Subgroup of Reproductive Functions of Progesterone Mediated by Progesterone Receptor-B Isoform

Biserka Mulac‐Jeričević(Baylor College of Medicine), Robert A. Mullinax(Baylor College of Medicine), Francesco J. DeMayo(Baylor College of Medicine), John P. Lydon(Baylor College of Medicine), Orla M. Conneely(Baylor College of Medicine)
Science
September 8, 2000
Cited by 703

Abstract

Progesterone regulates reproductive function through two intracellular receptors, progesterone receptor-A (PR-A) and progesterone receptor-B (PR-B), that arise from a single gene and function as transcriptional regulators of progesterone-responsive genes. Although in vitro studies show that PR isoforms can display different transcriptional regulatory activities, their physiological significance is unknown. By selective ablation of PR-A in mice, we show that the PR-B isoform modulates a subset of reproductive functions of progesterone by regulation of a subset of progesterone-responsive target genes. Thus, PR-A and PR-B are functionally distinct mediators of progesterone action in vivo and should provide suitable targets for generation of tissue-selective progestins.


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