Evidence for direct estrogen regulation of the human gonadotropin-releasing hormone gene

Sally Radovick, C. M. Ticknor, Y. Nakayama, A. C. Notides, A. Rahman, B. D. Weintraub, G. B. Cutler, Fredric Wondisford

Research output: Contribution to journalArticle

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Abstract

This study is an attempt to determine whether estrogen could directly regulate human gonadotropin-releasing hormone (GnRH) gene expression. Human GnRH expression vectors were constructed by fusing various 5' flanking regions of the human GnRH gene upstream of the luciferase reporter gene (LUC) or the thymidine kinase promoter linked to the chloramphenicol acetyltransferase reporter gene (CAT). These constructs were transiently transfected into a human choriocarcinoma cell line (JEG-3) and LUC or CAT activity was measured after either no treatment or treatment with various concentrations of estradiol. A stimulatory estrogen response element (ERE) was localized to a 32-bp region between -547 and -516 bp. To determine whether estrogen receptor bound to this region of the gene, we performed DNase I footprinting using purified calf uterine estrogen receptor. DNase I footprinting demonstrates a strong footprint between -567 and -514 bp of the human GnRH gene. In addition, an avidin-biotin complex DNA-binding assay demonstrated that a biotinylated DNA fragment containing -541 to -517 bp of the human GnRH gene bound 35S-labeled estrogen receptor as well as a biotinylated DNA fragment containing the xenopus vitellogenin ERE. On the other hand, the negative control biotinylated DNA fragment derived from adenovirus 5 bound insignificant amounts of 35S-labeled estrogen receptor. Both the GnRH ERE and vitellogenin ERE bound 35S-labeled estrogen receptor with high affinity (~ 1 nM). These data indicate that the human GnRH gene contains an ERE sufficient to mediate a stimulatory response to estrogen in heterologous cells. Based upon these data we hypothesize that the human GnRH gene might also be directly regulated by estrogen in the hypothalamus, and that this regulation may explain the GnRH hypersecretion observed at the time of the preovulatory luteinizing hormone (LH) surge.

Original languageEnglish (US)
Pages (from-to)1649-1655
Number of pages7
JournalJournal of Clinical Investigation
Volume88
Issue number5
DOIs
StatePublished - Jan 1 1991

Fingerprint

Gonadotropin-Releasing Hormone
Estrogens
Response Elements
Estrogen Receptors
Genes
Vitellogenins
Deoxyribonuclease I
DNA
Reporter Genes
Choriocarcinoma
Chloramphenicol O-Acetyltransferase
Thymidine Kinase
Avidin
5' Flanking Region
Biotin
Luteinizing Hormone
Xenopus
Luciferases
Adenoviridae
Hypothalamus

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Keywords

  • Estrogen
  • Gene regulation
  • GnRH
  • Hypothalamus

Cite this

Radovick, Sally ; Ticknor, C. M. ; Nakayama, Y. ; Notides, A. C. ; Rahman, A. ; Weintraub, B. D. ; Cutler, G. B. ; Wondisford, Fredric. / Evidence for direct estrogen regulation of the human gonadotropin-releasing hormone gene. In: Journal of Clinical Investigation. 1991 ; Vol. 88, No. 5. pp. 1649-1655.
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abstract = "This study is an attempt to determine whether estrogen could directly regulate human gonadotropin-releasing hormone (GnRH) gene expression. Human GnRH expression vectors were constructed by fusing various 5' flanking regions of the human GnRH gene upstream of the luciferase reporter gene (LUC) or the thymidine kinase promoter linked to the chloramphenicol acetyltransferase reporter gene (CAT). These constructs were transiently transfected into a human choriocarcinoma cell line (JEG-3) and LUC or CAT activity was measured after either no treatment or treatment with various concentrations of estradiol. A stimulatory estrogen response element (ERE) was localized to a 32-bp region between -547 and -516 bp. To determine whether estrogen receptor bound to this region of the gene, we performed DNase I footprinting using purified calf uterine estrogen receptor. DNase I footprinting demonstrates a strong footprint between -567 and -514 bp of the human GnRH gene. In addition, an avidin-biotin complex DNA-binding assay demonstrated that a biotinylated DNA fragment containing -541 to -517 bp of the human GnRH gene bound 35S-labeled estrogen receptor as well as a biotinylated DNA fragment containing the xenopus vitellogenin ERE. On the other hand, the negative control biotinylated DNA fragment derived from adenovirus 5 bound insignificant amounts of 35S-labeled estrogen receptor. Both the GnRH ERE and vitellogenin ERE bound 35S-labeled estrogen receptor with high affinity (~ 1 nM). These data indicate that the human GnRH gene contains an ERE sufficient to mediate a stimulatory response to estrogen in heterologous cells. Based upon these data we hypothesize that the human GnRH gene might also be directly regulated by estrogen in the hypothalamus, and that this regulation may explain the GnRH hypersecretion observed at the time of the preovulatory luteinizing hormone (LH) surge.",
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Radovick, S, Ticknor, CM, Nakayama, Y, Notides, AC, Rahman, A, Weintraub, BD, Cutler, GB & Wondisford, F 1991, 'Evidence for direct estrogen regulation of the human gonadotropin-releasing hormone gene', Journal of Clinical Investigation, vol. 88, no. 5, pp. 1649-1655. https://doi.org/10.1172/JCI115479

Evidence for direct estrogen regulation of the human gonadotropin-releasing hormone gene. / Radovick, Sally; Ticknor, C. M.; Nakayama, Y.; Notides, A. C.; Rahman, A.; Weintraub, B. D.; Cutler, G. B.; Wondisford, Fredric.

In: Journal of Clinical Investigation, Vol. 88, No. 5, 01.01.1991, p. 1649-1655.

Research output: Contribution to journalArticle

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AU - Radovick, Sally

AU - Ticknor, C. M.

AU - Nakayama, Y.

AU - Notides, A. C.

AU - Rahman, A.

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