Steroid hormones and vitamins including glucocorticoids and vitamin A derivatives act to induce cellular differentiation by directly modulating gene transcription and are often associated with the inhibition of cell growth. Nuclear receptors bind to hormones and vitamins and activate hormone responsive genes by recruiting an acetylase co-activation complex. The broad long- term objectives of this proposal are: (a) to decipher novel regulatory mechanisms involved in receptor and coactivator function; (b) to identify new components of the receptor coactivation-complex; and (c) to dissect the regulatory properties of the complex that translate a hormonal signal into transcriptional and physiological responses. To achieve the above goals, the following Specific Aims will be pursued: (I) To test the hypothesis that both nuclear receptor interaction domains of CBP/p300 are necessary for nuclear receptor mediated gene activation. (II) To determine the roles of the histone acetyltransferase (HAT)- associated domains of CBP/p300 in transcriptional activation and to test the hypothesis that additional proteins are necessary for HAT-mediated transactivation. (III) To test the hypothesis that constant region 2 (CR2) and constant region 3 (CR3) of adenoviral oncoprotein E1A function as the HAT-inhibitory domains and to determine the mechanism of transcription inhibition by E 1 A. A combination of in vitro binding, site directed mutagenesis, deletion analysis, and mammalian cell transfection based in vivo assays will be utilized to address the above Specific Aims. Yeast two-hybrid screens will be employed to identify and characterize novel CBP/p300 regulatory proteins. These studies are clinically significant because: (a) nuclear receptor agonists and antagonists are useful in treatment of breast, and prostate cancer, leukemia, diabetes, and cardiovascular diseases; and (b) chromosomal translocations and amplification of nuclear receptors and their cofactors have been implicated in leukemia and breast cancer suggesting abnormal targeting or regulation of the activities of receptors or their coactivators may play important roles in leukemia and oncogenesis. The accomplishment of the Specific Aims described above geared towards achieving the long- term goals should provide a better understanding of the role of nuclear receptors and coactivators in transcription and in human diseases including cancer.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
7R01DK057079-06
Application #
7175649
Study Section
Endocrinology Study Section (END)
Program Officer
Margolis, Ronald N
Project Start
2000-08-01
Project End
2007-07-31
Budget Start
2005-12-01
Budget End
2007-07-31
Support Year
6
Fiscal Year
2004
Total Cost
$16,379
Indirect Cost
Name
Northwestern University at Chicago
Department
Obstetrics & Gynecology
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Macfarlan, Todd; Parker, J Brandon; Nagata, Kyosuke et al. (2006) Thanatos-associated protein 7 associates with template activating factor-Ibeta and inhibits histone acetylation to repress transcription. Mol Endocrinol 20:335-47
Macfarlan, Todd; Kutney, Sara; Altman, Brian et al. (2005) Human THAP7 is a chromatin-associated, histone tail-binding protein that represses transcription via recruitment of HDAC3 and nuclear hormone receptor corepressor. J Biol Chem 280:7346-58
Curtis, Anne M; Seo, Sang-beom; Westgate, Elizabeth J et al. (2004) Histone acetyltransferase-dependent chromatin remodeling and the vascular clock. J Biol Chem 279:7091-7
Kutney, Sara N; Hong, Rui; Macfarlan, Todd et al. (2004) A signaling role of histone-binding proteins and INHAT subunits pp32 and Set/TAF-Ibeta in integrating chromatin hypoacetylation and transcriptional repression. J Biol Chem 279:30850-5
Hong, Rui; Macfarlan, Todd; Kutney, Sara N et al. (2004) The identification of phosphorylation sites of pp32 and biochemical purification of a cellular pp32-kinase. Biochemistry 43:10157-65
Hong, Rui; Chakravarti, Debabrata (2003) The human proliferating Cell nuclear antigen regulates transcriptional coactivator p300 activity and promotes transcriptional repression. J Biol Chem 278:44505-13
van Leeuwen, Hans; Okuwaki, Mitsuru; Hong, Rui et al. (2003) Herpes simplex virus type 1 tegument protein VP22 interacts with TAF-I proteins and inhibits nucleosome assembly but not regulation of histone acetylation by INHAT. J Gen Virol 84:2501-10
Seo, Sang-beom; Macfarlan, Todd; McNamara, Peter et al. (2002) Regulation of histone acetylation and transcription by nuclear protein pp32, a subunit of the INHAT complex. J Biol Chem 277:14005-10
Cervoni, Nadia; Detich, Nancy; Seo, Sang-Beom et al. (2002) The oncoprotein Set/TAF-1beta, an inhibitor of histone acetyltransferase, inhibits active demethylation of DNA, integrating DNA methylation and transcriptional silencing. J Biol Chem 277:25026-31
Li, Fusheng; Macfarlan, Todd; Pittman, Randall N et al. (2002) Ataxin-3 is a histone-binding protein with two independent transcriptional corepressor activities. J Biol Chem 277:45004-12

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