Differential requirement for Gata1 DNA binding and transactivation between primitive and definitive stages of hematopoiesis in zebrafish

Author:

Belele Christiane L.1,English Milton A.1,Chahal Jagman1,Burnetti Anthony1,Finckbeiner Steven M.1,Gibney Gretchen2,Kirby Martha1,Sood Raman1,Liu P. Paul1

Affiliation:

1. Genetics and Molecular Biology Branch and

2. Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD

Abstract

AbstractThe transcription factor Gata1 is required for the development of erythrocytes and megakaryocytes. Previous studies with a complementation rescue approach showed that the zinc finger domains are required for both primitive and definitive hematopoiesis. Here we report a novel zebrafish gata1 mutant with an N-ethyl-N-nitrosourea–induced point mutation in the C-finger (gata1T301K). The Gata1 protein with this mutation bound to its DNA target sequence with reduced affinity and transactivated inefficiently in a reporter assay. gata1T301K/T301K fish had a decreased number of erythrocytes during primitive hematopoiesis but normal adult hematopoiesis. We crossed the gata1T301K/T301K fish with those carrying the R339X mutation, also known as vlad tepes (vlt), which abolishes DNA binding and transactivation activities. As we reported previously, gata1vlt/vlt embryos were “bloodless” and died approximately 11 to 15 days after fertilization. Interestingly, the gata1T301K/vlt fish had nearly a complete block of primitive hematopoiesis, but they resumed hematopoiesis between 7 and 14 days after fertilization and grew to phenotypically normal fish with normal adult hematopoiesis. Our findings suggest that the impact of Gata1 on hematopoiesis correlates with its DNA-binding ability and that primitive hematopoiesis is more sensitive to reduction in Gata1 function than definitive hematopoiesis.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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