{"id":{"repo_id":"utmb","oai_identifier":"oai:utmb-ir.tdl.org:2152.3/541"},"canonical_url":"https://search.dev.ndltd.org/etd/utmb/oai:utmb-ir.tdl.org:2152.3/541","repository":{"repo_id":"utmb","name":"University of Texas Medical Branch","base_url":"https://utmb-ir.tdl.org/server/oai/request"},"display":{"title":"Studies on Fortilin-Prohibitin Interaction","abstract":"Abstract: Apoptosis, programmed cell death, is a tightly regulated process that occurs in development, in tissue maintenance and turnover, and in regulating the immune system. Alterations in apoptosis regulation is known to be involved in various diseases including cancer, autoimmune diseases, and cardiovascular diseases including atherosclerosis initiation and maintenance. Fortilin is an antiapoptotic protein with a wide tissue distribution and a wide range of functions. fortilin has no sequence homology to other regulators of apoptosis, such as the Bcl-2 Proteins or the Inhibitors of Apoptosis proteins. In elucidating the mechanism of Fortilin-mediated cellular protection, fortilin protein interactions have been previously shown to modulate the cellular response to apoptotic stimuli. The goal of this dissertation is to investigate novel fortilin protein interactions in order to further shed light on the mechanism of fortilin mediated protection. In a proteomic screen fortilin was shown to interact with the anti-proliferative protein, prohibitin. I demonstrate that fortilin specifically interacts with this protein through in vitro studies. fortilin co-localizes with prohibitin in a perinuclear distribution and subcellular studies showed that fortilin and prohibitin are found in the nucleus, cytosol, and to a lesser degree in the endoplasmic reticulum. Fortilin was shown to mutually stabilize prohibitin. Finally, cells overexpressing fortilin and prohibitin attenuate the apoptosis response of cells compared to cells overexpressing either protein alone. In summary, these findings demonstrate a novel protein interaction between fortilin and prohibitin and shows a functional significance in modulating apoptosis after inducing cell stress.","abstract_html":"Abstract: Apoptosis, programmed cell death, is a tightly regulated process that occurs in development, in tissue maintenance and turnover, and in regulating the immune system. Alterations in apoptosis regulation is known to be involved in various diseases including cancer, autoimmune diseases, and cardiovascular diseases including atherosclerosis initiation and maintenance. Fortilin is an antiapoptotic protein with a wide tissue distribution and a wide range of functions. fortilin has no sequence homology to other regulators of apoptosis, such as the Bcl-2 Proteins or the Inhibitors of Apoptosis proteins. In elucidating the mechanism of Fortilin-mediated cellular protection, fortilin protein interactions have been previously shown to modulate the cellular response to apoptotic stimuli. The goal of this dissertation is to investigate novel fortilin protein interactions in order to further shed light on the mechanism of fortilin mediated protection. In a proteomic screen fortilin was shown to interact with the anti-proliferative protein, prohibitin. I demonstrate that fortilin specifically interacts with this protein through in vitro studies. fortilin co-localizes with prohibitin in a perinuclear distribution and subcellular studies showed that fortilin and prohibitin are found in the nucleus, cytosol, and to a lesser degree in the endoplasmic reticulum. Fortilin was shown to mutually stabilize prohibitin. Finally, cells overexpressing fortilin and prohibitin attenuate the apoptosis response of cells compared to cells overexpressing either protein alone. In summary, these findings demonstrate a novel protein interaction between fortilin and prohibitin and shows a functional significance in modulating apoptosis after inducing cell stress.","abstract_has_math":false,"creators":["Doan, Hung 1982-"],"institution":"The University of Texas Medical Branch at Galveston","degree_name":"Biochemistry and Molecular Biology (Doctoral)","degree_level":"Doctoral","degree_discipline":"Biochemistry","degree_department":null,"school":null,"contributors":[],"advisors":["Barral, Jose M"],"committee_chairs":[],"committee_members":["Fujise, Kenichi","Nesic-Taylor, Olivera","Wiktorowicz, John E","Goka, Thomas J"],"year":2013,"date_issued":"2013-06-03","date_published":"2013-06-03","updated_at":"2026-07-24T05:51:09Z","subjects":["Apoptosis","protein interactions"],"languages":["en_US"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/2152.3/541","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Barral, Jose M"]},{"key":"dc:contributor.committeemember","label":"Committee Member","values":["Fujise, Kenichi","Nesic-Taylor, Olivera","Wiktorowicz, John E","Goka, Thomas J"]},{"key":"dc:creator","label":"Author","values":["Doan, Hung 1982-"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2013-06-03T19:40:52Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2013-06-03T19:40:52Z"]},{"key":"dc:date.issued","label":"Date","values":["2013-06-03"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Biochemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Doctoral"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Biochemistry and Molecular Biology (Doctoral)"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["The University of Texas Medical Branch at Galveston"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Apoptosis","protein interactions"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en_US"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/2152.3/541"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Abstract: Apoptosis, programmed cell death, is a tightly regulated process that occurs in development, in tissue maintenance and turnover, and in regulating the immune system. Alterations in apoptosis regulation is known to be involved in various diseases including cancer, autoimmune diseases, and cardiovascular diseases including atherosclerosis initiation and maintenance. Fortilin is an antiapoptotic protein with a wide tissue distribution and a wide range of functions. fortilin has no sequence homology to other regulators of apoptosis, such as the Bcl-2 Proteins or the Inhibitors of Apoptosis proteins. In elucidating the mechanism of Fortilin-mediated cellular protection, fortilin protein interactions have been previously shown to modulate the cellular response to apoptotic stimuli. The goal of this dissertation is to investigate novel fortilin protein interactions in order to further shed light on the mechanism of fortilin mediated protection. In a proteomic screen fortilin was shown to interact with the anti-proliferative protein, prohibitin. I demonstrate that fortilin specifically interacts with this protein through in vitro studies. fortilin co-localizes with prohibitin in a perinuclear distribution and subcellular studies showed that fortilin and prohibitin are found in the nucleus, cytosol, and to a lesser degree in the endoplasmic reticulum. Fortilin was shown to mutually stabilize prohibitin. Finally, cells overexpressing fortilin and prohibitin attenuate the apoptosis response of cells compared to cells overexpressing either protein alone. In summary, these findings demonstrate a novel protein interaction between fortilin and prohibitin and shows a functional significance in modulating apoptosis after inducing cell stress."]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Studies on Fortilin-Prohibitin Interaction"]}]}],"canonical_facts":{"dc:contributor.advisor":["Barral, Jose M"],"dc:contributor.committeemember":["Fujise, Kenichi","Nesic-Taylor, Olivera","Wiktorowicz, John E","Goka, Thomas J"],"dc:creator":["Doan, Hung 1982-"],"dc:date.accessioned":["2013-06-03T19:40:52Z"],"dc:date.available":["2013-06-03T19:40:52Z"],"dc:date.issued":["2013-06-03"],"dc:description.abstract":["Abstract: Apoptosis, programmed cell death, is a tightly regulated process that occurs in development, in tissue maintenance and turnover, and in regulating the immune system. Alterations in apoptosis regulation is known to be involved in various diseases including cancer, autoimmune diseases, and cardiovascular diseases including atherosclerosis initiation and maintenance. Fortilin is an antiapoptotic protein with a wide tissue distribution and a wide range of functions. fortilin has no sequence homology to other regulators of apoptosis, such as the Bcl-2 Proteins or the Inhibitors of Apoptosis proteins. In elucidating the mechanism of Fortilin-mediated cellular protection, fortilin protein interactions have been previously shown to modulate the cellular response to apoptotic stimuli. The goal of this dissertation is to investigate novel fortilin protein interactions in order to further shed light on the mechanism of fortilin mediated protection. In a proteomic screen fortilin was shown to interact with the anti-proliferative protein, prohibitin. I demonstrate that fortilin specifically interacts with this protein through in vitro studies. fortilin co-localizes with prohibitin in a perinuclear distribution and subcellular studies showed that fortilin and prohibitin are found in the nucleus, cytosol, and to a lesser degree in the endoplasmic reticulum. Fortilin was shown to mutually stabilize prohibitin. Finally, cells overexpressing fortilin and prohibitin attenuate the apoptosis response of cells compared to cells overexpressing either protein alone. In summary, these findings demonstrate a novel protein interaction between fortilin and prohibitin and shows a functional significance in modulating apoptosis after inducing cell stress."],"dc:format.mimetype":["application/pdf"],"dc:identifier.uri":["http://hdl.handle.net/2152.3/541"],"dc:language.iso":["en_US"],"dc:subject":["Apoptosis","protein interactions"],"dc:title":["Studies on Fortilin-Prohibitin Interaction"],"thesis:degree_discipline":["Biochemistry"],"thesis:degree_level":["Doctoral"],"thesis:degree_name":["Biochemistry and Molecular Biology (Doctoral)"],"thesis:institution_name":["The University of Texas Medical Branch at Galveston"]},"updated_at":"2026-07-24T05:51:09Z"}