The synucleins
Synucleins are small, soluble proteins expressed primarily in neural tissue and in certain tumors. The family includes three known proteins: alpha-synuclein, beta-synuclein, and gamma-synuclein. All synucleins have in common a highly conserved alpha-helical lipid-binding motif with similarity to the...
Gespeichert in:
Veröffentlicht in: | Genome biology 2002-01, Vol.3 (1), p.REVIEWS3002-REVIEWS3002 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | REVIEWS3002 |
---|---|
container_issue | 1 |
container_start_page | REVIEWS3002 |
container_title | Genome biology |
container_volume | 3 |
creator | George, Julia M |
description | Synucleins are small, soluble proteins expressed primarily in neural tissue and in certain tumors. The family includes three known proteins: alpha-synuclein, beta-synuclein, and gamma-synuclein. All synucleins have in common a highly conserved alpha-helical lipid-binding motif with similarity to the class-A2 lipid-binding domains of the exchangeable apolipoproteins. Synuclein family members are not found outside vertebrates, although they have some conserved structural similarity with plant 'late-embryo-abundant' proteins. The alpha- and beta-synuclein proteins are found primarily in brain tissue, where they are seen mainly in presynaptic terminals. The gamma-synuclein protein is found primarily in the peripheral nervous system and retina, but its expression in breast tumors is a marker for tumor progression. Normal cellular functions have not been determined for any of the synuclein proteins, although some data suggest a role in the regulation of membrane stability and/or turnover. Mutations in alpha-synuclein are associated with rare familial cases of early-onset Parkinson's disease, and the protein accumulates abnormally in Parkinson's disease, Alzheimer's disease, and several other neurodegenerative illnesses. The current challenge is to understand the normal cellular function of these proteins and how they might contribute to the development of human disease. |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_150459</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71414969</sourcerecordid><originalsourceid>FETCH-LOGICAL-p193t-b9c14f2290028a1a0326422d1c980e1353bcd52735366681c1ee4a220809800c3</originalsourceid><addsrcrecordid>eNpVUMtKw0AUHUSxD_UTxJW7wL3zyszChRStQsFNBXfDZHJrI3mZSYT-vSlWsatz4LzgnLApylQmqYa30z3XKtEW9ITNYvwAQCu5PmcTRAPaCDVlV-st3cRdPYSSijpesLONLyNdHnDOXh8f1ounZPWyfF7cr5IWreiTzAaUG84tADcePQiuJec5BmuAUCiRhVzxdCRaa4MBiaTnHAyMBghizu5-etshqygPVPedL13bFZXvdq7xhTtW6mLr3psvhwqksmP-9pDvms-BYu-qIgYqS19TM0SXokRp9d54_X_ob-H3AfENKrtWVQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71414969</pqid></control><display><type>article</type><title>The synucleins</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>SpringerLink Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Springer Nature OA Free Journals</source><source>PubMed Central</source><creator>George, Julia M</creator><creatorcontrib>George, Julia M</creatorcontrib><description>Synucleins are small, soluble proteins expressed primarily in neural tissue and in certain tumors. The family includes three known proteins: alpha-synuclein, beta-synuclein, and gamma-synuclein. All synucleins have in common a highly conserved alpha-helical lipid-binding motif with similarity to the class-A2 lipid-binding domains of the exchangeable apolipoproteins. Synuclein family members are not found outside vertebrates, although they have some conserved structural similarity with plant 'late-embryo-abundant' proteins. The alpha- and beta-synuclein proteins are found primarily in brain tissue, where they are seen mainly in presynaptic terminals. The gamma-synuclein protein is found primarily in the peripheral nervous system and retina, but its expression in breast tumors is a marker for tumor progression. Normal cellular functions have not been determined for any of the synuclein proteins, although some data suggest a role in the regulation of membrane stability and/or turnover. Mutations in alpha-synuclein are associated with rare familial cases of early-onset Parkinson's disease, and the protein accumulates abnormally in Parkinson's disease, Alzheimer's disease, and several other neurodegenerative illnesses. The current challenge is to understand the normal cellular function of these proteins and how they might contribute to the development of human disease.</description><identifier>ISSN: 1465-6906</identifier><identifier>EISSN: 1474-760X</identifier><identifier>EISSN: 1465-6914</identifier><identifier>PMID: 11806835</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>alpha-Synuclein ; Amino Acid Sequence ; Animals ; beta-Synuclein ; Evolution, Molecular ; gamma-Synuclein ; Humans ; Models, Molecular ; Molecular Sequence Data ; Nerve Tissue Proteins - chemistry ; Nerve Tissue Proteins - genetics ; Neurodegenerative Diseases - genetics ; Phylogeny ; Protein Family Review ; Sequence Alignment ; Sequence Homology, Amino Acid ; Synucleins</subject><ispartof>Genome biology, 2002-01, Vol.3 (1), p.REVIEWS3002-REVIEWS3002</ispartof><rights>Copyright © 2001 BioMed Central Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC150459/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC150459/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11806835$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>George, Julia M</creatorcontrib><title>The synucleins</title><title>Genome biology</title><addtitle>Genome Biol</addtitle><description>Synucleins are small, soluble proteins expressed primarily in neural tissue and in certain tumors. The family includes three known proteins: alpha-synuclein, beta-synuclein, and gamma-synuclein. All synucleins have in common a highly conserved alpha-helical lipid-binding motif with similarity to the class-A2 lipid-binding domains of the exchangeable apolipoproteins. Synuclein family members are not found outside vertebrates, although they have some conserved structural similarity with plant 'late-embryo-abundant' proteins. The alpha- and beta-synuclein proteins are found primarily in brain tissue, where they are seen mainly in presynaptic terminals. The gamma-synuclein protein is found primarily in the peripheral nervous system and retina, but its expression in breast tumors is a marker for tumor progression. Normal cellular functions have not been determined for any of the synuclein proteins, although some data suggest a role in the regulation of membrane stability and/or turnover. Mutations in alpha-synuclein are associated with rare familial cases of early-onset Parkinson's disease, and the protein accumulates abnormally in Parkinson's disease, Alzheimer's disease, and several other neurodegenerative illnesses. The current challenge is to understand the normal cellular function of these proteins and how they might contribute to the development of human disease.</description><subject>alpha-Synuclein</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>beta-Synuclein</subject><subject>Evolution, Molecular</subject><subject>gamma-Synuclein</subject><subject>Humans</subject><subject>Models, Molecular</subject><subject>Molecular Sequence Data</subject><subject>Nerve Tissue Proteins - chemistry</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Neurodegenerative Diseases - genetics</subject><subject>Phylogeny</subject><subject>Protein Family Review</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Amino Acid</subject><subject>Synucleins</subject><issn>1465-6906</issn><issn>1474-760X</issn><issn>1465-6914</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUMtKw0AUHUSxD_UTxJW7wL3zyszChRStQsFNBXfDZHJrI3mZSYT-vSlWsatz4LzgnLApylQmqYa30z3XKtEW9ITNYvwAQCu5PmcTRAPaCDVlV-st3cRdPYSSijpesLONLyNdHnDOXh8f1ounZPWyfF7cr5IWreiTzAaUG84tADcePQiuJec5BmuAUCiRhVzxdCRaa4MBiaTnHAyMBghizu5-etshqygPVPedL13bFZXvdq7xhTtW6mLr3psvhwqksmP-9pDvms-BYu-qIgYqS19TM0SXokRp9d54_X_ob-H3AfENKrtWVQ</recordid><startdate>20020101</startdate><enddate>20020101</enddate><creator>George, Julia M</creator><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20020101</creationdate><title>The synucleins</title><author>George, Julia M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p193t-b9c14f2290028a1a0326422d1c980e1353bcd52735366681c1ee4a220809800c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>alpha-Synuclein</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>beta-Synuclein</topic><topic>Evolution, Molecular</topic><topic>gamma-Synuclein</topic><topic>Humans</topic><topic>Models, Molecular</topic><topic>Molecular Sequence Data</topic><topic>Nerve Tissue Proteins - chemistry</topic><topic>Nerve Tissue Proteins - genetics</topic><topic>Neurodegenerative Diseases - genetics</topic><topic>Phylogeny</topic><topic>Protein Family Review</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Amino Acid</topic><topic>Synucleins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>George, Julia M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Genome biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>George, Julia M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The synucleins</atitle><jtitle>Genome biology</jtitle><addtitle>Genome Biol</addtitle><date>2002-01-01</date><risdate>2002</risdate><volume>3</volume><issue>1</issue><spage>REVIEWS3002</spage><epage>REVIEWS3002</epage><pages>REVIEWS3002-REVIEWS3002</pages><issn>1465-6906</issn><eissn>1474-760X</eissn><eissn>1465-6914</eissn><abstract>Synucleins are small, soluble proteins expressed primarily in neural tissue and in certain tumors. The family includes three known proteins: alpha-synuclein, beta-synuclein, and gamma-synuclein. All synucleins have in common a highly conserved alpha-helical lipid-binding motif with similarity to the class-A2 lipid-binding domains of the exchangeable apolipoproteins. Synuclein family members are not found outside vertebrates, although they have some conserved structural similarity with plant 'late-embryo-abundant' proteins. The alpha- and beta-synuclein proteins are found primarily in brain tissue, where they are seen mainly in presynaptic terminals. The gamma-synuclein protein is found primarily in the peripheral nervous system and retina, but its expression in breast tumors is a marker for tumor progression. Normal cellular functions have not been determined for any of the synuclein proteins, although some data suggest a role in the regulation of membrane stability and/or turnover. Mutations in alpha-synuclein are associated with rare familial cases of early-onset Parkinson's disease, and the protein accumulates abnormally in Parkinson's disease, Alzheimer's disease, and several other neurodegenerative illnesses. The current challenge is to understand the normal cellular function of these proteins and how they might contribute to the development of human disease.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>11806835</pmid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1465-6906 |
ispartof | Genome biology, 2002-01, Vol.3 (1), p.REVIEWS3002-REVIEWS3002 |
issn | 1465-6906 1474-760X 1465-6914 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_150459 |
source | MEDLINE; DOAJ Directory of Open Access Journals; SpringerLink Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature OA Free Journals; PubMed Central |
subjects | alpha-Synuclein Amino Acid Sequence Animals beta-Synuclein Evolution, Molecular gamma-Synuclein Humans Models, Molecular Molecular Sequence Data Nerve Tissue Proteins - chemistry Nerve Tissue Proteins - genetics Neurodegenerative Diseases - genetics Phylogeny Protein Family Review Sequence Alignment Sequence Homology, Amino Acid Synucleins |
title | The synucleins |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T13%3A16%3A02IST&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=The%20synucleins&rft.jtitle=Genome%20biology&rft.au=George,%20Julia%20M&rft.date=2002-01-01&rft.volume=3&rft.issue=1&rft.spage=REVIEWS3002&rft.epage=REVIEWS3002&rft.pages=REVIEWS3002-REVIEWS3002&rft.issn=1465-6906&rft.eissn=1474-760X&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E71414969%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=71414969&rft_id=info:pmid/11806835&rfr_iscdi=true |