Hematopoiesis in the fetal liver is impaired by targeted mutagenesis of a gene encoding a non-DNA binding subunit of the transcription factor, polyomavirus enhancer binding protein 2/core binding factor

被引:164
作者
Niki, M
Okada, H
Takano, H
Kuno, J
Tani, K
Hibino, H
Asano, S
Ito, Y
Satake, M
Noda, T
机构
[1] JAPANESE FDN CANC RES,INST CANC,DEPT CELL BIOL,TOSHIMA KU,TOKYO 170,JAPAN
[2] TOHOKU UNIV,INST DEV AGING & CANC,DEPT MOL IMMUNOL,AOBA KU,SENDAI,MIYAGI 980,JAPAN
[3] UNIV TOKYO,INST MED SCI,DEPT HEMATOL ONCOL,MINATO KU,TOKYO 108,JAPAN
[4] KYOTO UNIV,INST VIRUS RES,DEPT VIRAL ONCOL,SAKYO KU,KYOTO 606,JAPAN
关键词
D O I
10.1073/pnas.94.11.5697
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The PebpbZ gene encodes a non-DNA binding subunit of the heterodimeric transcription factor, polyomavirus enhancer binding protein 2/core binding factor (PEBP2/CBF), and is rearranged in inversion of chromosome 16 associated with human acute myeloid leukemia, To investigate its physiological function, Pebpb2 was mutated by a targeting strategy to generate a null mutant, The homozygous mutation in mice proved lethal in embryos around embryonic day 12.5, apparently due to massive hemorrhaging in the central nervous system. In addition, definitive hematopoiesis in the liver was severely impaired, The observed phenotype was indistinguishable from that reported for homozygous disruption of AML1, which encodes a DNA binding subunit of PEBP2/CBF, Thus, the results indicate that the two subunits function together as a heterodimeric PEBP2/CBF in vivo and that PEBP2/CBF plays an essential role in the development of definitive hematopoiesis.
引用
收藏
页码:5697 / 5702
页数:6
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