Comparative Genomics and Protein Domain Graph Analyses Link Ubiquitination and RNA Metabolism
The human gene parkin, known to cause familial Parkinson disease, as well as several other genes, likely involved in other neurodegenerative diseases or in cancer, encode proteins of the RBR family of ubiquitin ligases. Here, we describe the structural diversity of the RBR family in order to infer t...
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Veröffentlicht in: | Journal of molecular biology 2006-03, Vol.357 (1), p.9-17 |
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creator | Lucas, J. Ignasi Arnau, Vicente Marín, Ignacio |
description | The human gene
parkin, known to cause familial Parkinson disease, as well as several other genes, likely involved in other neurodegenerative diseases or in cancer, encode proteins of the RBR family of ubiquitin ligases. Here, we describe the structural diversity of the RBR family in order to infer their functional roles. Of particular interest is a relationship detected between RBR-mediated ubiquitination and RNA metabolism: a few RBR proteins contain RNA binding domains and DEAH-box RNA helicase domains. Global protein domain graph analyses demonstrate that this connection is not RBR-specific, but instead many other proteins contain both ubiquitination and RNA-related domains. These proteins are present in animals, plants and fungi, suggesting that the link between these two cellular processes is ancient. Our results show that global bioinformatic approaches, involving comparative genomics and domain network analyses, may unearth novel functional relationships involving well-known and thoroughly studied groups of proteins. |
doi_str_mv | 10.1016/j.jmb.2005.12.068 |
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parkin, known to cause familial Parkinson disease, as well as several other genes, likely involved in other neurodegenerative diseases or in cancer, encode proteins of the RBR family of ubiquitin ligases. Here, we describe the structural diversity of the RBR family in order to infer their functional roles. Of particular interest is a relationship detected between RBR-mediated ubiquitination and RNA metabolism: a few RBR proteins contain RNA binding domains and DEAH-box RNA helicase domains. Global protein domain graph analyses demonstrate that this connection is not RBR-specific, but instead many other proteins contain both ubiquitination and RNA-related domains. These proteins are present in animals, plants and fungi, suggesting that the link between these two cellular processes is ancient. Our results show that global bioinformatic approaches, involving comparative genomics and domain network analyses, may unearth novel functional relationships involving well-known and thoroughly studied groups of proteins.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/j.jmb.2005.12.068</identifier><identifier>PMID: 16426638</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Algorithms ; Animals ; Cluster Analysis ; comparative genomics ; domain graph ; Genomics ; Humans ; Molecular Sequence Data ; Parkinson disease ; Protein Conformation ; Protein Structure, Tertiary ; RNA - metabolism ; Ubiquitin - metabolism ; ubiquitin ligases ; Ubiquitin-Protein Ligases - genetics</subject><ispartof>Journal of molecular biology, 2006-03, Vol.357 (1), p.9-17</ispartof><rights>2005 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c297t-26867fefbd74e127e01cbed18ce63f31e8d60292974cddee866e8083740c5c253</citedby><cites>FETCH-LOGICAL-c297t-26867fefbd74e127e01cbed18ce63f31e8d60292974cddee866e8083740c5c253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jmb.2005.12.068$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16426638$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lucas, J. Ignasi</creatorcontrib><creatorcontrib>Arnau, Vicente</creatorcontrib><creatorcontrib>Marín, Ignacio</creatorcontrib><title>Comparative Genomics and Protein Domain Graph Analyses Link Ubiquitination and RNA Metabolism</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>The human gene
parkin, known to cause familial Parkinson disease, as well as several other genes, likely involved in other neurodegenerative diseases or in cancer, encode proteins of the RBR family of ubiquitin ligases. Here, we describe the structural diversity of the RBR family in order to infer their functional roles. Of particular interest is a relationship detected between RBR-mediated ubiquitination and RNA metabolism: a few RBR proteins contain RNA binding domains and DEAH-box RNA helicase domains. Global protein domain graph analyses demonstrate that this connection is not RBR-specific, but instead many other proteins contain both ubiquitination and RNA-related domains. These proteins are present in animals, plants and fungi, suggesting that the link between these two cellular processes is ancient. Our results show that global bioinformatic approaches, involving comparative genomics and domain network analyses, may unearth novel functional relationships involving well-known and thoroughly studied groups of proteins.</description><subject>Algorithms</subject><subject>Animals</subject><subject>Cluster Analysis</subject><subject>comparative genomics</subject><subject>domain graph</subject><subject>Genomics</subject><subject>Humans</subject><subject>Molecular Sequence Data</subject><subject>Parkinson disease</subject><subject>Protein Conformation</subject><subject>Protein Structure, Tertiary</subject><subject>RNA - metabolism</subject><subject>Ubiquitin - metabolism</subject><subject>ubiquitin ligases</subject><subject>Ubiquitin-Protein Ligases - genetics</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkL1OwzAYRS0EoqXwACwoE1uC7aSOK6aqQEEqP0J0RJZjfxEuiV3stFLfHpdWYoPpLufc4SB0TnBGMGFXi2zRVhnFeJgRmmHGD1CfYD5KOcv5IepjTGlKec566CSEBY5gXvBj1COsoCwyffQ-ce1SetmZNSRTsK41KiTS6uTFuw6MTW5cK-NMvVx-JGMrm02AkMyM_Uzmlflamc7YqDv7Y70-jZNH6GTlGhPaU3RUyybA2X4HaH53-za5T2fP04fJeJYqOiq7lDLOyhrqSpcFEFoCJqoCTbgCltc5Aa4ZpqPIFkprAM4YcMzzssBqqOgwH6DL3e_Su68VhE60JihoGmnBrYJgZUQL_j9IMWeYjWgEyQ5U3oXgoRZLb1rpN4JgsY0vFiLGF9v4glAR40fnYn--qlrQv8a-dgSudwDEFmsDXgRlwCrQxoPqhHbmj_tvRHeUvQ</recordid><startdate>20060317</startdate><enddate>20060317</enddate><creator>Lucas, J. 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Ignasi</creatorcontrib><creatorcontrib>Arnau, Vicente</creatorcontrib><creatorcontrib>Marín, Ignacio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lucas, J. 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parkin, known to cause familial Parkinson disease, as well as several other genes, likely involved in other neurodegenerative diseases or in cancer, encode proteins of the RBR family of ubiquitin ligases. Here, we describe the structural diversity of the RBR family in order to infer their functional roles. Of particular interest is a relationship detected between RBR-mediated ubiquitination and RNA metabolism: a few RBR proteins contain RNA binding domains and DEAH-box RNA helicase domains. Global protein domain graph analyses demonstrate that this connection is not RBR-specific, but instead many other proteins contain both ubiquitination and RNA-related domains. These proteins are present in animals, plants and fungi, suggesting that the link between these two cellular processes is ancient. Our results show that global bioinformatic approaches, involving comparative genomics and domain network analyses, may unearth novel functional relationships involving well-known and thoroughly studied groups of proteins.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>16426638</pmid><doi>10.1016/j.jmb.2005.12.068</doi><tpages>9</tpages></addata></record> |
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subjects | Algorithms Animals Cluster Analysis comparative genomics domain graph Genomics Humans Molecular Sequence Data Parkinson disease Protein Conformation Protein Structure, Tertiary RNA - metabolism Ubiquitin - metabolism ubiquitin ligases Ubiquitin-Protein Ligases - genetics |
title | Comparative Genomics and Protein Domain Graph Analyses Link Ubiquitination and RNA Metabolism |
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