Previously, we found that chromatin remodeling was required for Th2 cytokine gene expression. As the remodeling enzyme bound to the affected loci, the role of the remodeling enzyme appears to be direct.? ? Progress:? ? We identified a transcription factor that associates with a remodeling enzyme in a cytokine-dependent manner.? ? We identified two transcription factors that recruit a remodeling enzyme to the Th2 locus.? ? We identified a transcription factor that facilitates binding of another transcription factor to the Th2 locus.? ? We identified the version of a remodeling complex that regulates Th2 gene expression and chromatin structure.? ? We identified another remodeling enzyme regulating activation-inducible genes in a T cell line.? ? Future: ? Remodeling and other cytokine loci.? Remodeling and other T cell fates.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Intramural Research (Z01)
Project #
1Z01AG000524-04
Application #
7732252
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
2008
Total Cost
$438,713
Indirect Cost
Name
National Institute on Aging
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Wurster, Andrea L; Pazin, Michael J (2012) ATP-dependent chromatin remodeling in T cells. Biochem Cell Biol 90:1-13
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Shogren-Knaak, Michael; Ishii, Haruhiko; Sun, Jian-Min et al. (2006) Histone H4-K16 acetylation controls chromatin structure and protein interactions. Science 311:844-7
Lynch, Mary; Chen, Li; Ravitz, Michael J et al. (2005) hnRNP K binds a core polypyrimidine element in the eukaryotic translation initiation factor 4E (eIF4E) promoter, and its regulation of eIF4E contributes to neoplastic transformation. Mol Cell Biol 25:6436-53
Lu, Jun; Pazin, Michael J; Ravid, Katya (2004) Properties of ets-1 binding to chromatin and its effect on platelet factor 4 gene expression. Mol Cell Biol 24:428-41
Ishii, Haruhiko; Sen, Ranjan; Pazin, Michael J (2004) Combinatorial control of DNase I-hypersensitive site formation and erasure by immunoglobulin heavy chain enhancer-binding proteins. J Biol Chem 279:7331-8