LXV SIGA Annual Congress
“From genes to fork: On Mendel’s footsteps”
06-09 September 2022
SESSION 6 - Genetics and beyond:from Mendel to epigenomics
ORAL COMMUNICATIONS6.01 | Impact of structural and epigenetic variation on quantitative traits during tomato domestication |
6.02 | Exploring a model for the formation of novel genes from transposons in plants |
6.03 | Fine mapping and characterization of Grain Number Increase-2 locus (GNI-A2) in durum wheat |
6.04 | Multienvironment assessment and GWAS of the Global Durum Genomic resource for resistance to yellow rust |
6.05 | A common set of genes responding to florigenic and photoperiodic induction at the shoot apical meristem of rice |
6.06 | The transcriptome of Citrus aurantium sequenced and assembled by using a hybrid approach: a novel basis to investigate the cross-protection mechanism of Citrus tristeza virus |
6.07 | Genetics of domestication in common bean (Phaseolus vulgaris L.): an approach for the analysis of candidate genes via TILLING-by-sequencing |
6.08 | Rice SEPALLATA genes OsMADS5 and OsMADS34 cooperate to limit inflorescence branching by repressing the TERMINAL FLOWER1-like gene RCN4. |
6.09 | Genetic structure of maize landraces from the Himalayan region |
6.10 | A transcriptomic study on peach floral and vegetative buds during winter dormancy |
6.11 | Metabolomics and genetic of buds development in Ficus carica L.: for an evolution from monoecy toward dioecy |
6.12 | The CRISPR/CAS9 editing of a WRKY gene and the overexpression of a lipoxygenase gene for improving pathogen resistance in maize |
6.13 | Shaping the role of Vitis R2R3-MYB C2 repressors in transcriptional regulation by integrating DAP-seq and GCN data |
6.14 | Effect of storage time on wine DNA assessed by SSR analysis |
6.15 | Engineered nanomaterial exposure effect on organelle genetic material in Arabidopsis thaliana |
6.16 | GreeNC 2.0: a comprehensive database of plant long non-coding RNAs |
6.17 | Mendelizing barley VRN-H1/FR-H1 and FR-H2 quantitative trait loci in alternative backgrounds |
6.18 | Characterization and valorization of maize landraces from Valle d'Aosta |
6.19 | Effect of grafting on DNA methylation in tomato grafted plants |
6.20 | High-definition mapping of maize seed traits combining genomics and automated phenotyping in a multiparent mapping population |
6.21 | Genomics-driven breeding for local adaptation of durum wheat is enhanced by farmers’ traditional knowledge |
6.22 | Real-time on-site diagnosis of quarantine pathogens in plant tissues by Nanopore-Based Sequencing |
6.23 | First genetic maps development and QTL analysis for flower color in Ranunculus asiaticus L. |
6.24 | Application of K-seq genotyping protocol in two large genomes ornamental species |
6.25 | First genomic insights into the Mandevilla genus |
6.26 | Identification of the quantitative trait loci controlling spike-related traits in durum wheat |
6.27 | Green flesh and tangerine CRISPR/Cas9 edited tomato lines obtained in the San Marzano Italian landrace |
6.28 | Systemin treated tomato plants transmit to the progeny an epigenetic defense signal |
6.29 | Genetic and ploidy diversity of pear germplasm of Lazio Region, Italy |
6.30 | Comprehensive assessment of tetraploid germplasm for plant developmental traits related to grain yield including spike fertility and grain size and shape |
6.31 | Epigenetic control of plant male sterility mediated by DNA methylation |
6.32 | Intravarietal genetic diversity of the grapevine (Vitis vinifera L.) cultivar 'Greco Bianco' |
6.33 | Genome-Wide identification and spatial expression analysis of histone modification gene families in the rubber dandelion Taraxacum kok-saghyz |
6.34 | Unravelling the role of the DNA methylation reshape upon the cold induced anthocyanin pigmentation in blood orange (Citrus sinensis L.) |
6.35 | Integrated approaches to investigate the genetic bases of Citrus clementina self-incompatibility |