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A Novel Glucocorticoid Receptor Binding Element within the Murine c-myc Promoter
Author(s) -
Tianlin Ma,
John A. Copland,
Allan R. Brasier,
E. Aubrey Thompson
Publication year - 2000
Publication title -
molecular endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1944-9917
pISSN - 0888-8809
DOI - 10.1210/mend.14.9.0524
Subject(s) - hormone response element , glucocorticoid receptor , biology , repressor , glucocorticoid , response element , reporter gene , microbiology and biotechnology , promoter , transcription factor , transcription (linguistics) , gene , gene expression , genetics , endocrinology , cancer , estrogen receptor , breast cancer , linguistics , philosophy
In the course of analyzing the murine c-myc promoter response to glucocorticoid, we have identified a novel glucocorticoid response element that does not conform to the consensus glucocorticoid receptor-binding sequence. This c-myc promoter element has the sequence CAGGGTACATGGCGTATGTGTG, which has very little sequence similarity to any known response element. Glucocorticoids activate c-myc/reporter constructs that contain this element. Deletion of these sequences from the c-myc promoter increases basal activity of the promoter and blocks glucocorticoid induction. Insertion of this element into SV40/reporters inhibits basal reporter gene activity in the absence of glucocorticoids. Glucocorticoids stimulate activity of reporters that contain this element. Recombinant glucocorticoid receptor binds to this element in vitro. An unidentified cellular repressor also binds to this element. The activated glucocorticoid receptor displaces this protein(s). We conclude that the glucocorticoid receptor binds to the c-myc promoter in competition with this protein, which is a repressor of transcription. To our knowledge, no glucocorticoid response element with such properties has ever been reported.

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