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ATAC-see reveals the accessible genome by transposase-mediated imaging and sequencing.
Chen, Xingqi; Shen, Ying; Draper, Will; Buenrostro, Jason D; Litzenburger, Ulrike; Cho, Seung Woo; Satpathy, Ansuman T; Carter, Ava C; Ghosh, Rajarshi P; East-Seletsky, Alexandra; Doudna, Jennifer A; Greenleaf, William J; Liphardt, Jan T; Chang, Howard Y.
Affiliation
  • Chen X; Center for Personal Dynamic Regulomes, Stanford University, Stanford, California, USA.
  • Shen Y; Center for Personal Dynamic Regulomes, Stanford University, Stanford, California, USA.
  • Draper W; Department of Bioengineering, Stanford University, Stanford, California, USA.
  • Buenrostro JD; Center for Personal Dynamic Regulomes, Stanford University, Stanford, California, USA.
  • Litzenburger U; Department of Genetics, Stanford University, Stanford, California, USA.
  • Cho SW; Center for Personal Dynamic Regulomes, Stanford University, Stanford, California, USA.
  • Satpathy AT; Center for Personal Dynamic Regulomes, Stanford University, Stanford, California, USA.
  • Carter AC; Center for Personal Dynamic Regulomes, Stanford University, Stanford, California, USA.
  • Ghosh RP; Center for Personal Dynamic Regulomes, Stanford University, Stanford, California, USA.
  • East-Seletsky A; Department of Bioengineering, Stanford University, Stanford, California, USA.
  • Doudna JA; Department of Molecular and Cell Biology, University of California, Berkeley, California, USA.
  • Greenleaf WJ; Department of Chemistry, University of California, Berkeley, Berkeley, California, USA.
  • Liphardt JT; Department of Molecular and Cell Biology, University of California, Berkeley, California, USA.
  • Chang HY; Department of Chemistry, University of California, Berkeley, Berkeley, California, USA.
Nat Methods ; 13(12): 1013-1020, 2016 Dec.
Article in En | MEDLINE | ID: mdl-27749837
ABSTRACT
Spatial organization of the genome plays a central role in gene expression, DNA replication, and repair. But current epigenomic approaches largely map DNA regulatory elements outside of the native context of the nucleus. Here we report assay of transposase-accessible chromatin with visualization (ATAC-see), a transposase-mediated imaging technology that employs direct imaging of the accessible genome in situ, cell sorting, and deep sequencing to reveal the identity of the imaged elements. ATAC-see revealed the cell-type-specific spatial organization of the accessible genome and the coordinated process of neutrophil chromatin extrusion, termed NETosis. Integration of ATAC-see with flow cytometry enables automated quantitation and prospective cell isolation as a function of chromatin accessibility, and it reveals a cell-cycle dependence of chromatin accessibility that is especially dynamic in G1 phase. The integration of imaging and epigenomics provides a general and scalable approach for deciphering the spatiotemporal architecture of gene control.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatin / Genome, Human / Transposases / High-Throughput Nucleotide Sequencing / Fluorescent Dyes / Heterocyclic Compounds, 4 or More Rings Limits: Humans Language: En Journal: Nat Methods Journal subject: TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2016 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatin / Genome, Human / Transposases / High-Throughput Nucleotide Sequencing / Fluorescent Dyes / Heterocyclic Compounds, 4 or More Rings Limits: Humans Language: En Journal: Nat Methods Journal subject: TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2016 Type: Article Affiliation country: United States