Searching journal content for articles similar to Takeshima et al. 19 (11): 1974.

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  1. ...GC skew defines distinct RNA polymerase pause sites in CpG island promoters Wendy A. Kellner 1 , 3 , 4 , Joshua S.K. Bell 1 , 3 and Paula M. Vertino 1 , 2 1Department of Radiation Oncology, Emory University School of Medicine, Atlanta...
  2. ...islands scores as the observed frequency of CpG dinucleotides compared to their expected frequency given the G + C content of a region. We found that these scores, when calculated for the 350 bases upstream of each gene, are significantly correlated with active tRNA genes (Spearman's rank correlation, P...
  3. ...), in regulation of non-L1 TE life cycle (Lexa et al. 2014), in distal interactions between promoters and enhancers (Hou et al. 2019; Williams et al. 2020), and in protecting CpG islands from methylation (Halder et al. 2010; Mao et al. 2018; Jara-Espejo and Peres Line 2020)—remain hypothetical. If G4s...
  4. ...RNA-polymerase-II-transcribed genes. Cell 151: 835–846. doi:10.1016/j.cell.2012.09.041 ↵Arab K, Karaulanov E, Musheev M, Trnka P, Schäfer A, Grummt I, Niehrs C. 2019. GADD45A binds R-loops and recruits TET1 to CpG island promoters. Nat Genet 51: 217–223. doi:10.1038/s41588-018-0306-6 ↵Ariel F, Lucero...
  5. ...frequently used as TSSs. Despite the absence of CpG islands, Ciona TATA-less promoters showed low expression specificity like CpG-associated human TATA-less promoters. By using TSS-seq, we also predicted trans -spliced gene TSSs and found that their downstream regions had higher G+T content than those...
  6. ..., Yamashita S, Shimazu T, Niwa T, Ushijima T. 2009. The presence of RNA polymerase II, active or stalled, predicts epigenetic fate of promoter CpG islands. Genome Res 19: 1974–1982. Widschwendter M, Fiegl H, Egle D, Mueller-Holzner E, Spizzo G, Marth C, Weisenberger DJ, Campan M, Young J, Jacobs I, et al...
  7. ...targets (Fig. 4C), suggesting that CpG density alone can be an excellent predictor of H3K4me3 levels. A corollary to this conclusion would be that CpG density, together with H3K27me3 levels, can predict bivalent chromatin (Fig. 4B,D). Indeed, a machine learning approach based on multinomial logistic...
  8. ...results, DNA methylation is a strong marker of an exon when these;140,000 human exons are considered (Supplemental Fig. S9A). The methylated CpGs were constructed for alternative and constitutive exons that are expressed sequence tag (EST)-based since the RNA-seq data provided reliable inclusion level...
  9. ...from wild-type HCT116 cells (Birney et al. 2007) showed that CpG sites that became hypermethylated in the HCT116 IDH1R132H/WT cells are depleted of RNA polymerase II (Pol II) binding and histone H3 lysine 4 trimethylation (H3K4me3) relative to sites that become hypomethylated or remain unchanged...
  10. ...1992). Conversely, recent analyses revealed the presence of GC-rich elements in eukaryotic origins, such as CpG islands (CGI) (Delgado et al. 1998; Prioleau 2009; Cayrou et al. 2011; Costas et al. 2011) and an Origin G-rich Repeated Element (OGRE) that can form G4 (Cayrou et al. 2011, 2012a). G4were...
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