Dataset mE1_CBP_Enhancers
| General Information | |||
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| Name | mE1_CBP_Enhancers | Species | D. melanogaster |
| Dataset type | genomic sequence feature | FlyBase ID | FBlc0000415 |
| Source & Content | |||
| Consists of |
Genomic sequences identified by ChIP-chip and ChIP-Seq.
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| Created by | |||
| Available from |
Not available as reagents.
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| Strain |
iso-1
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Stage & tissue | |
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Stage
Tissue/Position (including subcellular localization)
Reference
Comment:0-24 hr AEL
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| Cell Line |
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Recent Updates
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| Description |
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| FB2013_03 | |||
| FB2013_02 | |||
| All updates | Click here to see a list of all updates to this record from FB2010_08 and on. | ||
Description & Members
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| Description |
Genomic sequences identified as putative embryo-only enhancers by virtue of embryo-specific CBP-binding in ChIP assays. A
synthesis of ChIP-chip and ChIP-Seq data sets; DNA sequences identified by genomic tiling array or high-throughput sequencing.
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Experimental protocol
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| Vector | |||
| Sample preparation |
Flies were cultivated in cages. Eggs were collected after a two hour pre-egg laying. Embryos of the desired age interval were
collected and initially cross-linked in 1.8% formaldehyde for 15 minutes, then homogenized in buffered 1.8% formaladehyde
and cross-linked for another 15 minutes. Cross-linked material was collected by centrifugation, washed, lysed and sonicated
to an average size of 500bp.
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| Collection preparation |
Pre-cleared chromatin was incubated with antibodies specific to nej (CBP). Antibody-bound chromatin was immunoprecipitated with protein-A beads. Input and immunoprecipitated DNA was reverse-cross-linked,
purified and processed for microarray hybridization or high-throughput sequencing.
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| Mode of assay |
ChIP-chip
ChIP-Seq
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| Assay platform |
Agilent-019182 Drosophila melanogaster Whole Genome ChIP-on-Chip Set 244K, Microarray 1 of 3
Agilent-019183 Drosophila melanogaster Whole Genome ChIP-on-Chip Set 244K, Microarray 2 of 3
Agilent-019184 Drosophila melanogaster Whole Genome ChIP-on-Chip Set 244K, Microarray 3 of 3
Illumina Genome Analyzer
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| Data analysis |
Peak calling for ChIP-chip experiments was performed using MAT (Johnson et al. 2006. Proc. Natl. Acad. Sci. U.S.A. 103(33):
12457-12462). Peak calls from ChiP-Seq data were performed using MACS (Zhang et al. 2008. Genome Biol. 9(9): R137) or Peakseq
(Rozowsky et al. 2009. Nat. Biotechnol. 27(1): 66-75). Peaks from CBP ChIP-chip and ChIP-seq experiments were filtered to
exclude peaks falling between -500bp and +500bp of annotated promoters. CBP binding sites occuring at only one of the 12 developmental
stages analyzed were also removed. Peaks were merged and a final list of sites occuring only during embryogenesis was generated.
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Additional data
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More information is available under:
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| Associated files | |||
| Additional sites | |||
Synonyms & Secondary IDs
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| Reported As | |||
| Symbol Synonym |
CBP binding sites
CBP embryo only enhancer predictions
Embryo-specific CBP binding
enhancers
mE1_CBP_Enhancers
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| Secondary FlyBase IDs | |||
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References
( 3 )
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| Research paper |
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| Supplementary material |
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Recent Updates
Description & Members