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SRX14213599: GSM5906067: Liver_5932_MOET; Bos taurus; RNA-Seq
1 DNBSEQ (DNBSEQ-G400) run: 60.3M spots, 6G bases, 3.5Gb downloads

External Id: GSM5906067_r1
Submitted by: Applied Mathematics and Computer Science, Technical University of Denmark
Study: Transcriptomics of the liver and the muscle from in vitro or in vivo-produced dairy male calves
show Abstracthide Abstract
In cattle, the in vitro production (IVP) of embryos is becoming more relevant than embryos produced in vivo, i.e., after ovarian stimulation and embryo transfer (MOET). However, the effects of IVP on the developmental programming of specific organs in the postnatal calves are yet unknown. The objective of this study was to compare the hepatic and muscular transcriptomic modifications between IVP and MOET male calves of three months of age (n=4 per group). Tissue samples from liver and semitendinosus muscle were obtained at 3 months of age, and the extracted RNA was sequenced through RNAseq to determine differentially expressed genes (DEG; FDR<0.05). KEGG pathways enrichment analysis showed that DEG up-regulated in the liver and the muscle of the IVP calves were involved in oxidative phosphorylation and the tricarboxylic acid cycle. In contrast, ribosome and translation were up-regulated in the liver but down-regulated in the muscle of the IVP calves compared to the MOET calves (FDR<0.05). In conclusion, our findings indicated an altered hepatic and muscular energy regulation in phenotypically normal IVP calves compared to MOET calves. Overall design: Samples were obtained from the liver and muscle from three-month-old IVP calves (n=4) and control MOET calves (n=4). The samples in this study are from the same animals as the samples in GSE176219.
Sample: Liver_5932_MOET
SAMN26027316 • SRS12035597 • All experiments • All runs
Organism: Bos taurus
Library:
Name: GSM5906067
Instrument: DNBSEQ-G400
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Tissues samples were shipped in dry ice to the BGI TECH SOLUTIONS Company (Hong Kong), which performed the RNA extraction, quality control, library preparation and sequencing. All samples met the requirements for library preparation (adequate concentration and quantity, purity as OD260/280 = 1.8~2.0 and RIN > 7). RNA sequencing (RNAseq) was run in the RNA samples through non-stranded & polyA-selected mRNA library preparation and PE100 sequencing with 5Gb clean data per sample on DNBSEQ. After library preparation and sequencing, raw data with adapter sequences or low-quality sequences were filtered to remove contamination and obtain valid data. This step was completed by the SOAPnuke software developed by BGI Company.
Runs: 1 run, 60.3M spots, 6G bases, 3.5Gb
Run# of Spots# of BasesSizePublished
SRR1806187760,300,0426G3.5Gb2022-06-30

ID:
20079129

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