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SRX7050430: GSM4138018: Input_S2 line_FLAG-Usp_20E-1h; Drosophila melanogaster; ChIP-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 8.3M spots, 1.9G bases, 638.9Mb downloads

Submitted by: NCBI (GEO)
Study: Employing proximity-dependent ligation techniques to estimate EcR/Usp molecular partners in Drosophila
show Abstracthide Abstract
The subject of the current study is the finding of possible molecular partners of Drosophila EcR receptor. Two labelling enzymes (BioID2 and APEX2) were fused to EcR or Usp to biotin label the surrounding proteins. All fused proteins were expressed using the Act5C promoter in Drosophila S2 cells. To ensure functionality of the generated proteins, we verified their ability to bind EcR and Usp sites in the Drosophila genome with the ChIP-Seq. Our results demonstrate that EcR and Usp fusions can be recruited to genomic sites endogenous for the EcR/Usp proteins. Conversely, unfused BioID2 and APEX2 enzymes do not bind to EcR/Usp sites. A more in-depth study was conducted to clarify the association of EcR/Usp with one of the detected proteins, CP190, a well-described cofactor of Drosophila insulators. ChIP-Seq experiments revealed an enrichment of CP190 binding on transcription start and end sites of 20E-dependent genes but not at EcR/Usp-bound enhancers. Overall design: ChIP-Seqs by anti-3xFLAG antibodies were performed after 1 hour treatment with 20-hydroxyecdysone (20E) in S2 Schneider cells stably expressing 3xFLAG-EcR, 3xFLAG-EcR-BioID2, 3xFLAG-EcR-APEX2, 3xFLAG-Usp, 3xFLAG-Usp-APEX2, 3xFLAG-Usp-BioID2, 3xFLAG-BioID2, 3xFLAG-APEX2. ChIP-Seq by anti-CP190 and Rpb3 antibodies were performed after 1 hour treatment with 20E and in sham-treated (DMSO) S2 Schneider cells stably expressing 3xFLAG-EcR. ChIP-Seq by anti-CP190 antibodies were performed on white prepupae (Oregon-Modencode).
Sample: Input_S2 line_FLAG-Usp_20E-1h
SAMN13107762 • SRS5567499 • All experiments • All runs
Library:
Instrument: Illumina NovaSeq 6000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: PAIRED
Construction protocol: Crosslinking was performed with 1% formaldehyde for 10 min at RT and stopped by adding glycine. After washings, chromatin was lysed in SDS-containing buffer (50 mM HEPESKOH, pH 7.9; 140 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% Na deoxycholate, 0.1% SDS) with protease inhibitors cocktail (Roche) and sheared to 500-bp fragments by sonication. Sonicated chromatin was centrifuged twice at 16 000 g for 20 min, and used in immunoprecipitation experiments. For one experiment, about 5 ug of antibodies and 8 uL of MabSelect sepharose (GE healthcare) were taken; BSA were added to a final concentration of 1%. The precipitated chromatin was sequentially washed twice with SDS-containing buffer and with TE buffer (20mM Tris-HCl, pH 8.0; 1mM EDTA). Precipitated chromatin complexes were eluted by sequential incubation in two portions of elution buffer (50mM Tris-HCl, pH 8.0; 1mM EDTA, 1% SDS), 30 min each, at room temperature. The eluted chromatin solution was supplemented with 5 M NaCl (16 uL per 500 uL sample) and incubated at 65°C for 16 h on a thermoshaker for de-crosslinking. De-crosslinked chromatin was subjected to proteinase treatment (3 uL of proteinase K and 5 uL of 0.5M EDTA per 500 uL sample) and incubated at 55°C for 4 h on thermoshaker. DNA was extracted with a phenol/chloroform mixture and precipitated with isopropanol. The precipitate was dissolved in TE buffer and subjected to library preparation. DNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM4138018
Links:
Runs: 1 run, 8.3M spots, 1.9G bases, 638.9Mb
Run# of Spots# of BasesSizePublished
SRR103403648,261,4621.9G638.9Mb2020-03-17

ID:
9269462

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