Searching journal content for articles similar to Mak et al. 19 (6): 1014.

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  1. ...analyzed histone modification dynamics during epigenetic reprogramming in Japanese killifish, medaka (Oryzias latipes) embryos. Our data revealed that H3K27ac, H3K27me3, and H3K9me3 escape complete reprogramming, whereas H3K4 methylation is completely erased during cleavage stage. Furthermore, we...
  2. ...and changing chromatin state. This state is determined, in part, by the dynamic binding of proteins to the DNA. These proteins—including histones, transcription factors (TFs), and polymerases—interact with one another, the , and other molecules to allow the chromatin to adopt one of exceedingly many possible...
  3. ...(two each of H2A, H2B, H3, and H4) around which ∼147 bp of DNA is wrapped. Nucleosomes are organized into chromatin fibers that provide the dynamic organizational platform underpinning eukaryotic gene expression regulation. Formation of transcriptionally active and silent chromatin states depends...
  4. ...retain essential functions, their chromatin organization may differ from canonical centromeres.Concerted local open chromatin and transcriptional dynamics contribute to genomic stabilization following centromere misdivisionTo investigate how gene expression and chromatin structure respond to centromere...
  5. ..., Szenker E, Garrett N, Almouzni G, Gurdon JB. 2012. HIRA dependent H3.3 deposition is required for transcriptional reprogramming following nuclear transfer to Xenopus oocytes. Epigenetics Chromatin 5: 17. KimM, Park YK, Kang TW, Lee SH, Rhee YH, Park JL, Kim HJ, Lee D, Kim SY, Kim YS. 2013. Dynamic changes...
  6. ...syndrome, highlighting the complex genetic heterogeneity of the disease (de Greef et al. 2011; Thijssen et al. 2015). In ICF1 patients, DNA hypomethylation is apparent at specific heterochromatic regions, including the pericentromeric and subtelomeric repeats (Jeanpierre et al. 1993; Yehezkel et al. 2008...
  7. ...transcriptional shift observed in RNA-seq under infection conditions.At first glance, the contact maps show a clustering of subtelomeric regions, but do not display a Rabl conformation, in which centromeres cluster to the spindle-pole body (Rabl 1885). However, the precise positions of centromeres are needed...
  8. ...that Fkh1 can reprogram origin firing in late G1. This result also demonstrates that Fkh1OE can stimulate additional origin firing independently of Fkh2. To scrutinize this activity of Fkh1 within heterochromatin, we more closely examined the activity of originswithin subtelomeric heterochromatin...
  9. ...involvement in speciation remains unclear. We show that subtelomeric regions—regions that have a species-specific organization, are more divergent in sequence, and are enriched in genes and recombination hotspots—are significantly enriched for species-specific histone modifications that decorate transcription...
  10. ...-GFP in 3D7 parasites, we found that sexual stage commitment is governed by transcriptional reprogramming and stabilization of a subset of essential gametocyte transcripts. We also measured mRNA dynamics in F12 gametocyte-deficient parasites and demonstrate that the transcriptional program required...
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