Please use this identifier to cite or link to this item: doi:10.22028/D291-41957
Title: Stimulus-Induced Activation of the Glycoprotein Hormone α-Subunit Promoter in Human Placental Choriocarcinoma Cells: Major Role of a tandem cAMP Response Element
Author(s): Bürvenich, Lars
Rössler, Oliver G.
Thiel, Gerald
Language: English
Title: Current Issues in Molecular Biology
Volume: 46
Issue: 4
Pages: 3218-3235
Publisher/Platform: MDPI
Year of Publication: 2024
Free key words: CREB
designer receptor
forskolin
MEKK1
MKK6
PKA
glycoprotein hormone α-subunit
DDC notations: 610 Medicine and health
Publikation type: Journal Article
Abstract: The glycoprotein hormones LH, FSH, TSH and chorionic gonadotropin consist of a common α-subunit and a hormone-specific β-subunit. The α-subunit is expressed in the pituitary and the placental cells, and its expression is regulated by extracellular signal molecules. Much is known about the regulation of the α-subunit gene in the pituitary, but few studies have addressed the regulation of this gene in trophoblasts. The aim of this study was to characterize the molecular mechanism of stimulus-induced α-subunit gene transcription in JEG-3 cells, a cellular model for human trophoblasts, using chromatin-embedded reporter genes under the control of the α-subunit promoter. The results show that increasing the concentration of the second messengers cAMP or Ca2+, or expressing the catalytic subunit of cAMP-dependent protein kinase in the nucleus activated the α-subunit promoter. Similarly, the stimulation of p38 protein kinase activated the α-subunit promoter, linking α-subunit expression to stress response. The stimulation of a Gαq-coupled designer receptor activated the α-subunit promoter, involving the transcription factor CREB, linking α-subunit expression to hormonal stimulation and an increase in intracellular Ca2+. Deletion mutagenesis underscores the importance of a tandem cAMP response element within the glycoprotein hormone α-subunit promoter, which acts as a point of convergence for a multiple signaling pathway.
DOI of the first publication: 10.3390/cimb46040202
URL of the first publication: https://doi.org/10.3390/cimb46040202
Link to this record: urn:nbn:de:bsz:291--ds-419576
hdl:20.500.11880/37547
http://dx.doi.org/10.22028/D291-41957
ISSN: 1467-3045
Date of registration: 29-Apr-2024
Faculty: M - Medizinische Fakultät
Department: M - Medizinische Biochemie und Molekularbiologie
Professorship: M - Prof. Dr. Gerald Thiel
Collections:SciDok - Der Wissenschaftsserver der Universität des Saarlandes

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