Searching journal content for articles similar to Faure et al. 22 (11): 2163.

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  1. ...cis-regulatory elements. Here, CTCF binds in tandem with beta-catenin and TCF/LEF to increase cohesin stalling and induce the formation of chromatin loops that contribute to the upregulation of a subset of Wnt target genes (Fig. 7). This, to our knowledge, represents a previously unknown mechanism...
  2. ...DIVERSITY does not take into account the spatial distribution of the motifs in its model. However, in over two-thirds of the sequences, the distance between the two copies is <50 bp, suggesting cooperative binding.Unlike vertebrates, there is no evidence to support cohesin-CTCF-mediated chromatin loop formations...
  3. ...occupied than liver and brain, consistent with a ground-state pattern of CTCF binding that is elaborated during differentiation. CTCF binding sites without the canonical consensus motif were highly tissue specific. In brain, a third of CTCF and cohesin binding sites coincide, consistent with the potential...
  4. ..., Schuijers J, Lee TI, Zhao K, et al. 2014. Control of cell identity genes occurs in insulated neighborhoods in mammalian chromosomes. Cell 159: 374–387. Faure AJ, Schmidt D, Watt S, Schwalie PC, Wilson MD, Xu H, Ramsay RG, Odom DT, Flicek P. 2012. Cohesin regulates tissue-specific expression by stabilizing...
  5. ...characterized on a -wide scale. Here we performed chromatin interaction analysis with paired-end tag sequencing (ChIA-PET) of the cohesin subunit SMC1A in developing mouse limb. We identified 2264 SMC1A interactions, of which 1491 (65%) involved sites co-occupied by CTCF. SMC1A participates in tissue-specific...
  6. ...Cohesin-based chromatin interactions enable regulated gene expression within preexisting architectural compartments Vlad C. Seitan 1 , 7 , Andre J. Faure 2 , 7 , Ye Zhan 3 , Rachel Patton McCord 3 , Bryan R. Lajoie 3 , Elizabeth Ing...
  7. ...that predominantly bind at highly occupied “HOT” sites (Fig. 2B). ASB variants affecting cohesin complex members also had a higher degree of overlap with eQTLs (Fig. 4B) and were significantly enriched for mammalian sequence conservation (Fig. 3E). This suggests that genetic variants that alter three...
  8. ...and transcriptional regulation by mediating chromatin loop formation with cohesin, which acts as an insulator and contributes to the establishment of topologically associated domains (TADs) (Dixon et al. 2012; Nora et al. 2017). A large fraction of CTCF binding sites are shared across multiple cell types...
  9. ...acts directly or indirectly to regulate chromatin interactions, although how this histone modification modulates 3D chromatin architecture remains elusive. To decipher the impact of the dynamic deposition of H3K27me3 on the Arabidopsis thaliana nuclear interactome, we combined genetics, transcriptomics...
  10. ...of HNARs, acting synergistically. Nanog binds to the HNAR center, whereas the Pou5f3 stabilizes the flanks. The HNAR model will provide a useful tool for regulatory studies in a variety of biological systems.The development of multicellular organisms is first driven by maternal products and occurs...
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