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dc.contributor.advisorFrank Gertler.en_US
dc.contributor.authorKwiatkowski, Adam Vincent, 1974-en_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Biology.en_US
dc.date.accessioned2005-09-27T19:09:37Z
dc.date.available2005-09-27T19:09:37Z
dc.date.copyright2004en_US
dc.date.issued2005en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/28936
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, February 2005.en_US
dc.descriptionIncludes bibliographical references.en_US
dc.description.abstractRegulated actin assembly drives cells movement, adhesion and shape change. The EnaNASP family of proteins controls actin filament elongation and are important regulators of axon guidance and cell motility. In vertebrates, the family consists of Mena (Mammalian Enabled), VASP (Vasodilator Stimulated Phosphoprotein), and EVL (Ena-VASP-Like). This thesis work focused on understanding the vertebrate EnaNASP protein family by discovering pathways that regulate EnaNASP function and by defining the role of EnaNASP proteins in vertebrate development. Characterization of the EVL locus revealed a new EVL isoform. A protein interaction screen for new EnaNASP ligands produced Tuba, a novel scaffold protein that associates with EnaNASP proteins in vivo. Tuba is a unique guanine nucleotide exchange factor (GEF) for Cdc42 that binds dynamin and a number of actin regulatory proteins in addition to Ena/VASP proteins. A knockout of EVL was made to determine the requirement for EVL in mouse development. Genetic analysis of EnaNASP function in the mouse revealed a requirement for Ena/VASP proteins in neuronal layering, spinal and cranial nerve formation, and cardiovascular development.en_US
dc.description.statementofresponsibilityby Adam Vincent Kwiatkowski.en_US
dc.format.extent151 leavesen_US
dc.format.extent7733059 bytes
dc.format.extent7753347 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypeapplication/pdf
dc.language.isoen_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/1721.1/7582
dc.subjectBiology.en_US
dc.titleCharacterization of Tuba, a novel Ena/VASP ligand, and function of Ena/VASP proteins in mouse developmenten_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.identifier.oclc60552457en_US


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