Searching journal content for articles similar to Hashimoto et al. 26 (10): 1430.

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  1. ...to access gene promoters. Many key genes were accessible at the two-cell stage or earlier. For example, Arntl is associated with the rhythmic opening of chromatin at promoters and regulates DNA accessibility for other TFs (Menet et al. 2014); Nfya forms a histone-like structure binding to DNA and promotes...
  2. ...-specific functions. The transcriptional regulatory logic defined in this study is summarized. The size of the TR and TRM above the chromatin and of the boxes below the chromatin correlates with the occurrence of binding and DNA motif at the distinct classes of CRM, respectively. Refer to Discussion for details...
  3. ...investigates the mechanisms by which mammalian cells coordinate DNA replication with transcription and chromatin assembly. In yeast, DNA replication initiates within nucleosome-free regions, but studies in mammalian cells have not revealed a similar relationship. Here, we have used genome-wide massively...
  4. ...: antluiz@bu.edu , jgalag@bu.edu Abstract The comprehension of protein and DNA binding in vivo is essential to understand gene regulation. Chromatin immunoprecipitation followed by sequencing (ChIP-seq) provides a global map of the regulatory binding network. Most ChIP-seq analysis tools focus...
  5. ...of a specific factor to DNA. However, there are several different mechanisms by which a factor can be recruited to the DNA and be identified in a ChIP–chip assay ( Kato et al. 2004 ). Three types of interactions between a transcription factor and its binding site on DNA include: (1) direct binding...
  6. .... , Davidson, E.H. ( 2005 ) Logic functions of the genomic cis -regulatory code . Proc. Natl. Acad. Sci. 102 : 4954 – 4959 . ↵ Johnson, D.S. , Mortazavi, A. , Myers, R.M. , Wold, B. ( 2007 ) Genome-wide mapping of in vivo protein-DNA interactions . Science 316 : 1497 – 1502 . ↵ Khambata-Ford, S. , Liu, Y...
  7. ...(GR). Previous models have proposed that DNA binding motifs and sites of chromatin accessibility predetermine GR binding and activity. However, there are vast excesses of both features relative to the number of GR binding sites. Thus, these features alone are unlikely to account for the specificity...
  8. ...in chromatin marks and our ATAC-seq peaks, we used stratified LDscore regression (Supplemental Materials; Finucane et al. 2015).Neural network models for chromatin accessibilityTo predict the chromatin activity of a genomic locus across three cell types (iPSC, LCL, and iPSC-CM) from the DNA sequence, we used...
  9. ...by coordinated actions of genomic regions that control the activity of multiple sequence-specific DNA binding proteins. Using -wide approaches to interrogate chromatin function, we here identify the elements that regulate tissue recovery in Drosophila imaginal discs, which show a high regenerative capacity after...
  10. ...curves in Fig. 2E). Since primary DNA sequence can influence nucleosome placement (Tillo and Hughes 2009), we hypothesized that theGC-rich peakwithin CBRs might represent a nucleosome positioning signal. We therefore determined the predicted nucleosome occupancy over all replicated CBRs using...
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