulating pectin methyl esterification during disease remains largely unknown. Our findings point to pectin methylesterase inhibitors as protectors of cell wall integrity in plant immunity. The potential mechanisms of modification, perception and signal transduction of pectin methyl esterification during fungal infection will be discussed.

 

Biography

Johanna Lethin had completed her Bachelor degree from Southwest Bap­tist University in Bolivar, Missouri, USA in Biology and Master’s degree from Halmstad University in Biomedical science, scholarship worker for CropTai­lor AB where my work was to find high Beta glucan oat lines from a mutag­enized Swedish oat population.

 


Abstract

Over the last few decades, on average ca 2000 ha of irrigated agricultural land has been lost every day due to high salinity levels. The size of high salinity areas has been growing from 45 million ha in the early 1990s to its current volume of 62 million ha. Globally, 3.1% of the total land mass is affected by salinity, with over half of the world’s countries afflicted. Presently, about one-fifth of the world’s irrigated lands are too salty for agriculture. Clearly, this negative trend has to be broken. Our aim is to develop wheat (Triticum aestivum L.) varieties with increased salinity tolerance. Starting from Gom-25, a commonly grown in Bangladesh variety already fairly well adapted to salt and heat stress, we introduced ca 1 million mutations per genome by EMS (Ethyl Methane Sulphonate) and raised a population of ca 1800 lines. Mutated wheat lines with an increased salinity tolerance are now selected from this population. The aim is to reuse some parts of the one million ha area of salt contaminated land in Bangladesh.

 

Biography

FahadAl-Qurainy is the professor, expertise in Department of Botany and Microbiology at King Saud University. He publishes more than 60 articles related to plants.

 


Abstract

The cryopreservation of pre-embryonic callus of date palm (Phoenix dactylifera L.) cv. Sagai investigated through encapsulation-dehydration, vitrification and encapsulation -vitrification the maximum regrowth (53.33%) of encapsulated cryopreserved (+LN) embryogenic calli was noted when pre-embryos mass was incubated with 0.5 M of sucrose for two days followed by 6 h air dehydration. The greatest survival (80%) of encapsulated cryopreserved embryonic clump was resulted when calli were incubated with 0.3 or 0.7 M of sucrose for two days followed by 4 h of dehydration, or with 0.5 M of sucrose for two days without air dehydration or 2 h of dehydration. After cryopreservation using encapsulation-vitrification protocol, the highest survival rate (86.67%) and the maximum regrowth (46.67%) achieved when the encapsulated-vitrified cryopreserved calli treated with 100% plant vitrification solution 2 (PVS2) at 25ËšC for 60 min. After cryopreservation using vitrification protocol, the highest recovery 53.33% attained when the vitrified cryopreserved embryogenic calli treated with PVS2 at 25ËšC for 30 min. The maximum (40%) regrowth of vitrified cryopreserved embryogenic calli observed when the vitrified cryopreserved embryogenic calli subjected to PVS2 at 25ËšC for 60 min. The results obtained during this study for regrowth after cryopreservation of Sagai were above the minimum expected for a cryopreserved germplasm bank. The regeneration and regrowth were more than 30% in all the methods applied for Sagai.