Analysis of gene regulation in the beta-globin loci has been instructive in establishing a number of the founding principles for the differential, tissue-specific transcriptional control of vertebrate genes. The PI proposes to continue analysis of the cis-regulatory mechanisms and trans-acting factors involved in regulating the chicken and human beta-globin gene clusters, in particular to address the underlying mechanisms responsible for erythroid tissue- and developmental stage-specific transcriptional control (""""""""hemoglobin switching""""""""). This application proposes three lines of study to investigate cis- regulatory mechanisms that are responsible for globin gene switching using different experimental approaches: stable or transient transfection of mutated chicken beta-globin gene-bearing constructs into definitive or primitive chicken erythroid cells, and transgeneic mouse experiments in which a variety of mutated yeast artificial chromosomes (YACs) bearing the human beta-globin locus have been incorporated into the murine germ line. Both strategies focus on elucidating the underlying mechanisms controlling the differential expression of beta- globin locus genes during development, with particular emphasis on whether or, and if so how, regulatory sequence competition among distal and gene proximal transcriptional control elements of locus dictate developmental stage-specific expression. The proposal will also examine the question of whether or not developmental stage-specific transcription factor binding to the beta/epsilon-globin gene enhancer differentially contributes to chicken beta-globin gene switching.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL024415-21
Application #
6017211
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1979-07-01
Project End
2000-07-31
Budget Start
1999-06-01
Budget End
2000-07-31
Support Year
21
Fiscal Year
1999
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
Cui, Shuaiying; Tanabe, Osamu; Sierant, Michael et al. (2015) Compound loss of function of nuclear receptors Tr2 and Tr4 leads to induction of murine embryonic ?-type globin genes. Blood 125:1477-87
Cui, Shuaiying; Lim, Kim-Chew; Shi, Lihong et al. (2015) The LSD1 inhibitor RN-1 induces fetal hemoglobin synthesis and reduces disease pathology in sickle cell mice. Blood 126:386-96
Shi, Lihong; Sierant, M C; Gurdziel, Katherine et al. (2014) Biased, non-equivalent gene-proximal and -distal binding motifs of orphan nuclear receptor TR4 in primary human erythroid cells. PLoS Genet 10:e1004339
Shi, Lihong; Lin, Yu-Hsuan; Sierant, M C et al. (2014) Developmental transcriptome analysis of human erythropoiesis. Hum Mol Genet 23:4528-42
Cui, Shuaiying; Tanabe, Osamu; Lim, Kim-Chew et al. (2014) PGC-1 coactivator activity is required for murine erythropoiesis. Mol Cell Biol 34:1956-65
Suzuki, Mikiko; Yamazaki, Hiromi; Mukai, Harumi Y et al. (2013) Disruption of the Hbs1l-Myb locus causes hereditary persistence of fetal hemoglobin in a mouse model. Mol Cell Biol 33:1687-95
Shi, Lihong; Cui, Shuaiying; Engel, James D et al. (2013) Lysine-specific demethylase 1 is a therapeutic target for fetal hemoglobin induction. Nat Med 19:291-4
Hosoya, Tomonori; Clifford, Mary; Losson, RĂ©gine et al. (2013) TRIM28 is essential for erythroblast differentiation in the mouse. Blood 122:3798-807
Campbell, Andrew D; Cui, Shuaiying; Shi, Lihong et al. (2011) Forced TR2/TR4 expression in sickle cell disease mice confers enhanced fetal hemoglobin synthesis and alleviated disease phenotypes. Proc Natl Acad Sci U S A 108:18808-13
Cui, Shuaiying; Kolodziej, Katarzyna E; Obara, Naoshi et al. (2011) Nuclear receptors TR2 and TR4 recruit multiple epigenetic transcriptional corepressors that associate specifically with the embryonic ?-type globin promoters in differentiated adult erythroid cells. Mol Cell Biol 31:3298-311

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