Searching journal content for articles similar to Squazzo et al. 16 (7): 890.

Displaying results 1-10 of 17
For checked items
  1. ...gene clusters. In contrast, -wide profiles of the Drosophila show that H3K27me3 covers large genomic domains containing silent genes that included genic and intergenic regions ( Schwartz et al. 2006 ; Beisel et al. 2007 ). Mammalian chromosomes are known to be longitudinally organized in a manner...
  2. ...binding events connect enhancers to their target genes by looping out the intervening DNA, thereby reducing the effective distance and increasing the probability of interactions between linearly distant genomic regulatory regions. We therefore searched for genes where this configuration has the potential...
  3. ...Figure 4. PR-DUB and PRC1/2 share a limited set of bivalent target genes. (A) Euler diagram showing the overlap between BAP1, SUZ12, and RING1B binding regions in wild-type proliferating mESCs. (B) Hidden Markov analysis for the 1457 BAP1-bound regions positions not associated with SUZ12 or RING1B in m...
  4. ...IP-seq signals for 5hmC, H3K27me3, SUZ12, and H3K4me3 around ±7 kb from the center of Class 2 and Class 3a IS. Cayrou et al. 1878 Genome Research www..org Figure 5. Sequencemotifs at origins. (A,B) Distribution of OGRE sites around IS inmouse (A) and human (B) ES cells. PWM-based scanning of 1-kb regions on both...
  5. ...) demonstrated that the amino terminus of histone H3 is recognized by the Nurf55-Suz12 submodule of PRC2 and that this binding is blocked by marks of active chromatin, namely, K4me3 and K36me2/3. Although the mechanism of such “crosstalk” is sometimes reasonably obvious, more often it is not, as illustrated...
  6. ...and differentiated cells. (A) Genomic distribution of hypomethylated regions (HMR) in H1 ESCs and B cells. Colors in each bar indicate whether an HMR is shared between the two cell types, specific to one, or shared but expanding, i.e., significantly larger in one cell type than in the other. (B) Overlap between i...
  7. ...binds to silenced regions of the in a cell-type-specific manner . Genome Res. 16 : 890 – 900 . ↵ Tolhuis, B. , Palstra, R.J. , Splinter, E. , Grosveld, F. , de Laat, W. ( 2002 ) Looping and interaction between hypersensitive sites in the active beta-globin locus . Mol. Cell 10 : 1453 – 1465 . ↵ Wurtele...
  8. ...course of differentiation. Antibodies were used against (1) H3K27me3, a repressive mark; (2) SUZ12, a member of the PRC2 complex and a mark of chromatin silencing; (3) H3K4me3, a mark for active chromatin state; and (4) Pol II, a mark of active transcription.In accord with published studies (Boyer et al...
  9. ...important developmental regulators inmouse embryonic stem (ES) cells (Boyer et al. 2006) and are in part cell-type specific (Bracken et al. 2006; Mikkelsen et al. 2007; Mohn et al. 2008). Although DNA binding 6These authors contributed equally to this work. 7Corresponding authors E-mail dirk@fmi.ch E...
  10. ...is organized as a highly dynamic structure in a cell-type–specific manner and is tightly coupled with gene transcription (Cavalli and Misteli 2013; Sawyer and Dundr 2017; Wang et al. 2017; Watson and Tsai 2017). Chromatin domains can be subdivided into transcriptionally active and inactive territories based...
For checked items

Preprint Server