Profiling genome-wide chromatin methylation with engineered posttranslation apparatus within living cells Journal Article


Authors: Wang, R.; Islam, K.; Liu, Y.; Zheng, W.; Tang, H.; Lailler, N.; Blum, G.; Deng, H.; Luo, M.
Article Title: Profiling genome-wide chromatin methylation with engineered posttranslation apparatus within living cells
Abstract: Protein methyltransferases (PMTs) have emerged as important epigenetic regulators in myriad biological processes in both normal physiology and disease conditions. However, elucidating PMT-regulated epigenetic processes has been hampered by ambiguous knowledge about in vivo activities of individual PMTs particularly because of their overlapping but nonredundant functions. To address limitations of conventional approaches in mapping chromatin modification of specific PMTs, we have engineered the chromatin-modifying apparatus and formulated a novel technology, termed clickable chromatin enrichment with parallel DNA sequencing (CliEn-seq), to probe genome-wide chromatin modification within living cells. The three-step approach of CliEn-seq involves in vivo synthesis of S-adenosyl-l-methionine (SAM) analogues from cell-permeable methionine analogues by engineered SAM synthetase (methionine adenosyltransferase or MAT), in situ chromatin modification by engineered PMTs, subsequent enrichment and sequencing of the uniquely modified chromatins. Given critical roles of the chromatin-modifying enzymes in epigenetics and structural similarity among many PMTs, we envision that the CliEn-seq technology is generally applicable in deciphering chromatin methylation events of individual PMTs in diverse biological settings. © 2012 American Chemical Society.
Keywords: human cell; methylation; genes; biosynthesis; methyltransferases; protein processing; epigenetics; chromatin; in-vivo; dna sequence; alkylation; amino acids; enzyme synthesis; dna sequences; protein methyltransferase; s adenosylmethionine; biological process; living cell; biological settings; methionine adenosyltransferase; s adenosyl l methionines; cell-permeable; chromatin modification; conventional approach; parallel-dna; structural similarity; synthetases; three-step approach
Journal Title: Journal of the American Chemical Society
Volume: 135
Issue: 3
ISSN: 0002-7863
Publisher: American Chemical Society  
Date Published: 2013-01-23
Start Page: 1048
End Page: 1056
Language: English
DOI: 10.1021/ja309412s
PROVIDER: scopus
PMCID: PMC3582175
PUBMED: 23244065
DOI/URL:
Notes: --- - "Export Date: 1 March 2013" - "CODEN: JACSA" - "Source: Scopus"
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MSK Authors
  1. Weihong Zheng
    11 Zheng
  2. Minkui Luo
    70 Luo
  3. Kabirul Islam
    9 Islam
  4. Gil Blum
    15 Blum
  5. Rui Wang
    8 Wang
  6. Nathalie Josette Lailler
    12 Lailler