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dc.identifier.urihttp://hdl.handle.net/1951/59925
dc.identifier.urihttp://hdl.handle.net/11401/71466
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeDissertation
dcterms.abstractThe six-layered mammalian neocortex derives from a pseudostratified neuroepithelium by a series of cell divisions of neuronal progenitors, neuroepithelial and radial glial cells. Neurogenesis, a major event in the developing neocortex, relies on the ability of radial glial cells (RGCs) to switch from proliferative self-expanding to differentiative neurongenerating/progenitor self-renewing divisions. However, the molecular mechanisms that control this switch in a correct temporal manner are not well understood. In this thesis, I demonstrated that the DOCK180 family member DOCK7, an activator of Rac GTPases, plays an important role in the regulation of RGC proliferation versus differentiation. Silencing of DOCK7 in RGCs of developing mouse embryos hampers neuronal differentiation and maintains cells as cycling progenitors. Conversely, DOCK7 overexpression promotes RGC differentiation into basal progenitors and neurons. Using different approaches, including live-cell imaging experiments, I obtained evidence that DOCK7 influences RGC fate and neurogenesis by controlling the apically directed interkinetic nuclear migration (INM) process of RGCs. Importantly, DOCK7 exerts its effects on INM and neurogenesis independently of its GEF activity towards Rac, but instead does so by antagonizing the microtubule growth-promoting function of the centrosome-associated protein TACC3. Taken together, DOCK7 interacts with TACC3 to control INM, as such governing RGC fate and genesis of neurons during cortical development.
dcterms.available2013-05-22T17:35:51Z
dcterms.available2015-04-24T14:47:40Z
dcterms.contributorMills, Alea Aen_US
dcterms.contributorVan Aelst, Linda , Tsirka, Styliani-Anna Een_US
dcterms.contributorDubnau, Joshuaen_US
dcterms.contributorTurner, Glenn.en_US
dcterms.creatorYANG, YUTING ROSA
dcterms.dateAccepted2013-05-22T17:35:51Z
dcterms.dateAccepted2015-04-24T14:47:40Z
dcterms.dateSubmitted2013-05-22T17:35:51Z
dcterms.dateSubmitted2015-04-24T14:47:40Z
dcterms.descriptionDepartment of Molecular and Cellular Biologyen_US
dcterms.extent116 pg.en_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierYANG_grad.sunysb_0771E_11067en_US
dcterms.identifierhttp://hdl.handle.net/1951/59925
dcterms.identifierhttp://hdl.handle.net/11401/71466
dcterms.issued2012-08-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2013-05-22T17:35:51Z (GMT). No. of bitstreams: 1 YANG_grad.sunysb_0771E_11067.pdf: 3615494 bytes, checksum: 9cc072376a5cdffd0354bc97fa33ad7b (MD5) Previous issue date: 1en
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dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectNeurosciences--Cellular biology--Molecular biology
dcterms.titleDOCK7 interacts with TACC3 to regulate interkinetic nuclear migration and genesis of neurons from cortical neuronal progenitors
dcterms.typeDissertation


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