This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.During Th2 differentiation, positive and negative regulatory elements work cooperatively in the Th2 cytokine locus to bring about changes in chromatin structure that facilitate coordinated cytokine gene expression in a lineage-specific fashion. The overall goal of this study is to understand the interplay among cis-elements that coordinates this gene expression. We will create a model system in which the role that various cis-elements play in transcriptional regulation within the Th2 cytokine locus can be examined. Their completion will lay the groundwork for successfully addressing the overall scientific goal.
The first aim i s to identify trans-factor binding sites serving structural or functional roles in mediating transcriptional activity in the locus. We will focus on binding sites for two important Th2-related factors, GATA3 and STAT6. Biochemical and molecular biological approaches will be used to fulfill the objectives of this aim.
The second aim i s to generate a reporter system to evaluate the role of elements within the Th2 cytokine locus in regulating coordinated expression of IL4, IL5, and IL13. This reporter will be utilized to assess transcription of the genes simultaneously as well as assess the role of cis-elements, individually and in combination, on their regulation.Appropriate Th2 differentiation is critical for proper immune homeostasis and antigen responsiveness. Dysregulated T cell polarization has been implicated in allergic diseases and autoimmunity. Information gleaned from these studies will contribute to our understanding of Th2 differentiation and hopefully enable the ultimate goal, to intervene in this process and to avoid or correct these pathological manifestations.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR024214-02
Application #
7721038
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2008-07-01
Project End
2009-06-30
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
2
Fiscal Year
2008
Total Cost
$215,629
Indirect Cost
Name
University of Kansas
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
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