Searching journal content for articles similar to Armstrong et al. 28 (11): 1688.

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  1. ...Cell-type- and chromosome-specific chromatin landscapes and DNA replication programs of Drosophila testis tumor stem cell–like cells Jennifer A. Urban1, Daniel Ringwalt1, John M. Urban2,3, Wingel Xue1,5, Ryan Gleason1, Keji Zhao4 and Xin Chen1,2 1Department of Biology, The Johns Hopkins University...
  2. ..., the establishment of centromeric chromatin and its subsequent propagation through many generations depends on a variety of factors that are often species specific. These include centromere-specific DNA sequence elements, replication timing, and transcriptional status of centromere DNA, as well as the influence...
  3. ...in instructing cell type–specific gene expression patterns (Niwa 2018; Stadhouders et al. 2019). In addition, chromatin undergoes covalent histone modifications and DNA methylation, which further recruit chromatin modifying factors to impart precise catalysis of transcription and enhance or repress gene...
  4. ..., indicating that the chromatin fiber is more open and less compact than in the domains of low expression. This is in line with similar observations based on the expression of endogenous genes in Drosophila embryos (Sexton et al. 2012). Since both chromatin composition and chromosomal conformation could...
  5. ...with spatial organization of chromatin in the nucleus; early and late RDs reside in distinct nuclear compartments (Nakamura et al. 1986; Nakayasu 1989; O'Keefe et al. 1992), and cytogenetic visualization of pulse-labeled DNA synthesis reveals distinct punctate replication foci whose structure remains stable...
  6. ...activity. Although PcG recruitment mechanisms differ between mammals and Drosophila, it has previously been suggested that the process of transcription through Polycomb response elements (PREs) removes PcG complexes from chromatin (Schmitt et al. 2005). At the vestigial PRE, it was reported...
  7. ...reported that 42% of TADs are shared between Kc167 cells and 16-h embryos. Active chromatin and transcription but not architectural proteins dCTCF and Su(Hw) are typical for TAD boundaries and inter-TAD regions Previous studies revealed that TAD boundaries in 16-h Drosophila embryos (Sexton et al. 2012...
  8. ...control of -wide nucleosome positioning and developmental gene expression and its requirement for a ChromodomainHelicase-DNA binding (CHD) Type III chromatin remodeling protein. Nucleosome positions can be described by several physical parameters: occupancy, the relative enrichment or depletion...
  9. ...(Recombination In K) heterochromatin, which lose H3K9me2 and undergo mitotic and meiotic recombination (Ellermeier et al. 2010; Zaratiegui et al. 2011). Mouse dnmt3l mutants also have altered DNA methylation and chromatin signatures and increased DSB initiation within retrotransposons, which is associated...
  10. ...that are mostly inactiveor expressed at a low level (Guelenet al. 2008). Lamins can also interact with shorter chromatin domains in HeLa cells (Euskirchen et al. 2011), and inmice and yeast, short DNA sequences canmediate localization of loci to the nuclear periphery (Ahmed et al. 2010; Brickner et al. 2012...
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