Academic Journal

TRPM3-Induced Gene Transcription Is under Epigenetic Control

التفاصيل البيبلوغرافية
العنوان: TRPM3-Induced Gene Transcription Is under Epigenetic Control
المؤلفون: Gerald Thiel, Oliver G. Rössler
المصدر: Pharmaceuticals, Vol 15, Iss 7, p 846 (2022)
بيانات النشر: MDPI AG, 2022.
سنة النشر: 2022
المجموعة: LCC:Medicine
LCC:Pharmacy and materia medica
مصطلحات موضوعية: AP-1, A485, BET proteins, bromodomain, Elk-1, interleukin-8, Medicine, Pharmacy and materia medica, RS1-441
الوصف: Transient receptor potential M3 (TRPM3) cation channels regulate numerous biological functions, including gene transcription. Stimulation of TRPM3 channels with pregnenolone sulfate activates stimulus-responsive transcription factors, which bind to short cognate sequences in the promoters of their target genes. In addition, coregulator proteins are involved that convert the chromatin into a configuration that is permissive for gene transcription. In this study, we determined whether TRPM3-induced gene transcription requires coactivators that change the acetylation pattern of histones. We used compound A485, a specific inhibitor of the histone acetyltransferases CBP and p300. In addition, the role of bromodomain proteins that bind to acetylated lysine residues of histones was analyzed. We used JQ1, an inhibitor of bromodomain and extra terminal domain (BET) family proteins. The results show that both compounds attenuated the activation of AP-1 and CREB-regulated gene transcription following stimulation of TRPM3 channels. Inhibition of CBP/p300 and BET proteins additionally reduced the transcriptional activation potential of the transcription factors c-Fos and Elk-1. Transcriptional upregulation of the interleukin-8 gene was attenuated by A485 and JQ1, indicating that proinflammatory cytokine expression is controlled by CBP/p300 and bromodomain proteins. We conclude that TRPM3-induced signaling involves transcriptional coactivators and acetyl-lysine-bound bromodomain proteins for activating gene transcription.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1424-8247
Relation: https://www.mdpi.com/1424-8247/15/7/846; https://doaj.org/toc/1424-8247
DOI: 10.3390/ph15070846
URL الوصول: https://doaj.org/article/11b73d7125f44024a05cff7f6ff6765b
رقم الانضمام: edsdoj.11b73d7125f44024a05cff7f6ff6765b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14248247
DOI:10.3390/ph15070846