{"id":{"repo_id":"houston","oai_identifier":"oai:uh-ir.tdl.org:10657/1918"},"canonical_url":"https://search.dev.ndltd.org/etd/houston/oai:uh-ir.tdl.org:10657/1918","repository":{"repo_id":"houston","name":"University of Houston","base_url":"https://uh-ir.tdl.org/server/oai/request"},"display":{"title":"Phosphorylation of Glucocorticoid Receptor tau1c Transactivation Domain Enhances Binding to CREB Binding Protein (CBP) TAZ2 and a Microfluidic, High Throughput Protein Crystal Growth Method for Microgravity","abstract":"The glucocorticoid receptor (GR) N-terminal domain (NTD) contains a transactivation domain (activation function 1; AF-1). Although GR AF-1 is phosphorylated, effects of GR phosphorylation upon AF-1 activity and cofactor recruitment are not clear. Most GR AF-1 activity is confined to an unstructured domain called tau1c (amino acids 187-244) that contains three phosphorylation sites and binds to a cysteine rich fragment (CH3) of the co-activator CREB binding protein (CBP). Because CH3 overlaps the CBP transcriptional adaptor zinc binding (TAZ) 2 domain, implicated in phosphorylation dependent binding to other unstructured transcription factor domains, we investigated if GR interacts with TAZ2 and whether this binding event is modulated by phosphorylation. We find that GR tau1c is required for enhancement of GR function and GR/CBP association in cultured cells. Tau1c interacts with TAZ2 in vitro with reasonable affinity and peptide mapping reveals CBP binding determinants throughout tau1c. Phosphorylation at GR S203, not involved in transactivation, does not affect tau1c binding to TAZ2. However, phosphorylation at S211 and S226, markers of GR transcriptional activity, enhances TAZ2 binding in a synergistic fashion. We propose that GR tau1c phosphorylation could promote CBP recruitment and enhance AF-1 activity.","abstract_html":"The glucocorticoid receptor (GR) N-terminal domain (NTD) contains a transactivation domain (activation function 1; AF-1). Although GR AF-1 is phosphorylated, effects of GR phosphorylation upon AF-1 activity and cofactor recruitment are not clear. Most GR AF-1 activity is confined to an unstructured domain called tau1c (amino acids 187-244) that contains three phosphorylation sites and binds to a cysteine rich fragment (CH3) of the co-activator CREB binding protein (CBP). Because CH3 overlaps the CBP transcriptional adaptor zinc binding (TAZ) 2 domain, implicated in phosphorylation dependent binding to other unstructured transcription factor domains, we investigated if GR interacts with TAZ2 and whether this binding event is modulated by phosphorylation. We find that GR tau1c is required for enhancement of GR function and GR/CBP association in cultured cells. Tau1c interacts with TAZ2 in vitro with reasonable affinity and peptide mapping reveals CBP binding determinants throughout tau1c. Phosphorylation at GR S203, not involved in transactivation, does not affect tau1c binding to TAZ2. However, phosphorylation at S211 and S226, markers of GR transcriptional activity, enhances TAZ2 binding in a synergistic fashion. We propose that GR tau1c phosphorylation could promote CBP recruitment and enhance AF-1 activity.","abstract_has_math":false,"creators":["Carruthers, Carl W., Jr. 1971-"],"institution":"University of Houston","degree_name":"Doctor of Philosophy","degree_level":"Doctoral","degree_discipline":"Biochemistry","degree_department":null,"school":null,"contributors":[],"advisors":["Gustafsson, Jan-Åke"],"committee_chairs":[],"committee_members":["Webb, Paul","Fox, Robert O.","Schwartz, Robert J.","Moore, David"],"year":2014,"date_issued":"2014-12","date_published":"2014-12","updated_at":"2026-07-24T02:31:52Z","subjects":["Phosphorylation","Glucocorticoids","Glucocorticoid receptors","Tau1c","Transactivation","CBP","Transcriptional adaptor zinc binding (TAZ) 2"],"languages":["eng"],"rights":["The author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s)."],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/10657/1918","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Gustafsson, Jan-Åke"]},{"key":"dc:contributor.committeemember","label":"Committee Member","values":["Webb, Paul","Fox, Robert O.","Schwartz, Robert J.","Moore, David"]},{"key":"dc:creator","label":"Author","values":["Carruthers, Carl W., Jr. 1971-"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2017-07-20T19:16:14Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2017-07-20T19:16:14Z"]},{"key":"dc:date.issued","label":"Date","values":["2014-12"]},{"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":["Doctor of Philosophy"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Houston"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Phosphorylation","Glucocorticoids","Glucocorticoid receptors","Tau1c","Transactivation","CBP","Transcriptional adaptor zinc binding (TAZ) 2"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["eng"]},{"key":"dc:rights","label":"Dc Rights","values":["The author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s)."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10657/1918"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["The glucocorticoid receptor (GR) N-terminal domain (NTD) contains a transactivation domain (activation function 1; AF-1). Although GR AF-1 is phosphorylated, effects of GR phosphorylation upon AF-1 activity and cofactor recruitment are not clear. Most GR AF-1 activity is confined to an unstructured domain called tau1c (amino acids 187-244) that contains three phosphorylation sites and binds to a cysteine rich fragment (CH3) of the co-activator CREB binding protein (CBP). Because CH3 overlaps the CBP transcriptional adaptor zinc binding (TAZ) 2 domain, implicated in phosphorylation dependent binding to other unstructured transcription factor domains, we investigated if GR interacts with TAZ2 and whether this binding event is modulated by phosphorylation. We find that GR tau1c is required for enhancement of GR function and GR/CBP association in cultured cells. Tau1c interacts with TAZ2 in vitro with reasonable affinity and peptide mapping reveals CBP binding determinants throughout tau1c. Phosphorylation at GR S203, not involved in transactivation, does not affect tau1c binding to TAZ2. However, phosphorylation at S211 and S226, markers of GR transcriptional activity, enhances TAZ2 binding in a synergistic fashion. We propose that GR tau1c phosphorylation could promote CBP recruitment and enhance AF-1 activity."]},{"key":"dc:format.mimetype","label":"Dc Format Mimetype","values":["application/pdf"]},{"key":"dc:title","label":"Title","values":["Phosphorylation of Glucocorticoid Receptor tau1c Transactivation Domain Enhances Binding to CREB Binding Protein (CBP) TAZ2 and a Microfluidic, High Throughput Protein Crystal Growth Method for Microgravity"]}]}],"canonical_facts":{"dc:contributor.advisor":["Gustafsson, Jan-Åke"],"dc:contributor.committeemember":["Webb, Paul","Fox, Robert O.","Schwartz, Robert J.","Moore, David"],"dc:creator":["Carruthers, Carl W., Jr. 1971-"],"dc:date.accessioned":["2017-07-20T19:16:14Z"],"dc:date.available":["2017-07-20T19:16:14Z"],"dc:date.issued":["2014-12"],"dc:description.abstract":["The glucocorticoid receptor (GR) N-terminal domain (NTD) contains a transactivation domain (activation function 1; AF-1). Although GR AF-1 is phosphorylated, effects of GR phosphorylation upon AF-1 activity and cofactor recruitment are not clear. Most GR AF-1 activity is confined to an unstructured domain called tau1c (amino acids 187-244) that contains three phosphorylation sites and binds to a cysteine rich fragment (CH3) of the co-activator CREB binding protein (CBP). Because CH3 overlaps the CBP transcriptional adaptor zinc binding (TAZ) 2 domain, implicated in phosphorylation dependent binding to other unstructured transcription factor domains, we investigated if GR interacts with TAZ2 and whether this binding event is modulated by phosphorylation. We find that GR tau1c is required for enhancement of GR function and GR/CBP association in cultured cells. Tau1c interacts with TAZ2 in vitro with reasonable affinity and peptide mapping reveals CBP binding determinants throughout tau1c. Phosphorylation at GR S203, not involved in transactivation, does not affect tau1c binding to TAZ2. However, phosphorylation at S211 and S226, markers of GR transcriptional activity, enhances TAZ2 binding in a synergistic fashion. We propose that GR tau1c phosphorylation could promote CBP recruitment and enhance AF-1 activity."],"dc:format.mimetype":["application/pdf"],"dc:identifier.uri":["http://hdl.handle.net/10657/1918"],"dc:language.iso":["eng"],"dc:rights":["The author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s)."],"dc:subject":["Phosphorylation","Glucocorticoids","Glucocorticoid receptors","Tau1c","Transactivation","CBP","Transcriptional adaptor zinc binding (TAZ) 2"],"dc:title":["Phosphorylation of Glucocorticoid Receptor tau1c Transactivation Domain Enhances Binding to CREB Binding Protein (CBP) TAZ2 and a Microfluidic, High Throughput Protein Crystal Growth Method for Microgravity"],"thesis:degree_discipline":["Biochemistry"],"thesis:degree_level":["Doctoral"],"thesis:degree_name":["Doctor of Philosophy"],"thesis:institution_name":["University of Houston"]},"updated_at":"2026-07-24T02:31:52Z"}