Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene
NACP-Rep1, a polymorphic microsatellite upstream of the alpha-synuclein gene ( SNCA), consisting of the nucleotides (TC)(x)(T)(2)(TC)(y)(TA)(z)(CA)(w), has five alleles originally defined by 2-bp differences in (CA)(w). Different NACP-Rep1 alleles have been associated with sporadic Parkinson's...
Gespeichert in:
Veröffentlicht in: | Human genetics 2003-10, Vol.113 (5), p.426-431 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 431 |
---|---|
container_issue | 5 |
container_start_page | 426 |
container_title | Human genetics |
container_volume | 113 |
creator | CHIBA-FALEK, Ornit TOUCHMAN, Jeffrey W NUSSBAUM, Robert L |
description | NACP-Rep1, a polymorphic microsatellite upstream of the alpha-synuclein gene ( SNCA), consisting of the nucleotides (TC)(x)(T)(2)(TC)(y)(TA)(z)(CA)(w), has five alleles originally defined by 2-bp differences in (CA)(w). Different NACP-Rep1 alleles have been associated with sporadic Parkinson's disease in some, but not all, studies and can effect expression driven by the SNCA promoter over a three-fold range in the neuroblastoma cell line, SH-SY5Y. By analyzing children in CEPH families in which parents appeared to be homozygous for a NACP-Rep1 allele, we found that there are sequence differences within same-sized NACP-Rep1 alleles, contributed mainly by variation of the (TC)(y)(TA)(z) portion of the microsatellite repeat. To test whether these sequence differences might impact on promoter function we determined the effect of two sequence variant alleles, both of size "1", using the luciferase reporter system. There was only a very small expression difference between these two variant alleles. This finding implies that the overall length of the NACP-Rep1 allele plays the main role in the transcription regulation by the NACP-Rep1 element and suggests that functional differences due to sequence heterogeneity within NACP-Rep1 alleles of the same length are probably not confounding factors in association studies based on alleles defined by length. |
doi_str_mv | 10.1007/s00439-003-1002-9 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_75700250</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>75700250</sourcerecordid><originalsourceid>FETCH-LOGICAL-p237t-fdeb6fa973661f890901b14c9634d823b7f6aee72bafbd4699c52d9271e567ac3</originalsourceid><addsrcrecordid>eNpF0M9KAzEQBvAgiq3VB_Aiuegtmj-7SXMsxapQVKSel9nsRCPpbt3sCn0sX8RncsWKlxnm48ccPkJOBb8UnJurxHmmLONcseGWzO6RsciUZEJytU_GXGWcaSPMiByl9Ma5yK3MD8lISCuVnsoxWS362nWhqSFSGMY2hUQbT0PdtcAgRozB0Q9oA_woCh29n80f2RNuxIBo94r065Olbd27iEPwgjUekwMPMeHJbk_I8-J6Nb9ly4ebu_lsyTZSmY75CkvtwRqltfBTyy0Xpcic1SqrplKVxmtANLIEX1aZttblsrLSCMy1Aacm5OL376Zt3ntMXbEOyWGMUGPTp8LkZqgl5wM828G-XGNVbNqwhnZb_PUwgPMdgOQg-hZqF9K_y4XOlLLqGyDibKo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75700250</pqid></control><display><type>article</type><title>Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>CHIBA-FALEK, Ornit ; TOUCHMAN, Jeffrey W ; NUSSBAUM, Robert L</creator><creatorcontrib>CHIBA-FALEK, Ornit ; TOUCHMAN, Jeffrey W ; NUSSBAUM, Robert L</creatorcontrib><description>NACP-Rep1, a polymorphic microsatellite upstream of the alpha-synuclein gene ( SNCA), consisting of the nucleotides (TC)(x)(T)(2)(TC)(y)(TA)(z)(CA)(w), has five alleles originally defined by 2-bp differences in (CA)(w). Different NACP-Rep1 alleles have been associated with sporadic Parkinson's disease in some, but not all, studies and can effect expression driven by the SNCA promoter over a three-fold range in the neuroblastoma cell line, SH-SY5Y. By analyzing children in CEPH families in which parents appeared to be homozygous for a NACP-Rep1 allele, we found that there are sequence differences within same-sized NACP-Rep1 alleles, contributed mainly by variation of the (TC)(y)(TA)(z) portion of the microsatellite repeat. To test whether these sequence differences might impact on promoter function we determined the effect of two sequence variant alleles, both of size "1", using the luciferase reporter system. There was only a very small expression difference between these two variant alleles. This finding implies that the overall length of the NACP-Rep1 allele plays the main role in the transcription regulation by the NACP-Rep1 element and suggests that functional differences due to sequence heterogeneity within NACP-Rep1 alleles of the same length are probably not confounding factors in association studies based on alleles defined by length.</description><identifier>ISSN: 0340-6717</identifier><identifier>EISSN: 1432-1203</identifier><identifier>DOI: 10.1007/s00439-003-1002-9</identifier><identifier>PMID: 12923682</identifier><identifier>CODEN: HUGEDQ</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>alpha-Synuclein ; Base Sequence ; Biological and medical sciences ; Classical genetics, quantitative genetics, hybrids ; DNA Primers ; Female ; Fundamental and applied biological sciences. Psychology ; Genes, Reporter ; Genetic Variation - genetics ; Genetics of eukaryotes. Biological and molecular evolution ; Genotype ; Human ; Humans ; Luciferases - genetics ; Luciferases - metabolism ; Male ; Microsatellite Repeats - genetics ; Molecular Sequence Data ; Nerve Tissue Proteins - genetics ; Neuroblastoma ; Pedigree ; Synucleins ; Transfection ; Tumor Cells, Cultured</subject><ispartof>Human genetics, 2003-10, Vol.113 (5), p.426-431</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15164339$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12923682$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CHIBA-FALEK, Ornit</creatorcontrib><creatorcontrib>TOUCHMAN, Jeffrey W</creatorcontrib><creatorcontrib>NUSSBAUM, Robert L</creatorcontrib><title>Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene</title><title>Human genetics</title><addtitle>Hum Genet</addtitle><description>NACP-Rep1, a polymorphic microsatellite upstream of the alpha-synuclein gene ( SNCA), consisting of the nucleotides (TC)(x)(T)(2)(TC)(y)(TA)(z)(CA)(w), has five alleles originally defined by 2-bp differences in (CA)(w). Different NACP-Rep1 alleles have been associated with sporadic Parkinson's disease in some, but not all, studies and can effect expression driven by the SNCA promoter over a three-fold range in the neuroblastoma cell line, SH-SY5Y. By analyzing children in CEPH families in which parents appeared to be homozygous for a NACP-Rep1 allele, we found that there are sequence differences within same-sized NACP-Rep1 alleles, contributed mainly by variation of the (TC)(y)(TA)(z) portion of the microsatellite repeat. To test whether these sequence differences might impact on promoter function we determined the effect of two sequence variant alleles, both of size "1", using the luciferase reporter system. There was only a very small expression difference between these two variant alleles. This finding implies that the overall length of the NACP-Rep1 allele plays the main role in the transcription regulation by the NACP-Rep1 element and suggests that functional differences due to sequence heterogeneity within NACP-Rep1 alleles of the same length are probably not confounding factors in association studies based on alleles defined by length.</description><subject>alpha-Synuclein</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>DNA Primers</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Reporter</subject><subject>Genetic Variation - genetics</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Genotype</subject><subject>Human</subject><subject>Humans</subject><subject>Luciferases - genetics</subject><subject>Luciferases - metabolism</subject><subject>Male</subject><subject>Microsatellite Repeats - genetics</subject><subject>Molecular Sequence Data</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Neuroblastoma</subject><subject>Pedigree</subject><subject>Synucleins</subject><subject>Transfection</subject><subject>Tumor Cells, Cultured</subject><issn>0340-6717</issn><issn>1432-1203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0M9KAzEQBvAgiq3VB_Aiuegtmj-7SXMsxapQVKSel9nsRCPpbt3sCn0sX8RncsWKlxnm48ccPkJOBb8UnJurxHmmLONcseGWzO6RsciUZEJytU_GXGWcaSPMiByl9Ma5yK3MD8lISCuVnsoxWS362nWhqSFSGMY2hUQbT0PdtcAgRozB0Q9oA_woCh29n80f2RNuxIBo94r065Olbd27iEPwgjUekwMPMeHJbk_I8-J6Nb9ly4ebu_lsyTZSmY75CkvtwRqltfBTyy0Xpcic1SqrplKVxmtANLIEX1aZttblsrLSCMy1Aacm5OL376Zt3ntMXbEOyWGMUGPTp8LkZqgl5wM828G-XGNVbNqwhnZb_PUwgPMdgOQg-hZqF9K_y4XOlLLqGyDibKo</recordid><startdate>20031001</startdate><enddate>20031001</enddate><creator>CHIBA-FALEK, Ornit</creator><creator>TOUCHMAN, Jeffrey W</creator><creator>NUSSBAUM, Robert L</creator><general>Springer</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>20031001</creationdate><title>Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene</title><author>CHIBA-FALEK, Ornit ; TOUCHMAN, Jeffrey W ; NUSSBAUM, Robert L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p237t-fdeb6fa973661f890901b14c9634d823b7f6aee72bafbd4699c52d9271e567ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>alpha-Synuclein</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Classical genetics, quantitative genetics, hybrids</topic><topic>DNA Primers</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes, Reporter</topic><topic>Genetic Variation - genetics</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Genotype</topic><topic>Human</topic><topic>Humans</topic><topic>Luciferases - genetics</topic><topic>Luciferases - metabolism</topic><topic>Male</topic><topic>Microsatellite Repeats - genetics</topic><topic>Molecular Sequence Data</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Neuroblastoma</topic><topic>Pedigree</topic><topic>Synucleins</topic><topic>Transfection</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CHIBA-FALEK, Ornit</creatorcontrib><creatorcontrib>TOUCHMAN, Jeffrey W</creatorcontrib><creatorcontrib>NUSSBAUM, Robert L</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>Human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CHIBA-FALEK, Ornit</au><au>TOUCHMAN, Jeffrey W</au><au>NUSSBAUM, Robert L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene</atitle><jtitle>Human genetics</jtitle><addtitle>Hum Genet</addtitle><date>2003-10-01</date><risdate>2003</risdate><volume>113</volume><issue>5</issue><spage>426</spage><epage>431</epage><pages>426-431</pages><issn>0340-6717</issn><eissn>1432-1203</eissn><coden>HUGEDQ</coden><abstract>NACP-Rep1, a polymorphic microsatellite upstream of the alpha-synuclein gene ( SNCA), consisting of the nucleotides (TC)(x)(T)(2)(TC)(y)(TA)(z)(CA)(w), has five alleles originally defined by 2-bp differences in (CA)(w). Different NACP-Rep1 alleles have been associated with sporadic Parkinson's disease in some, but not all, studies and can effect expression driven by the SNCA promoter over a three-fold range in the neuroblastoma cell line, SH-SY5Y. By analyzing children in CEPH families in which parents appeared to be homozygous for a NACP-Rep1 allele, we found that there are sequence differences within same-sized NACP-Rep1 alleles, contributed mainly by variation of the (TC)(y)(TA)(z) portion of the microsatellite repeat. To test whether these sequence differences might impact on promoter function we determined the effect of two sequence variant alleles, both of size "1", using the luciferase reporter system. There was only a very small expression difference between these two variant alleles. This finding implies that the overall length of the NACP-Rep1 allele plays the main role in the transcription regulation by the NACP-Rep1 element and suggests that functional differences due to sequence heterogeneity within NACP-Rep1 alleles of the same length are probably not confounding factors in association studies based on alleles defined by length.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><cop>New York, NY</cop><pub>Springer</pub><pmid>12923682</pmid><doi>10.1007/s00439-003-1002-9</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0340-6717 |
ispartof | Human genetics, 2003-10, Vol.113 (5), p.426-431 |
issn | 0340-6717 1432-1203 |
language | eng |
recordid | cdi_proquest_miscellaneous_75700250 |
source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | alpha-Synuclein Base Sequence Biological and medical sciences Classical genetics, quantitative genetics, hybrids DNA Primers Female Fundamental and applied biological sciences. Psychology Genes, Reporter Genetic Variation - genetics Genetics of eukaryotes. Biological and molecular evolution Genotype Human Humans Luciferases - genetics Luciferases - metabolism Male Microsatellite Repeats - genetics Molecular Sequence Data Nerve Tissue Proteins - genetics Neuroblastoma Pedigree Synucleins Transfection Tumor Cells, Cultured |
title | Functional analysis of intra-allelic variation at NACP-Rep1 in the α-synuclein gene |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T23%3A05%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Functional%20analysis%20of%20intra-allelic%20variation%20at%20NACP-Rep1%20in%20the%20%CE%B1-synuclein%20gene&rft.jtitle=Human%20genetics&rft.au=CHIBA-FALEK,%20Ornit&rft.date=2003-10-01&rft.volume=113&rft.issue=5&rft.spage=426&rft.epage=431&rft.pages=426-431&rft.issn=0340-6717&rft.eissn=1432-1203&rft.coden=HUGEDQ&rft_id=info:doi/10.1007/s00439-003-1002-9&rft_dat=%3Cproquest_pubme%3E75700250%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=75700250&rft_id=info:pmid/12923682&rfr_iscdi=true |