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      Pinning down ploidy in paleopolyploid plants

      research-article
      , ,
      BMC Genomics
      BioMed Central
      RECOMB-CG - 2017 : The Fifteenth RECOMB Comparative Genomics Satellite Conference (RECOMB-CG 2017)
      04-06 October 2017
      Whole genome duplication, Gene loss, Birth and death process, Multinomial model, Paralog gene tree, Sequence divergence, Brassica rapa

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          Abstract

          Background

          Fractionation is the genome-wide process of losing one gene per duplicate pair following whole genome multiplication (doubling, tripling, …). This is important in the evolution of plants over tens of millions of years, because of their repeated cycles of genome multiplication and fractionation. One type of evidence in the study of these processes is the frequency distribution of similarities between the two genes, over all the duplicate pairs in the genome.

          Results

          We study modeling and inference problems around the processes of fractionation and whole genome multiplication focusing first on the frequency distribution of similarities of duplicate pairs in the genome. Our birth-and-death model accounts for repeated duplication, triplication or other multiplication events, as well as fractionation rates among multiple progeny of a single gene specific to each event. It also has a biologically and combinatorially well-motivated way of handling the tendency for at least one sibling to survive fractionation. The method settles previously unexplored questions about the expected number of gene pairs tracing their ancestry back to each multiplication event. We exemplify the algebraic concepts inherent in our models and on Brassica rapa, whose evolutionary history is well-known. We demonstrate the quantitative analysis of high-similarity gene pairs and triples to confirm the known ploidies of events in the lineage of B. rapa.

          Conclusions

          Our birth-and-death model accounts for the similarity distribution of paralogs in terms of multiple rounds of whole genome multiplication and fractionation. An analysis of high-similarity gene triples confirms the recent Brassica triplication.

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          Most cited references6

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          The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla.

          The analysis of the first plant genomes provided unexpected evidence for genome duplication events in species that had previously been considered as true diploids on the basis of their genetics. These polyploidization events may have had important consequences in plant evolution, in particular for species radiation and adaptation and for the modulation of functional capacities. Here we report a high-quality draft of the genome sequence of grapevine (Vitis vinifera) obtained from a highly homozygous genotype. The draft sequence of the grapevine genome is the fourth one produced so far for flowering plants, the second for a woody species and the first for a fruit crop (cultivated for both fruit and beverage). Grapevine was selected because of its important place in the cultural heritage of humanity beginning during the Neolithic period. Several large expansions of gene families with roles in aromatic features are observed. The grapevine genome has not undergone recent genome duplication, thus enabling the discovery of ancestral traits and features of the genetic organization of flowering plants. This analysis reveals the contribution of three ancestral genomes to the grapevine haploid content. This ancestral arrangement is common to many dicotyledonous plants but is absent from the genome of rice, which is a monocotyledon. Furthermore, we explain the chronology of previously described whole-genome duplication events in the evolution of flowering plants.
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            How to usefully compare homologous plant genes and chromosomes as DNA sequences.

            There are four sequenced and publicly available plant genomes to date. With many more slated for completion, one challenge will be to use comparative genomic methods to detect novel evolutionary patterns in plant genomes. This research requires sequence alignment algorithms to detect regions of similarity within and among genomes. However, different alignment algorithms are optimized for identifying different types of homologous sequences. This review focuses on plant genome evolution and provides a tutorial for using several sequence alignment algorithms and visualization tools to detect useful patterns of conservation: conserved non-coding sequences, false positive noise, subfunctionalization, synteny, annotation errors, inversions and local duplications. Our tutorial encourages the reader to experiment online with the reviewed tools as a companion to the text.
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              Finding and comparing syntenic regions among Arabidopsis and the outgroups papaya, poplar, and grape: CoGe with rosids.

              In addition to the genomes of Arabidopsis (Arabidopsis thaliana) and poplar (Populus trichocarpa), two near-complete rosid genome sequences, grape (Vitis vinifera) and papaya (Carica papaya), have been recently released. The phylogenetic relationship among these four genomes and the placement of their three independent, fractionated tetraploidies sum to a powerful comparative genomic system. CoGe, a platform of multiple whole or near-complete genome sequences, provides an integrative Web-based system to find and align syntenic chromosomal regions and visualize the output in an intuitive and interactive manner. CoGe has been customized to specifically support comparisons among the rosids. Crucial facts and definitions are presented to clearly describe the sorts of biological questions that might be answered in part using CoGe, including patterns of DNA conservation, accuracy of annotation, transposability of individual genes, subfunctionalization and/or fractionation of syntenic gene sets, and conserved noncoding sequence content. This précis of an online tutorial, CoGe with Rosids (http://tinyurl.com/4a23pk), presents sample results graphically.
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                Author and article information

                Contributors
                sankoff@uottawa.ca
                Conference
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                8 May 2018
                8 May 2018
                2018
                : 19
                Issue : Suppl 5 Issue sponsor : Publication of this supplement has not been supported by sponsorship. Information about the source of funding for publication charges can be found in the individual articles. The articles have undergone the journal's standard peer review process for supplements. The Supplement Editors declare that they have no competing interests.
                : 287
                Affiliations
                ISNI 0000 0001 2182 2255, GRID grid.28046.38, Department of Mathematics and Statistics, , University of Ottawa, ; 585 King Edward, Ottawa, K1N 6N5 Canada
                Article
                4624
                10.1186/s12864-018-4624-y
                5998896
                29745846
                18b6137b-3a84-4f4d-97c5-4fa3fce0c30c
                © The Author(s) 2018

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                RECOMB-CG - 2017 : The Fifteenth RECOMB Comparative Genomics Satellite Conference
                RECOMB-CG 2017
                Barcelona, Spain
                04-06 October 2017
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                Research
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                © The Author(s) 2018

                Genetics
                whole genome duplication,gene loss,birth and death process,multinomial model,paralog gene tree,sequence divergence,brassica rapa

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