The long term goal of this research is to understand the molecular mechanisms underlying the regulation of the homeotic genes during development. Specifically, we will investigate the regulation of the homeotic genes by the trithorax locus (trx) in Drosophila melanogaster. Genetic and molecular evidence suggests that trx encodes a positive trans-acting regulator of many of the homeotic genes in the Bithorax Complex (BX-C) and Antennapedia Complex (ANT-C). The trx gene product is required to establish and maintain the normal level of expression of these genes in their appropriate segments. We will investigate how trx exerts its effects on the homeotic genes by molecular cloning of the trx DNA sequences and by characterizing the structure of its RNA and protein products. We will also determine the effects of trx mutations on the expression of selected homeotic gene products. The major strategy for cloning trx will be chromosomal walking. Determination of the location and physical extent of the locus will involve molecular mapping of trx mutations and rescue of trx mutations by P element-mediated transformation. The primary structure of the trx gene and its RNA and protein products will be determined by Northern analysis, S1 nuclease protection, primer extension and DNA sequencing of trx cDNA clones and corresponding genomic DNA. Temporal and spatial expression patterns of trx will be determined by in situ hybridization of trx gene probes to tissue sections and by immunofluorescent staining of embryos with anti-trx antibodies. The effects of trx mutations on homeotic gene expression will also use these methods, with the available probes for selected homeotic gene products. The results of these studies will provide the foundation for further experiments to determine whether trx protein(s) interacts directly with the homeotic genes and address how trx functions in the positive regulation of these genes to effects their proper spatial expression during development.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM039255-05
Application #
2179713
Study Section
Genetics Study Section (GEN)
Project Start
1988-04-01
Project End
1995-08-31
Budget Start
1992-04-01
Budget End
1995-08-31
Support Year
5
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Case Western Reserve University
Department
Genetics
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Tie, Feng; Banerjee, Rakhee; Fu, Chen et al. (2016) Polycomb inhibits histone acetylation by CBP by binding directly to its catalytic domain. Proc Natl Acad Sci U S A 113:E744-53
Du, Juan; Zhang, Junzheng; He, Tao et al. (2016) Stuxnet Facilitates the Degradation of Polycomb Protein during Development. Dev Cell 37:507-19
Tie, Feng; Banerjee, Rakhee; Saiakhova, Alina R et al. (2014) Trithorax monomethylates histone H3K4 and interacts directly with CBP to promote H3K27 acetylation and antagonize Polycomb silencing. Development 141:1129-39
Mason-Suares, Heather; Tie, Feng; Yan, Christopher M et al. (2013) Polycomb silencing of the Drosophila 4E-BP gene regulates imaginal disc cell growth. Dev Biol 380:111-24
Tie, Feng; Banerjee, Rakhee; Conrad, Patricia A et al. (2012) Histone demethylase UTX and chromatin remodeler BRM bind directly to CBP and modulate acetylation of histone H3 lysine 27. Mol Cell Biol 32:2323-34
Stepanik, Vincent A; Harte, Peter J (2012) A mutation in the E(Z) methyltransferase that increases trimethylation of histone H3 lysine 27 and causes inappropriate silencing of active Polycomb target genes. Dev Biol 364:249-58
Tie, Feng; Banerjee, Rakhee; Stratton, Carl A et al. (2009) CBP-mediated acetylation of histone H3 lysine 27 antagonizes Drosophila Polycomb silencing. Development 136:3131-41
Kurzhals, Rebeccah L; Tie, Feng; Stratton, Carl A et al. (2008) Drosophila ESC-like can substitute for ESC and becomes required for Polycomb silencing if ESC is absent. Dev Biol 313:293-306
Tie, Feng; Stratton, Carl A; Kurzhals, Rebeccah L et al. (2007) The N terminus of Drosophila ESC binds directly to histone H3 and is required for E(Z)-dependent trimethylation of H3 lysine 27. Mol Cell Biol 27:2014-26
Tie, Feng; Siebold, Alex P; Harte, Peter J (2005) The N-terminus of Drosophila ESC mediates its phosphorylation and dimerization. Biochem Biophys Res Commun 332:622-32

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