Searching journal content for articles similar to Teif et al. 24 (8): 1285.

Displaying results 1-10 of 14
For checked items
  1. ...are linked to active chromatin remodeling and reduced DNA methylation. Nucleosomes lost or gained in CLL marks differential binding of 3D chromatin organizers such as CTCF as well as immune response–related transcription factors and delineated mechanisms of epigenetic deregulation. The principal component...
  2. ...binding, DNA methylation, and gene expression in DKO ESCs and developed biophysical models to predict differential CTCF binding. Methylation-sensitive nucleosome repositioning accounted for a significant portion of CTCF binding loss in DKO ESCs, whereas unmethylated and nucleosome-depleted CpG islands...
  3. ..., dissociates from chromatin during mitosis. Along these lines, CTCF becomes highly phosphorylated in mitosis (Dovat et al. 2002; Dephoure et al. 2008; Rizkallah and Hurt 2009), and in vitro assays show that DNA binding capability of phosphorylated CTCF is dramatically reduced (Jantz and Berg 2004; Sekiya et al...
  4. ...show that localization of a TF to the chromatin does not necessarily imply DNA sequence-specific binding in mitosis (Fig. 7A). This is exemplified by SOX2 and, as shown by others, by CTCF (Oomen et al. 2019): While these TFs are both chromosomally retained, they are largely evicted from the sites...
  5. ...of nucleosomes during mitosis.The cell cycle is a dynamic orchestrated process that involves major changes to the chromatin structure (Raynaud et al. 2014) and the expression of hundreds of genes (Spellman et al. 1998; Cho et al. 2001; Whitfield et al. 2002; Bar-Joseph et al. 2008). During the cell cycle, DNA...
  6. ...differentiation in an immune response. [Supplemental material is available for this article.] Epigenetic modifications play important roles in regulating cellular differentiation events. One such epigenetic modification, DNA methylation, occurs on cytosine residues primarily at CpG dinucleotides in mammals...
  7. ...HSCs and CD36+ cells using MNase-seq as describedpreviously (Schones et al. 2008). As shown in Figure 1A, nucleosomes were well positioned surrounding the binding sites of the constitutively expressed insulator protein, CTCF, and little difference was detected after differentiation. In striking contrast...
  8. ..., independent features. This may be due to the popularity of “single-profile” methods which provide rich data for only one aspect of chromatin at a time (Box 1). However, features such as chromatin accessibility (Fig. 1A), DNA methylation (Fig. 1B), compartments (Fig. 1C), CTCF loops, E–P, and other...
    OPEN ACCESS ARTICLE
  9. .... Furthermore, we used dC9Sun-D3A to demonstrate the binding sensitivity to DNA methylation for CTCF and NRF1 in situ. Overall, this modular dC9Sun-D3A system enables precise DNA methylation deposition with the lowest off-target DNA methylation levels reported to date, allowing accurate functional determination...
  10. ...influence nucleosome stability in a direct or indirect manner. This is consistent with reports showing (1) that nucleosomes found at hydroxymethylated CTCF binding sites are more sensitive to MNase digestion (Teif et al. 2014), and (2) that nucleosomes formed in vitro on a hydroxymethylated DNA template...
For checked items

Preprint Server