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Sergei Denissov

Researcher at Radboud University Nijmegen

Publications -  9
Citations -  2983

Sergei Denissov is an academic researcher from Radboud University Nijmegen. The author has contributed to research in topics: Chromatin & Gene. The author has an hindex of 8, co-authored 9 publications receiving 2756 citations.

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Selective Anchoring of TFIID to Nucleosomes by Trimethylation of Histone H3 Lysine 4

TL;DR: Experiments reveal crosstalk between histone modifications and the transcription factor TFIID, which has important implications for regulation of RNA polymerase II-mediated transcription in higher eukaryotes.
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Quantitative Interaction Proteomics and Genome-wide Profiling of Epigenetic Histone Marks and Their Readers

TL;DR: The authors' data reveal a highly adapted interplay between chromatin marks and their associated protein complexes, and reading specific trimethyl-lysine sites by specialized complexes appears to be a widespread mechanism to mediate gene expression.
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Genome-wide profiling of PPARgamma:RXR and RNA polymerase II occupancy reveals temporal activation of distinct metabolic pathways and changes in RXR dimer composition during adipogenesis.

TL;DR: This study uses chromatin immunoprecipitation combined with deep sequencing to generate genome-wide maps of PPARgamma and retinoid X receptor (RXR)-binding sites, and RNA polymerase II (RNAPII) occupancy at very high resolution throughout adipocyte differentiation of 3T3-L1 cells, and indicates that a hitherto unrecognized high number of adipocyte genes of distinctly regulated pathways are directly activated by PPARGamma:RxR.
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Mll2 is required for h3k4 trimethylation on bivalent promoters in embryonic stem cells, whereas mll1 is redundant

TL;DR: It is shown that Mll2, one of the six Set1/Trithorax-type H3K4 methyltransferases in mammals, is required for trimethylation of bivalent promoters in mouse embryonic stem cells and proposed that MLL2 is the pioneer trimethyltransferase for promoter definition in the naïve epigenome and that Polycomb group action on bivalent promoter blocks the premature establishment of active, Set1C-bound, promoters.
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Genome-wide pattern of TCF7L2/TCF4 chromatin occupancy in colorectal cancer cells.

TL;DR: Through a DNA array-based genome-wide analysis of TCF4 chromatin occupancy, 6,868 high-confidenceTCF4-binding sites are identified in the LS174T colorectal cancer cell line and significantly correlate with Wnt-responsive gene expression profiles derived from primary human adenomas.