Searching journal content for articles similar to van Heeringen et al. 24 (3): 401.

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  1. ...active ICRs or together with H3K27me3 at transcriptionally inactive ones (Sanz et al. 2008; Henckel et al. 2009; Maupetit-Méhouas et al. 2016).When the maintenance of gamete-derived methylation asymmetry is temporary: the transient gDMRsAlong with ubiquitous gDMRs/ICRs, other regions that exhibit...
  2. ...reproductive technology, and the Human Sperm Bank and the Helsinki Declaration. Our research followed the guiding principles of the human embryonic stem cell ethics issued by the MOST and MOH of China and was regularly reviewed by the medical ethics committee of The First Affiliated Hospital of Zhengzhou...
  3. ...levels reflect a graded concentration originating from strong sites. This suggests that PRC2 and H3K27 methylation spread along a gradient unique to XCI. We propose that XCI is governed by a hierarchy of defined Polycomb stations that spread H3K27 methylation in cis . Footnotes ↵ 4...
  4. ...and developmental promoters and enhancers in zebrafish sperm lack DNA methylation and contain H3K4me3, H2A.Z/FV, H3K27ac, and (at developmental genes) H3K27me3 (Wu et al. 2011; Murphy et al. 2018; Zhang et al. 2018). Additionally, histone chromatin marks and DNA methylation are reprogrammed during pre-ZGA zebrafish...
  5. ...3 signal are weak domains in young cells, and genes that show a loss of H3K27me3 signal are strong domains in young cells. (G,H) Genome browser tracks of genes that are differentially methylated in enterocytes, showing a loss (G) and gain (H) in H3K27me3 signal with age.To map age-dependent changes...
  6. ...) DNase I H3K4me1 H3K4me3 H3K27me3 SINEs LINEs rep timing (late > early) Hi-C PC1 (B > A) H3K9me2 CpG methylation (%) H3K9me3 H4K20me3 PAD nPAD 100 Figure 2. Pericentromeric association segregates repressed chromatin from active chromatin. (A) Sat4C profile of Chromosome 17 with designated PADs (red...
  7. ...(Supplemental Fig. S4D). Thus, although H3K27me3 may restrict the activation of silenced genes on the Xi, it is not sufficient to explain the delay in reactivation of late genes. Additionally, on the Xi, H3K36me3 and H3K4me3 were depleted on all classes of genes. DNA methylation (Milagre et al. 2017) was also...
  8. ...is independent of compartment-driven repression (Fig. 3F). However, FAC domains are almost completely absent from the annotation of the embryonic stem cell line H1-hESC, consistent with previous observations that H3K27me3 does not form domains in embryonic stem cells but rather occurs only at so-called poised...
  9. ...factor (Cadoret et al. 2008), but this enrichment was minimal. Histone modifications such as methylation of H3K4 or acetylation of H3K9 and H3K27 exhibited minor but statistically significant enrichment in replication initiation. CpG methylation, replication, and gene expression To further explore...
  10. ..., such as H3K4 mono- and trimethylation and H3K36 trimethylation, with little or no signal for the repressive modifications H3K27 trimethylation or H3K9 trimethylation (Fig. 4). This analysis was conducted for TAL1 OSs in G1E cells, ER4 cells, Ter119+ erythroblasts, and megakaryocytes, for which the histone...
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