Estrogen Regulation of Gene Expression and Analysis of the Role of the Coregulator, Repressor of Estrogen Receptor Activity (Rea)
Park, Seongeun
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https://hdl.handle.net/2142/87229
Description
Title
Estrogen Regulation of Gene Expression and Analysis of the Role of the Coregulator, Repressor of Estrogen Receptor Activity (Rea)
Author(s)
Park, Seongeun
Issue Date
2004
Doctoral Committee Chair(s)
Katzenellenbogen, Benita S.
Department of Study
Molecular and Integrative Physiology
Discipline
Molecular and Integrative Physiology
Degree Granting Institution
University of Illinois at Urbana-Champaign
Degree Name
Ph.D.
Degree Level
Dissertation
Keyword(s)
Biology, Molecular
Language
eng
Abstract
To elucidate the functional activities of REA in diverse estrogen target tissues in vivo, I have used targeted disruption to ablate the REA gene in mice. Genotyping revealed that homozygous animals are not viable, suggesting a crucial role for REA in early development. The viability of heterozygous animals is similar to that of wild type, and female heterozygous animals have an increased body weight relative to age-matched wild-type animals beginning after puberty. Studies in immature heterozygous animals revealed a greater uterine weight gain in response to estradiol (E2) and a greater stimulation of E2 up-regulated genes and a loss of down regulation in genes normally suppressed by E2 in the uterus. Analysis of the histology of the uterus and mammary gland in REA wild type and heterozygous mice revealed gene dosage developmental effects of REA and changes in E2-responsiveness. Studies using mouse embryo fibroblasts (MEFs) revealed that REA heterozygous MEFs displayed a greater transcriptional response to E2. These studies demonstrate that REA is a significant modulator of estrogen responsiveness in vivo.
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