» Articles » PMID: 20110178

Loss of GATA1 and Gain of FLI1 Expression During Thrombocyte Maturation

Overview
Specialty Hematology
Date 2010 Jan 30
PMID 20110178
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

In this paper, we characterized expression of GATA1 and FLI1 gene promoters in thrombocytes of zebrafish transgenic lines, G1-GM2 and TG(fli1:EGFP)y1 that carry transgenes of GATA1 and FLI1 gene promoters driving GFP. We found two discrete populations of thrombocytes verified by morphology, labeled with GFP in both G1-GM2 and TG(fli1:EGFP)y1 lines: (1) the more intensely labeled GFP+ thrombocyte, and (2) the less intensely labeled GFP+ thrombocytes. The more intensely labeled GFP+ thrombocyte in G1-GM2 line and the less intensely labeled GFP+ thrombocytes in the TG(fli1:EGFP)y1 line corresponded to young thrombocytes. These results showed that young thrombocytes have higher GATA1 promoter activity, while mature thrombocytes have more FLI1 gene promoter transcription. This finding suggests that there is a gradual loss of GATA1 and gain of FLI1 expression as the thrombocytes mature, and this overexpression of FLI1 may help maintain the thrombocyte lineage. Furthermore, the presence of transcriptional factors similar to those found in megakaryocytes raises the possibility that vertebrate thrombocytes may be the forerunners of mammalian megakaryocytes and, therefore, could serve as a model to study megakaryocyte maturation.

Citing Articles

Piggyback knockdown screening of unique genes of zebrafish young thrombocytes identifies eight novel genes in thrombopoiesis.

Fallatah W, Mary J, Dhinoja S, Vallabhaneni S, Jagadeeswaran P Sci Rep. 2025; 15(1):5180.

PMID: 39939668 PMC: 11822207. DOI: 10.1038/s41598-025-88866-9.


Definitive hematopoiesis is dispensable to sustain erythrocytes and macrophages during zebrafish ontogeny.

Elsaid R, Mikdache A, Castillo K, Salloum Y, Diabangouaya P, Gros G iScience. 2024; 27(2):108922.

PMID: 38327794 PMC: 10847700. DOI: 10.1016/j.isci.2024.108922.


One Host-Multiple Applications: Zebrafish () as Promising Model for Studying Human Cancers and Pathogenic Diseases.

Dudziak K, Nowak M, Sozoniuk M Int J Mol Sci. 2022; 23(18).

PMID: 36142160 PMC: 9499349. DOI: 10.3390/ijms231810255.


Current insights into the role of Fli-1 in hematopoiesis and malignant transformation.

Ben-David Y, Gajendran B, Sample K, Zacksenhaus E Cell Mol Life Sci. 2022; 79(3):163.

PMID: 35412146 PMC: 11072361. DOI: 10.1007/s00018-022-04160-1.


Zebrafish for thrombocytopoiesis- and hemostasis-related researches and disorders.

Meng P, Wu L, Lin Q, Zhang Y Blood Sci. 2022; 2(2):44-49.

PMID: 35402814 PMC: 8975081. DOI: 10.1097/BS9.0000000000000043.


References
1.
Orkin S, Shivdasani R, Fujiwara Y, McDevitt M . Transcription factor GATA-1 in megakaryocyte development. Stem Cells. 2000; 16 Suppl 2:79-83. DOI: 10.1002/stem.5530160710. View

2.
Gregory M, Hanumanthaiah R, Jagadeeswaran P . Genetic analysis of hemostasis and thrombosis using vascular occlusion. Blood Cells Mol Dis. 2003; 29(3):286-95. DOI: 10.1006/bcmd.2002.0568. View

3.
Eisbacher M, Holmes M, Newton A, Hogg P, Khachigian L, Crossley M . Protein-protein interaction between Fli-1 and GATA-1 mediates synergistic expression of megakaryocyte-specific genes through cooperative DNA binding. Mol Cell Biol. 2003; 23(10):3427-41. PMC: 154245. DOI: 10.1128/MCB.23.10.3427-3441.2003. View

4.
Long Q, Meng A, Wang H, Jessen J, Farrell M, Lin S . GATA-1 expression pattern can be recapitulated in living transgenic zebrafish using GFP reporter gene. Development. 1997; 124(20):4105-11. DOI: 10.1242/dev.124.20.4105. View

5.
Shattil S, Leavitt A . All in the family: primary megakaryocytes for studies of platelet alphaIIbbeta3 signaling. Thromb Haemost. 2001; 86(1):259-65. View