Literature DB >> 2856398

Tissue-specific regulation of pituitary proopiomelanocortin gene transcription by corticotropin-releasing hormone, 3',5'-cyclic adenosine monophosphate, and glucocorticoids.

J P Gagner1, J Drouin.   

Abstract

The release of pituitary hormones derived from POMC is under multihormonal and tissue-specific control in the anterior and intermediate lobes of the pituitary where the same single-copy POMC gene is expressed. In order to assess the tissue-specificity of POMC regulation at the gene level, we have previously shown that glucocorticoids inhibit POMC gene transcription in the anterior but not in the intermediate pituitary. In the present work, we have investigated the role of corticotropin-releasing hormone (CRH) and cAMP in the differential regulation of anterior and intermediate pituitary POMC gene transcription. Using pituitary cells in primary culture and nuclear run-on transcription assays, we found that cAMP increases POMC gene transcription rate to the same extent in both anterior and intermediate pituitary cells while CRH only increases anterior pituitary POMC transcription rate. This observation contrasts with the stimulation of ACTH and alpha MSH release from anterior and intermediate pituitary cells, respectively, by both CRH and cAMP. In the anterior pituitary, both CRH and cAMP stimulated as well as basal POMC transcription rates are inhibited by glucocorticoids. In the anterior pituitary, both CRH stimulation and glucocorticoid inhibition of POMC transcription are rapid and do not require de novo protein synthesis. Thus, we report that transcription of the POMC gene is differentially regulated by CRH, cAMP, and glucocorticoids in anterior and intermediate pituitary tissues, in much the same way as the control of POMC processing and release.

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Year:  1987        PMID: 2856398     DOI: 10.1210/mend-1-10-677

Source DB:  PubMed          Journal:  Mol Endocrinol        ISSN: 0888-8809


  12 in total

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2.  Antagonism between Nur77 and glucocorticoid receptor for control of transcription.

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3.  Novel dimeric Nur77 signaling mechanism in endocrine and lymphoid cells.

Authors:  A Philips; S Lesage; R Gingras; M H Maira; Y Gauthier; P Hugo; J Drouin
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Review 4.  The Jeremiah Metzger Lecture. From POMC to functional diversity of neural peptides: the key importance of convertases.

Authors:  M Chretien; L Gasper; S Benjannet; M Mbikay; C Lazure; N G Seidah
Journal:  Trans Am Clin Climatol Assoc       Date:  1991

5.  Role of Brg1 and HDAC2 in GR trans-repression of the pituitary POMC gene and misexpression in Cushing disease.

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6.  Pituitary-specific expression and glucocorticoid regulation of a proopiomelanocortin fusion gene in transgenic mice.

Authors:  Y Tremblay; I Tretjakoff; A Peterson; T Antakly; C X Zhang; J Drouin
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7.  Interleukin-6 regulation of kappa opioid receptor gene expression in primary sertoli cells.

Authors:  S Jenab; P L Morris
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Review 8.  POMC: The Physiological Power of Hormone Processing.

Authors:  Erika Harno; Thanuja Gali Ramamoorthy; Anthony P Coll; Anne White
Journal:  Physiol Rev       Date:  2018-10-01       Impact factor: 37.312

9.  Glucocorticoid receptor binding to a specific DNA sequence is required for hormone-dependent repression of pro-opiomelanocortin gene transcription.

Authors:  J Drouin; M A Trifiro; R K Plante; M Nemer; P Eriksson; O Wrange
Journal:  Mol Cell Biol       Date:  1989-12       Impact factor: 4.272

10.  TIF1beta/KAP-1 is a coactivator of the orphan nuclear receptor NGFI-B/Nur77.

Authors:  Juliette Rambaud; Julien Desroches; Aurélio Balsalobre; Jacques Drouin
Journal:  J Biol Chem       Date:  2009-03-25       Impact factor: 5.157

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