JunB mediates enhancer/promoter activity of COL1A2 following TGF-β induction
M Ponticos, C Harvey, T Ikeda, D Abraham… - Nucleic acids …, 2009 - academic.oup.com
M Ponticos, C Harvey, T Ikeda, D Abraham, G Bou-Gharios
Nucleic acids research, 2009•academic.oup.comTranscriptional control of the genes coding for collagen type I is regulated by a complex
interaction between a distal enhancer and a proximal promoter. In this study, we have
dissected the molecular mechanism of this interaction by defining a specific sequence within
the enhancer that respond in fibroblasts to transforming growth factor-β (TGF-β). We show
that TGF-β activates COL1A2 gene via a non-canonical (Smad-independent) signalling
pathway, which requires enhancer/promoter co-operation. This interaction involves …
interaction between a distal enhancer and a proximal promoter. In this study, we have
dissected the molecular mechanism of this interaction by defining a specific sequence within
the enhancer that respond in fibroblasts to transforming growth factor-β (TGF-β). We show
that TGF-β activates COL1A2 gene via a non-canonical (Smad-independent) signalling
pathway, which requires enhancer/promoter co-operation. This interaction involves …
Abstract
Transcriptional control of the genes coding for collagen type I is regulated by a complex interaction between a distal enhancer and a proximal promoter. In this study, we have dissected the molecular mechanism of this interaction by defining a specific sequence within the enhancer that respond in fibroblasts to transforming growth factor-β (TGF-β). We show that TGF-β activates COL1A2 gene via a non-canonical (Smad-independent) signalling pathway, which requires enhancer/promoter co-operation. This interaction involves exchange of cJun/Jun B transcription factor occupancy of a critical enhancer site resulting in the stabilization of enhancer/promoter coalescence. Moreover, using transgenesis, we show that interference in this mechanism results in the abolition of COL1A2 fibroblast expression in vivo . These data are therefore relevant to the control of collagen type I in vivo both in embryonic development, in adult connective tissue homeostasis, and in tissue repair and scarring pathologies.
