Comparative genomic analysis of male and female poplars

Poster (download) Elena Pushkova1, George Krasnov2, Roman Novakovskiy3, Nadezhda Bolsheva4, Nataliya Melnikova5, Alexey Dmitriev61Engelhardt Institute of Molecular Biology, RAS, Moscow, Russia, pushkova18@gmail.com2Engelhardt Institute of Molecular Biology, RAS, Moscow, Russia, gskrasnov@mail.ru3Engelhardt Institute of Molecular Biology, RAS, Moscow, Russia, 0legovich46@mail.ru4Engelhardt Institute of Molecular Biology, RAS, Moscow, Russia, nlbolsheva@mail.ru5Engelhardt Institute of Molecular Biology, RAS, Moscow, Russia, mnv-4529264@yandex.ru6Engelhardt Institute of Molecular Biology, RAS, Moscow, Russia, alex_245@mail.ru In the genomic analysis of trees, species belonging to the Populus genera serve as model objects. In our work, we carried out sequencing of the genome of male and female plants of Populus x sibirica, which are widespread in the Moscow region. Achieve high quality de novo In assemblies, we used a combination of two platforms, namely Oxford Nanopore and Illumina, to obtain long and high-precision short read operations, respectively. In general, using the MinION sequencer, we got 18 GB with an average N50 of 25 kb for each genotype, while using the HiSeq 2500 tool, we got from 36 to 52 million paired 125 + 125 readings for male and female plants. The Shasta assembler provided the best assembly results: N50 values ​​were around 0.5 MB, and integrity was above 95% according to BUSCO. Analysis of the high-quality genomes of male and female P. x sibirica trees makes it possible to identify genes associated with poplar sex, which will facilitate the determination of its sex determination mechanism.

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Genome Assembly and Annotation of Nothobranchius rachovii killifish

Zulfiia Guvatova1, George Krasnov2, Anastasiya Snezhkina3, Artemy Tokarev4, Maria Fedorova5, Anna Kudryavtseva61Center for Precision Genome Editing and Genetic Technologies for Biomedicine Engelhardt Institute of Molecular Biology, Russian Academy of Sciences Moscow, Russia, guvatova.zulfiya@mail.ru2Center for Precision Genome Editing and Genetic Technologies for Biomedicine Engelhardt Institute of Molecular Biology, Russian Academy of Sciences Moscow, Russia, gskrasnov@mail.ru3Center for Precision Genome Editing and Genetic Technologies for Biomedicine Engelhardt Institute of Molecular Biology, Russian Academy of Sciences Moscow, Russia, leftger@rambler.ru4Artemy Tokarev Veterinary biology faculty MSAVM&B – MVA named after K.I. Skryabin Moscow, Russia, artemiy.tokarev@mail.ru5Laboratory of Postgenomic Research Engelhardt Institute of Molecular Biology, Russian Academy of Sciences Moscow, Russia, fedorowams@yandex.ru6Center for Precision Genome Editing and Genetic Technologies for Biomedicine Engelhardt Institute of Molecular Biology, Russian Academy of Sciences Moscow, Russia, rhizamoeba@mail.ru Nothobranchius rachovii is a species of freshwater annual killifish native to Africa. This organism is an attractive model in aging studies because of short lifetime and rapid maturation. In this study, we present draft genome assembly of this organism based on Nanopore reads and polished with Illumina reads. We tested four popular Nanopore reads assemblers (Flye, MaSuRCA, Shasta, wtdbg2) and two polishers (Pilon and MaSuRCA-polish tool). We selected the best combination of these tools in terms of contig length and assembly completeness.

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Comparative genomics and quantitative proteomics reveal differentially produced proteins underlying virulence and host specificity in Bacillus thuringiensis

Poster (download) Yury Malovichko1, Maria Belousova2, Elena Lukasheva3, Daria Gorbach4, Ekaterina Romanovskaya5, Christian Ihling6, Andrej Frolov7, Anton Nizhnikov8, Kirill Antonets91All-Russian Research Institute of Agricultural Microbiology, yu.malovichko@arriam.ru2All-Russian Research Institute of Agricultural Microbiology, m.belousova@arriam.ru3St. Petersburg State University, elena_lukasheva@mail.ru4St. Petersburg State University, daria.gorba4@yandex.ru5St. Petersburg State University, e.romanovskaya@spbu.ru6Martin-Luther Universität Halle-Wittenberg, christian.ihling@pharmazie.uni-halle.de7Martin-Luther Universität Halle-Wittenberg, Andrej.Frolov@ipb-halle.de8All-Russian Research Institute of Agricultural Microbiology, a.nizhnikov@arriam.ru9All-Russian Research Institute of Agricultural Microbiology, k.antonets@arriam.ru Bacillus thuringiensis is a Gram-positive spore-forming bacterium known for its insecticidal activities. Although its features of high virulence and exceptional host specificity are wiely known and have conditioned its use as a source of novel biopesticides, molecular mechanisms underlying these traits remain elusive and are usually attributed to its repertoire of proteinaceous toxins. In this work we used combined proteogenomic approach to dissect <>. We used three different strains of B. thuringiensis belonging to the var. thuringiensis, darmstadtiensis and israeliensis and one derivate of B. thuringiensis var israeliensis, which lost the ability to produce Cry-toxins. By using hybrid Oxford Nanopore and Illumina sequencing we achieved replicon-level genome assemblies of the studied strains which, upon annotation, facilitated comparison of virulence factor repertoires and putative reasons of virulence loss in derivate strain, Further application of quantitative HPLC-Orbitrap-MS and proteome level-comparison between vegetative and sporulating cultures allowed us to identify the proteins, which were differentially produced in the strains at each stage. While proteins differentially produced at vegetative stage related mostly to cell metabolism with few virulence factors captured, those identified in spores included different spore coat proteins, flotillin-like proteins involved in in cell differentiation, exosporium proteins and a wide set of virulence factors including proteinaceous Cry toxins. Taking together the data obtained in this study indicate the impact of the accessory genes produced at various stages of colony development on pathogenicity-associated phenotypic traits in strains with different host ranges. To our knowledge, this is the first proteogenomic study of B. thuringiensis aimed to compare both genomic and proteomic profiles between serovars.

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