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SRX2564149: GSM2492002: Nup98-2; Drosophila melanogaster; ChIP-Seq
1 ILLUMINA (NextSeq 500) run: 43.9M spots, 3G bases, 1.4Gb downloads

Submitted by: NCBI (GEO)
Study: Nuclear Pores provide a scaffold for induced enhancer promoter contacts
show Abstracthide Abstract
We found that in addition to promoters, multiple Nups bind enhancers and insulators in the Drosophila genome. We identified a functional role for Nup98 in mediating enhancer-promoter looping at ecdysone-inducible genes. These genes were found to be stably associated with nuclear pores before and after activation. Interestingly, although changing the levels of Nup98 disrupted induced enhancer-promoter contact, it did not affect transcriptional activation. Instead, loss of Nup98-mediated enhancer-promoter contact affected the primed response to subsequent transcriptional activation or transcriptional memory. In support of the enhancer-looping role, we found Nup98 to gain and retain physical interactions with several architectural proteins upon stimulation with ecdysone. Overall design: Characterization of Nup98 occupancy by ChIP-Seq in drosophila embryonic S2 cells. Drosophila brains were also dissected from 3rd instar larvae and ChIP-Seq were performed using Nup93, Elys, Nup98, H3K27ac and H3K27m3 antibodies. Control S2 cells and Nup93 and Elys knockdown cells were used to test antibodies specificity.
Sample: Nup98-2
SAMN06336848 • SRS1980879 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: Lysates from embryonic cells or 3rd instar brains were clarified from sonicated nuclei and histone-DNA or Nup-DNA complexes were isolated with specific antibody Libraries were prepared according to Illumina's instructions for NextSeq® 500/550 High Output Kit v2 (FC-404-2005).
Experiment attributes:
GEO Accession: GSM2492002
Links:
Runs: 1 run, 43.9M spots, 3G bases, 1.4Gb
Run# of Spots# of BasesSizePublished
SRR525926843,930,4483G1.4Gb2017-03-31

ID:
3706541

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