Searching journal content for articles similar to Tantin et al. 18 (4): 631.

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  1. ...TF dimers that bind rigidly spacedmotif complexes. The inflexibility of these motif complexes implies that dimerization on DNA frequently imposes strict constraints on the relative spatial conformation of the participating TFs. As in the case of OCT4 and SOX2, a small number of additional motif...
  2. ...factor involved in regulating circadian rhythms. Overall, the genome-wide determination and analysis of GR:DNA binding and transcriptional response to hormone reveals new insights into the complexities of gene regulatory activities managed by GR. Footnotes ↵ 4 Corresponding author. E...
  3. ...the PET sequencing strategy, in which short and paired tags are extracted from the ends of long DNA fragments for ultra-high-throughput sequencing. The PET sequences can be accurately mapped to the reference , thus demarcating the genomic boundaries of PET-represented DNA fragments and revealing...
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  4. ...but not in transfected NIH3T3 mouse fibroblasts, which do not express SOX2, POU5F1, or NANOG ( Fig. 4B ). Furthermore, while most of the SOX2-IP’d DNAs aligned with genomic regions enriched for H3K4me3, the distal elements tended to do so only in ES cells, but not in NP cells or MEFs ( Fig. 4C ; Supplemental Fig. 3...
  5. ..., USA The pluripotency control regions (PluCRs) are defined as genomic regions that are bound by POU5F1, SOX2, and NANOG in vivo. We utilized a high-throughput binding assay to record more than 270,000 different DNA/protein binding measurements along incrementally tiled windows of DNA within these Plu...
  6. ...and ChIP signal. Evidence from these statistical analyses in wild-type cells, and comparisons to maps of TF binding in Rad21 -cohesin haploinsufficient mouse liver, suggests that cohesin helps to stabilize large protein–DNA complexes. Finally, we observe that the presence of mirrored CTCF binding events...
  7. ...sought to reconstruct the genomic repressor network that controls gene transcription in ESC. ChIP DNAs prepared from REST and five of its cofactors were subjected to high-throughput sequencing. For each experiment 11.2–15.8 million sequence reads were uniquely mapped to the mouse . In order to find...
  8. ...not be as easily visualized. OCT4 and SUZ12 have a common set of target genes in embryonic cells None of the components of the PRC2/3/4 are site-specific DNA-binding proteins, and therefore it is not clear how specific regions of the mammalian are targeted for interaction with the PRCs. The DNA-binding factor AEBP...
  9. ...in the same cells. Open chromatin common to all seven cell types tended to be at or near transcription start sites and to be coincident with CTCF binding sites, while open chromatin sites found in only one cell type were typically located away from transcription start sites and contained DNA motifs recognized...
  10. ...of DNA-binding motifs that are actually bound by the TFs from ChIP-seq data for POU5F1, SOX2, and NANOG in H1 hESCs, in either SE constituents or sets of random genomic sequences of the same size. (E) Venn diagram showing the average numbers, across 84 samples, of: 1. TFs having motifs that are expressed...
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