FK506-binding protein 52 is essential to uterine reproductive physiology controlled by the progesterone receptor A isoform

Mol Endocrinol. 2006 Nov;20(11):2682-94. doi: 10.1210/me.2006-0024. Epub 2006 Jul 27.

Abstract

FK506-binding protein 52 (FKBP52) is a tetratricopeptide repeat protein that associates with steroid receptors in complexes containing heat shock protein 90. To investigate the role of FKBP52 in steroid-regulated physiology, we generated FKBP52-deficient mice. FKBP52 (-/-) females are sterile due to a complete failure of implantation, a process that requires estrogen (ER) and progesterone receptors (PR). Because the uterus expresses two forms of PR, PR-A and PR-B, we investigated all three receptors as potential targets of FKBP52 action. FKBP52 (-/-) uteri showed a normal growth response to estradiol, and unaltered expression of genes controlled by ER and PR-B. In contrast, FKBP52 (-/-) uteri were neither able to express two PR-A-regulated genes, nor undergo decidualization in response to progesterone, suggesting that FKBP52 specifically regulates PR-A at this organ. Analysis of uterine PR heterocomplexes showed preferential association of FKBP52 with PR-A compared with PR-B. Loss of FKBP52 neither disrupted the PR-A/heat shock protein 90 interaction, nor impaired uterine PR-A hormone-binding function, demonstrating the essential role of FKBP52 in PR-A action to be downstream of the hormone-binding event. Transcription studies in +/+ and -/- mouse embryonic fibroblast cells showed a near-complete loss of PR-A activity at mouse mammary tumor virus and synthetic progesterone response element promoters, although partial reductions of ER and PR-B were also observed. Partial disruptions of ovulation and mammary development were also found in FKBP52 (-/-) females. Taken as a whole, our results show FKBP52 to be an essential regulator of PR-A action in the uterus, while being a nonessential but contributory regulator of steroid receptors in the mammary and ovary. These data may now provide the basis for selective targeting of steroid-regulated physiology through tetratricopeptide repeat proteins.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Embryo Implantation / genetics
  • Embryo, Mammalian / cytology
  • Female
  • Gene Deletion
  • Infertility, Female / genetics
  • Male
  • Mammary Glands, Animal / growth & development
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Ovulation / genetics
  • Progesterone / metabolism
  • Protein Binding
  • Protein Isoforms / physiology
  • Receptors, Estrogen / metabolism
  • Receptors, Progesterone / metabolism
  • Receptors, Progesterone / physiology*
  • Reproduction / physiology*
  • Tacrolimus Binding Proteins / genetics
  • Tacrolimus Binding Proteins / physiology*
  • Transcriptional Activation
  • Uterus / physiology*

Substances

  • Protein Isoforms
  • Receptors, Estrogen
  • Receptors, Progesterone
  • progesterone receptor A
  • Progesterone
  • Tacrolimus Binding Proteins
  • tacrolimus binding protein 4