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Calcineurin controls gene transcription following stimulation of a Gαq-coupled designer receptor
Abstract
Stimulation of Gaq-coupled receptors triggers the activation of gene transcription via a rise of intracellular Ca 2+ . To investigate the role of the Ca 2+ /calmodulin-dependent phosphatase calcineurin in regulating transcription following Gαq-coupled receptor stimulation, we used a gain-of-function approach and expressed ΔCnA, a constitutively active mutant of calcineurin A. Furthermore, we expressed hM3Dq, a designer receptor that is specifically coupled to Gαq and can be activated by the pharmacological compound clozapine-N-oxide. Stimulation of hM3Dq or expression of ΔCnA induced transcription of a reporter gene controlled by the calcineurin substrate nuclear factor of activated T cells (NFAT), suggesting that calcineurin increased NFAT-regulated gene transcription. In contrast, expression of ΔCnA attenuated hM3Dq-induced biosynthesis of the transcription factors c-Fos and Egr-1 and reduced both c-Fos and Egr-1 promoter activities. A dissection of the c-Fos and Egr-1 promoters revealed that calcineurin inhibited serum response element-mediated transcription. In particular, the expression of ΔCnA reduced the transcriptional activity of the ternary complex factor Elk-1 following stimulation of hM3Dq receptors. Furthermore, ΔCnA reduced the transcriptional activity of the transcription factor CREB and thus attenuated transcription mediated by the cAMP response element. In summary, we show that calcineurin functions as a positive and negative modulator of gene transcription.
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“Previous studies have reported that c-Fos expression is negatively regulated by Ppp3ca [28].”
From Engineered Extracellular Vesicles Loaded with MiR-100-5p Antagonist Selectively Target the Lesioned Region to Promote Recovery from Brain Damage (2025) · cites this paper as [28]
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Cited by
Cheng, Y., Gai, C., Zhao, Y., Li, T., Song, Y., Luo, Q., Xin, D., Jiang, Z., Chen, W., Liu, D., et al. (2025) · Neuroscience Bulletin · doi:10.1007/s12264-025-01376-6 · Cited by 5
Metadata
- Authors
- Langfermann, D. S., Schmidt, T., Rössler, O. G., & Thiel, G.
- Venue
- Experimental Cell Research
- Publisher
- Elsevier BV
- Published
- 2019-10
- Volume
- 383
- Issue
- 2
- Pages
- 111553
- ISSN
- 0014-4827
- Cited by
- 11
- References
- 0
- Language
- en
- Funders
- Universität des Saarlandes
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