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Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina

A new non-alpha (n alpha) member of the nicotinic acetylcholine receptor (nAChR) gene family designated GFn alpha-2 has been identified in goldfish retina by cDNA cloning. This cDNA clone encodes a protein with structural features common to all nAChR subunits sequenced to date; however, unlike all k...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2115429/
https://www.ncbi.nlm.nih.gov/pubmed/2465296
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collection PubMed
description A new non-alpha (n alpha) member of the nicotinic acetylcholine receptor (nAChR) gene family designated GFn alpha-2 has been identified in goldfish retina by cDNA cloning. This cDNA clone encodes a protein with structural features common to all nAChR subunits sequenced to date; however, unlike all known alpha-subunits of the receptor, it lacks the cysteine residues believed to be involved in acetylcholine binding. Northern blot analysis shows multiple transcripts hybridizing to the GFn alpha-2 cDNA in goldfish retina but undetectable levels of hybridizable RNA in brain, muscle, or liver. S1 nuclease protection experiments indicate that multiple mRNAs are expressed in retina with regions identical or very similar to the GFn alpha-2 sequence. In situ hybridization shows that the gene encoding GFn alpha-2 is expressed predominantly in the ganglion cell layer of the retina.
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spelling pubmed-21154292008-05-01 Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina J Cell Biol Articles A new non-alpha (n alpha) member of the nicotinic acetylcholine receptor (nAChR) gene family designated GFn alpha-2 has been identified in goldfish retina by cDNA cloning. This cDNA clone encodes a protein with structural features common to all nAChR subunits sequenced to date; however, unlike all known alpha-subunits of the receptor, it lacks the cysteine residues believed to be involved in acetylcholine binding. Northern blot analysis shows multiple transcripts hybridizing to the GFn alpha-2 cDNA in goldfish retina but undetectable levels of hybridizable RNA in brain, muscle, or liver. S1 nuclease protection experiments indicate that multiple mRNAs are expressed in retina with regions identical or very similar to the GFn alpha-2 sequence. In situ hybridization shows that the gene encoding GFn alpha-2 is expressed predominantly in the ganglion cell layer of the retina. The Rockefeller University Press 1989-02-01 /pmc/articles/PMC2115429/ /pubmed/2465296 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina
title Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina
title_full Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina
title_fullStr Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina
title_full_unstemmed Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina
title_short Identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina
title_sort identification of a novel nicotinic acetylcholine receptor structural subunit expressed in goldfish retina
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2115429/
https://www.ncbi.nlm.nih.gov/pubmed/2465296