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Series GSE245312 Query DataSets for GSE245312
Status Public on Nov 30, 2023
Title Characterization of regeneration initiating cells during Xenopus laevis tail regeneration [scRNA-Seq]
Organism Xenopus laevis
Experiment type Expression profiling by high throughput sequencing
Summary In this experiment, we revealed the critical steps for regeneration initiation. We discovered Regeneration Initiating Cells (RICs) using single cell and spatial transcriptomics of the regenerating Xenopus laevis tail. RICs are formed transiently from the basal epidermal cells and are critical for the modification of the surrounding extracellular matrix to allow for migration of other cell types that promote regeneration. Absence or deregulation of RICs leads to excessive extracellular matrix deposition and regeneration defects.
 
Overall design Single cell experiment was performed using 0, 1, 3, 12 hours post amputation (hpa) of Xenopus laevis tail at stage 40. Embryos were anesthetized and the regenerating part was dissected and collected. Tail pieces from 50 embryos were collected per one sample.
 
Contributor(s) Abaffy P, Zucha D, Naraine R, Kraus D, Sindelka R
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Submission date Oct 13, 2023
Last update date Nov 30, 2023
Contact name Radek Sindelka
E-mail(s) Radek.Sindelka@ibt.cas.cz
Organization name Institute of Biotechnology, Czech Academy of Science, v.v.i.
Lab Laboratory of Gene Expression
Street address Průmyslová 595
City Vestec by Prague
ZIP/Postal code 25250
Country Czech Republic
 
Platforms (1)
GPL28901 Illumina NovaSeq 6000 (Xenopus laevis)
Samples (1)
GSM7840723 0, 1, 3, 12 hpa regeneration
This SubSeries is part of SuperSeries:
GSE245320 Characterization of regeneration initiating cells during Xenopus laevis tail regeneration
Relations
BioProject PRJNA1027818

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE245312_RAW.tar 140.9 Mb (http)(custom) TAR (of MTX, TSV, XLSX)
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Raw data are available in SRA

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