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SRX9849197: GSM5019865: differentiation DM3; Bubalus bubalis; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 30.1M spots, 9G bases, 3.6Gb downloads

Submitted by: NCBI (GEO)
Study: Transcriptomics analysis of proliferation and differentiation of buffalo muscle stem cells
show Abstracthide Abstract
Buffalo breeding has become an important branch of beef cattle industry. It is of great significance to study buffalo meat production and meat quality. However, the important role of mRNA and lncRNA molecules in muscle stem cells (MuSCs) development in buffalo has not been explored. Then, we performed mRNA and lncRNA expression profiling analysis on the proliferation and differentiation of MuSCs in buffalo. The results showed that there were 4,820 differentially genes, 12,227 mRNAs, and 1,352 lncRNAs. These differentially expressed mRNAs are enriched in biological processes such as cell cycle, p53 signaling pathway, RNA transport, and Calcium signaling pathway and others. We also identified a number of genes, such as MCMC4, SERDINE1, ISLR, LOC102394806, and LOC102403551, and found that interference with MYLPF expression significantly inhibited the differentiation of MuSCs. In conclusion, our research revealed the role of mRNA and lncRNA expression in the differentiation of buffalo MuSCs. This study can be used as an important reference for the study of RNA regulation during muscle development in buffalo. Overall design: Profiles of mRNAs and non-coding RNAs during the proliferation(GM) and differentiation(DM) of buffalo muscle stem cells
Sample: differentiation DM3
SAMN17313764 • SRS8030721 • All experiments • All runs
Organism: Bubalus bubalis
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Cells were removed, flash frozen on dry ice, and RNA was harvested using Trizol reagent(Invitrogen,Carlsbad,CA,USA). 3 μg RNA per sample was used as the initial material for RNA sample preparation. PolyA-Seq libraries were prepared following the described protocol at RiboBio (Guangzhou, China) in accordance to the manufacturer's instructions. The identification of mRNAs and lncRNAs were carried out with reference to RiboBio's technical methods. RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM5019865
Links:
Runs: 1 run, 30.1M spots, 9G bases, 3.6Gb
Run# of Spots# of BasesSizePublished
SRR1343563930,123,6919G3.6Gb2021-07-29

ID:
12896373

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