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Phosphorylation of Estrogen Receptor ? at serine 118 directs recruitment of promoter complexes and gene-specific transcription.


ABSTRACT: Phosphorylation of estrogen receptor ? (ER?) is important for receptor function, although the role of specific ER? phosphorylation sites in ER?-mediated transcription remains to be fully evaluated. Transcriptional activation by ER? involves dynamic, coordinate interactions with coregulators at promoter enhancer elements to effect gene expression. To determine whether ER? phosphorylation affects recruitment of unique protein complexes at gene-specific promoters, changes in ER? Ser118 phosphorylation were assessed for effects on receptor and coregulator recruitment and transcription of ER?-regulated genes. Chromatin immunoprecipitation assays to measure promoter association found a 17?-estradiol (E2)-dependent recruitment of ER? at 150 min to ER?-regulated promoters, whereas ER? phosphorylated at Ser118 was dissociated from promoters after E2 treatment. Mutation of Ser118 to alanine (S118A) altered unliganded and ligand-induced association of ER? and p160 coregulators with ER? target promoters when compared with wild-type (WT)-ER? transfection. S118A and WT-ER? exhibited a similar level of recruitment to the estrogen response element-driven pS2 promoter and induced pS2 mRNA after E2 treatment. Although WT-ER? was recruited to c-myc and cyclin D1 promoters after E2 treatment and induced mRNA expression, S118A exhibited reduced interaction with c-myc and cyclin D1 promoters, and E2 did not induce c-myc and cyclin D1 mRNA. In addition, S118A resulted in increased recruitment of steroid receptor coactivator-1, glucocorticoid receptor interacting protein-1, and activated in breast cancer-1 to pS2, c-myc, and cyclin D1 irrespective of the presence of E2. Together, these data indicate that site specific phosphorylation of ER? directs gene-specific recruitment of ER? and transcriptional coregulators to ER? target gene promoters.

SUBMITTER: Duplessis TT 

PROVIDER: S-EPMC3100622 | biostudies-literature | 2011 Jun

REPOSITORIES: biostudies-literature

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Phosphorylation of Estrogen Receptor α at serine 118 directs recruitment of promoter complexes and gene-specific transcription.

Duplessis Tamika T TT   Williams Christopher C CC   Hill Steven M SM   Rowan Brian G BG  

Endocrinology 20110419 6


Phosphorylation of estrogen receptor α (ERα) is important for receptor function, although the role of specific ERα phosphorylation sites in ERα-mediated transcription remains to be fully evaluated. Transcriptional activation by ERα involves dynamic, coordinate interactions with coregulators at promoter enhancer elements to effect gene expression. To determine whether ERα phosphorylation affects recruitment of unique protein complexes at gene-specific promoters, changes in ERα Ser118 phosphorylat  ...[more]

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