Literature DB >> 23768074

Differential contribution of CBP:CREB binding to corticotropin-releasing hormone expression in the infant and adult hypothalamus.

Jessica L Cope1, Limor Regev1, Yuncai Chen2, Aniko Korosi1, Courtney J Rice1, Sung Ji1, George A Rogge3, Marcelo A Wood3, Tallie Z Baram1,2.   

Abstract

Corticotropin-releasing hormone (CRH) contributes crucially to the regulation of central and peripheral responses to stress. Because of the importance of a finely tuned stress system, CRH expression is tightly regulated in an organ- and brain region-specific manner. Thus, in the hypothalamus, CRH is constitutively expressed and this expression is further enhanced by stress; however, the underlying regulatory mechanisms are not fully understood. The regulatory region of the crh gene contains several elements, including the cyclic-AMP response element (CRE), and the role of the CRE interaction with the cyclic-AMP response element binding protein (CREB) in CRH expression has been a focus of intensive research. Notably, whereas thousands of genes contain a CRE, the functional regulation of gene expression by the CRE:CREB system is limited to ∼100 genes, and likely requires additional proteins. Here, we investigated the role of a member of the CREB complex, CREB binding protein (CBP), in basal and stress-induced CRH expression during development and in the adult. Using mice with a deficient CREB-binding site on CBP, we found that CBP:CREB interaction is necessary for normal basal CRH expression at the mRNA and protein level in the nine-day-old mouse, prior to onset of functional regulation of hypothalamic CRH expression by glucocorticoids. This interaction, which functions directly on crh or indirectly via regulation of other genes, was no longer required for maintenance of basal CRH expression levels in the adult. However, CBP:CREB binding contributed to stress-induced CRH expression in the adult, enabling rapid CRH synthesis in hypothalamus. CBP:CREB binding deficiency did not disrupt basal corticosterone plasma levels or acute stress-evoked corticosterone release. Because dysregulation of CRH expression occurs in stress-related disorders including depression, a full understanding of the complex regulation of this gene is important in both health and disease.

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Year:  2013        PMID: 23768074      PMCID: PMC3869921          DOI: 10.3109/10253890.2013.806907

Source DB:  PubMed          Journal:  Stress        ISSN: 1025-3890            Impact factor:   3.493


  109 in total

1.  Hypophysiotropic neurons of the paraventricular nucleus respond in spatially, temporally, and phenotypically differentiated manners to acute vs. repeated restraint stress: rapid publication.

Authors:  Victor Viau; Paul E Sawchenko
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2.  Solution structure of the KIX domain of CBP bound to the transactivation domain of CREB: a model for activator:coactivator interactions.

Authors:  I Radhakrishnan; G C Pérez-Alvarado; D Parker; H J Dyson; M R Montminy; P E Wright
Journal:  Cell       Date:  1997-12-12       Impact factor: 41.582

3.  The transcriptional coactivators p300 and CBP are histone acetyltransferases.

Authors:  V V Ogryzko; R L Schiltz; V Russanova; B H Howard; Y Nakatani
Journal:  Cell       Date:  1996-11-29       Impact factor: 41.582

4.  Evidence for a local site of action for glucocorticoids in inhibiting CRF and vasopressin expression in the paraventricular nucleus.

Authors:  P E Sawchenko
Journal:  Brain Res       Date:  1987-02-17       Impact factor: 3.252

5.  The effects of restraint or hypertonic saline stress on corticotrophin-releasing factor, arginine vasopressin, and proenkephalin A mRNAs in the CFY, Sprague-Dawley and Wistar strains of rat.

Authors:  M S Harbuz; D S Jessop; S L Lightman; H S Chowdrey
Journal:  Brain Res       Date:  1994-12-19       Impact factor: 3.252

Review 6.  HPA axis responsiveness to stress: implications for healthy aging.

Authors:  Greti Aguilera
Journal:  Exp Gerontol       Date:  2010-09-09       Impact factor: 4.032

Review 7.  Neurobiology of the stress response early in life: evolution of a concept and the role of corticotropin releasing hormone.

Authors:  K L Brunson; S Avishai-Eliner; C G Hatalski; T Z Baram
Journal:  Mol Psychiatry       Date:  2001-11       Impact factor: 15.992

8.  CREB-binding protein controls response to cocaine by acetylating histones at the fosB promoter in the mouse striatum.

Authors:  Amir A Levine; Zhonghui Guan; Angel Barco; Shiqin Xu; Eric R Kandel; James H Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  2005-12-27       Impact factor: 11.205

9.  Immune challenge and immobilization stress induce transcription of the gene encoding the CRF receptor in selective nuclei of the rat hypothalamus.

Authors:  S Rivest; N Laflamme; R E Nappi
Journal:  J Neurosci       Date:  1995-04       Impact factor: 6.167

10.  Sequence of stress-induced alterations in indices of synaptic and transcriptional activation in parvocellular neurosecretory neurons.

Authors:  K J Kovács; P E Sawchenko
Journal:  J Neurosci       Date:  1996-01       Impact factor: 6.167

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2.  The Effect of Acute and Repeated Stress on CRH-R1 and CRH-R2 mRNA Expression in Pituitaries of Wild Type and CRH Knock-Out Mice.

Authors:  Vera Klenerova; Richard Kvetnansky; Sixtus Hynie
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Review 3.  Corticotropin releasing factor in neuroplasticity.

Authors:  Limor Regev; Tallie Z Baram
Journal:  Front Neuroendocrinol       Date:  2013-10-19       Impact factor: 8.606

Review 4.  Examining the contribution of histone modification to sex differences in learning and memory.

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Journal:  Learn Mem       Date:  2019-08-15       Impact factor: 2.460

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