Abstract
Nucleosomes are the basic packaging units of chromatin, modulating accessibility of regulatory proteins to DNA and thus influencing eukaryotic gene regulation. Elaborate chromatin remodelling mechanisms have evolved that govern nucleosome organization at promoters, regulatory elements, and other functional regions in the genome. Analyses of chromatin landscape have uncovered a variety of mechanisms, including DNA sequence preferences, that can influence nucleosome positions. To identify major determinants of nucleosome organization in the human genome, we used deep sequencing to map nucleosome positions in three primary human cell types and in vitro. A majority of the genome showed substantial flexibility of nucleosome positions, whereas a small fraction showed reproducibly positioned nucleosomes. Certain sites that position in vitro can anchor the formation of nucleosomal arrays that have cell type-specific spacing in vivo. Our results unveil an interplay of sequence-based nucleosome preferences and non-nucleosomal factors in determining nucleosome organization within mammalian cells.
MeSH Terms
CD4-Positive T-Lymphocytes/metabolism
CD8-Positive T-Lymphocytes/metabolism
Cells, Cultured
Chromatin Assembly and Disassembly/physiology
Gene Expression Regulation
Genome, Human/genetics
Granulocytes/metabolism
High-Throughput Nucleotide Sequencing
Humans
Micrococcal Nuclease/metabolism
Nucleosomes/chemistry,genetics,metabolism
Organ Specificity
Transcription, Genetic
Chemicals
Nucleosomes
Micrococcal Nuclease
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Valouev Anton
Department of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, California 94305, USA.
Johnson Steven M
Boyd Scott D
Smith Cheryl L
Fire Andrew Z
Sidow Arend
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