TY - JOUR
T1 - α(2D/A)-Adrenergic receptor gene induction in the retina by phorbol ester
T2 - Involvement of an AP-2 element
AU - Venkataraman, Venkateswar
AU - Duda, Teresa
AU - Sharma, Rameshwar K.
PY - 1999
Y1 - 1999
N2 - Background: The α2-adrenergic receptor (α2-AR) expressed in the bovine retina has been demonstrated to be of the α(2D) subtype. The bovine α(2D)-adrenergic receptor (α(2D/A)-AR) gene has been cloned and characterized. This report describes the induction of this gene by phorbol- 12, 13-myristate acetate (PMA), an activator of protein kinase C (PKC). Results: Treatment of the bovine retina for 60 min with PMA (1 μM) resulted in significant and similar increases in α(2D/A)-AR mRNA level and gene transcription. This indicates that PMA causes α(2D/A)-AR gene induction and that this induction takes place directly at the transcriptional level. In C6 cells, treatment with PMA at a concentration which was as low as 0.1 μM induced endogenous α(2D/A)-AR mRNA after 60 min. Luciferase reporter assays in C6 cells mapped the PMA-responsive element to a region between -247 bp and -163 bp on the α(2D/A)-AR promoter. Electrophoretic mobility shift assays showed an increased binding of nuclear factor(s) from PMA-treated bovine retina to this promoter region. Competition assays indicate that an AP-2 element may be involved in the PMA-dependent induction. Conclusion: These findings demonstrate for the first time, the direct induction of the α(2D/A)-AR gene by PMA and support a role for an AP-2 element in the induction mechanism.
AB - Background: The α2-adrenergic receptor (α2-AR) expressed in the bovine retina has been demonstrated to be of the α(2D) subtype. The bovine α(2D)-adrenergic receptor (α(2D/A)-AR) gene has been cloned and characterized. This report describes the induction of this gene by phorbol- 12, 13-myristate acetate (PMA), an activator of protein kinase C (PKC). Results: Treatment of the bovine retina for 60 min with PMA (1 μM) resulted in significant and similar increases in α(2D/A)-AR mRNA level and gene transcription. This indicates that PMA causes α(2D/A)-AR gene induction and that this induction takes place directly at the transcriptional level. In C6 cells, treatment with PMA at a concentration which was as low as 0.1 μM induced endogenous α(2D/A)-AR mRNA after 60 min. Luciferase reporter assays in C6 cells mapped the PMA-responsive element to a region between -247 bp and -163 bp on the α(2D/A)-AR promoter. Electrophoretic mobility shift assays showed an increased binding of nuclear factor(s) from PMA-treated bovine retina to this promoter region. Competition assays indicate that an AP-2 element may be involved in the PMA-dependent induction. Conclusion: These findings demonstrate for the first time, the direct induction of the α(2D/A)-AR gene by PMA and support a role for an AP-2 element in the induction mechanism.
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U2 - 10.1046/j.1365-2443.1999.00249.x
DO - 10.1046/j.1365-2443.1999.00249.x
M3 - Article
C2 - 10320481
AN - SCOPUS:0032588040
SN - 1356-9597
VL - 4
SP - 161
EP - 173
JO - Genes to Cells
JF - Genes to Cells
IS - 3
ER -