Absence of fetal liver hematopoiesis in mice deficient in transcriptional coactivator core binding factor beta.
- 29 October 1996
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 93 (22) , 12359-12363
- https://doi.org/10.1073/pnas.93.22.12359
Abstract
Core binding factor beta (CBF beta) is considered to be a transcriptional coactivator that dimerizes with transcription factors core binding factor alpha 1 (CBFA1), -2, and -3, and enhances DNA binding capacity of these transcription factors. CBF beta and CBFA2, which is also called acute myeloid leukemia 1 gene, are frequently involved in chromosomal translocations in human leukemia. To elucidate the function of CBF beta, mice carrying a mutation in the Cbfb locus were generated. Homozygous mutant embryos died between embryonic days 11.5-13.5 due to hemorrhage in the central nervous system. Mutant embryos had primitive erythropoiesis in yolk sac but lacked definitive hematopoiesis in fetal liver. In the yolk sac of mutant embryos, no erythroid or myeloid progenitors of definitive hematopoietic origin were detected, and the expression of flk-2/flt-3, the marker gene for early precursor cells of definitive hematopoiesis, was absent. These data suggest that Cbfb is essential for definitive hematopoiesis in liver, especially for the commitment to early hematopoietic precursor cells.Keywords
This publication has 32 references indexed in Scilit:
- The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusionBlood, 1995
- Transcription factor NF-E2 is required for platelet formation independent of the actions of thrombopoeitin/MGDF in megakaryocyte developmentCell, 1995
- Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia [see comments]Blood, 1995
- The leukemic core binding factor beta-smooth muscle myosin heavy chain (CBF beta-SMMHC) chimeric protein requires both CBF beta and myosin heavy chain domains for transformation of NIH 3T3 cells.Proceedings of the National Academy of Sciences, 1995
- Emergence of multipotent hemopoietic cells in the yolk sac and paraaortic splanchnopleura in mouse embryos, beginning at 8.5 days postcoitus.Proceedings of the National Academy of Sciences, 1995
- Cellular and molecular characterization of the role of the flk-2/flt-3 receptor tyrosine kinase in hematopoietic stem cells.1994
- Novel insights into erythroid development revealed through in vitro differentiation of GATA-1 embryonic stem cells.Genes & Development, 1994
- PEBP2 alpha B/mouse AML1 consists of multiple isoforms that possess differential transactivation potentials.Molecular and Cellular Biology, 1994
- Lack of N Regions in Antigen Receptor Variable Region Genes of TdT-Deficient LymphocytesScience, 1993
- The 3;21 translocation in myelodysplasia results in a fusion transcript between the AML1 gene and the gene for EAP, a highly conserved protein associated with the Epstein-Barr virus small RNA EBER 1.Proceedings of the National Academy of Sciences, 1993