SOX18 directly interacts with MEF2C in endothelial cells

Brett M. Hosking, S. C.Mary Wang, Shen Liang Chen, Sarah Penning, Peter Koopman, George E.O. Muscat

Research output: Contribution to journalArticlepeer-review

50 Scopus citations

Abstract

Recently, we demonstrated that mutations in the Sry-related HMG box gene Sox18 underlie vascular and hair follicle defects in the mouse allelic mutants ragged (Ra) and RaJ. Ra mice display numerous anomalies in the homozygote including, oedema, peritoneal secretions, and are almost completely naked. Sox18 and the MADS box transcription factor, Mef2C, are expressed in developing endothelial cells. Null mutants in Sox18 and Mef2c display overlapping phenotypic abnormalities, hence, we investigated the relationship between these two DNA binding proteins. We report here the direct interaction between MEF2C and SOX18 proteins, and establish that these proteins are coexpressed in vivo in endothelial cell nuclei. MEF2C expression potentiates SOX18-mediated transcription in vivo and regulates the function of the SOX18 activation domain. Interestingly, MEF2C fails to interact or co-activate transcription with the Ra or RaJ mutant SOX18 proteins. These results suggest that MEF2C and SOX18 may be important partners directing the transcriptional regulation of vascular development.

Original languageEnglish
Pages (from-to)493-500
Number of pages8
JournalBiochemical and Biophysical Research Communications
Volume287
Issue number2
DOIs
StatePublished - 21 Sep 2001

Keywords

  • Endothelial
  • MEF2C
  • Protein-protein interaction
  • Ragged
  • Sox18
  • Transcription
  • Vasculogenesis

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