Sox9 regulates Papss2 mRNA expression through derepression of the transcriptional repressor, C/EBPβ, in chondrogenic cells

Abstract

Objectives

Previously, we showed that Papss2 expression is regulated by Sox9 in primary chondrocytes and a chondrogenic cell line, ATDC5. Here we explore molecular mechanisms whereby Sox9 regulates mouse Papss2 mRNA expression.

Methods

Luciferase reporter assays were performed in ATDC5 cells to identify Sox9-responsive elements in the mouse Papss2 gene. Electromobility shift assays, mobility shift competition assays, and super shift assays were used to characterize protein binding to a 32 bp Sox9-responsive element. Western blot and co-immunoprecipitation assays were used to determine the effects of Sox9 on C/EBPβ protein levels and binding of Sox9 to C/EBPβ.

Results

An evolutionarily conserved 509 bp Sox9-responsive DNA element was identified in the Papss2 gene, which was subsequently narrowed down to 32 bp. Putative SoxE and C/EBPβ binding sites were identified within this 32 bp. Increasing amounts of C/EBPβ resulted in attenuation of Sox9-mediated activation of the responsive element indicating C/EBPβ acts as a transcriptional repressor. Three protein-DNA complexes containing C/EBPβ were identified on the Sox9-responsive element under conditions when Papss2 expression was low. With high Sox9 expression, when Papss2 expression was stimulated, the formation of C/EBPβ containing protein-DNA complexes was inhibited, Sox9 and C/EBPβ protein-protein binding was observed, and overall cellular C/EBPβ protein levels were reduced.

Conclusion

We propose that Sox9 acts to derepress C/EBPβ-inhibited transcription of Papss2 by first interacting with C/EBPβ to prevent it from binding DNA, then reducing C/EBPβ expression.