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SRX13584935: GSM5769461: Day5_DTR_Utricle_scATACseq; Danio rerio; ATAC-seq
1 ILLUMINA (NextSeq 550) run: 50.5M spots, 4.9G bases, 1.2Gb downloads

External Id: GSM5769461_r1
Submitted by: Shawn Burgess, NHGRI, NIH
Study: A regulatory network of Sox and Six transcription factors initiate a cell fate transformation during hearing regeneration in adult zebrafish
show Abstracthide Abstract
Using adult zebrafish inner ears as a model for sensorineural regeneration, we performed a targeted ablation of the mechanosensory receptors in the saccule and utricle and characterized the single-cell epigenome and transcriptome at consecutive time-points following hair cell death. Overall design: To elucidate the transcriptional regulatory network that controls tissue regeneration, we characterized the gene expression profiles (scRNA-seq) and the map of accessible regions (scATAC-seq) associated with the response to hair cell ablation in adult zebrafish sensory epithelia. We dissected out saccules and utricles at three time points: Days 4, 5 and 7 post-DT, and each were processed separately in both scRNA-seq and scATAC-seq experiments. Untreated Tg(myo6b:DTR) transgenic zebrafish and wild-type DT injected (and untreated) zebrafish lacking the Tg(myo6b:DTR) transgene were used as non-regenerating controls. Cell suspensions of isolated sensory epithelia were subjected to single cell sequencing for both their transcriptome and open chromatin regions using 10X Genomics Chromium Single Cell Gene Expression and Single Cell ATAC Sequencing. We also include biological triplicates of untreated wild-type saccules and utricles for bulk ATAC-seq.
Sample: Day5_DTR_Utricle_scATACseq
SAMN24588408 • SRS11474983 • All experiments • All runs
Organism: Danio rerio
Library:
Name: GSM5769461
Instrument: NextSeq 550
Strategy: ATAC-seq
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: For single-cell experiments, non-regenerating (untreated) and regenerating inner ears (saccule and utricle) were dissected at consecutive time-points and dissociated into single-cells using trypsin and collagenase. For bulk ATAC-seq experiments, untreated inner ears (saccule and utricle) were harvested and samples prepared in triplicate. Nuclei were extracted and chromatin digested by tn5 transposase. DNA fragments were extracted and then amplified by PCR. Libraries were amplified by PCR with indexed primers. For scRNA-seq, cDNA libraries were generatated with Chromium Controller and Chromium Single Cell 3' GEM, Library and Gel Bead Kit V3 (10x Genomics). For scATAC-seq, libraries were generated with the Chromium Controller and Chromium Single Cell ATAC Library & Gel Bead Kit (1000111, 10X Genomics). For bulk ATAC-seq, libraries were generated using Nextera DNA Library Preparation Kit (Catalog # FC-121-1030). Transposed DNA were amplified by PCR with indexed primers and libraries were purified.
Runs: 1 run, 50.5M spots, 4.9G bases, 1.2Gb
Run# of Spots# of BasesSizePublished
SRR1741326850,486,8854.9G1.2Gb2022-07-19

ID:
18873848

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