BTB-Kelch Proteins and TAk1 Kinase N Immune Function

dc.contributor.advisorChen, Zhijian J.en
dc.creatorLiu, Hong-Hsingen
dc.date.accessioned2010-07-12T17:59:20Z
dc.date.available2010-07-12T17:59:20Z
dc.date.issued2006-12-19
dc.description.abstractBTB-kelch proteins are putative components of E3 ligases with a BTB domain at the N terminus and several kelch repeats at the C terminus. KLHL6 and mKELCH are two members of this family. Conditional ablation of Klhl6 in B cells resulted in mild developmental phenotypes in bone marrow precursors. The number of peripheral B cells was decreased by half, and responded defectively in germinal center formation after antigen stimulations. mKELCH is a novel protein cloned from hearts. Knocked-in LacZ expressed predominantly at muscles and several photosensitive organs. TAK1 is a member of MAPKKK. Deletion of TAK1 prevented the maturation of CD4+ or CD8+ single positive thymocytes, leading to reduction of T cells in peripheral tissues. Thymocytes lacking TAK1 failed to activate NF-κB and JNK, and were prone to apoptosis upon stimulation. All three mouse models have provided important evidences in elucidating biological functions for each protein in vivo.en
dc.format.digitalOriginborn digitalen
dc.format.mediumElectronicen
dc.format.mimetypeapplication/pdfen
dc.identifier.oclc424500398
dc.identifier.urihttps://hdl.handle.net/2152.5/414
dc.language.isoenen
dc.subjectMAP Kinase Kinase Kinasesen
dc.subjectThymus Glanden
dc.subjectImmunityen
dc.titleBTB-Kelch Proteins and TAk1 Kinase N Immune Functionen
dc.typeThesisen
dc.type.genredissertationen
dc.type.materialTexten
thesis.date.available2006-12-19
thesis.degree.departmentGraduate School of Biomedical Sciencesen
thesis.degree.disciplineIntegrative Biologyen
thesis.degree.grantorUT Southwestern Medical Centeren
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophyen

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