AI Article Synopsis

  • CCAAT/enhancer-binding proteins (C/EBPs) play a role in regulating cell functions, with C/EBPbeta and C/EBPdelta influencing osteocalcin promoter activity in rat osteoblasts.
  • C/EBPdelta was specifically shown to increase osteocalcin expression in mice, enhancing transcription from the osteocalcin II promoter, while C/EBPbeta did not have a similar effect.
  • The study concluded that C/EBPdelta regulates osteocalcin OG2 promoter activity by physically interacting with Runx2, leading to enhanced binding at the OSE2 element, which is essential for promoter activation.

Article Abstract

CCAAT/enhancer-binding proteins (C/EBPs) are involved in the regulation of cell proliferation, differentiation, and control of metabolic function. Although the roles of C/EBPs in osteoblasts are largely unknown, both C/EBPbeta and -delta have been shown to enhance rat osteocalcin promoter activity through the synergistic activation of Runx2 at the C/EBP element. Here we show that in the mouse, C/EBPdelta increases the expression of osteocalcin whereas C/EBPbeta does not. This increased expression was found to occur at the transcriptional level, as demonstrated by the increased transcriptional activity from mouse osteocalcin II (OG2) promoter by C/EBPdelta. Although we found three putative C/EBP sites in the -637/+/-34 region of the OG2 promoter, none of these sites showed binding activity with in vitro translated C/EBP proteins. Notably, we show that C/EBPdelta physically interacts with Runx2 and that C/EBPdelta overexpression increases binding between the Runx2-C/EBPdelta complex and the OSE2 element, a critical osteoblast-specific cis-acting element in the OG2 promoter. Consistent with these DNA binding data, a mutation in OSE2 abrogated the stimulatory effect of C/EBPdelta on this promoter activity. Finally, chromatin immunoprecipitation analysis in MC3T3-E1 cells showed in vivo occupancy of the OG2 promoter by Runx2 and C/EBPdelta. In conclusion, C/EBPdelta was found to regulate mouse osteocalcin OG2 promoter activity indirectly by interacting with Runx2 in the context of the OSE2 element and this subsequently resulted in the cooperative activation of the OG2 promoter.

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Source
http://dx.doi.org/10.1677/jme.1.01944DOI Listing

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