Transcriptional profiling of murine osteoblast differentiation based on RNA-seq expression analyses
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
29653293
DOI
10.1016/j.bone.2018.04.006
PII: S8756-3282(18)30152-2
Knihovny.cz E-zdroje
- Klíčová slova
- Alternative splicing, Bone cells, Non-coding RNA, RNAseq, Topological domains,
- MeSH
- alternativní sestřih MeSH
- buněčná diferenciace genetika MeSH
- kultivované buňky MeSH
- lebka fyziologie MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- osteoblasty fyziologie MeSH
- osteogeneze genetika MeSH
- RNA analýza MeSH
- stanovení celkové genové exprese MeSH
- transkriptom genetika MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- RNA MeSH
Osteoblastic differentiation is a multistep process characterized by osteogenic induction of mesenchymal stem cells, which then differentiate into proliferative pre-osteoblasts that produce copious amounts of extracellular matrix, followed by stiffening of the extracellular matrix, and matrix mineralization by hydroxylapatite deposition. Although these processes have been well characterized biologically, a detailed transcriptional analysis of murine primary calvaria osteoblast differentiation based on RNA sequencing (RNA-seq) analyses has not previously been reported. Here, we used RNA-seq to obtain expression values of 29,148 genes at four time points as murine primary calvaria osteoblasts differentiate in vitro until onset of mineralization was clearly detectable by microscopic inspection. Expression of marker genes confirmed osteogenic differentiation. We explored differential expression of 1386 protein-coding genes using unsupervised clustering and GO analyses. 100 differentially expressed lncRNAs were investigated by co-expression with protein-coding genes that are localized within the same topologically associated domain. Additionally, we monitored expression of 237 genes that are silent or active at distinct time points and compared differential exon usage. Our data represent an in-depth profiling of murine primary calvaria osteoblast differentiation by RNA-seq and contribute to our understanding of genetic regulation of this key process in osteoblast biology.
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