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Keywords
(8)
Dna Binding
Dna Binding Protein
Intracellular Signaling
quantitative rt-pcr
Regulatory Element
Rna Interference
bone morphogenetic protein 2
Ovarian Cancer
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Mechanisms of bone morphogenetic protein 2 (BMP2) stimulated inhibitor of DNA binding 3 ( Id3) transcription
Mechanisms of bone morphogenetic protein 2 (BMP2) stimulated inhibitor of DNA binding 3 ( Id3) transcription,10.1016/j.mce.2010.10.019,Molecular and C
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Mechanisms of bone morphogenetic protein 2 (BMP2) stimulated inhibitor of DNA binding 3 ( Id3) transcription
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Catherine C. Ho
,
Xiang Zhou
,
Yuji Mishina
,
Daniel J. Bernard
Bone morphogenetic protein 2
(BMP2) stimulates expression of the inhibitors of
DNA binding
(Id) 1, 2, and 3 in a variety of cell types. Here, we examined mechanisms mediating BMP2-stimulated Id3 transcription in murine gonadotropes. Using a combination of quantitative RT-PCR, promoter-reporter analyses, over-expression, and
RNA interference
approaches, we demonstrate that BMP2 signals via the BMPR2 and BMPR1A (ALK3) receptors and
intracellular signaling
proteins SMADs 1 and 5 to stimulate Id3 transcription. We further define a novel 6-bp cis-element mediating BMP2- and SMAD-dependent transcription, though this site does not appear to bind SMADs directly. A specific
DNA binding protein
complex binds to this element, but its constituent protein(s) remain undetermined. Recently, a more distal enhancer was shown to mediate BMP4-induction of the human ID3 gene in
ovarian cancer
cells. This enhancer is conserved in the murine gene and we demonstrate its role in BMP2-induced Id3 promoter activity in gonadotropes. Conversely, the proximal cis-element defined here is also conserved in human ID3 and we demonstrate its functional role in BMP2-induction of ID3 transcription. Finally, we show that the two regulatory elements also mediate BMP2-induction of Id3 promoter activity in murine fibroblasts. Collectively, we have defined a general mechanism whereby BMP2 regulates Id3/ID3 transcription in different cell types and in different species.
Journal:
Molecular and Cellular Endocrinology - MOL CELL ENDOCRINOL
, vol. 332, no. 1, pp. 242-252, 2011
DOI:
10.1016/j.mce.2010.10.019
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