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SRX8279272: GSM4520625: RNA-seq_WntMo_M3; Gallus gallus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 21.1M spots, 1.8G bases, 643.6Mb downloads

Submitted by: NCBI (GEO)
Study: The connectome of neural crest enhancers reveals regulatory features of signaling systems
show Abstracthide Abstract
The neural crest is a migratory stem cell population that gives rise to a wide array of cell types. The formation and differentiation of neural crest cells are controlled by a complex transcriptional network, which endows these cells with unique features such as multipotency and stemness. During migration, signaling systems modulate subcircuits within this network to ensure that neural crest cells differentiate at the right time and place. The wingless (Wnt) signaling pathway, in particular, plays an important role in defining developmental potential of these cells but, surprisingly few direct Wnt-target genes have been identified in the neural crest transcriptional network. To address this, we generated a high-resolution contact map of active enhancers in the neural crest and identified the direct targets of Wnt signaling in the neural crest genome via CUT&RUN for its nuclear effectors LEF1 and CTNNB1 (bCat). Overall design: CUT&RUN data for Wnt signaling nuclear factors LEF1 and CTNNB1, and CTCF in chick neural crest cells at specification stage (HH9) CUT&RUN data for LEF1 in chick neural crest cells at specification stage (HH9) upon Wnt knockdown RNA-seq on neural crest cells upon Wnt knockdown. H2K27ac HiChIP for dissected neural folds and whole embryos at HH9
Sample: RNA-seq_WntMo_M3
SAMN14845423 • SRS6605674 • All experiments • All runs
Organism: Gallus gallus
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Loss of function assays were performed after bilateral injections with their respective controls. Wnt knockdown was performed by the combined inhibition of Wnt 1 and 4 by morpholinos. For RNA expression levels, paired single neural folds were finely dissected and total RNA isolated with the RNAqueous-Micro Total RNA Isolation Kit (Thermo Fisher Scientific, #AM1931) according to the kit's protocol. RNA was poly(A) selected using the NEBNext Poly(A) mRNA Magnetic Isolation Module (New England Biolabs, E7490). TruSeq-barcoded RNAseq libraries were generated with the NEBNext Ultra II Directional RNA Library Prep Kit (New England Biolabs, E7760) and sequenced on an Illumina NextSeq500 instrument.
Experiment attributes:
GEO Accession: GSM4520625
Links:
Runs: 1 run, 21.1M spots, 1.8G bases, 643.6Mb
Run# of Spots# of BasesSizePublished
SRR1171997521,142,2731.8G643.6Mb2021-04-04

ID:
10781851

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