Searching journal content for articles similar to Qiu et al. 26 (2): 211.

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  1. ...to explore interactions that involve more than one mutant. For example, SWI4 and SWI6 are key TFs enacting G1/S-specific transcription, and together they form a complex to bind to and regulate genes involved in DNA synthesis and repair (Sidorova and Breeden 1993). The individual deletions of SWI4 (swi4Δ...
  2. ...-in orientations in vitro (Song et al. 2011, 2014). However, to what extent nucleosomes modulate CPD deamination in other sequence contexts and across the of intact cells remains unclear.Genome-wide sequencing methods have emerged as powerful tools to understand how different genomic and chromatin contexts impact...
  3. .... Genome-wide mapping of nucleosome positioning and DNA methylation within individual DNA molecules. Genome Res 22: 2497–2506. doi:10.1101/gr.143008.112 ↵Kouzine F, Gupta A, Baranello L, Wojtowicz D, Ben-Aissa K, Liu J, Przytycka TM, Levens D. 2013. Transcription-dependent dynamic supercoiling is a short...
  4. ...of DNA to transcription factors. It is catalyzed by ATP-dependent chromatin remodeling complexes such as the SWI/SNF and NuRD remodelers, both of which bind to numerous common target gene promoters as revealed by the chromatin occupancy profiles of their ATPase subunits (BRG1–SWI/SNF and CHD4–Nu...
  5. ....” The presence of KDM1A/HDACs is required to antagonize the activities of the methyltransferases and acetyltransferases (HATs) and maintain an optimal histone modification landscape. The equilibrium of these counteractions likely defines the activity of an enhancer. When an enhancer is decommissioned upon...
  6. ..., Bruhm DC, Jensen SØ, Medina JE, Hruban C, White JR, et al. 2019. Genome-wide cell-free DNA fragmentation in patients with cancer. Nature 570: 385–389. doi:10.1038/s41586-019-1272-6 ↵De Coster W, Weissensteiner MH, Sedlazeck FJ. 2021. Towards population-scale long-read sequencing. Nat Rev Genet 22: 572...
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  7. ...particle.Because the SWI/SNF ACR plays a role in altering nucleosome positions and evicting nucleosomes, we used the CPD-seq data to test whether the SWI/SNF complex is specifically required for repair in nucleosomes. High-resolution analysis of repair in WT cells near the transcription start sites (TSSs...
  8. ...the nucleosome maps in NBCs with the binding sites of BRG1, the ATPase of the SWI/SNF chromatin remodeling complex (Abraham et al. 2013). Nucleosomes that did not change locations between conditions were depleted of BRG1 in NBCs, whereas shifted nucleosomes (>20% change of their start/end coordinates) were...
  9. ...undergo obligatory remodeling to evict existing nucleosomes and allow break-recognition factors to access and signal for repair complexes to assemble and mend the broken DNA. Although repair of the broken DNA ensures that integrity is preserved, chromatin architecture must also be restored to preserve...
  10. ...of H3K9me3 and H3K27me3 in the nondiapause (C), prediapause (D), and diapause (E) stages. (F–H) Venn diagram shows the number of genes with H3K9me3 peaks, H3K27me3 peaks, or both at the nondiapause (F), prediapause (G), and diapause (H) stages. (I–K) Genome-wide correlation plots showing correlation...
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