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Series GSE26602 Query DataSets for GSE26602
Status Public on Feb 23, 2011
Title Genome-Wide And Phase-Specific DNA-Binding Rhythms Of BMAL1 Control Circadian Output Functions In Mouse Liver
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Using chromatin immuno-precipitation (ChIP) combined with deep sequencing (ChIP-seq) we obtained a time resolved and genome-wide map of BMAL1 binding in mouse liver, which allowed to identify over two thousand binding sites with peak binding narrowly centered around Zeitgeber time (ZT) 6. Annotation of BMAL1 targets confirms carbohydrate and lipid metabolism as the major output of the circadian clock in mouse liver. Moreover, transcription regulators are largely overrepresented, several of which also exhibit circadian activity. Genes of the core circadian oscillator stand out as strongly bound, often at promoter and distal sites. Genomic sequence analysis of the sites identified E- boxes and tandem E1-E2 consensus elements. Electromobility shift assays (EMSA) showed that E1-E2 sites are bound by a dimer of BMAL1/CLOCK heterodimers with a spacing-dependent cooperative interaction that was further validated in transactivation assays. BMAL1 target genes showed cyclic mRNA expression profiles with a phase distribution centered at ZT10. Importantly, sites with E1-E2 elements showed tighter phases both in binding and mRNA accumulation. Finally, comparing the temporal accumulation of precursor mRNA and mature mRNA helped distinguish direct BMAL1 targets from targets with more complex regulation, and showed how transcriptional and post-transcriptional regulation contribute differentially to circadian expression phase. Together, our analysis of a dynamic protein-DNA interactome uncovered how genes of the core circadian oscillator are wired together and drive phase-specific circadian output programs in a complex tissue.
 
Overall design ChIP-Seq of BMAL1 in mouse liver during one circadian cycle at 4 hour time resolution presented in this Series (GSE26602).

mRNA profiling data used in this study are already published (Kornmann et al, PLoS Biol 2007) and have been deposited on ArrayExpress repository (accession number: E-MEXP-842).
 
Contributor(s) Rey G, Cesbron F, Rougemont J, Reinke H, Brunner M, Naef F
Citation(s) 21364973
Submission date Jan 13, 2011
Last update date May 15, 2019
Contact name Guillaume Rey
E-mail(s) guillaume.rey@unige.ch
Organization name University of Geneva
Street address Campus Biotech, Chemin des Mines 9
City Geneva
ZIP/Postal code 1202
Country Switzerland
 
Platforms (1)
GPL9185 Illumina Genome Analyzer (Mus musculus)
Samples (13)
GSM654880 BMAL1_ZT02_ChIP-Seq_rep1
GSM654881 BMAL1_ZT02_ChIP-Seq_rep2
GSM654882 BMAL1_ZT06_ChIP-Seq_rep1
Relations
SRA SRP005305
BioProject PRJNA136207

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE26602_BMAL1_ZT02.bedgraph.gz 197.9 Mb (ftp)(http) BEDGRAPH
GSE26602_BMAL1_ZT06.bedgraph.gz 148.5 Mb (ftp)(http) BEDGRAPH
GSE26602_BMAL1_ZT10.bedgraph.gz 219.6 Mb (ftp)(http) BEDGRAPH
GSE26602_BMAL1_ZT14.bedgraph.gz 261.0 Mb (ftp)(http) BEDGRAPH
GSE26602_BMAL1_ZT18.bedgraph.gz 225.4 Mb (ftp)(http) BEDGRAPH
GSE26602_BMAL1_ZT22.bedgraph.gz 203.4 Mb (ftp)(http) BEDGRAPH
GSE26602_input.bedgraph.gz 141.1 Mb (ftp)(http) BEDGRAPH
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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