首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >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
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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

机译:定向转录编码非DNA结合亚基的基因(多瘤病毒增强子结合蛋白2 /核心结合因子)的定向诱变会损害胎儿肝脏的造血功能

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摘要

The Pebpb2 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.
机译:Pebpb2基因编码异二聚体转录因子,多瘤病毒增强子结合蛋白2 /核心结合因子(PEBP2 / CBF)的非DNA结合亚基,并在与人类急性髓细胞白血病相关的16号染色体的倒置中重新排列。为了研究其生理功能,通过靶向策略将Pebpb2突变以产生无效突变体。小鼠纯合突变在胚胎第12.5天左右被证明具有致死性,这显然是由于中枢神经系统大出血所致。此外,肝脏的确定性造血功能严重受损。观察到的表型与报道的纯合子破坏AML1没有区别,后者编码PEBP2 / CBF的DNA结合亚基。因此,结果表明,这两个亚基在体内起异二聚体PEBP2 / CBF的作用,并且PEBP2 / CBF在确定性造血过程中起着至关重要的作用。

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