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High-throughput Mapping of the Chromatin Structure of Human Promoters

ABSTRACT: Understanding how chromatin structure affects cellular functions such as transcription and replication in human cells has been limited by a lack of sufficient nucleosome positioning data. We describe a high-resolution microarray approach combined with a novel analysis algorithm to examine the translational nucleosome positions in 3,692 promoters within seven human cell lines. Unlike unexpressed genes without transcription pre-initiation complexes at their promoters, expressed genes or genes containing pre-initiation complexes exhibit characteristic nucleosome-free regions at their transcription start sites. Coupling these data to ChIP-chip analyses reveals that the melanocyte master transcriptional regulator MITF binds predominantly to nucleosome-free regions, supporting the model that nucleosomes limit sequence accessibility. This study thus presents the first global view of human nucleosome positioning and provides a high-throughput tool for analyzing chromatin structure in development and disease. Keywords: Nucleosome positions, MNase digestion, cell type comparison

ORGANISM(S): Homo sapiens

PROVIDER: GSE6385 | GEO | 2007/01/15

SECONDARY ACCESSION(S): PRJNA99559

REPOSITORIES: GEO

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Project description:Abstract: In the yeast S. pombe, multiple chromatin-modifying enzymes are required for heterochromatin formation, yet how their actions alter chromatin structure to block access to DNAby the transcriptional machinery is unknown. We constructed high-resolution nucleosome occupancy maps of heterochromatic regions in wild-type strains and in mutants lacking the H3K9 methyltransferase Clr4 or one of the two activities of the silencing effector complex SHREC. Fourier analysis reveals that these enzymes do not increase the regularity of nucleosome spacing. Rather, their principal effect was to induce the elimination of nucleosome-free regions (NFRs). Both NFRs associated with transcription initiation sites as well as those not associated with promoters are affected. As in S. cerevisiae, repressed genes in euchromatin retain their NFRs. Thus, NFR elimination cannot be explained as a secondary consequence of repression. The maps also show that TFIIIC boundary elements have NFRs resistant to silencing, suggesting a potential role in preventing lateral spread of heterochromatin. NFR elimination offers a mechanism by which heterochromatin restricts access of the transcriptional machinery to DNA. Nucleosome positions in either heterochromatin or euchromatin were mapped in various mutants to determine whether chromatin structure is altered upon heterochromatic silencing. Eight strains were assayed for nucleosome positioning in heterochromatin while two strains were assayed for nucleosome positioning in euchromatin. Two biological replicates were assayed for each strain. No dye swaps were done. RNA transcripts were also mapped using the heterochromatin tiling arrays to determine where RNA transcripts accumulate in heterochromatin. Three strains were assayed for transcripts in heterochromatin by hybridizing cy5-labeled cDNA created from total RNA against cy3-labeled cDNA created from RNA synthesized from sonicated genomic DNA. Two biological replicates were assayed for each strain.

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High-throughput Mapping of the Chromatin Structure of Human Promoters

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