γ‐Aminobutyric AcidA Receptor Heterogeneity Is Increased by Alternative Splicing of a Novel β‐Subunit Gene Transcript

: DNA sequences encoding two variants of a novel γ‐aminobutyric acidA (GABAA) receptor β subunit were isolated from an embryonic chicken whole‐brain cDNA library and a chicken genomic library. The coding regions of these variants only differ from each other by the absence or presence of 12 bp in the...

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Veröffentlicht in:Journal of neurochemistry 1991-04, Vol.56 (4), p.1437-1440
Hauptverfasser: Bateson, Alan N., Lasham, Annette, Darlison, Mark G.
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container_end_page 1440
container_issue 4
container_start_page 1437
container_title Journal of neurochemistry
container_volume 56
creator Bateson, Alan N.
Lasham, Annette
Darlison, Mark G.
description : DNA sequences encoding two variants of a novel γ‐aminobutyric acidA (GABAA) receptor β subunit were isolated from an embryonic chicken whole‐brain cDNA library and a chicken genomic library. The coding regions of these variants only differ from each other by the absence or presence of 12 bp in the region that encodes the presumed intracellular loop between transmembrane domains M3 and M4; the encoded subunits have been named β4 and β4′, respectively. The predicted mature polypeptides are 72–77% identical to the previously characterized mammalian and chicken β1,β2, and β3 subunits. Analysis of the β4‐subunit gene reveals that the different transcripts encoding the two variants arise by the use of one of two 5′‐donor splice sites that are separated by 12 bp. This is the first demonstration of alternative splicing of a GABAA receptor subunit gene transcript and represents a further mechanism for the generation of GABAA receptor heterogeneity.
doi_str_mv 10.1111/j.1471-4159.1991.tb11443.x
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The coding regions of these variants only differ from each other by the absence or presence of 12 bp in the region that encodes the presumed intracellular loop between transmembrane domains M3 and M4; the encoded subunits have been named β4 and β4′, respectively. The predicted mature polypeptides are 72–77% identical to the previously characterized mammalian and chicken β1,β2, and β3 subunits. Analysis of the β4‐subunit gene reveals that the different transcripts encoding the two variants arise by the use of one of two 5′‐donor splice sites that are separated by 12 bp. This is the first demonstration of alternative splicing of a GABAA receptor subunit gene transcript and represents a further mechanism for the generation of GABAA receptor heterogeneity.</description><subject>Alternative splicing</subject><subject>Aminoacid receptors (glycine, glutamate, gaba)</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>cDNA and genomic DNA cloning</subject><subject>Cell receptors</subject><subject>Cell structures and functions</subject><subject>Chicken brain</subject><subject>Chickens</subject><subject>Cloning, Molecular</subject><subject>DNA</subject><subject>DNA, Recombinant</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Variation</subject><subject>Molecular and cellular biology</subject><subject>Molecular Sequence Data</subject><subject>Novel receptor β subunit</subject><subject>Receptor heterogeneity</subject><subject>Receptors, GABA-A - genetics</subject><subject>RNA Splicing</subject><subject>RNA, Messenger - genetics</subject><subject>Transcription, Genetic</subject><subject>γ‐Aminobutyric acidA receptor</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkU9u1DAUhy0EKkPhCEgWEuwS_G9sZ4WiEbSDqiLRsrZsz0vlUSYJsdM2YsMROAu9Rw_Rk5CoEfXmLb6ffk9-H0LvKMnp9D7ucyoUzQRdFzktCponR6kQPL99hlb_0XO0IoSxjBPBXqJXMe4JoVJIeoSOqBaaabJCv-7vHn7_KQ-had2Qxj54XPqwK_F38NCltsenkKBvr6CBkEa8jXjb-B5shB12Iy7riTY2hWvAF10dfGiucFthi8_ba6jx_d-p_mJwQxMSPplK8GVvm-j70KXX6EVl6whvlnmMfnz5fLk5zc6-nWw35VnWsYKpjFqhdMUd84qsFXXKF14CAUo92TlrtRdeWldJwlXBrF9zwkjFQDNbeW0VP0YfHnu7vv05QEzmEKKHurYNtEM0mggpZSGn4NslOLgD7EzXh4PtR7Nca-LvF26jt3U1_cSH-BQrNOd0PS_89Ji7CTWMT5yYWZ_Zm9mRmR2ZWZ9Z9Jlb8_V8QwVX_B_TppNL</recordid><startdate>199104</startdate><enddate>199104</enddate><creator>Bateson, Alan N.</creator><creator>Lasham, Annette</creator><creator>Darlison, Mark G.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>199104</creationdate><title>γ‐Aminobutyric AcidA Receptor Heterogeneity Is Increased by Alternative Splicing of a Novel β‐Subunit Gene Transcript</title><author>Bateson, Alan N. ; Lasham, Annette ; Darlison, Mark G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2927-1a478f3b2c70571b7c9c6e0e11c0dbaa8c4c6abf603792ac53020f2e82afc8a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Alternative splicing</topic><topic>Aminoacid receptors (glycine, glutamate, gaba)</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>cDNA and genomic DNA cloning</topic><topic>Cell receptors</topic><topic>Cell structures and functions</topic><topic>Chicken brain</topic><topic>Chickens</topic><topic>Cloning, Molecular</topic><topic>DNA</topic><topic>DNA, Recombinant</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Variation</topic><topic>Molecular and cellular biology</topic><topic>Molecular Sequence Data</topic><topic>Novel receptor β subunit</topic><topic>Receptor heterogeneity</topic><topic>Receptors, GABA-A - genetics</topic><topic>RNA Splicing</topic><topic>RNA, Messenger - genetics</topic><topic>Transcription, Genetic</topic><topic>γ‐Aminobutyric acidA receptor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bateson, Alan N.</creatorcontrib><creatorcontrib>Lasham, Annette</creatorcontrib><creatorcontrib>Darlison, Mark G.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bateson, Alan N.</au><au>Lasham, Annette</au><au>Darlison, Mark G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>γ‐Aminobutyric AcidA Receptor Heterogeneity Is Increased by Alternative Splicing of a Novel β‐Subunit Gene Transcript</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1991-04</date><risdate>1991</risdate><volume>56</volume><issue>4</issue><spage>1437</spage><epage>1440</epage><pages>1437-1440</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: DNA sequences encoding two variants of a novel γ‐aminobutyric acidA (GABAA) receptor β subunit were isolated from an embryonic chicken whole‐brain cDNA library and a chicken genomic library. The coding regions of these variants only differ from each other by the absence or presence of 12 bp in the region that encodes the presumed intracellular loop between transmembrane domains M3 and M4; the encoded subunits have been named β4 and β4′, respectively. The predicted mature polypeptides are 72–77% identical to the previously characterized mammalian and chicken β1,β2, and β3 subunits. Analysis of the β4‐subunit gene reveals that the different transcripts encoding the two variants arise by the use of one of two 5′‐donor splice sites that are separated by 12 bp. This is the first demonstration of alternative splicing of a GABAA receptor subunit gene transcript and represents a further mechanism for the generation of GABAA receptor heterogeneity.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>1848280</pmid><doi>10.1111/j.1471-4159.1991.tb11443.x</doi><tpages>4</tpages></addata></record>
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subjects Alternative splicing
Aminoacid receptors (glycine, glutamate, gaba)
Animals
Base Sequence
Biological and medical sciences
cDNA and genomic DNA cloning
Cell receptors
Cell structures and functions
Chicken brain
Chickens
Cloning, Molecular
DNA
DNA, Recombinant
Fundamental and applied biological sciences. Psychology
Genetic Variation
Molecular and cellular biology
Molecular Sequence Data
Novel receptor β subunit
Receptor heterogeneity
Receptors, GABA-A - genetics
RNA Splicing
RNA, Messenger - genetics
Transcription, Genetic
γ‐Aminobutyric acidA receptor
title γ‐Aminobutyric AcidA Receptor Heterogeneity Is Increased by Alternative Splicing of a Novel β‐Subunit Gene Transcript
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