Literature DB >> 11273702

An expressed sequence tag (EST) data mining strategy succeeding in the discovery of new G-protein coupled receptors.

T Wittenberger1, H C Schaller, S Hellebrand.   

Abstract

We have developed a comprehensive expressed sequence tag database search method and used it for the identification of new members of the G-protein coupled receptor superfamily. Our approach proved to be especially useful for the detection of expressed sequence tag sequences that do not encode conserved parts of a protein, making it an ideal tool for the identification of members of divergent protein families or of protein parts without conserved domain structures in the expressed sequence tag database. At least 14 of the expressed sequence tags found with this strategy are promising candidates for new putative G-protein coupled receptors. Here, we describe the sequence and expression analysis of five new members of this receptor superfamily, namely GPR84, GPR86, GPR87, GPR90 and GPR91. We also studied the genomic structure and chromosomal localization of the respective genes applying in silico methods. A cluster of six closely related G-protein coupled receptors was found on the human chromosome 3q24-3q25. It consists of four orphan receptors (GPR86, GPR87, GPR91, and H963), the purinergic receptor P2Y1, and the uridine 5'-diphosphoglucose receptor KIAA0001. It seems likely that these receptors evolved from a common ancestor and therefore might have related ligands. In conclusion, we describe a data mining procedure that proved to be useful for the identification and first characterization of new genes and is well applicable for other gene families. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11273702     DOI: 10.1006/jmbi.2001.4520

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  47 in total

1.  A semiautomated approach to gene discovery through expressed sequence tag data mining: discovery of new human transporter genes.

Authors:  Shoshana Brown; Jean L Chang; Wolfgang Sadée; Patricia C Babbitt
Journal:  AAPS PharmSci       Date:  2003

2.  The G-protein-coupled receptor, GPR84, is important for eye development in Xenopus laevis.

Authors:  Kimberly J Perry; Verity R Johnson; Erica L Malloch; Lisa Fukui; Jason Wever; Alvin G Thomas; Paul W Hamilton; Jonathan J Henry
Journal:  Dev Dyn       Date:  2010-11       Impact factor: 3.780

3.  A point mutation in the UDP-glucose pyrophosphorylase gene results in decreases of UDP-glucose and inactivation of glycogen synthase.

Authors:  Juan-Carlos Higuita; Alberto Alape-Girón; Monica Thelestam; Abram Katz
Journal:  Biochem J       Date:  2003-03-15       Impact factor: 3.857

Review 4.  International Union of Pharmacology LVIII: update on the P2Y G protein-coupled nucleotide receptors: from molecular mechanisms and pathophysiology to therapy.

Authors:  Maria P Abbracchio; Geoffrey Burnstock; Jean-Marie Boeynaems; Eric A Barnard; José L Boyer; Charles Kennedy; Gillian E Knight; Marta Fumagalli; Christian Gachet; Kenneth A Jacobson; Gary A Weisman
Journal:  Pharmacol Rev       Date:  2006-09       Impact factor: 25.468

5.  The role of G-protein receptor 84 in experimental neuropathic pain.

Authors:  Louise S C Nicol; John M Dawes; Federica La Russa; Athanasios Didangelos; Anna K Clark; Clive Gentry; John Grist; John B Davies; Marzia Malcangio; Stephen B McMahon
Journal:  J Neurosci       Date:  2015-06-10       Impact factor: 6.167

6.  GPR124 regulates microtubule assembly, mitotic progression, and glioblastoma cell proliferation.

Authors:  Allison E Cherry; Juan Jesus Vicente; Cong Xu; Richard S Morrison; Shao-En Ong; Linda Wordeman; Nephi Stella
Journal:  Glia       Date:  2019-05-06       Impact factor: 7.452

7.  GPR171 is a hypothalamic G protein-coupled receptor for BigLEN, a neuropeptide involved in feeding.

Authors:  Ivone Gomes; Dipendra K Aryal; Jonathan H Wardman; Achla Gupta; Khatuna Gagnidze; Ramona M Rodriguiz; Sanjai Kumar; William C Wetsel; John E Pintar; Lloyd D Fricker; Lakshmi A Devi
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-16       Impact factor: 11.205

8.  Several classical mouse inbred strains, including DBA/2, NOD/Lt, FVB/N, and SJL/J, carry a putative loss-of-function allele of Gpr84.

Authors:  Carlos J Perez; Aline Dumas; Luc Vallières; Jean-Louis Guénet; Fernando Benavides
Journal:  J Hered       Date:  2013-04-24       Impact factor: 2.645

9.  GPR84 and TREM-1 Signaling Contribute to the Pathogenesis of Reflux Esophagitis.

Authors:  Heba Abdel-Aziz; Mathias Schneider; Winfried Neuhuber; Abdel Meguid Kassem; Saleem Khailah; Jürgen Müller; Hadeel Gamal Eldeen; Ahmed Khairy; Mohamed T Khayyal; Anastasiia Shcherbakova; Thomas Efferth; Gudrun Ulrich-Merzenich
Journal:  Mol Med       Date:  2016-05-09       Impact factor: 6.354

10.  Medium-chain fatty acid-sensing receptor, GPR84, is a proinflammatory receptor.

Authors:  Masakatsu Suzuki; Sachiko Takaishi; Miyuki Nagasaki; Yoshiko Onozawa; Ikue Iino; Hiroaki Maeda; Tomoaki Komai; Tomiichiro Oda
Journal:  J Biol Chem       Date:  2013-02-28       Impact factor: 5.157

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