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SRX18393604: GSM6757766: OreR, 2to3, mnase, 1; Drosophila melanogaster; MNase-Seq
1 ILLUMINA (NextSeq 500) run: 59.8M spots, 9.1G bases, 3.6Gb downloads

External Id: GSM6757766_r1
Submitted by: Zeitlinger, Stowers Institute for Medical Research
Study: Chromatin accessibility in the Drosophila embryo is determined by transcription factor pioneering and enhancer activation [Mnase-seq]
show Abstracthide Abstract
Spatiotemporal gene regulation during embryonic development is driven by cis-regulatory DNA sequences called enhancers. Enhancers are activated through a combination of transcription factors (TFs) that bind to short sequence motifs within these sequences, but the order of events by which TFs read out motifs is not clear. Some TFs can only bind chromatin that is already accessible, while other TFs called pioneers can open chromatin themselves. Identifying motifs and the order by which they drive chromatin accessibility is very challenging. The recent implementation of convolutional neural networks, which learn complex cis-regulatory sequence rules that are predictive for genomics data, provides an unprecedented opportunity to dissect this problem. Here, we trained base-resolution deep learning models and applied them to high-resolution TF binding and chromatin accessibility data from the well-studied early Drosophila embryo. We uncover a clear hierarchical relationship between the pioneer Zelda and the TFs involved in the spatiotemporal patterning of the embryo, consistent with Zelda being a pioneer. However, the models predict that patterning TFs can also augment chromatin accessibility in a context-specific manner. Using a series of Drosophila mutant strains, we find that the two types of TFs increase chromatin accessibility by distinct mechanisms. Zelda's pioneering is proportional to motif affinity, while the patterning TFs specifically increase chromatin accessibility when they mediate enhancer activation. This was conclusive because Dorsal can function both as activator and repressor, and the effect on chromatin accessibility depended on Dorsal's transactivation effect and not on its binding per se. In conclusion, chromatin accessibility occurs in two phases: one through pioneering, which makes regions first accessible but not necessarily active, and a second when the correct combination of transcription factors lead to enhancer activation. Overall design: Micrococcal nuclease DNA sequencing (MNase-seq) in 2-3 hour after egg laying (AEL) Drosophila melanogaster embryos.
Sample: OreR, 2to3, mnase, 1
SAMN31886424 • SRS15877718 • All experiments • All runs
Library:
Name: GSM6757766
Instrument: NextSeq 500
Strategy: MNase-Seq
Source: GENOMIC
Selection: MNase
Layout: PAIRED
Construction protocol: For each MNase digestion, 100 hand-sorted 2-3 h AEL Drosophila embryos were used. Nuclei were extracted by douncing in PBS with 0.1% IGEPAL CA-630. The nuclei were harvested by centrifugation and resuspended gently in MNase Digestion Buffer (PBS with 0.1% Triton X-100 and 1 mM CaCl2). MNase digestion was performed with 100 U MNase (NEB, M0247S) for 30 minutes at 37°C. The reaction was stopped with 20 mM EGTA. The nuclei were treated with 50 µg/ml RNase A (Thermo Scientific, EN0531) for 1 hour at 37 °C and 1000 rpm, and subsequently incubated overnight at 65 °C and 1000 rpm with 200 µg/ml Proteinase K (Invitrogen, 100005393) and 0.5% SDS for reverse cross-linking. DNA was extracted using phenol-chloroform (VWR, K169). MNase-seq libraries were constructed from 10 ng purified DNA using the High Throughput Library Prep Kit from KAPA Biosystems (KK8234) according to the manufacturer's instructions. MNase-seq for nucleosome occupancy using standard Illumina protocols.
Runs: 1 run, 59.8M spots, 9.1G bases, 3.6Gb
Run# of Spots# of BasesSizePublished
SRR2242412959,845,0419.1G3.6Gb2022-12-20

ID:
25416562

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