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  1. ...of imprinted genes H13/Nap1l5 (Wood et al. 2008; Cowley et al. 2012). No studies have 287 investigated DNA modifications regulating cell-type specific IPA site usage in its endogenous 288 state. We therefore examined how endogenous DNA methylation state impacts IPA site selection 289 across immune cells...
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  2. ...not only for clinical management but also for monitoring tumor risk associated with some imprinting disorders.View larger version: In this window In a new window Figure 2. Diagnostic applications of haplotype-aware methylation analysis. Haplotype assignment after phasing significantly enhances...
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  3. ...establish a mechanistic link between SETD3-mediated ACTB methylation and SMARCA4-dependent chromatin regulation, it is plausible that SETD3 expression levels or ACTBmethylation status could influence tumor growth, invasiveness, or therapy responsiveness in colorectal cancer. Although we did not address...
  4. ...methylation of the supernumerary X Chromosome could play a marginal role in regulating the global transcriptome at the pluripotent stage.MethodsFibroblast reprogramming into iPSCsFibroblasts were obtained from the NIGMS Human Genetic Cell Repository at the Coriell Institute for Medical Research (Supplemental...
  5. .... 1987; Li et al. 2018), genomic imprinting (Li et al. 1993; Suzuki et al. 2007; Court et al. 2014), X-Chromosome inactivation (Sharp et al. 2011), and transcription repression (Moore et al. 2013). As a result, variations in DNA methylation have been associated with human diseases such as aging...
  6. ...in conditions where H3K9 methylation is low, such as in female primordial germ cells (Huang et al. 2021) or H3K9 methyltransferase-deficient cells (Fukuda et al. 2023). These findings may suggest that SUV39H1/2 and H3K27 methyltransferases also inhibit CTCF binding at transposons. To explore this, we examined...
  7. ...and stochastic accumulation of epigenetic changes, such as DNA methylation variability, with advancing age. Although increasingly recognized for its potential role in aging biology, its extent, biological significance, and population specificity remain insufficiently characterized. Here, we present the first...
  8. ...&Tag to map a variety of histone PTMs, including the euchromatin marks H3K9ac, H3K14ac, and H3K27ac, facultative heterochromatin mark H3K27me3, and constitutive heterochromatin marks H3K9me2 and H3K9me3. We also used ChIP-seq to profile the H3K9 methylation binding protein CBX1.Scaling all LADs to a uniform...
  9. ...and exists until zygotic activation (ZGA) (Dahl et al. 2016; Zhang et al. 2016). Additionally, the repressive mark H3K27me3 transmitted from oocytes regulates DNA methylation-independent imprinting in embryos (Inoue et al. 2017).Epigenetic reprogramming of nonmammalian vertebrates is largely distinct from...
  10. ..., late, and very late during reprogramming. Early genes are activated before the onset of late pluripotency genes activation. Early genes are located genomically closer to genes that escape XCI, unlike genes reactivating late. Early genes also show increased pluripotency transcription factor (TF) binding...
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