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10.1371/journal.pone.0152683

http://scihub22266oqcxt.onion/10.1371/journal.pone.0152683
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C4816323!4816323 !27031353
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suck abstract from ncbi


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pmid27031353
      PLoS+One 2016 ; 11 (3 ): e0152683
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  • Cas9 Functionally Opens Chromatin #MMPMID27031353
  • Barkal AA ; Srinivasan S ; Hashimoto T ; Gifford DK ; Sherwood RI
  • PLoS One 2016[]; 11 (3 ): e0152683 PMID27031353 show ga
  • Using a nuclease-dead Cas9 mutant, we show that Cas9 reproducibly induces chromatin accessibility at previously inaccessible genomic loci. Cas9 chromatin opening is sufficient to enable adjacent binding and transcriptional activation by the settler transcription factor retinoic acid receptor at previously unbound motifs. Thus, we demonstrate a new use for Cas9 in increasing surrounding chromatin accessibility to alter local transcription factor binding.
  • |*CRISPR-Cas Systems [MESH]
  • |*Transcriptional Activation [MESH]
  • |Animals [MESH]
  • |CRISPR-Associated Proteins/genetics/*metabolism [MESH]
  • |Cell Line [MESH]
  • |Chromatin/genetics/*metabolism [MESH]
  • |Genetic Loci [MESH]
  • |Genome [MESH]
  • |Mice [MESH]
  • |Mouse Embryonic Stem Cells/metabolism [MESH]
  • |Mutation [MESH]


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