Literature DB >> 23443545

Tet-mediated covalent labelling of 5-methylcytosine for its genome-wide detection and sequencing.

Liang Zhang1, Keith E Szulwach, Gary C Hon, Chun-Xiao Song, Beomseok Park, Miao Yu, Xingyu Lu, Qing Dai, Xiao Wang, Craig R Street, Huiping Tan, Jung-Hyun Min, Bing Ren, Peng Jin, Chuan He.   

Abstract

5-methylcytosine is an epigenetic mark that affects a broad range of biological functions in mammals. The chemically inert methyl group prevents direct labelling for subsequent affinity purification and detection. Therefore, most current approaches for the analysis of 5-methylcytosine still have limitations of being either density-biased, lacking in robustness and consistency, or incapable of analysing 5-methylcytosine specifically. Here we present an approach, TAmC-Seq, which selectively tags 5-methylcytosine with an azide functionality that can be further labelled with a biotin for affinity purification, detection and genome-wide mapping. Using this covalent labelling approach, we demonstrate high sensitivity and specificity for known methylated loci, as well as increased CpG dinucleotide coverage at lower sequencing depth as compared with antibody-based enrichment, providing an improved efficiency in the 5-methylcytosine enrichment and genome-wide profiling.

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Year:  2013        PMID: 23443545      PMCID: PMC3679896          DOI: 10.1038/ncomms2527

Source DB:  PubMed          Journal:  Nat Commun        ISSN: 2041-1723            Impact factor:   14.919


  34 in total

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  18 in total

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5.  DNA-methyltransferase1 (DNMT1) binding to CpG rich GABAergic and BDNF promoters is increased in the brain of schizophrenia and bipolar disorder patients.

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7.  Simultaneous single-molecule epigenetic imaging of DNA methylation and hydroxymethylation.

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Review 10.  Integrating DNA methylation dynamics into a framework for understanding epigenetic codes.

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