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Locking the genome: nuclear organization and cell fate

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CURRENT OPINION IN GENETICS & DEVELOPMENT
卷 21, 期 2, 页码 167-174

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CURRENT BIOLOGY LTD
DOI: 10.1016/j.gde.2011.01.023

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  1. Novartis Research Foundation
  2. NCCR Frontiers in Genetics
  3. FP7 Network of Excellence, 'Epigenome'
  4. NIH [R01GM056264]
  5. John D and Catherine T MacArthur Foundation
  6. Harvard University

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The differentiation of pluripotent or totipotent cells into various differentiated cell types is accompanied by a restriction of gene expression patterns, alteration in histone and DNA methylation, and changes in the gross nuclear organization of eu- and heterochromatic domains. Several recent studies have coupled genome-wide mapping of histone modifications with changes in gene expression. Other studies have examined changes in the subnuclear positioning of tissue-specific genes upon transcriptional induction or repression. Here we summarize intriguing correlations of the three phenomena, which suggest that in some cases causal relationships may exist.

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