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      Developmental remodelling of non-CG methylation at satellite DNA repeats

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          Abstract

          In vertebrates, DNA methylation predominantly occurs at CG dinucleotides however, widespread non-CG methylation (mCH) has been reported in mammalian embryonic stem cells and in the brain. In mammals, mCH is found at CAC trinucleotides in the nervous system, where it is associated with transcriptional repression, and at CAG trinucleotides in embryonic stem cells, where it positively correlates with transcription. Moreover, CAC methylation appears to be a conserved feature of adult vertebrate brains. Unlike any of those methylation signatures, here we describe a novel form of mCH that occurs in the TGCT context within zebrafish mosaic satellite repeats. TGCT methylation is inherited from both male and female gametes, remodelled during mid-blastula transition, and re-established during gastrulation in all embryonic layers. Moreover, we identify DNA methyltransferase 3ba (Dnmt3ba) as the primary enzyme responsible for the deposition of this mCH mark. Finally, we observe that TGCT-methylated repeats are specifically associated with H3K9me3-marked heterochromatin suggestive of a functional interplay between these two gene-regulatory marks. Altogether, this work provides insight into a novel form of vertebrate mCH and highlights the substrate diversity of vertebrate DNA methyltransferases.

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          Trimmomatic: a flexible trimmer for Illumina sequence data

          Motivation: Although many next-generation sequencing (NGS) read preprocessing tools already existed, we could not find any tool or combination of tools that met our requirements in terms of flexibility, correct handling of paired-end data and high performance. We have developed Trimmomatic as a more flexible and efficient preprocessing tool, which could correctly handle paired-end data. Results: The value of NGS read preprocessing is demonstrated for both reference-based and reference-free tasks. Trimmomatic is shown to produce output that is at least competitive with, and in many cases superior to, that produced by other tools, in all scenarios tested. Availability and implementation: Trimmomatic is licensed under GPL V3. It is cross-platform (Java 1.5+ required) and available at http://www.usadellab.org/cms/index.php?page=trimmomatic Contact: usadel@bio1.rwth-aachen.de Supplementary information: Supplementary data are available at Bioinformatics online.
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            The Sequence Alignment/Map format and SAMtools

            Summary: The Sequence Alignment/Map (SAM) format is a generic alignment format for storing read alignments against reference sequences, supporting short and long reads (up to 128 Mbp) produced by different sequencing platforms. It is flexible in style, compact in size, efficient in random access and is the format in which alignments from the 1000 Genomes Project are released. SAMtools implements various utilities for post-processing alignments in the SAM format, such as indexing, variant caller and alignment viewer, and thus provides universal tools for processing read alignments. Availability: http://samtools.sourceforge.net Contact: rd@sanger.ac.uk
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              Fast gapped-read alignment with Bowtie 2.

              As the rate of sequencing increases, greater throughput is demanded from read aligners. The full-text minute index is often used to make alignment very fast and memory-efficient, but the approach is ill-suited to finding longer, gapped alignments. Bowtie 2 combines the strengths of the full-text minute index with the flexibility and speed of hardware-accelerated dynamic programming algorithms to achieve a combination of high speed, sensitivity and accuracy.
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                Author and article information

                Contributors
                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                16 December 2020
                04 December 2020
                04 December 2020
                : 48
                : 22
                : 12675-12688
                Affiliations
                Genomics and Epigenetics Division, Garvan Institute of Medical Research , Sydney, New South Wales 2010, Australia
                St Vincent's Clinical School, Faculty of Medicine, University of New South Wales , Sydney, New South Wales 2010, Australia
                Genomics and Epigenetics Division, Garvan Institute of Medical Research , Sydney, New South Wales 2010, Australia
                St Vincent's Clinical School, Faculty of Medicine, University of New South Wales , Sydney, New South Wales 2010, Australia
                Genomics and Epigenetics Division, Garvan Institute of Medical Research , Sydney, New South Wales 2010, Australia
                St Vincent's Clinical School, Faculty of Medicine, University of New South Wales , Sydney, New South Wales 2010, Australia
                School of Biological and Chemical Sciences, Queen Mary University of London , London, E1 4NS, UK
                Genomics and Epigenetics Division, Garvan Institute of Medical Research , Sydney, New South Wales 2010, Australia
                School of Biotechnology and Biomolecular Sciences, University of New South Wales , Sydney, New South Wales 2052, Australia
                Author notes
                To whom correspondence should be addressed. Tel: +61 2 9295 8343; Fax: +61 2 9295 8101; Email: o.bogdanovic@ 123456garvan.org.au
                Author information
                http://orcid.org/0000-0001-5680-0056
                Article
                gkaa1135
                10.1093/nar/gkaa1135
                7736785
                33271598
                807fe75b-a2df-40c5-94e6-3fca204492fd
                © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@ 123456oup.com

                History
                : 06 November 2020
                : 03 November 2020
                : 25 June 2020
                Page count
                Pages: 14
                Funding
                Funded by: Australian Research Council, DOI 10.13039/501100000923;
                Award ID: DP190103852
                Funded by: NHMRC, DOI 10.13039/501100000925;
                Award ID: APP1162993
                Funded by: CINSW;
                Award ID: CDF181229
                Categories
                AcademicSubjects/SCI00010
                Gene regulation, Chromatin and Epigenetics

                Genetics
                Genetics

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