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Control of embryonic stem cell lineage commitment by core promoter factor, TAF3.

Cell | Sep 2, 2011

http://www.ncbi.nlm.nih.gov/pubmed/21884934

Deciphering the molecular basis of pluripotency is fundamental to our understanding of development and embryonic stem cell function. Here, we report that TAF3, a TBP-associated core promoter factor, is highly enriched in ES cells. In this context, TAF3 is required for endoderm lineage differentiation and prevents premature specification of neuroectoderm and mesoderm. In addition to its role in the core promoter recognition complex TFIID, genome-wide binding studies reveal that TAF3 localizes to a subset of chromosomal regions bound by CTCF/cohesin that are selectively associated with genes upregulated by TAF3. Notably, CTCF directly recruits TAF3 to promoter distal sites and TAF3-dependent DNA looping is observed between the promoter distal sites and core promoters occupied by TAF3/CTCF/cohesin. Together, our findings support a new role of TAF3 in mediating long-range chromatin regulatory interactions that safeguard the finely-balanced transcriptional programs underlying pluripotency.

Pubmed ID: 21884934 RIS Download

Mesh terms: Animals | Cell Cycle Proteins | Cell Proliferation | Chromosomal Proteins, Non-Histone | Embryonic Stem Cells | Endoderm | Gene Expression Regulation, Developmental | Homeodomain Proteins | Humans | Mice | Promoter Regions, Genetic | Repressor Proteins | Teratoma | Transcription Factor TFIID | Transcription, Genetic

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Associated grants

  • Agency: NCI NIH HHS, Id: R37 CA025417
  • Agency: NCI NIH HHS, Id: R37 CA025417-34
  • Agency: Howard Hughes Medical Institute, Id:

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