The goal of this proposal is the elucidation of the genetic pathway underlying embryonic hematopoiesis in a vertebrate species. We choose to study the regulation of GATA-1, one of the earlist expressed genes required for erythroid development, as an entry point to decipher this pathway. Presently, little is known regarding factors that function early to initiate GATA-1 expression or that cooperate with GATA-1 to establish the erythroid lineage during vertebrate embryogenesis. The use of an in vivo system that allows one to integrate approaches of experimental embryology, genetics and molecular biology would greatly facilitate identification of these factors. We seek to identify these factors in the zebrafish, were chemical mutagenesis screens recently have led to the isolation of several mutants defective in embryonic blood cell formation. By injecting DNA constructs containing the GATA-1 promoter ligated to the green fluorescent protein (GFP) reporter gene, we have generated GATA-1-GFP transgenic fish that faithfully recapitulate the GATA-1 expression pattern in living embryos. These fish make it possible to observe continuously the dynamic expression patterns of GATA-1 in vivo and to isolate GATA-1 expressing cells for in vitro studies. Using this system, coupled to genetic analysis of embryonic blood mutations, we have developed approaches that allow rapid identification of novel genes that are expressed specifically in hematopoietic progenitor cells during embryongenesis. We propose to characterize the novel hematopoietic genes that we have already identified and to identify additional candidates. Their potential roles in hematopoietic development will be examined in wild type embryos and in embryos with defects in blood development. Given the fact that the expression pattern and sequences of many important hematopoietic genes are well conserved between fish, mice and humans, our studies should ultimately lead to a better understanding of the molecular and genetic bases underlying initial specification of mammalian hematopoietic progenitor cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK054508-02
Application #
2872259
Study Section
Hematology Subcommittee 2 (HEM)
Program Officer
Badman, David G
Project Start
1998-03-06
Project End
2003-01-31
Budget Start
1999-02-15
Budget End
2000-01-31
Support Year
2
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Medical College of Georgia (MCG)
Department
Other Basic Sciences
Type
Schools of Medicine
DUNS #
City
Augusta
State
GA
Country
United States
Zip Code
30912
Lin, Sijie; Zhao, Yan; Nel, Andre E et al. (2013) Zebrafish: an in vivo model for nano EHS studies. Small 9:1608-18
Veldman, Matthew B; Zhao, Chengjian; Gomez, Gustavo A et al. (2013) Transdifferentiation of fast skeletal muscle into functional endothelium in vivo by transcription factor Etv2. PLoS Biol 11:e1001590
Zhao, Yan; Lin, Shuo (2013) Essential role of SH3-domain GRB2-like 3 for vascular lumen maintenance in zebrafish. Arterioscler Thromb Vasc Biol 33:1280-6
Gomez, Gustavo; Lee, Jae-Hyung; Veldman, Matthew B et al. (2012) Identification of vascular and hematopoietic genes downstream of etsrp by deep sequencing in zebrafish. PLoS One 7:e31658
Huang, Haigen; Lindgren, Anne; Wu, Xinrong et al. (2012) High-throughput screening for bioactive molecules using primary cell culture of transgenic zebrafish embryos. Cell Rep 2:695-704
Zhang, Ying; Morimoto, Kenji; Danilova, Nadia et al. (2012) Zebrafish models for dyskeratosis congenita reveal critical roles of p53 activation contributing to hematopoietic defects through RNA processing. PLoS One 7:e30188
Veldman, Matthew B; Lin, Shuo (2012) Etsrp/Etv2 is directly regulated by Foxc1a/b in the zebrafish angioblast. Circ Res 110:220-9
Danilova, Nadia; Sakamoto, Kathleen M; Lin, Shuo (2011) Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects. Br J Haematol 152:217-28
Zhong, Hanbing; Wang, Danyang; Wang, Nan et al. (2011) Combinatory action of VEGFR2 and MAP kinase pathways maintains endothelial-cell integrity. Cell Res 21:1080-7
Ren, Xi; Gomez, Gustavo A; Zhang, Bo et al. (2010) Scl isoforms act downstream of etsrp to specify angioblasts and definitive hematopoietic stem cells. Blood 115:5338-46

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