Searching journal content for articles similar to Festuccia et al. 29 (2): 250.

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  1. ...RNA 3′ ends and maps transcriptionally engaged Pol II. G4 signals overlapped with the TSSs and Pol II pausing sites at promoter regions (Fig. 1I,J), indicating that G4s may participate in the early stages of transcription.Because G4-CUT&Tag could detect the G4 signals at enhancers (Fig. 1E), we...
  2. ...of meiotic folding are linked to recombination activity. We apply an integrative bioinformatics approach to analyze how three-dimensional (3D) chromosomal organization during meiosis relates to rates of double-strand-break (DSB) and crossover (CO) formation at PRDM9 binding peaks. We show that active...
  3. ...-strandedness, which is most pronounced at transcript end sites, is dependent on high AT content and symmetrically positioned nucleosomes. We propose that sharp transitions in sequence composition at functional genomic elements constitute a common regulatory code and that DNA structure and propagation of torsional...
  4. ...contribute to the observed loss of TADs and CTCF loops during mitosis and reveals that CTCF sites, key architectural cis-elements, display cell cycle stage–dependent dynamics in factor binding and nucleosome positioning.Several studies have observed a key role of CCCTC-binding factor (CTCF) in organizing...
  5. ...understand the role of mitotic histone modifications and nucleosome de-positioning, we investigated the global dynamics and genomic organization of histone modifications in mitosis and in interphase. Using HeLa-S3 cells as a model system, our study incorporated a synchronization approach that enables...
  6. ...with independent observations in a mouse blood progenitor cell line, in which the retained CTCF binding has been implicated in faster transcription reactivation, when involving promoters, and more generally in fast restoration of 3D contacts after mitosis (Zhang et al. 2019). Together, these reports suggest...
  7. ...1 in Saccharomyces cerevisiae (Gkikopoulos et al. 2011), results in gross -wide alteration of their nucleosomal patterns. Transcription factors contribute to chromatin organization through the recruitment of remodelers to promoters (Yudkovsky et al. 1999; Korber et al. 2004) and also through...
  8. ...) leads to rapid loss of transcription in yeast. This has, for example, enabled the determination of mRNA half-lives and establishing the role of Pol II activity in nucleosome positioning (Adams and Gross 1991; Grigull et al. 2004; Sun et al. 2013; Hsieh et al. 2015; Vasseur et al. 2016; Lauinger et al...
  9. ...Mitosis entails global alterations to chromosome structure and nuclear architecture, concomitant with transient silencing of transcription. How cells transmit transcriptional states through mitosis remains incompletely understood. While many nuclear factors dissociate from mitotic chromosomes...
  10. ...they communicate.Enhancers: functional elements characterized by a stereotyped chromatin architectureEnhancers are one variety of cis-regulatory element encoded in Metazoan s. They are characterized by a stereotyped pattern of transcription factor binding, transcription initiation, and chromatin organization (Fig...
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