Literature DB >> 7721899

The cyclic AMP response element in the calcitonin/calcitonin gene-related peptide gene promoter is necessary but not sufficient for its activation by nerve growth factor.

A Watson1, D Latchman.   

Abstract

The gene encoding calcitonin gene-related peptide (CGRP) is inducible by nerve growth factor (NGF) in primary dorsal root ganglion neurons. By transfecting these primary neurons, we have defined a region of the CGRP promoter from -140 to -72 relative to the transcriptional start site which is essential for its inducibility by NGF as well as by cyclic AMP and which can confer these responses on a heterologous promoter. A cyclic AMP response element (CRE) within this region is essential for both these responses which are abolished by site-directed mutagenesis of this element. In contrast to the intact fragment the isolated CRE can confer responsiveness to cyclic AMP but not NGF on a heterologous promoter. The reasons for the different role of the CRE in the response of the CGRP promoter to cyclic AMP and NGF are discussed.

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Year:  1995        PMID: 7721899     DOI: 10.1074/jbc.270.16.9655

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  9 in total

1.  Distinct signalling pathways mediate the cAMP response element (CRE)-dependent activation of the calcitonin gene-related peptide gene promoter by cAMP and nerve growth factor.

Authors:  K Freeland; Y Z Liu; D S Latchman
Journal:  Biochem J       Date:  2000-01-15       Impact factor: 3.857

2.  Regulation of the neural-specific gene VGF in PC12 cells. Identification of transcription factors interacting with NGF-responsive elements.

Authors:  P V Luc; J A Wagner
Journal:  J Mol Neurosci       Date:  1997-06       Impact factor: 3.444

3.  Nerve growth factor antiserum induces axotomy-like changes in neuropeptide expression in intact sympathetic and sensory neurons.

Authors:  A M Shadiack; Y Sun; R E Zigmond
Journal:  J Neurosci       Date:  2001-01-15       Impact factor: 6.167

4.  A dominant-negative inhibitor of CREB reveals that it is a general mediator of stimulus-dependent transcription of c-fos.

Authors:  S Ahn; M Olive; S Aggarwal; D Krylov; D D Ginty; C Vinson
Journal:  Mol Cell Biol       Date:  1998-02       Impact factor: 4.272

Review 5.  Thyroid parafollicular cells. An accessible model for the study of serotonergic neurons.

Authors:  A F Russo; M S Clark; P L Durham
Journal:  Mol Neurobiol       Date:  1996-12       Impact factor: 5.590

6.  Acid activation of Trpv1 leads to an up-regulation of calcitonin gene-related peptide expression in dorsal root ganglion neurons via the CaMK-CREB cascade: a potential mechanism of inflammatory pain.

Authors:  Masako Nakanishi; Kenji Hata; Tomotaka Nagayama; Teruhisa Sakurai; Toshihiko Nishisho; Hiroki Wakabayashi; Toru Hiraga; Shigeyuki Ebisu; Toshiyuki Yoneda
Journal:  Mol Biol Cell       Date:  2010-06-09       Impact factor: 4.138

7.  Depolarization stimulates initial calcitonin gene-related peptide expression by embryonic sensory neurons in vitro.

Authors:  X Ai; S E MacPhedran; A K Hall
Journal:  J Neurosci       Date:  1998-11-15       Impact factor: 6.167

8.  Activation of extracellular signal-regulated protein kinase 5 is essential for cystitis- and nerve growth factor-induced calcitonin gene-related peptide expression in sensory neurons.

Authors:  Sharon J Yu; Chun-mei Xia; Jarren C Kay; Li-Ya Qiao
Journal:  Mol Pain       Date:  2012-06-28       Impact factor: 3.395

9.  Targeted mutation of EphB1 receptor prevents development of neuropathic hyperalgesia and physical dependence on morphine in mice.

Authors:  Yuan Han; Xue-Song Song; Wen-Tao Liu; Mark Henkemeyer; Xue-Jun Song
Journal:  Mol Pain       Date:  2008-11-21       Impact factor: 3.395

  9 in total

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