Literature DB >> 7754520

Evolutionary history of the ligand-gated ion-channel superfamily of receptors.

M O Ortells1, G G Lunt.   

Abstract

The fast-acting ligand-gated ion channels (LGICs) constitute a group that encompasses nicotinic ACh, 5-HT3, GABAA and glycine receptors. Undoubtedly, they all share a common evolutionary ancestor, and the group can therefore be considered to be a gene superfamily. Because the members of the superfamily are all receptors, it is reasonable to suppose that their common ancestor must also have been some type of receptor, and because the receptors are made of similar subunits, the ancestor was probably homo-oligomeric. Although we failed to find a group of proteins that are related evolutionarily to this superfamily, the analysis of the evolutionary relationships within the superfamily is possible and can give rise to information about the evolution of the structure and function of present-day receptors and indeed of the nervous system itself.

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Year:  1995        PMID: 7754520     DOI: 10.1016/0166-2236(95)93887-4

Source DB:  PubMed          Journal:  Trends Neurosci        ISSN: 0166-2236            Impact factor:   13.837


  128 in total

1.  LGICdb: the ligand-gated ion channel database.

Authors:  N Le Novère; J P Changeux
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

Review 2.  General anaesthetic actions on ligand-gated ion channels.

Authors:  M D Krasowski; N L Harrison
Journal:  Cell Mol Life Sci       Date:  1999-08-15       Impact factor: 9.261

3.  Neuronal alpha-bungarotoxin receptors are alpha7 subunit homomers.

Authors:  R C Drisdel; W N Green
Journal:  J Neurosci       Date:  2000-01-01       Impact factor: 6.167

4.  Structural determinants of fast desensitization and desensitization-deactivation coupling in GABAa receptors.

Authors:  M T Bianchi; K F Haas; R L Macdonald
Journal:  J Neurosci       Date:  2001-02-15       Impact factor: 6.167

Review 5.  Mechanisms of GABAA receptor assembly and trafficking: implications for the modulation of inhibitory neurotransmission.

Authors:  Josef T Kittler; Kristina McAinsh; Stephen J Moss
Journal:  Mol Neurobiol       Date:  2002 Oct-Dec       Impact factor: 5.590

6.  Caenorhabditis elegans levamisole resistance genes lev-1, unc-29, and unc-38 encode functional nicotinic acetylcholine receptor subunits.

Authors:  J T Fleming; M D Squire; T M Barnes; C Tornoe; K Matsuda; J Ahnn; A Fire; J E Sulston; E A Barnard; D B Sattelle; J A Lewis
Journal:  J Neurosci       Date:  1997-08-01       Impact factor: 6.167

7.  Neuronal nicotinic threonine-for-leucine 247 alpha7 mutant receptors show different gating kinetics when activated by acetylcholine or by the noncompetitive agonist 5-hydroxytryptamine.

Authors:  E Palma; L Maggi; F Eusebi; R Miledi
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-02       Impact factor: 11.205

8.  N,N-disubstituted piperazines: synthesis and affinities at alpha4beta2(*) and alpha7(*) neuronal nicotinic acetylcholine receptors.

Authors:  Jianhong Chen; Seth Norrholm; Linda P Dwoskin; Peter A Crooks; Donglu Bai
Journal:  Bioorg Med Chem Lett       Date:  2003-01-06       Impact factor: 2.823

9.  Conformation-dependent hydrophobic photolabeling of the nicotinic receptor: electrophysiology-coordinated photochemistry and mass spectrometry.

Authors:  John F Leite; Michael P Blanton; Mona Shahgholi; Dennis A Dougherty; Henry A Lester
Journal:  Proc Natl Acad Sci U S A       Date:  2003-10-20       Impact factor: 11.205

10.  Evidence for a diverse Cys-loop ligand-gated ion channel superfamily in early bilateria.

Authors:  Joseph A Dent
Journal:  J Mol Evol       Date:  2006-04-01       Impact factor: 2.395

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