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SRX14677356: GSM5987806: Liver, sh931 (RNA-seq); Mesocricetus auratus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 72.4M spots, 21.8G bases, 9.9Gb downloads

External Id: GSM5987806_r1
Submitted by: Biobix, Lab of Bioinformatics and Computational Genomics, Dept. Of Mathematical Modelling, Statistics and Bioinformatics, Ghent University
Study: Liver transcriptomic and methylomic analyses identify transcriptional MAPK regulation in facultative hibernation of Syrian hamster [RNA-Seq]
show Abstracthide Abstract
Hibernation consist of alternating torpor/arousal phases, during which animals cope with repetitive hypothermia and ischemia-reperfusion. Due to limited transcriptomic and methylomic information for facultative hibernators, we here conducted RNA and whole genome bisulfite sequencing in liver of hibernating Syrian hamster (Mesocricetus auratus). Gene Ontology analysis was performed on 844 differentially expressed genes (DEGs) and confirmed the Liver, shift in metabolic fuel utilization, inhibition of RNA transcription and cell cycle regulation as found in seasonal hibernators. We Liver, show a so far unreported suppression of MAPK and PP1 pathways. Notably, hibernating hamsters Liver, showed upregulation of MAPK inhibitors (DUSPs and SPRYs) and reduced levels of MAPK induced transcription factors. Promoter methylation was found to modulate the expression of genes targeted by these transcription factors. In conclusion, we document gene regulation between hibernation phases, which may aid the identification of pathways and targets to prevent organ damage in transplantation or ischemia-reperfusion. Overall design: RNA Sequencing profiles for 9 Syrian Hamsters in the following hibernation stages: euthermic, torpor late and arousal early.
Sample: Liver, sh931 (RNA-seq)
SAMN27112555 • SRS12441500 • All experiments • All runs
Library:
Name: GSM5987806
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Liver was flushed with physiological salt solution, removed and snap-frozen in liquid nitrogen and stored at −80 °C. Total RNA was extracted from liver tissue samples of three animals per hibernation phase using Nucleospin (Machery Nagel, Düren, Germany). Concentrations were measured using Nanodrop and processed for RNA sequencing (RNAseq) by NXTGNT (www.nxtgnt.com). RNA quality was checked using a Bioanalyzer RNA 6000 nano chip assay and Ribogreen assay (Invitrogen, Carlsbad, CA, USA). 437ng RNA per sample was used for further analysis. cDNA libraries were prepared for sequencing using Truseq stranded mRNA library prep (Illumina, San Diego, CA. USA) according to protocol. Sequencing was performed on a NextSeq500 High output flow cell, generating single-end 75bp reads.
Runs: 1 run, 72.4M spots, 21.8G bases, 9.9Gb
Run# of Spots# of BasesSizePublished
SRR1854757672,407,65521.8G9.9Gb2023-05-02

ID:
20988645

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