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      The Arabidopsis lyrata genome sequence and the basis of rapid genome size change

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          Abstract

          We present the 207 Mb genome sequence of the outcrosser Arabidopsis lyrata, which diverged from the self-fertilizing species A. thaliana about 10 million years ago. It is generally assumed that the much smaller A. thaliana genome, which is only 125 Mb, constitutes the derived state for the family. Apparent genome reduction in this genus can be partially attributed to the loss of DNA from large-scale rearrangements, but the main cause lies in the hundreds of thousands of small deletions found throughout the genome. These occurred primarily in non-coding DNA and transposons, but protein-coding multi-gene families are smaller in A. thaliana as well. Analysis of deletions and insertions still segregating in A. thaliana indicates that the process of DNA loss is ongoing, suggesting pervasive selection for a smaller genome.

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          Most cited references51

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          Identification of common molecular subsequences.

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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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              The Sorghum bicolor genome and the diversification of grasses.

              Sorghum, an African grass related to sugar cane and maize, is grown for food, feed, fibre and fuel. We present an initial analysis of the approximately 730-megabase Sorghum bicolor (L.) Moench genome, placing approximately 98% of genes in their chromosomal context using whole-genome shotgun sequence validated by genetic, physical and syntenic information. Genetic recombination is largely confined to about one-third of the sorghum genome with gene order and density similar to those of rice. Retrotransposon accumulation in recombinationally recalcitrant heterochromatin explains the approximately 75% larger genome size of sorghum compared with rice. Although gene and repetitive DNA distributions have been preserved since palaeopolyploidization approximately 70 million years ago, most duplicated gene sets lost one member before the sorghum-rice divergence. Concerted evolution makes one duplicated chromosomal segment appear to be only a few million years old. About 24% of genes are grass-specific and 7% are sorghum-specific. Recent gene and microRNA duplications may contribute to sorghum's drought tolerance.
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                Author and article information

                Journal
                9216904
                2419
                Nat Genet
                Nature genetics
                1061-4036
                1546-1718
                22 March 2011
                10 April 2011
                May 2011
                1 November 2011
                : 43
                : 5
                : 476-481
                Affiliations
                [1 ]Molecular and Computational Biology, University of Southern California, Los Angeles, California 90089, USA.
                [2 ]Department of Plant Systems Biology, VIB, 9052 Gent, Belgium.
                [3 ]Department of Plant Biotechnology and Genetics, Ghent University, 9052 Gent, Belgium.
                [4 ]Department of Ecology and Evolution, University of Chicago, Chicago, Illinois 60637, USA.
                [5 ]Center for Genome Research and Biocomputing, Oregon State University, Corvallis, Oregon 97331, USA.
                [6 ]Department of Horticulture, Oregon State University, Corvallis, Oregon 97331, USA.
                [7 ]Department of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany.
                [8 ]US Department of Energy Joint Genome Institute, Walnut Creek, California 94598, USA.
                [9 ]Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon 97331, USA.
                [10 ]HudsonAlpha Genome Sequencing Center, Hudson Alpha Institute for Biotechnology, Huntsville, Alabama 35806, USA.
                [11 ]Munich Information Center for Protein Sequences/Institute for Bioinformatics and Systems Biology, Helmholtz Center Munich, 85764 Neuherberg, Germany.
                [12 ]Department of Ecology and Evolutionary Biology, University of California Irvine, Irvine, California 92697, USA.
                [13 ]Department of Plant Biology, Cornell University, Ithaca, New York 14853, USA.
                [14 ] Gregor Mendel Institute, Austrian Academy of Science, 1030 Vienna, Austria.
                Author notes
                [§ ]To whom correspondence should be addressed. weigel@ 123456weigelworld.org (D.W.); ya-long.guo@ 123456hotmail.com (Y.-L.G.).
                [*]

                These authors contributed equally to this work.

                [¶]

                Present addresses: Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey 08544, USA (T.T.H.); Dow AgroSciences, Portland, Oregon 97224, USA (E.G.B.); Department of Biology, University of Utah, Salt Lake City, Utah, USA (R.M.C.); Graduate University for Advanced Studies, Hayama, Kanagawa, 240-0193, Japan (J.A.F.); Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, Massachusetts 02138, USA (J.D.H.); Center for Genomic Regulation, 08003 Barcelona, Spain (S.O.); Department of Plant Developmental Biology, Max Planck Institute for Plant Breeding Research, 50829 Cologne, Germany (K.S.); Department of Molecular Biology, Max Planck Institute for Developmental Biology, 72076 Tübingen, Germany (X.W.).

                Article
                nihpa282063
                10.1038/ng.807
                3083492
                21478890
                18f2d534-de0e-42ad-8c83-5bdf6f4219af

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                History
                Funding
                Funded by: National Institute of General Medical Sciences : NIGMS
                Award ID: R01 GM083068-04 ||GM
                Categories
                Article

                Genetics
                Genetics

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