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PLoS Genet


Title:Cell cycle-specified fluctuation of nucleosome occupancy at gene promoters
Author(s):Hogan GJ; Lee CK; Lieb JD;
Address:"Department of Biology and Carolina Center for Genome Sciences, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America"
Journal Title:PLoS Genet
Year:2006
Volume:20060808
Issue:9
Page Number:e158 -
DOI: 10.1371/journal.pgen.0020158
ISSN/ISBN:1553-7404 (Electronic) 1553-7390 (Print) 1553-7390 (Linking)
Abstract:"The packaging of DNA into nucleosomes influences the accessibility of underlying regulatory information. Nucleosome occupancy and positioning are best characterized in the budding yeast Saccharomyces cerevisiae, albeit in asynchronous cell populations or on individual promoters such as PHO5 and GAL1-10. Using FAIRE (formaldehyde-assisted isolation of regulatory elements) and whole-genome microarrays, we examined changes in nucleosome occupancy throughout the mitotic cell cycle in synchronized populations of S. cerevisiae. Perhaps surprisingly, nucleosome occupancy did not exhibit large, global variation between cell cycle phases. However, nucleosome occupancy at the promoters of cell cycle-regulated genes was reduced specifically at the cell cycle phase in which that gene exhibited peak expression, with the notable exception of S-phase genes. We present data that establish FAIRE as a high-throughput method for assaying nucleosome occupancy. For the first time in any system, nucleosome occupancy was mapped genome-wide throughout the cell cycle. Fluctuation of nucleosome occupancy at promoters of most cell cycle-regulated genes provides independent evidence that periodic expression of these genes is controlled mainly at the level of transcription. The promoters of G2/M genes are distinguished from other cell cycle promoters by an unusually low baseline nucleosome occupancy throughout the cell cycle. This observation, coupled with the maintenance throughout the cell cycle of the stereotypic nucleosome occupancy states between coding and non-coding loci, suggests that the largest component of variation in nucleosome occupancy is 'hard wired,' perhaps at the level of DNA sequence"
Keywords:"Cell Adhesion Molecules/genetics Cell Cycle/*physiology Cyclin B/metabolism Cyclins/metabolism G1 Phase G2 Phase Genes, Fungal/*genetics Histones/metabolism Lipoproteins/metabolism Microarray Analysis Mitosis Molecular Sequence Data Mutation/genetics Nucl;"
Notes:"MedlineHogan, Gregory J Lee, Cheol-Koo Lieb, Jason D eng R01 GM072518/GM/NIGMS NIH HHS/ R01 GM072518-01A1/GM/NIGMS NIH HHS/ R01 GM072518-02/GM/NIGMS NIH HHS/ GM072518/GM/NIGMS NIH HHS/ Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't 2006/09/28 PLoS Genet. 2006 Sep 22; 2(9):e158. doi: 10.1371/journal.pgen.0020158. Epub 2006 Aug 8"

 
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