Expression of multiple catechol-o-methyltransferase (COMT) mRNA variants in human brain
Catechol‐o‐methyltransferase (COMT) is important for modulating dopamine levels, prefrontal cortex (PFC) function, and several psychiatric phenotypes. A single COMT mRNA has been described in human brain, which gives rise to membrane‐bound (MB)‐ and soluble (S)‐COMT proteins. In addition, we have re...
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Veröffentlicht in: | American journal of medical genetics. Part B, Neuropsychiatric genetics Neuropsychiatric genetics, 2007-09, Vol.144B (6), p.834-839 |
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description | Catechol‐o‐methyltransferase (COMT) is important for modulating dopamine levels, prefrontal cortex (PFC) function, and several psychiatric phenotypes. A single COMT mRNA has been described in human brain, which gives rise to membrane‐bound (MB)‐ and soluble (S)‐COMT proteins. In addition, we have recently described a novel COMT protein isoform in the human PFC, suggesting that there are more COMT gene products expressed than are currently appreciated. Therefore, we have investigated whether variant COMT mRNAs are present in human brain. We used reverse transcription‐PCR (RT‐PCR) to screen systematically for variant COMT mRNAs in human frontal cortex. Intron‐spanning primers were used for exon‐to‐exon PCR reactions; additionally, specific primers were designed to sequences in the NCBI Aceview database. The identity of amplicons was confirmed by sequencing, and their regional distributions and 3′ untranslated regions (UTRs) were characterised using RT‐PCR. We detected 7 COMT variant mRNAs, resulting from both insertions and deletions within the known COMT brain transcript. Several of the variants alter the predicted coding sequence. Three of these variants correspond to sequences within the Aceview database and could be reliably amplified, while the remaining four do not correspond to any expressed sequence tags and were amplified only once. The regional distributions of these transcripts are described. The results demonstrate multiple COMT mRNAs in human brain, revealing an additional complexity to the biology of COMT. The alternate gene products may be of significant functional importance, and differentially impacted by polymorphisms within the COMT gene. © 2007 Wiley‐Liss, Inc. |
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A single COMT mRNA has been described in human brain, which gives rise to membrane‐bound (MB)‐ and soluble (S)‐COMT proteins. In addition, we have recently described a novel COMT protein isoform in the human PFC, suggesting that there are more COMT gene products expressed than are currently appreciated. Therefore, we have investigated whether variant COMT mRNAs are present in human brain. We used reverse transcription‐PCR (RT‐PCR) to screen systematically for variant COMT mRNAs in human frontal cortex. Intron‐spanning primers were used for exon‐to‐exon PCR reactions; additionally, specific primers were designed to sequences in the NCBI Aceview database. The identity of amplicons was confirmed by sequencing, and their regional distributions and 3′ untranslated regions (UTRs) were characterised using RT‐PCR. We detected 7 COMT variant mRNAs, resulting from both insertions and deletions within the known COMT brain transcript. Several of the variants alter the predicted coding sequence. Three of these variants correspond to sequences within the Aceview database and could be reliably amplified, while the remaining four do not correspond to any expressed sequence tags and were amplified only once. The regional distributions of these transcripts are described. The results demonstrate multiple COMT mRNAs in human brain, revealing an additional complexity to the biology of COMT. The alternate gene products may be of significant functional importance, and differentially impacted by polymorphisms within the COMT gene. © 2007 Wiley‐Liss, Inc.</description><identifier>ISSN: 1552-4841</identifier><identifier>EISSN: 1552-485X</identifier><identifier>DOI: 10.1002/ajmg.b.30539</identifier><identifier>PMID: 17477346</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Adult and adolescent clinical studies ; Base Sequence ; Biological and medical sciences ; Brain - enzymology ; Catechol O-Methyltransferase - genetics ; DNA Primers - genetics ; dopamine ; Fetus - enzymology ; Gene Expression ; Genetic Variation ; Humans ; Medical genetics ; Medical sciences ; Molecular Sequence Data ; mRNA splicing ; prefrontal cortex ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychoses ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; Schizophrenia ; Tissue Distribution</subject><ispartof>American journal of medical genetics. 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Part B, Neuropsychiatric genetics</title><addtitle>Am. J. Med. Genet</addtitle><description>Catechol‐o‐methyltransferase (COMT) is important for modulating dopamine levels, prefrontal cortex (PFC) function, and several psychiatric phenotypes. A single COMT mRNA has been described in human brain, which gives rise to membrane‐bound (MB)‐ and soluble (S)‐COMT proteins. In addition, we have recently described a novel COMT protein isoform in the human PFC, suggesting that there are more COMT gene products expressed than are currently appreciated. Therefore, we have investigated whether variant COMT mRNAs are present in human brain. We used reverse transcription‐PCR (RT‐PCR) to screen systematically for variant COMT mRNAs in human frontal cortex. Intron‐spanning primers were used for exon‐to‐exon PCR reactions; additionally, specific primers were designed to sequences in the NCBI Aceview database. The identity of amplicons was confirmed by sequencing, and their regional distributions and 3′ untranslated regions (UTRs) were characterised using RT‐PCR. We detected 7 COMT variant mRNAs, resulting from both insertions and deletions within the known COMT brain transcript. Several of the variants alter the predicted coding sequence. Three of these variants correspond to sequences within the Aceview database and could be reliably amplified, while the remaining four do not correspond to any expressed sequence tags and were amplified only once. The regional distributions of these transcripts are described. The results demonstrate multiple COMT mRNAs in human brain, revealing an additional complexity to the biology of COMT. The alternate gene products may be of significant functional importance, and differentially impacted by polymorphisms within the COMT gene. © 2007 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Adult and adolescent clinical studies</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Brain - enzymology</subject><subject>Catechol O-Methyltransferase - genetics</subject><subject>DNA Primers - genetics</subject><subject>dopamine</subject><subject>Fetus - enzymology</subject><subject>Gene Expression</subject><subject>Genetic Variation</subject><subject>Humans</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>mRNA splicing</subject><subject>prefrontal cortex</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>Schizophrenia</subject><subject>Tissue Distribution</subject><issn>1552-4841</issn><issn>1552-485X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90M9v0zAUwHELgdgY3DgjX0AgkWLHdl58rKoRfnQbmioNcbEc94V6OEmxE1j_ezJathsn-_B570lfQp5zNuOM5e_sdft9Vs8EU0I_IMdcqTyTpfr68O4v-RF5ktI1YxMCeEyOOEgAIYtjcnV6s42Yku872je0HcPgtwGpswO6TR-yPmtx2OzCEG2XGow2IX29uDhbvaHt5fmc_rLR225I1Hd0M7a2o3W0vntKHjU2JHx2eE_I6v3pavEhW15UHxfzZeakLnWGwBu5xlJbXPM1cpcXWgoGyFytiwKcQtuAYDk0ypVYsFI7ACmQ167UhTghr_Zrt7H_OWIaTOuTwxBsh_2YTM65FABsgm_30MU-pYiN2Ubf2rgznJnbjua2o6nN344Tf3HYO9Ytru_xIdwEXh6ATc6GZqrjfLp3moFSAiYn9u63D7j771Ez_3RW_Tuf7ad8GvDmbsrGH6YAAcpcnVdm-UVefq6Wlfkm_gDe95sj</recordid><startdate>20070905</startdate><enddate>20070905</enddate><creator>Tunbridge, Elizabeth M.</creator><creator>Lane, Tracy A.</creator><creator>Harrison, Paul J.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20070905</creationdate><title>Expression of multiple catechol-o-methyltransferase (COMT) mRNA variants in human brain</title><author>Tunbridge, Elizabeth M. ; Lane, Tracy A. ; Harrison, Paul J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4989-e71f4de89aed1de1c2694307e0cb9667c5eaf73027f5c8e6089c7743e1bc8963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Adult and adolescent clinical studies</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Brain - enzymology</topic><topic>Catechol O-Methyltransferase - genetics</topic><topic>DNA Primers - genetics</topic><topic>dopamine</topic><topic>Fetus - enzymology</topic><topic>Gene Expression</topic><topic>Genetic Variation</topic><topic>Humans</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Molecular Sequence Data</topic><topic>mRNA splicing</topic><topic>prefrontal cortex</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>Schizophrenia</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tunbridge, Elizabeth M.</creatorcontrib><creatorcontrib>Lane, Tracy A.</creatorcontrib><creatorcontrib>Harrison, Paul J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>American journal of medical genetics. Part B, Neuropsychiatric genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tunbridge, Elizabeth M.</au><au>Lane, Tracy A.</au><au>Harrison, Paul J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of multiple catechol-o-methyltransferase (COMT) mRNA variants in human brain</atitle><jtitle>American journal of medical genetics. Part B, Neuropsychiatric genetics</jtitle><addtitle>Am. J. Med. Genet</addtitle><date>2007-09-05</date><risdate>2007</risdate><volume>144B</volume><issue>6</issue><spage>834</spage><epage>839</epage><pages>834-839</pages><issn>1552-4841</issn><eissn>1552-485X</eissn><abstract>Catechol‐o‐methyltransferase (COMT) is important for modulating dopamine levels, prefrontal cortex (PFC) function, and several psychiatric phenotypes. A single COMT mRNA has been described in human brain, which gives rise to membrane‐bound (MB)‐ and soluble (S)‐COMT proteins. In addition, we have recently described a novel COMT protein isoform in the human PFC, suggesting that there are more COMT gene products expressed than are currently appreciated. Therefore, we have investigated whether variant COMT mRNAs are present in human brain. We used reverse transcription‐PCR (RT‐PCR) to screen systematically for variant COMT mRNAs in human frontal cortex. Intron‐spanning primers were used for exon‐to‐exon PCR reactions; additionally, specific primers were designed to sequences in the NCBI Aceview database. The identity of amplicons was confirmed by sequencing, and their regional distributions and 3′ untranslated regions (UTRs) were characterised using RT‐PCR. We detected 7 COMT variant mRNAs, resulting from both insertions and deletions within the known COMT brain transcript. Several of the variants alter the predicted coding sequence. Three of these variants correspond to sequences within the Aceview database and could be reliably amplified, while the remaining four do not correspond to any expressed sequence tags and were amplified only once. The regional distributions of these transcripts are described. The results demonstrate multiple COMT mRNAs in human brain, revealing an additional complexity to the biology of COMT. The alternate gene products may be of significant functional importance, and differentially impacted by polymorphisms within the COMT gene. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17477346</pmid><doi>10.1002/ajmg.b.30539</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Adult and adolescent clinical studies Base Sequence Biological and medical sciences Brain - enzymology Catechol O-Methyltransferase - genetics DNA Primers - genetics dopamine Fetus - enzymology Gene Expression Genetic Variation Humans Medical genetics Medical sciences Molecular Sequence Data mRNA splicing prefrontal cortex Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics Schizophrenia Tissue Distribution |
title | Expression of multiple catechol-o-methyltransferase (COMT) mRNA variants in human brain |
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