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  1. ...et al. 2014). Nucleosome positioning is highly dynamic, and its regulation is crucial to control chromatin accessibility, recruitment of chromatin modifiers, and transcription factors (Jiang and Pugh 2009; Prendergast and Semple 2011; Bartholomew 2014; Kornberg and Lorch 2020). In most s, genes...
  2. ...results are consistent with a model in which nucleosome fragility is encoded at the promoters of OPN-type genes, potentiating the high transcriptional plasticity observed at these sites. The presence of these promoter structures in yeast, human, and now C. elegans suggests a well-conserved strategy...
  3. ...or intragenic regions. These consensus clusters were generally of lower abundance, which is consistent with previous studies based on other techniques (Miura et al. 2006; Arribere and Gilbert 2013; Malabat et al. 2015). Given the pervasive nature of transcription in eukaryotes, they could be cryptic promoters...
  4. ...to form chromatin. Transcriptionally active euchromatin or repressive heterochromatin is regulated in part by the addition or removal of histone post-translational modifications (PTMs) by “writer” and “eraser” enzymes, respectively. Nucleosomal PTMs are recognized by a variety of “reader” proteins...
  5. ...highly transcribed genes results from multiple rounds of transcription, in which each round of transcription mediates a fixed amount of H3K36 methylation per nucleosome across the population of cells. Additionally, the linear rate of H3K36me3 gain across protein-coding genes also suggests that Set2...
  6. ...RNAmediated histonemodifications (Allo et al. 2009) and the SWI/SNF nucleosome remodelling complex (Batsche et al. 2006) affect splicing in such a manner. It is, therefore, conceivable that differences in intragenic CGI methylation might alter transcript processing in specific cell types. Further studies are now required...
  7. ...modifications and variant turnover; more importantly, nucleosome physical organization directly regulates the accessibility of DNA to binding proteins such as transcription factors (He et al. 2010). Micrococcal nuclease (MNase) preferably digests chromatin at DNA sites that are not occupied by nucleosomes while...
  8. ...by Illumina sequencing of mononucleosomal DNA isolated from mid-log cultures. For each species’ chromatin map, we determined the normalized nucleosome occupancy per base pair, correcting for differences in sequencing depth and MNase digestion level (see Methods). In order to investigate the sequence...
  9. ...forms a barrier against which nucleosomes are packed, resulting in uniform positioning, which decays at farther distances from the barrier. We present evidence for a novel 3′ NFR that is present at >95% of all genes. 3′ NFRs may be important for transcription termination and anti-sense initiation. We...
  10. ...and nucleosome occupancy levels relative to nonoverlapping regions of the same genes. Nucleosome occupancy was highly correlated with Pol II abundance across overlapping regions and with concomitant increases in local alternative exon usage. These results are consistent with an antisense transcription...
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