6533b821fe1ef96bd127b03e
RESEARCH PRODUCT
Comparative genomics and protein domain graph analyses link ubiquitination and RNA metabolism.
Ignacio MarínJ. Ignasi LucasVicente Arnausubject
Comparative genomicsGeneticsbiologyProtein ConformationUbiquitinUbiquitin-Protein LigasesProtein domainMolecular Sequence DataRNAGenomicsF-box proteinRNA Helicase AParkinUbiquitin ligaseProtein Structure TertiaryStructural Biologybiology.proteinAnimalsCluster AnalysisHumansRNAMolecular BiologyGeneAlgorithmsdescription
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.
year | journal | country | edition | language |
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2006-03-01 | Journal of molecular biology |