The specific aims of this proposal are designed to investigate the mechanisms by which the GATA transcription factor family regulates tissue-specific transcription during T lymphocyte and neuronal development. We originally identified a group of related transcription factors [the chicken GATA (cGATA) factor family]. More recent studies in a large number of laboratories have shown that homologs for each member of the family exists in all vertebrate species. These factors are themselves tissue-specifically regulated and bind to very similar cis- regulatory consensus sequences of genes expressed in a restricted set of tissues. Using the cloned transcription factor genes and cDNAs, as well as antibodies which recognize unique functional domains of these trans- activating proteins, we propose to investigate several aspects of GATA factor transcriptional activation. In the first series of experiments, we plan to empirically determine the biophysical parameters governing binding of the factors to their highest affinity site(s), and to then test whether binding sites encountered in genetically defined cis- regulatory sequences of neuronal and T cell genes bind the predicted factor family member. The role of GATA factor regulation in T lymphocyte differentiation and determination in hematopoietic cell culture models (cGATA-3 and mGATA-3) and in transgenic mice (mGATA-3) will be examined. We will ask whether the T lymphocyte-restricted transcription units encoding the T cell receptor delta gene, the HIV-1 genome and the murine lck gene are regulated by GATA-3, and whether or not the neuronal- specific nalpha acetylcholinesterase receptor gene is directly regulated by cGATA-2 and/or cGATA-3 in the CNS. We will also investigate the potentially determinative role(s) that specific GATA factors may play in T lymphocyte and CNS development in vivo, in chickens by examining the consequences of conditional GATA factor expression on lymphocyte differentiation (in transformed preB/preT cells) and in mice by examining the effects of targeted disruption of the mGATA-3 gene. The single copy Drosophila GATA factor gene will be studied (in order to incorporate the wealth of genetic background information available in this organism) to define the hierarchy of genes which regulate expression of the dGATA gene during embryonic development as well as to identify potential targets for its activity in the nervous system. These experiments will provide fundamental insight into how the earliest events which are specified by this family of transcription factors in the nervous system and in T cells may be achieved, and how the genetic processes which are regulated by this transcription factor gene family may go awry during altered embryonic development.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM028896-11
Application #
2175305
Study Section
Molecular Biology Study Section (MBY)
Project Start
1983-03-01
Project End
1996-11-30
Budget Start
1994-12-01
Budget End
1995-11-30
Support Year
11
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
City
Evanston
State
IL
Country
United States
Zip Code
60201
Moriguchi, Takashi; Yu, Lei; Otsuki, Akihito et al. (2016) Gata3 Hypomorphic Mutant Mice Rescued with a Yeast Artificial Chromosome Transgene Suffer a Glomerular Mesangial Cell Defect. Mol Cell Biol 36:2272-81
Udager, Aaron M; Prakash, Ajay; Saenz, David A et al. (2014) Proper development of the outer longitudinal smooth muscle of the mouse pylorus requires Nkx2-5 and Gata3. Gastroenterology 146:157-165.e10
Lim, Kim-Chew; Hosoya, Tomonori; Brandt, William et al. (2012) Conditional Gata2 inactivation results in HSC loss and lymphatic mispatterning. J Clin Invest 122:3705-17
Ku, Chia-Jui; Hosoya, Tomonori; Maillard, Ivan et al. (2012) GATA-3 regulates hematopoietic stem cell maintenance and cell-cycle entry. Blood 119:2242-51
Hosoya-Ohmura, Sakie; Lin, Yu-Hsuan; Herrmann, Mary et al. (2011) An NK and T cell enhancer lies 280 kilobase pairs 3' to the gata3 structural gene. Mol Cell Biol 31:1894-904
Duncan, Jeremy S; Lim, Kim-Chew; Engel, James D et al. (2011) Limited inner ear morphogenesis and neurosensory development are possible in the absence of GATA3. Int J Dev Biol 55:297-303
Hosoya, Tomonori; Maillard, Ivan; Engel, James D (2010) From the cradle to the grave: activities of GATA-3 throughout T-cell development and differentiation. Immunol Rev 238:110-25
Maeda, Atsuko; Moriguchi, Takashi; Hamada, Michito et al. (2009) Transcription factor GATA-3 is essential for lens development. Dev Dyn 238:2280-91
Hosoya, Tomonori; Kuroha, Takashi; Moriguchi, Takashi et al. (2009) GATA-3 is required for early T lineage progenitor development. J Exp Med 206:2987-3000
Hoshino, Tomofumi; Shimizu, Ritsuko; Ohmori, Shinya et al. (2008) Reduced BMP4 abundance in Gata2 hypomorphic mutant mice result in uropathies resembling human CAKUT. Genes Cells 13:159-70

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