The transcription factor snail regulates osteogenic differentiation by repressing Runx2 expression

  • Su Jin Park
  • , Seung Hyun Jung
  • , Gadi Jogeswar
  • , Hyun Mo Ryoo
  • , Jong In Yook
  • , Han Seok Choi
  • , Yumie Rhee
  • , Cheol Hee Kim
  • , Sung Kil Lim

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

Osteoblasts originate from mesenchymal stem cells by the coordinated activities of different signaling pathways that regulate the expression of osteoblast-specific genes. Runt-related transcription factor 2 (Runx2) is the master transcription factor for osteoblast differentiation. Despite the importance of Runx2 in the developing skeleton, how Runx2 expression is regulated remains a pivotal question. Snail, a zinc finger transcription factor, is essential for triggering epithelial-to-mesenchymal transitions (EMTs) during embryonic development and tumor progression. Here, we report that Runx2 expression is significantly up- or down-regulated relative to Snail expression. We demonstrate that Snail binds to the Runx2 promoter and that repression of Runx2 transcription by Snail is dependent on specific E-box sequence within the promoter. With antisense morpholino oligonucleotide (MO)-mediated knockdown of Snail expression in zebrafish, we observed alterations in osteogenic potential. These results indicate that Snail plays a crucial role in osteogenic differentiation by acting as a direct Runx2 repressor.

Original languageEnglish
Pages (from-to)1498-1507
Number of pages10
JournalBone
Volume46
Issue number6
DOIs
StatePublished - Jun 2010

Keywords

  • E-box
  • Osteogenic differentiation
  • Runx2
  • Snail

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