Analysis of clathrin vesicle transport from the <italic>trans</italic> Golgi network to the late endosome.
dc.contributor.author | Abazeed, Mohamed | |
dc.contributor.advisor | Fuller, Robert S. | |
dc.date.accessioned | 2016-08-30T16:23:39Z | |
dc.date.available | 2016-08-30T16:23:39Z | |
dc.date.issued | 2008 | |
dc.identifier.uri | http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqm&rft_dat=xri:pqdiss:3304908 | |
dc.identifier.uri | https://hdl.handle.net/2027.42/126995 | |
dc.description.abstract | Vesicle transport from the <italic>trans</italic>-Golgi network (TGN) to the late endosome/prevacuolar compartment (PVC) represents a conserved, clathrin-dependent sorting event that separates lysosomal from secretory cargo molecules and is also required for localization of integral membrane proteins to the TGN. The principal aim of this thesis has been the development of a cell-free assay that authentically reconstitutes the transport of membrane proteins from the TGN to the late endosome/PVC. The cell-free reaction exhibits features consistent with authentic membrane fusion reactions including dependence on time, temperature, ATP, and cytosol. Molecular analysis indicates that factors required for formation of clathrin-coated vesicles at the TGN (the Chc1p clathrin heavy chain, the Vps1p dynamin homolog, the Gga clathrin adaptor) and for vesicle fusion at the PVC (the Pep12p t-SNARE, the Vps21p rab protein, the Vps45p SM (Sec1/Munc18) protein) are required for cell-free transport. We used the TGN-PVC transport assay to determine the roles of clathrin adaptors Gga and AP-1 in TGN-PVC transport. We find that the Gga1/2 proteins, and not AP-1, function in the direct transport of two TGN transmembrane proteins, Kex2p and Vps10p, from the TGN to the PVC. To characterize the role of the yeast Gga proteins in TGN to PVC transport, we employ directed yeast two-hybrid and in vitro binding experiments to identify interactions between the sequences in the C-tails of TGN cargo molecules and Gga1/2p. Together, these experiments demonstrate that sequences in the cytosolic tails of Kex2p and Vps10p bind to the VHS domain of the Gga1/2p adaptor. Details of these experiments as well as further studies directed toward identifying the binding regions that mediate these interactions are described. Finally, we show that truncated forms of Gga proteins are able to form homo- and hetero-dimers and that sequence elements in the Gga hinge domain function to block both cargo binding and dimer formation. All together, these results establish the first cell-free assay reconstitution of TGN to late endosome/PVC transport in any system and describe new insights into the process of molecular recruitment of cargo proteins into Gga-containing clathrin coated vesicles at the TGN. | |
dc.format.extent | 174 p. | |
dc.language | English | |
dc.language.iso | EN | |
dc.subject | Analysis | |
dc.subject | Clathrin Vesicle | |
dc.subject | Endosome | |
dc.subject | Endosomes | |
dc.subject | Kex2p | |
dc.subject | Late | |
dc.subject | Pep12p | |
dc.subject | Prevacuolar Compartment | |
dc.subject | Trans-golgi Network | |
dc.subject | Transport | |
dc.subject | Yeast | |
dc.title | Analysis of clathrin vesicle transport from the <italic>trans</italic> Golgi network to the late endosome. | |
dc.type | Thesis | |
dc.description.thesisdegreename | PhD | en_US |
dc.description.thesisdegreediscipline | Biological Sciences | |
dc.description.thesisdegreediscipline | Cellular biology | |
dc.description.thesisdegreegrantor | University of Michigan, Horace H. Rackham School of Graduate Studies | |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/126995/2/3304908.pdf | |
dc.owningcollname | Dissertations and Theses (Ph.D. and Master's) |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.