Searching journal content for articles similar to Sammons et al. 25 (2): 179.

Displaying results 1-9 of 9
For checked items
  1. ...the gene regulatory network of the cancer .One of the most important and well-studied guardians of genomic integrity, TP53 (protein product of TP53, also known as p53), leverages regulatory opportunities provided by TEs for its function. One group of TE families, human endogenous retroviruses (ERVs...
  2. ...events lead to chromatin opening and potential enhancer activation, suggesting TP53 pioneer-factor activity (Younger and Rinn 2017). For the majority of these binding events, though, TP53 is not required for chromatin accessibility (Karsli Uzunbas et al. 2019). TP63, on the other hand, plays an extensive...
  3. ...RE, Appella E, Hager GL, Nagaich AK. 2010. p53 binding to nucleosomal DNA depends on the rotational positioning of DNA response element. J Biol Chem 285: 1321–1332. doi:10.1074/jbc.M109.081182 ↵Sammons MA, Zhu J, Drake AM, Berger SL. 2015. TP53 engagement with the occurs in distinct local chromatin...
  4. ....aerts@med.kuleuven.be Abstract Transcription factors regulate their target genes by binding to regulatory regions in the genome. Although the binding preferences of TP53 are known, it remains unclear what distinguishes functional enhancers from nonfunctional binding. In addition, the genome is scattered with recognition...
  5. ...novo sites), showing context-dependent pioneer activity of this receptor (John et al. 2011; Johnson et al. 2018). To assess the chromatin environment of GRtetra binding sites, we measured (1) chromatin accessibility by the assay for transposase-accessible chromatin (ATAC)-seq and (2) the binding...
  6. ...development and progression. ESR1 genomic action is thought to operate under tight epigenetic control, with its chromatin binding and subsequent transcriptional output heavily reliant on the pioneer transcription factor FOXA1, which renders chromatin accessible for ESR1 binding. However, the exact...
  7. ...type, as well as understanding how the specificity of such a network is encoded in the DNA sequence of genomic enhancers. Profiling accessible chromatin via DNase I hypersensitive sequencing (DNase-seq) or via the assay for transposase-accessible chromatin using sequencing (ATAC-seq) represents...
  8. ..., the TP53 motif showed evidence of reduced footprinting depth and local chromatin accessibility (Supplemental Fig. S2). Given the enrichment of these TF motifs, we next determined whether any of the transcription factors which recognize these motifs are up-regulated in EAC. Again, we used RNA-seq data...
  9. ...correspond to overlapping motifs. Predicted and known dimers are compact, i.e., tightly spaced. Rigid and compact transcription factor dimers Genome Research 1313 www..org limited ability of chromatin openness to confer binding specificity upon pioneer TFs. Our results suggest that multiple homodimeric...
For checked items

Preprint Server