دورية أكاديمية

Selective recruitment of p160 coactivators on glucocorticoid-regulated promoters in Schwann cells.

التفاصيل البيبلوغرافية
العنوان: Selective recruitment of p160 coactivators on glucocorticoid-regulated promoters in Schwann cells.
المؤلفون: Grenier, Julien, Trousson, Amalia, Chauchereau, Anne, Amazit, Larbi, Lamirand, Audrey, Leclerc, Philippe, Guiochon-Mantel, Anne, Schumacher, Michael, Massaad, Charbel
المساهمون: Stéroïdes et système nerveux : physiopathologie moléculaire et clinique, Institut National de la Santé et de la Recherche Médicale (INSERM), Faculté de Médecine Paris-Sud, Université Paris-Sud - Paris 11 (UP11), Génétique oncologique (GO - UMR 8125), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Centre National de la Recherche Scientifique (CNRS), Récepteurs stéroïdiens : physiopathologie endocrinienne et métabolique, Université Paris-Sud - Paris 11 (UP11)-IFR93-Institut National de la Santé et de la Recherche Médicale (INSERM), IFR de Bicêtre, Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de génétique moléculaire, pharmacogénétique et hormonologie, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Bicêtre AP-HP, Le Kremlin-Bicêtre, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
المصدر: ISSN: 0888-8809 ; Molecular Endocrinology -Baltimore- ; https://hal.science/hal-01939763Test ; Molecular Endocrinology -Baltimore-, 2004, 18 (12), pp.2866-79. ⟨10.1210/me.2004-0241⟩.
بيانات النشر: HAL CCSD
Endocrine Society
سنة النشر: 2004
مصطلحات موضوعية: [SDV.CAN]Life Sciences [q-bio]/Cancer, [SDV.BBM.MN]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular Networks [q-bio.MN], [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology
الوصف: International audience ; In the nervous system, glucocorticoid hormones play a major role during development and throughout life. We studied the mechanisms of action of the glucocorticoid receptor (GR) and its interactions with p160 coactivator family members [steroid receptor coactivator (SRC)-1 (a and e), SRC-2 and SRC-3] in mouse Schwann cells (MSC80). We found that the three p160s were expressed in MSC80 cells. We have shown by functional overexpression and RNA interference experiments that the recruitment of these coactivators by the GR is promoter dependent. A minimal promoter containing two glucocorticoid response elements, (GRE)2-TATA, recruits SRC-1 (a and e) and SRC-3, whereas SRC-2 is excluded. Within the context of the more complex mouse mammary tumor virus promoter, GR recruits SRC-1e and SRC-2, whereas SRC-1a and SRC-3 are not implicated. Furthermore, we have identified cytosolic aspartate aminotransferase as a GR target gene in MSC80 cells by microarray experiments. The GR recruits exclusively SRC-1e in the context of the cytosolic aspartate aminotransferase promoter. Because SRC-1 is the omnipresent coactivator of GR, we further investigated the interactions between GR and this coactivator in Schwann cells by reporter assays and immunocytochemistry experiments with deleted forms of SRC-1. We have shown that SRC-1 unexpectedly interacts with GR via its two nuclear receptor binding domains, thus providing a novel mechanism of GR signaling within the nervous system.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/15331759; hal-01939763; https://hal.science/hal-01939763Test; PUBMED: 15331759
DOI: 10.1210/me.2004-0241
الإتاحة: https://doi.org/10.1210/me.2004-0241Test
https://hal.science/hal-01939763Test
رقم الانضمام: edsbas.E2B63E7
قاعدة البيانات: BASE