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dc.contributor.authorGilbert, Wendy
dc.date.accessioned2015-10-02T16:49:49Z
dc.date.available2015-10-02T16:49:49Z
dc.date.issued2011-01
dc.identifier.issn09680004
dc.identifier.urihttp://hdl.handle.net/1721.1/99128
dc.description.abstractRibosomes are highly conserved macromolecular machines that are responsible for protein synthesis in all living organisms. Work published in the past year has shown that changes to the ribosome core can affect the mechanism of translation initiation that is favored in the cell, which potentially leads to specific changes in the relative efficiencies with which different proteins are made. Here, I examine recent data from expression and proteomic studies that suggest that cells make slightly different ribosomes under different growth conditions, and discuss genetic evidence that such differences are functional. In particular, I argue that eukaryotic cells probably produce ribosomes that lack one or more core ribosomal proteins (RPs) under some conditions, and that core RPs contribute differentially to translation of distinct subpopulations of mRNAs.en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.tibs.2010.12.002en_US
dc.rightsCreative Commons Attribution-Noncommercial-NoDerivativesen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleFunctional specialization of ribosomes?en_US
dc.typeArticleen_US
dc.identifier.citationGilbert, Wendy V. “Functional Specialization of Ribosomes?” Trends in Biochemical Sciences 36, no. 3 (March 2011): 127–132.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorGilbert, Wendyen_US
dc.relation.journalTrends in Biochemical Sciencesen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsGilbert, Wendy V.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2807-9657
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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