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Cell Growth and Development

Defective Gene Expression, S Phase Progression, and Maturation during Hematopoiesis in E2F1/E2F2 Mutant Mice

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Pages 3607-3622 | Received 24 Jul 2002, Accepted 21 Feb 2003, Published online: 27 Mar 2023
 

Abstract

E2F plays critical roles in cell cycle progression by regulating the expression of genes involved in nucleotide synthesis, DNA replication, and cell cycle control. We show that the combined loss of E2F1 and E2F2 in mice leads to profound cell-autonomous defects in the hematopoietic development of multiple cell lineages. E2F2 mutant mice show erythroid maturation defects that are comparable with those observed in patients with megaloblastic anemia. Importantly, hematopoietic defects observed in E2F1/E2F2 double-knockout (DKO) mice appear to result from impeded S phase progression in hematopoietic progenitor cells. During DKO B-cell maturation, differentiation beyond the large pre-BII-cell stage is defective, presumably due to failed cell cycle exit, and the cells undergo apoptosis. However, apoptosis appears to be the consequence of failed maturation, not the cause. Despite the accumulation of hematopoietic progenitor cells in S phase, the combined loss of E2F1 and E2F2 results in significantly decreased expression and activities of several E2F target genes including cyclin A2. Our results indicate specific roles for E2F1 and E2F2 in the induction of E2F target genes, which contribute to efficient expansion and maturation of hematopoietic progenitor cells. Thus, E2F1 and E2F2 play essential and redundant roles in the proper coordination of cell cycle progression with differentiation which is necessary for efficient hematopoiesis.

ACKNOWLEDGMENTS

J.D. is supported by grants from the NIH (CA77314) and the ACS (RSG LIB-101051), and by a Scholar Award from the Leukemia and Lymphoma Society. C.J.H. is supported by NIH/NHLBI 2 RO1 HL61382-04.

We thank D. Johnson, G. Shapiro, D. DeRyckere, and J. Hagman for critical review of the manuscript and B. Schaefer, S. Field, S. Orkin, and M. Greenberg for mice. We also thank K. Helm and M. Ashton of the Cancer Center Flow Cytometry Core (supported by grant 2 P30 CA 46934-09).

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