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      Comparative population genomics reveals the domestication history of the peach, Prunus persica , and human influences on perennial fruit crops

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          Abstract

          Background

          Recently, many studies utilizing next generation sequencing have investigated plant evolution and domestication in annual crops. Peach, Prunus persica, is a typical perennial fruit crop that has ornamental and edible varieties. Unlike other fruit crops, cultivated peach includes a large number of phenotypes but few polymorphisms. In this study, we explore the genetic basis of domestication in peach and the influence of humans on its evolution.

          Results

          We perform large-scale resequencing of 10 wild and 74 cultivated peach varieties, including 9 ornamental, 23 breeding, and 42 landrace lines. We identify 4.6 million SNPs, a large number of which could explain the phenotypic variation in cultivated peach. Population analysis shows a single domestication event, the speciation of P. persica from wild peach. Ornamental and edible peach both belong to P. persica , along with another geographically separated subgroup, Prunus ferganensis.

          We identify 147 and 262 genes under edible and ornamental selection, respectively. Some of these genes are associated with important biological features. We perform a population heterozygosity analysis in different plants that indicates that free recombination effects could affect domestication history. By applying artificial selection during the domestication of the peach and facilitating its asexual propagation, humans have caused a sharp decline of the heterozygote ratio of SNPs.

          Conclusions

          Our analyses enhance our knowledge of the domestication history of perennial fruit crops, and the dataset we generated could be useful for future research on comparative population genomics.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s13059-014-0415-1) contains supplementary material, which is available to authorized users.

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          Most cited references51

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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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            Rapid isolation of high molecular weight plant DNA.

            A method is presented for the rapid isolation of high molecular weight plant DNA (50,000 base pairs or more in length) which is free of contaminants which interfere with complete digestion by restriction endonucleases. The procedure yields total cellular DNA (i.e. nuclear, chloroplast, and mitochondrial DNA). The technique is ideal for the rapid isolation of small amounts of DNA from many different species and is also useful for large scale isolations.
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              A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase.

              Grain weight is one of the most important components of grain yield and is controlled by quantitative trait loci (QTLs) derived from natural variations in crops. However, the molecular roles of QTLs in the regulation of grain weight have not been fully elucidated. Here, we report the cloning and characterization of GW2, a new QTL that controls rice grain width and weight. Our data show that GW2 encodes a previously unknown RING-type protein with E3 ubiquitin ligase activity, which is known to function in the degradation by the ubiquitin-proteasome pathway. Loss of GW2 function increased cell numbers, resulting in a larger (wider) spikelet hull, and it accelerated the grain milk filling rate, resulting in enhanced grain width, weight and yield. Our results suggest that GW2 negatively regulates cell division by targeting its substrate(s) to proteasomes for regulated proteolysis. The functional characterization of GW2 provides insight into the mechanism of seed development and is a potential tool for improving grain yield in crops.
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                Author and article information

                Contributors
                wyandck@126.com
                zhengzhijun01@gmail.com
                wlirong2009@sina.com
                liuxin@genomics.cn
                zhugengrui@126.com
                weichaof@sina.com
                chengshf@genomics.cn
                zengpeng@genomics.org.cn
                scccw7216@163.com
                morningtoyou@126.com
                feixue1039@gmail.com
                zhongxiao@genomics.cn
                xiaoliwang1984@163.com
                zhaopei1226@163.com
                bianchao@genomics.cn
                zhuyinling@genomics.cn
                zhangjh1201@163.com
                619409148@qq.com
                chinachen000@gmail.com
                275163098@qq.com
                haojingxiao@163.com
                jay20075267@163.com
                huangguodong@genomics.cn
                liyuxiang@genomics.cn
                1816868738@qq.com
                ytguojian@163.com
                xuxun@genomics.cn
                wangj@genomics.org.cn
                Journal
                Genome Biol
                Genome Biology
                BioMed Central (London )
                1465-6906
                1465-6914
                31 July 2014
                31 July 2014
                2014
                : 15
                : 7
                : 415
                Affiliations
                [ ]Zhengzhou Fruit Research Institute, Chinese Academy of Agriculture Sciences, Zhengzhou, 450009 China
                [ ]The Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (Fruit Tree Breeding Technology), Ministry of Agriculture, Zhengzhou, 450009 China
                [ ]BGI-Shenzhen, Shenzhen, 518083 China
                [ ]MetaGene Genomics Institute, Hangzhou, 310011 China
                [ ]State Key Laboratory of Agricultural Genomics, BGI-Shenzhen, Shenzhen, 518083 China
                [ ]Key Laboratory of Genomics, Ministry of Agriculture, BGI-Shenzhen, Shenzhen, 518083 China
                Article
                415
                10.1186/s13059-014-0415-1
                4174323
                25079967
                c0533ccd-2c17-42e1-a408-3a78a3243248
                © Cao et al.; licensee BioMed Central ltd 2014

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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.

                History
                : 25 February 2014
                : 15 July 2014
                Categories
                Research
                Custom metadata
                © The Author(s) 2014

                Genetics
                Genetics

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