Searching journal content for articles similar to Hagey et al. 26 (7): 908.

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  1. ...and hypomethylated 4q-D4Z4 array causes an impairment of D4Z4 interactome, leading to a chromatin switch toward an active state (mainly enhancer and promoter regions), which in turn results in the transcriptional up-regulation of the atrophic genes.We propose that the genetic deletion of 4q-D4Z4 array in FSHD1...
  2. ...reported that 42% of TADs are shared between Kc167 cells and 16-h embryos. Active chromatin and transcription but not architectural proteins dCTCF and Su(Hw) are typical for TAD boundaries and inter-TAD regions Previous studies revealed that TAD boundaries in 16-h Drosophila embryos (Sexton et al. 2012...
  3. ...regulatory regions. Other studies have shown that demethylation at enhancers is associated with gene reactivation during differentiation (Mahé et al. 2017). However we do not know whether DNA methylation changes at enhacers is simply the readout of transcription factor availability or the mechanisms...
  4. ...tissues, for collared flycatcher, pied flycatcher, and their F1 hybrids.A characteristic signature of spermatogenesis is spurious transcription as a result of a permissive chromatin environment during this process (Soumillon et al. 2013). Thus, if spermatogenesis is interrupted at an early stage in the F1...
  5. ...Corresponding authors: saurabhagarwal23@gmail.com, biren@ucsd.edu, siwase@umich.eduAbstractTranscriptional enhancers enable exquisite spatiotemporal control of gene expression in metazoans. Enrichment of monomethylation of histone H3 lysine 4 (H3K4me1) is a major chromatin signature of transcriptional enhancers...
  6. ...of the VEGFA transcriptional program and angiogenesis. Collectively these results revealed that extracellular stimuli rapidly reconfigure the chromatin landscape to coordinately regulate biological responses.Divergent gene programs control distinct cell identities and biological functions. Environmental...
  7. ...). The model that has emerged from these findings posits that cell-specific pioneer factor binding creates a chromatin landscape that predetermines GR binding (John et al. 2011; Biddie and John 2014). It has also been reported that GR can act as a pioneer factor at a minority of binding sites, which have...
  8. ...endothelial cells. NF-κB, the transcription factor complex driving the response, interferes with the regulatory machinery by binding active enhancers already in interaction with gene promoters. Notably, >50% of these enhancers do not encode canonical NF-κB binding motifs. Using a combination of genomics...
  9. ...and signaling molecules that act in concert to provide this cell population with its defining features (Sauka-Spengler and Bronner-Fraser 2008b). In order to interrogate such a complex regulatory program, we and others have assembled a multistep neural crest GRN that integrates transcriptional inputs...
  10. ...where the same local region also harbored enhancer chromatin signatures. These enhancer-marked DMRs comprised 30% of the tissue-specific DMRs, >70% of the cell type-specific DMRs, and >40% of the individual-specific DMR landscape. Results Summary of the M&M algorithm Differentially methylated regions...
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