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dc.contributor.advisorSusan Lindquist.en_US
dc.contributor.authorBrown, Jessica C. Sen_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Biology.en_US
dc.date.accessioned2009-04-29T14:46:13Z
dc.date.available2009-04-29T14:46:13Z
dc.date.copyright2008en_US
dc.date.issued2008en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/45147
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 2008.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractSeveral well-characterized fungal proteins act as prions, proteins capable of multiple conformations, each with different activities, at least one of which is selfpropagating. We report a protein-based heritable element that confers resistance to glucosamine, [GAR⁺]. Genetically it resembles other yeast prions: it appears spontaneously at a rate higher than mutations and is transmissible by non-Mendelian, cytoplasmic inheritance. However, [GAR⁺] is in other ways profoundly different from known prions. [GAR⁺] propagation involves Pmal, the plasma membrane protein pump, and [GAR⁺] formation is induced by Stdl, a member of the Snf3/Rgt2 glucose signaling pathway. Also, [GAR⁺] does not appear to involve the formation of an amyloid template and the prion state represents only a fraction of the Pmal protein in the cell,· consistent with the prion form constituting a complex between Pmal and Stdl, a much lower abundance protein. [GAR⁺] propagation is subject to a strong species barrier, as substitution of PMAl from other Saccharomyces species blocks propagation to s.. cerevisiae PMAl. Direct competition between [gar-] and [GAR⁺] cells indicate that cells carrying [GAR⁺] have an advantage under certain environmental conditions. [GAR⁺] appears spontaneously in a yeast isolated from a variety of sources and can be induced by co-culturing yeast and a number of Staphylococcus species. Overall, [GAR⁺] expands the conceptual framework for self-propagating protein-based elements of inheritance to include non-amyloid, potentially multicomponent systems such as transmembrane proteins and signal transducers.en_US
dc.description.statementofresponsibilityby Jessica C. S. Brown.en_US
dc.format.extent195 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectBiology.en_US
dc.title[GAR⁺] : a novel type of prion involved in glucose signaling and environmental sensing in S. cerevisiaeen_US
dc.title.alternativeNovel type of prion involved in glucose signaling and environmental sensing in S. cerevisiaeen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.identifier.oclc313768758en_US


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