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SRX7156505: GSM4162191: Sample 14: 1404F1L; Sus scrofa; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 22.1M spots, 3.4G bases, 1.5Gb downloads

Submitted by: NCBI (GEO)
Study: Longissimus dorsi muscle transcriptome in pure (Iberian x Iberian) and crossbred (Iberian x Large White) pig fetuses at gestation day 77
show Abstracthide Abstract
Growth is dependent on genotype and diet, even at early developmental stages. In this study, we investigated the effects of genotype, sex, and body weight on the fetal muscle transcriptome of purebred Iberian and crossbred Iberian x Large White pigs sharing the same uterine environment. RNA sequencing was performed on 16 purebred and crossbred fetuses with high body weight (340±14g and 415±14g, respectively) and 16 with low body weight (246±14g and 311±14g, respectively), on gestational day 77. Genotype had the greatest effect on gene expression, with 645 genes identified as differentially expressed (DE) between purebred and crossbred animals. Functional analysis showed differential regulation of pathways involved in energy and lipid metabolism, muscle development, and tissue disorders. In purebred animals, fetal body weight was associated with 35 DE genes involved in development, lipid metabolism and adipogenesis. In crossbred animals, fetal body weight was associated with 60 DE genes involved in muscle development, viability, and immunity. Interestingly, the results suggested an interaction genotype*weight for some DE genes. Fetal sex had only a modest effect on gene expression. This study allowed the identification of genes, metabolic pathways, biological functions and regulators related to fetal genotype, weight and sex, in animals sharing the same uterine environment. Our findings contribute to a better understanding of the molecular events that influence prenatal muscle development and highlight the complex interactions affecting transcriptional regulation during development. Overall design: In total 32 longissimus dorsi samples were analyzed, 8 coming from males and 8 coming from females within each genotype
Sample: Sample 14: 1404F1L
SAMN13292008 • SRS5663751 • All experiments • All runs
Organism: Sus scrofa
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was extracted from 50-100mg samples of muscle using the RiboPure TM of High Quality total RNA kit (Ambion, Austin, TX, USA) following the manufacturer's recommendations. RNA was quantified using a NanoDrop-100 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA). The quality of the RNA was evaluated using the RNA Integrity Number (RIN) value from the Agilent 2100 Bioanalyzer device (Agilent technologies, Santa Clara, CA, USA). The RIN values ranged from 7.8 to 9.8 Sequencing libraries were made using the mRNA-Seq sample preparation kit (Illumina Inc., Cat. # RS-100-0801) according to manufacturer's protocol. Each library was sequenced using TruSeq SBS Kit v3-HS, in paired end mode with the read length 2x76bp on a on a HiSeq2000 sequence analyzer (Illumina, Inc). Images from the instrument were processed using the manufacturer's software to generate FASTQ sequence files.
Experiment attributes:
GEO Accession: GSM4162191
Links:
Runs: 1 run, 22.1M spots, 3.4G bases, 1.5Gb
Run# of Spots# of BasesSizePublished
SRR1046201222,081,6073.4G1.5Gb2020-01-07

ID:
9401448

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