Searching journal content for articles similar to Brönner et al. 27 (7): 1174.

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  1. ...is mediated using several factors including chromatin modifiers. However, factors that avoid the intrusion of silencing signals into protein-coding genes are poorly understood. Here we show that a plant specific paralog of RNA polymerase (Pol) II, named Pol IV, is involved in avoidance of facultative...
  2. ...strategies likely compensate for the absence of classical methylation marks. For instance, short double-stranded RNAs induce RNA silencing through distinct mechanisms (Meister and Tuschl 2004). Telomere-associated factors such as DNA helicase Dna2p, telomerase Dot1, and ubiquitinase Dot4p may also contribute...
  3. ...and suggest the possibility of transcription from heterochromatic regions, as well as a role for post-transcriptional regulation.Chromatin state of gene targets of small RNA pathwaysThe disconnect between chromatin state and transcript abundance for many of the pregametic, spermatogenesis, and oogenesis...
  4. ...RNA bait library specifically targeting 4650 regions that accumulate H3K27me3 and included a subset of loci differentially methylated between shoots and roots (Supplemental Fig. S9). The comparison of both Hi-C and C-Hi-C matrixes allowed us to identify a significant enrichment of chromatin contacts...
  5. ...in both the mRNA levels and protein levels and do not affect the cell cycle (the efficiency of knockdown achieved here is similar to the ones reported by other studies in Drosophila cells [Supplemental Fig. S1; Schwartz et al. 2012; Ramírez et al. 2018; Zenk et al. 2021]). High-resolution contact maps...
  6. ...sequencing (WGBS), and gene expression by RNA-seq. The major limiting factor for such multi-omics characterization was the high amount of starting material needed from each individual patient. To overcome this limitation, we also analyzed the chromatin regulatory landscape of an extended series of MM...
  7. ...over long distances. In line with the globally dispersed distribution of RNA polymerase II in A. thaliana nuclear space, actively transcribed genes do not show a strong tendency to associate with each other. In general, there are often contacts between 5′ and 3′ ends of genes, forming local chromatin...
  8. ...IP-seq enrichment profiles showing ChIP/input ratios (scale −0.4 to +0.4 centered on 0), LADs mapped with EDD, and RNA-seq gene expression profiles (scale 0–1000 FPKM). (B) Number of LADs identified at each differentiation stage. (C) Median LAD lengths at all differentiation time points confounded (All) and at each...
  9. ...to direct these heterochromatic structural states, often overlapping with defense mechanisms against foreign nucleic acids. A prominent example is RNA interference (RNAi) (Fire et al. 1998), which can not only degrade RNA, but can also induce transcriptional gene silencing. In fact, short interfering RNA...
  10. ...with accumulation of RNA polymerase II (Pol II), suggesting that H2Bub1 levels within gene bodies reflect changes in Pol II elongation rates that are probably associated with cotranscriptional splicing. In support of this notion, we find a significant correlation between H2Bub1 levels and experimentally measured...
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