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Mol. Cells 2010; 29(1): 29-33

Published online December 10, 2009

https://doi.org/10.1007/s10059-010-0007-1

© The Korean Society for Molecular and Cellular Biology

Hoxc8 Represses BMP-Induced Expression of Smad6

Myengmo Kang1, Jinwoong Bok1, Custer C. Deocaris, Hyoung Woo Park, and Myoung Hee Kim*

Department of Anatomy, Embryology Laboratory, Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul 120-752, Korea, 1These authors contributed equally to this work.

Correspondence to : *Correspondence: mhkim1@yuhs.ac

Received: June 2, 2009; Revised: September 25, 2009; Accepted: October 20, 2009

Abstract

Proper regulation of bone morphogenetic protein (BMP) signaling is critical for correct patterning and morphogenesis of various tissues and organs. A well known feedback mechanism is a BMP-mediated induction of Smad6, an inhibitor of BMP signaling. Hoxc8, one of the Hox family transcription factors, has also been shown to negatively regulate BMP-mediated gene ex-pression. Here we add another level of Hoxc8 regulation on BMP signaling. Our results show that Hoxc8, when over-expressed in C3H10T1/2 or C2C12 cells, suppressed basal Smad6 promoter activity and its mRNA expression. Activation of Smad6 transcription either by BMP2 treatment or Smad1 over-expression was also abolished by Hoxc8. When chromatin was precipitated from mouse embryos with anti-Smad1 or anti-Hoxc8 antibody, Smad6 promoter sequence was enriched, suggesting that Hoxc8 proteins make complexes with Smad1 in the Smad6 promoter region. Yet, a lack of Hox binding motifs in the Smad6 promoter sequence suggests that instead of directly binding to the DNA, Hoxc8 may regulate Smad6 expression via an indirect mechanism. Our results suggest that the Smad6-mediated negative feedback mechanism on BMP signaling may be balanced by the repression of Smad6 expression by Hoxc8.

Keywords bone morphogenetic protein (BMP), Hoxc8, Smad1, Smad6

Article

Research Article

Mol. Cells 2010; 29(1): 29-33

Published online January 31, 2010 https://doi.org/10.1007/s10059-010-0007-1

Copyright © The Korean Society for Molecular and Cellular Biology.

Hoxc8 Represses BMP-Induced Expression of Smad6

Myengmo Kang1, Jinwoong Bok1, Custer C. Deocaris, Hyoung Woo Park, and Myoung Hee Kim*

Department of Anatomy, Embryology Laboratory, Brain Korea 21 Project for Medical Science, Yonsei University College of Medicine, Seoul 120-752, Korea, 1These authors contributed equally to this work.

Correspondence to:*Correspondence: mhkim1@yuhs.ac

Received: June 2, 2009; Revised: September 25, 2009; Accepted: October 20, 2009

Abstract

Proper regulation of bone morphogenetic protein (BMP) signaling is critical for correct patterning and morphogenesis of various tissues and organs. A well known feedback mechanism is a BMP-mediated induction of Smad6, an inhibitor of BMP signaling. Hoxc8, one of the Hox family transcription factors, has also been shown to negatively regulate BMP-mediated gene ex-pression. Here we add another level of Hoxc8 regulation on BMP signaling. Our results show that Hoxc8, when over-expressed in C3H10T1/2 or C2C12 cells, suppressed basal Smad6 promoter activity and its mRNA expression. Activation of Smad6 transcription either by BMP2 treatment or Smad1 over-expression was also abolished by Hoxc8. When chromatin was precipitated from mouse embryos with anti-Smad1 or anti-Hoxc8 antibody, Smad6 promoter sequence was enriched, suggesting that Hoxc8 proteins make complexes with Smad1 in the Smad6 promoter region. Yet, a lack of Hox binding motifs in the Smad6 promoter sequence suggests that instead of directly binding to the DNA, Hoxc8 may regulate Smad6 expression via an indirect mechanism. Our results suggest that the Smad6-mediated negative feedback mechanism on BMP signaling may be balanced by the repression of Smad6 expression by Hoxc8.

Keywords: bone morphogenetic protein (BMP), Hoxc8, Smad1, Smad6

Mol. Cells
May 31, 2023 Vol.46 No.5, pp. 259~328
COVER PICTURE
The alpha-helices in the lamin filaments are depicted as coils, with different subdomains distinguished by various colors. Coil 1a is represented by magenta, coil 1b by yellow, L2 by green, coil 2a by white, coil 2b by brown, stutter by cyan, coil 2c by dark blue, and the lamin Ig-like domain by grey. In the background, cells are displayed, with the cytosol depicted in green and the nucleus in blue (Ahn et al., pp. 309-318).

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