Literature DB >> 10407191

Two related G protein-coupled receptors: the distribution of GPR7 in rat brain and the absence of GPR8 in rodents.

D K Lee1, T Nguyen, C A Porter, R Cheng, S R George, B F O'Dowd.   

Abstract

GPR7 and GPR8, orphan G protein-coupled receptor (GPCR) genes, expressed in the brain and periphery share highest sequence identity to each other and significant similarity with opioid and somatostatin receptors. To further our knowledge of GPR7's physiological function, we performed in situ hybridization analyses of rat brain to reveal specific patterns of expression in the brain. GPR7 mRNA was found to be discretely localized in areas of the amygdala, hippocampus, hypothalamus and cortex. We previously reported that GPR7 was highly conserved in both human and rodent orthologs while GPR8 was not found in the rodent [9]. We speculated that GPR8 originated after the divergence of the human and rodent. Using primers designed from human GPR8, we isolated lemur GPR8 and subsequently aligned human, monkey, and lemur GPR8 orthologs to design primers recognizing highly conserved regions of GPR8. Using these primers, orthologs of GPR7 and GPR8 were isolated by the PCR from rabbit, tree shrew, and flying lemur, as well as GPR7 in the rat. Subsequent analysis of the clones obtained demonstrated that both GPR7 and GPR8 sequences were highly conserved amongst the species studied, but a rodent GPR8 was not isolated. The absence of a GPR8 gene in the rodent suggests that GPR8 originated from gene duplication of GPR7 after the rodent line diverged from the rabbit, tree shrew, flying lemur, lemur, monkey and human lines. In addition, the taxonomic distribution of GPR8 is consistent with molecular studies grouping rabbits with primates, tree shrews and flying lemurs rather than with rodents. Copyright 1999 Elsevier Science B.V.

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Year:  1999        PMID: 10407191     DOI: 10.1016/s0169-328x(99)00171-0

Source DB:  PubMed          Journal:  Brain Res Mol Brain Res        ISSN: 0169-328X


  21 in total

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Review 2.  Analgesic neuropeptide W suppresses seizures in the brain revealed by rational repositioning and peptide engineering.

Authors:  Brad R Green; Misty Smith; Karen L White; H Steve White; Grzegorz Bulaj
Journal:  ACS Chem Neurosci       Date:  2010-11-18       Impact factor: 4.418

3.  Neuropeptide W-Induced Hypophagia is Mediated Through Corticotropin-Releasing Hormone-Containing Neurons.

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Journal:  J Mol Neurosci       Date:  2015-02-19       Impact factor: 3.444

4.  Neuropeptide B-deficient mice demonstrate hyperalgesia in response to inflammatory pain.

Authors:  Michele A Kelly; Carsten T Beuckmann; S Clay Williams; Christopher M Sinton; Toshiyuki Motoike; James A Richardson; Robert E Hammer; Mary G Garry; Masashi Yanagisawa
Journal:  Proc Natl Acad Sci U S A       Date:  2005-06-27       Impact factor: 11.205

5.  Neuropeptide W as a stress mediator in the hypothalamus.

Authors:  Michio Niimi; Koji Murao
Journal:  Endocrine       Date:  2005-06       Impact factor: 3.633

6.  Design, synthesis and SAR analysis of novel potent and selective small molecule antagonists of NPBWR1 (GPR7).

Authors:  Mariangela Urbano; Miguel Guerrero; Jian Zhao; Subash Velaparthi; S Adrian Saldanha; Peter Chase; Zhiwei Wang; Olivier Civelli; Peter Hodder; Marie-Therese Schaeffer; Steven Brown; Hugh Rosen; Edward Roberts
Journal:  Bioorg Med Chem Lett       Date:  2012-10-02       Impact factor: 2.823

7.  SAR analysis of novel non-peptidic NPBWR1 (GPR7) antagonists.

Authors:  Miguel Guerrero; Mariangela Urbano; Marie-Therese Schaeffer; Steven Brown; Hugh Rosen; Edward Roberts
Journal:  Bioorg Med Chem Lett       Date:  2012-12-20       Impact factor: 2.823

8.  Mesolimbic neuropeptide W coordinates stress responses under novel environments.

Authors:  Toshiyuki Motoike; Jeffrey M Long; Hirokazu Tanaka; Christopher M Sinton; Amber Skach; S Clay Williams; Robert E Hammer; Takeshi Sakurai; Masashi Yanagisawa
Journal:  Proc Natl Acad Sci U S A       Date:  2016-05-02       Impact factor: 11.205

9.  Neuropeptide W increases mean arterial pressure as a result of behavioral arousal.

Authors:  Alicia T Pate; Gina L C Yosten; Willis K Samson
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2013-08-07       Impact factor: 3.619

10.  Targeted disruption of GPR7, the endogenous receptor for neuropeptides B and W, leads to metabolic defects and adult-onset obesity.

Authors:  Makoto Ishii; Hong Fei; Jeffrey M Friedman
Journal:  Proc Natl Acad Sci U S A       Date:  2003-08-18       Impact factor: 11.205

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