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      Characterization of disease resistance genes in the Brassica napus pangenome reveals significant structural variation

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          Summary

          Methods based on single nucleotide polymorphism ( SNP), copy number variation ( CNV) and presence/absence variation ( PAV) discovery provide a valuable resource to study gene structure and evolution. However, as a result of these structural variations, a single reference genome is unable to cover the entire gene content of a species. Therefore, pangenomics analysis is needed to ensure that the genomic diversity within a species is fully represented. Brassica napus is one of the most important oilseed crops in the world and exhibits variability in its resistance genes across different cultivars. Here, we characterized resistance gene distribution across 50 B. napus lines. We identified a total of 1749 resistance gene analogs ( RGAs), of which 996 are core and 753 are variable, 368 of which are not present in the reference genome (cv. Darmor‐ bzh). In addition, a total of 15 318 SNPs were predicted within 1030 of the RGAs. The results showed that core R‐genes harbour more SNPs than variable genes. More nucleotide binding site‐leucine‐rich repeat ( NBSLRR) genes were located in clusters than as singletons, with variable genes more likely to be found in clusters. We identified 106 RGA candidates linked to blackleg resistance quantitative trait locus ( QTL). This study provides a better understanding of resistance genes to target for genomics‐based improvement and improved disease resistance.

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          Plant pathogens and integrated defence responses to infection.

          Plants cannot move to escape environmental challenges. Biotic stresses result from a battery of potential pathogens: fungi, bacteria, nematodes and insects intercept the photosynthate produced by plants, and viruses use replication machinery at the host's expense. Plants, in turn, have evolved sophisticated mechanisms to perceive such attacks, and to translate that perception into an adaptive response. Here, we review the current knowledge of recognition-dependent disease resistance in plants. We include a few crucial concepts to compare and contrast plant innate immunity with that more commonly associated with animals. There are appreciable differences, but also surprising parallels.
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            Multiple reference genomes and transcriptomes for Arabidopsis thaliana

            Genetic differences between Arabidopsis thaliana accessions underlie the plant’s extensive phenotypic variation, and until now these have been interpreted largely in the context of the annotated reference accession Col-0. Here we report the sequencing, assembly and annotation of the genomes of 18 natural A. thaliana accessions, and their transcriptomes. When assessed on the basis of the reference annotation, one-third of protein-coding genes are predicted to be disrupted in at least one accession. However, re-annotation of each genome revealed that alternative gene models often restore coding potential. Gene expression in seedlings differed for nearly half of expressed genes and was frequently associated with cis variants within 5 kilobases, as were intron retention alternative splicing events. Sequence and expression variation is most pronounced in genes that respond to the biotic environment. Our data further promote evolutionary and functional studies in A. thaliana, especially the MAGIC genetic reference population descended from these accessions.
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              De novo assembly of soybean wild relatives for pan-genome analysis of diversity and agronomic traits.

              Wild relatives of crops are an important source of genetic diversity for agriculture, but their gene repertoire remains largely unexplored. We report the establishment and analysis of a pan-genome of Glycine soja, the wild relative of cultivated soybean Glycine max, by sequencing and de novo assembly of seven phylogenetically and geographically representative accessions. Intergenomic comparisons identified lineage-specific genes and genes with copy number variation or large-effect mutations, some of which show evidence of positive selection and may contribute to variation of agronomic traits such as biotic resistance, seed composition, flowering and maturity time, organ size and final biomass. Approximately 80% of the pan-genome was present in all seven accessions (core), whereas the rest was dispensable and exhibited greater variation than the core genome, perhaps reflecting a role in adaptation to diverse environments. This work will facilitate the harnessing of untapped genetic diversity from wild soybean for enhancement of elite cultivars.
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                Author and article information

                Contributors
                jacqueline.batley@uwa.edu.au
                Journal
                Plant Biotechnol J
                Plant Biotechnol. J
                10.1111/(ISSN)1467-7652
                PBI
                Plant Biotechnology Journal
                John Wiley and Sons Inc. (Hoboken )
                1467-7644
                1467-7652
                10 October 2019
                April 2020
                : 18
                : 4 ( doiID: 10.1111/pbi.v18.4 )
                : 969-982
                Affiliations
                [ 1 ] UWA School of Biological Sciences and the UWA Institute of Agriculture Faculty of Science The University of Western Australia Crawley WA Australia
                Author notes
                [*] [* ] Correspondence (Tel +61 08 6488 5929; email jacqueline.batley@ 123456uwa.edu.au )
                Author information
                https://orcid.org/0000-0002-2158-4485
                https://orcid.org/0000-0001-8530-3067
                https://orcid.org/0000-0002-6100-1790
                https://orcid.org/0000-0001-7599-6760
                https://orcid.org/0000-0002-5391-5824
                Article
                PBI13262
                10.1111/pbi.13262
                7061875
                31553100
                bb0a4400-1638-45c4-910a-df060398d54f
                © 2019 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 08 January 2019
                : 30 August 2019
                : 13 September 2019
                Page count
                Figures: 3, Tables: 4, Pages: 14, Words: 12394
                Funding
                Funded by: Australian Research Council ARC , open-funder-registry 10.13039/501100000923;
                Award ID: FT130100604
                Award ID: DP1601004497
                Award ID: LP140100537
                Award ID: LP160100030
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                April 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.7 mode:remove_FC converted:09.03.2020

                Biotechnology
                brassica napus,pangenome,rgaugury,presence/absence variation,resistance gene
                Biotechnology
                brassica napus, pangenome, rgaugury, presence/absence variation, resistance gene

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