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      DNA methylome analysis provides evidence that the expansion of the tea genome is linked to TE bursts

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          Summary

          DNA methylation is essential for gene regulation, imprinting and silencing of transposable elements ( TEs). Although bursts of transposable elements are common in many plant lineages, how plant DNA methylation is related to transposon bursts remains unclear. Here we explore the landscape of DNA methylation of tea, a species thought to have experienced a recent transposon burst event. This species possesses more transposable elements than any other sequenced asterids (potato, tomato, coffee, pepper and tobacco). The overall average DNA methylation levels were found to differ among the tea, potato and tomato genomes, and methylation at CHG sequence sites was found to be significantly higher in tea than that in potato or tomato. Moreover, the abundant TEs resulting from burst events not only resulted in tea developing a very large genome size, but also affected many genes involved in importantly biological processes, including caffeine, theanine and flavonoid metabolic pathway genes. In addition, recently transposed TEs were more heavily methylated than ancient ones, implying that DNA methylation is proportionate to the degree of TE silencing, especially on recent active ones. Taken together, our results show that DNA methylation regulates transposon silencing and may play a role in genome size expansion.

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          Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning.

          Cytosine DNA methylation is important in regulating gene expression and in silencing transposons and other repetitive sequences. Recent genomic studies in Arabidopsis thaliana have revealed that many endogenous genes are methylated either within their promoters or within their transcribed regions, and that gene methylation is highly correlated with transcription levels. However, plants have different types of methylation controlled by different genetic pathways, and detailed information on the methylation status of each cytosine in any given genome is lacking. To this end, we generated a map at single-base-pair resolution of methylated cytosines for Arabidopsis, by combining bisulphite treatment of genomic DNA with ultra-high-throughput sequencing using the Illumina 1G Genome Analyser and Solexa sequencing technology. This approach, termed BS-Seq, unlike previous microarray-based methods, allows one to sensitively measure cytosine methylation on a genome-wide scale within specific sequence contexts. Here we describe methylation on previously inaccessible components of the genome and analyse the DNA methylation sequence composition and distribution. We also describe the effect of various DNA methylation mutants on genome-wide methylation patterns, and demonstrate that our newly developed library construction and computational methods can be applied to large genomes such as that of mouse.
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            Draft genome sequence of Camellia sinensis var. sinensis provides insights into the evolution of the tea genome and tea quality

            Significance A high-quality genome assembly of Camellia sinensis var. sinensis facilitates genomic, transcriptomic, and metabolomic analyses of the quality traits that make tea one of the world’s most-consumed beverages. The specific gene family members critical for biosynthesis of key tea metabolites, monomeric galloylated catechins and theanine, are indicated and found to have evolved specifically for these functions in the tea plant lineage. Two whole-genome duplications, critical to gene family evolution for these two metabolites, are identified and dated, but are shown to account for less amplification than subsequent paralogous duplications. These studies lay the foundation for future research to understand and utilize the genes that determine tea quality and its diversity within tea germplasm.
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              Single-base resolution methylomes of tomato fruit development reveal epigenome modifications associated with ripening.

              Ripening of tomato fruits is triggered by the plant hormone ethylene, but its effect is restricted by an unknown developmental cue to mature fruits containing viable seeds. To determine whether this cue involves epigenetic remodeling, we expose tomatoes to the methyltransferase inhibitor 5-azacytidine and find that they ripen prematurely. We performed whole-genome bisulfite sequencing on fruit in four stages of development, from immature to ripe. We identified 52,095 differentially methylated regions (representing 1% of the genome) in the 90% of the genome covered by our analysis. Furthermore, binding sites for RIN, one of the main ripening transcription factors, are frequently localized in the demethylated regions of the promoters of numerous ripening genes, and binding occurs in concert with demethylation. Our data show that the epigenome is not static during development and may have been selected to ensure the fidelity of developmental processes such as ripening. Crop-improvement strategies could benefit by taking into account not only DNA sequence variation among plant lines, but also the information encoded in the epigenome.
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                Author and article information

                Contributors
                yhongyu92@163.com
                haifengwang@fafu.edu.cn
                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
                15 October 2018
                April 2019
                : 17
                : 4 ( doiID: 10.1111/pbi.2019.17.issue-4 )
                : 826-835
                Affiliations
                [ 1 ] Henan Key Laboratory of Tea Plant Biology College of Life Science Xinyang Normal University Xinyang China
                [ 2 ] State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops College of Plant Protection Fujian Agriculture and Forestry University Fuzhou China
                [ 3 ] College of Horticulture Fujian Agriculture and Forestry University Fuzhou China
                [ 4 ] Agrobiological Gene Research Center Guangdong Academy of Agricultural Sciences Guangzhou China
                [ 5 ] Guangdong Provincial Key Laboratory of Plant Epigenetics College of Life Sciences and Oceanography Shenzhen University Shenzhen China
                [ 6 ] Department of Botany and Plant Sciences Institute of Integrative Genome Biology University of California Riverside CA USA
                Author notes
                [*] [* ] Correspondence (Tel +86‐591‐83850425; fax +86‐591‐86395943; email haifengwang@ 123456fafu.edu.cn and Tel +86‐376‐6391565; fax +86‐376‐6392538; email yhongyu92@ 123456163.com )
                [†]

                These authors contributed equally to this article.

                Author information
                http://orcid.org/0000-0001-7213-927X
                Article
                PBI13018
                10.1111/pbi.13018
                6419580
                30256509
                fa20216a-b6f6-46bd-9e37-011d7a31c544
                © 2018 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
                : 29 June 2018
                : 14 September 2018
                : 23 September 2018
                Page count
                Figures: 5, Tables: 1, Pages: 10, Words: 7313
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: 31501031
                Funded by: Program for Excellent Youth Talents
                Funded by: Program for New Century Excellent Talents in Fujian Province University
                Funded by: Pre‐eminent Youth Fund
                Funded by: Distinguished Young Scholars in Fujian Province
                Funded by: Youth Backbone Teachers Plant of XYNU
                Award ID: 2016GGJS‐13
                Funded by: Nanhu Scholars Program for Young Scholars of XYNU
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                pbi13018
                April 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.1 mode:remove_FC converted:15.03.2019

                Biotechnology
                dna methylation,tea methylome,genome expansion,te burst
                Biotechnology
                dna methylation, tea methylome, genome expansion, te burst

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