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Sample GSM7840817 Query DataSets for GSM7840817
Status Public on Nov 30, 2023
Title refr_72_hpa_D
Sample type SRA
 
Source name tail
Organism Xenopus laevis
Characteristics tissue: tail
time: 72 hours post amputation
condition: refractory
treatment: amputated
Treatment protocol Bulk RNA-Seq analysis was done to analyze the temporal changes in gene expression during the regeneration and refractory periods of 0, 0.5, 6 hpa and 3 dpa. The experiment was done in four biological repeats.
Growth protocol Xenopus laevis females were stimulated with 500 U of human chorionic gonadotropin (Sigma-Aldrich). Eggs were collected the following day and fertilized by testes suspension which were surgically obtained from the male. After the removal of jelly coats by the 2% cysteine treatment, embryos were incubated in 0.1x MBS until the experimental procedure. Embryonic stages were determined based on Nieuwkoop and Faber table. Embryos were immediately transferred to the 0.1x MMR solution with gentamycin. Solution was changed every day.
Extracted molecule total RNA
Extraction protocol All samples were stored at -80°C. Total RNA was extracted from 20 embryos per sample at the regenerative stage. Total RNA was extracted using TriReagent extraction and LiCl precipitation (Sigma) according to the manufacturer’s instructions. The concentration of total RNA was determined using a spectrophotometer (Nanodrop 2000; ThermoFisher Scientific), and the quality of RNA was assessed using a Fragment Analyzer (Agilent, Standard Sensitivity RNA analysis kit, DNF-471).
100 ng of total RNA was used for library preparation using the Lexogen SENSE Total RNA-Seq Library Prep Kit.
Library quality was tested by capillary electrophoresis on Fragment Analyzer (Agilent, NGS High Sensitivity kit DNF-474). The libraries were pooled and sequenced using Illumina NextSeq 500, 2x76 bp.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NextSeq 500
 
Data processing Reads were filtered for low quality reads and adaptor sequences, using TrimmomaticPE (v. 0.36), while ribosomal RNA reads were filtered out using Sortmerna (v. 2.1b) (default parameters).
The cleaned reads were then aligned using STAR (v. 2.7.9a) to the Xenopus laevis genome version 10.1 and annotation version XENLA_10.1_GCF.
A count table was then generated using the python script htseq-count (v. 0.6.1p1) with the parameter “–m union”. The counts were normalized and analyzed using DESeq2 (v. 1.32.0)[84] under R (v. 4.1.0).
Outlier samples were assessed by analyzing the PCA of the 500 most variable genes.
Assembly: Xenopus laevis genome version 10.1
Supplementary files format and content: 02_bulk_data_non_normalized_refrac.xlsx: non-normalized count data from the refractory experiment
Supplementary files format and content: 02_bulk_data_non_normalized_regen.xlsx: non-normalized count data from the regeneration experiment
Supplementary files format and content: 02_bulk_data_normalized_refrac.xlsx: median of ratios normalized data for the refractory dataset using DESeq2. Outlier samples were removed.
Supplementary files format and content: 02_bulk_data_normalized_regen.xlsx: median of ratios normalized data for the regeneration dataset using DESeq2. Outlier samples were removed.
 
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
 
Platform ID GPL21248
Series (2)
GSE245318 Characterization of regeneration initiating cells during Xenopus laevis tail regeneration [bulk RNA-Seq 2]
GSE245320 Characterization of regeneration initiating cells during Xenopus laevis tail regeneration
Relations
BioSample SAMN37810396
SRA SRX22090545

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA

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