The overall aim of this project is to understand the mechanisms that control alternative commitment of alpha/beta thymocytes to the CD4 or CD8 lineages and that ensure the precise correlation between coreceptor expression and TCR restriction to class I or II MHC. Although it is now widely accepted that alternate TCR signaling in response to engagement by class I or II ligands is responsible for initiating alternate lineage commitment, the intracellular pathways through which this is accomplished remain unknown. We have previously described a unique spontaneous mutant mouse, termed """"""""helper deficient"""""""" or HD, in which the correlation between coreceptor expression and MHC specificity breaks down, such that all thymocytes, in particular class II-restricted ones, adopt the CD8 lineage. We have now tentatively identified the defective gene as cKrox, a largely uncharacterized member of the POK subfamily of proteins, which are defined as containing both a Kr?ppel-like zinc finger and a BTB/POZ domain, the latter implicated in transcriptional repression. Based on this very recent finding, the current proposal focuses on defining the functional characteristics, regulation and cellular distribution of cKrox in developing thymocytes. We propose the following specific aims: 1) To definitively demonstrate that cKrox corresponds to the HD locus. 2) To determine how cKrox activity is differentially regulated in class I- versus class II-specific thymocytes. 3) To functionally dissect the roles of the zinc finger and BTB/POZ domains of cKrox in lineage commitment.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI042915-07
Application #
6892848
Study Section
Immunobiology Study Section (IMB)
Program Officer
Macchiarini, Francesca
Project Start
1999-06-01
Project End
2009-05-31
Budget Start
2005-06-01
Budget End
2006-05-31
Support Year
7
Fiscal Year
2005
Total Cost
$422,500
Indirect Cost
Name
Institute for Cancer Research
Department
Type
DUNS #
064367329
City
Philadelphia
State
PA
Country
United States
Zip Code
19111
Engel, Isaac; Zhao, Meng; Kappes, Dietmar et al. (2012) The transcription factor Th-POK negatively regulates Th17 differentiation in V?14i NKT cells. Blood 120:4524-32
Engel, Isaac; Hammond, Kirsten; Sullivan, Barbara A et al. (2010) Co-receptor choice by V alpha14i NKT cells is driven by Th-POK expression rather than avoidance of CD8-mediated negative selection. J Exp Med 207:1015-29
Park, Kyewon; He, Xi; Lee, Hyung-Ok et al. (2010) TCR-mediated ThPOK induction promotes development of mature (CD24-) gammadelta thymocytes. EMBO J 29:2329-41
He, Xi; Park, Kyewon; Wang, Haitao et al. (2008) CD4-CD8 lineage commitment is regulated by a silencer element at the ThPOK transcription-factor locus. Immunity 28:346-58
He, Xiao; Kappes, Dietmar J (2006) CD4/CD8 lineage commitment: light at the end of the tunnel? Curr Opin Immunol 18:135-42