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Nephroblastoma overexpressed (Nov) induces gremlin in ST‐2 stromal cell lines by post‐transcriptional mechanisms

TLDR
It is confirmed by demonstrating that downregulation of Nov destabilizes gremlin transcripts, and this effect is possibly mediated by AU‐rich elements present in the 3′‐UTR of gremlin.
Abstract
Nephroblastoma overexpressed (Nov) inhibits osteoblastogenesis in part because it binds bone morphogenetic protein (BMP)-2. In the present study, we investigated whether Nov regulated the expression of the BMP antagonist gremlin. Overexpression of Nov increased gremlin mRNA levels in ST-2 cells, and its downregulation by RNA interference decreased gremlin mRNA. Nov did not affect Grem1 transcription, but prolonged the half-life of gremlin mRNA in ST-2 cells, demonstrating that Nov acts by post-transcriptional mechanisms. This was confirmed by demonstrating that downregulation of Nov destabilizes gremlin transcripts. To assess whether the 3′-untranslated region (UTR) of gremlin mRNA mediated the effect of Nov, the decay of a chimeric cfos gremlin 3′-UTR construct was compared to that of cfos in ST-2 cells. The presence of the gremlin 3′-UTR prolonged the half-life of cfos and was responsible for the effect of Nov. To examine the binding of the gremlin 3′-UTR to ribonucleoproteins, radiolabeled gremlin RNA fragments were incubated with cytosolic extracts from Nov overexpressing and control cells. RNA electrophoretic mobility analysis revealed that Nov enhanced the binding of cytosolic proteins to the fragments spanning the 3′-UTR of gremlin between bases 1,358–1,557 and 1,158–1,357 from the transcriptional start. Mutations of AU-rich elements in these two RNA fragments prevented the formation of RNA–protein complexes induced by Nov. Nov did not alter the binding of cytosolic extracts to sequences present in the 5′-UTR or coding region of gremlin. In conclusion, Nov stabilizes gremlin transcripts, and this effect is possibly mediated by AU-rich elements present in the 3′-UTR of gremlin. J. Cell. Biochem. 112: 715–722, 2011. © 2010 Wiley-Liss, Inc.

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Cytoplasmic protein binds in vitro to a highly conserved sequence in the 5' untranslated region of ferritin heavy- and light-subunit mRNAs (RNA-protein complexes/iron/translational control)

TL;DR: It is proposed that intracellular iron levels regulate ferritin synthesis by causing changes in specific protein binding to the conserved sequence in the ferritIn heavy- and light-subunit mRNAs.
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Gremlin aggravates hyperglycemia-induced podocyte injury by a TGFβ/smad dependent signaling pathway.

TL;DR: Gremlin was clearly elevated in high glucose cultured mouse podocytes, and likely employed endogenous canonical TGFβ1/Smad signaling to induce podocyte injury.
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CCN3 modulates bone turnover and is a novel regulator of skeletal metastasis

TL;DR: The CCN family of proteins is composed of six secreted proteins, which are grouped together based on their structural similarity, and CCN3, a founding member of this family, and its role in regulating cells within the bone microenvironment is focused on.
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A perspective on anti-CCN2 therapy for chronic kidney disease.

TL;DR: This review aims to provide an overview of the current state of CCN2 research with a focus on anti-fibrotic therapy and shows promising results with minimal adverse side effects.
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CCN3 and DLL1 co-regulate osteogenic differentiation of mouse embryonic fibroblasts in a Hey1-dependent manner

TL;DR: It is suggested that CCN3 significantly inhibited the osteogenic differentiation of MEFs through the inhibition of BMP signaling and the mutual inhibition with DLL1, so as to inhibit the expression of Hey1, the target gene shared by BMP and Notch signaling pathways.
References
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Journal ArticleDOI

Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells

TL;DR: 21-nucleotide siRNA duplexes provide a new tool for studying gene function in mammalian cells and may eventually be used as gene-specific therapeutics.
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Isolation and characterization of rat and human glyceraldehyde-3-phosphate dehydrogenase cDNAs: genomic complexity and molecular evolution of the gene

TL;DR: Comparison of these two cDNA sequences with those of the chicken, Drosophila and yeast genes allows the analysis of the evolution of the GAPDH genes in detail.
Journal ArticleDOI

Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos

TL;DR: The activity of exogenous noggin RNA in embryonic axis induction and the localized expression of endogenous noggan transcripts suggest that noggins plays a role in normal dorsal development.
Journal ArticleDOI

Bone morphogenetic proteins, their antagonists, and the skeleton.

TL;DR: A large number of extracellular proteins that bind BMPs and prevent their binding to signaling receptors have emerged, indicating the existence and need of local feedback mechanisms to temper BMP cellular activities.
Journal ArticleDOI

Connective-tissue growth factor (CTGF) modulates cell signalling by BMP and TGF-beta.

TL;DR: Results show that CTGF inhibits BMP and activates TGF-β signals by direct binding in the extracellular space and can antagonize BMP4 activity by preventing its binding to BMP receptors and has the opposite effect, enhancement of receptor binding, on T GF-β1.
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