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转录共激活因子核心结合因子β缺陷小鼠中胎儿肝脏造血功能的缺失

Absence of fetal liver hematopoiesis in mice deficient in transcriptional coactivator core binding factor beta.

作者信息

Sasaki K, Yagi H, Bronson R T, Tominaga K, Matsunashi T, Deguchi K, Tani Y, Kishimoto T, Komori T

机构信息

Department of Medicine III, Osaka University Medical School, Japan.

出版信息

Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12359-63. doi: 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.

摘要

核心结合因子β(CBFβ)被认为是一种转录共激活因子,它与转录因子核心结合因子α1(CBFA1)、-2和-3形成二聚体,并增强这些转录因子的DNA结合能力。CBFβ和CBFA2(也称为急性髓系白血病1基因)经常参与人类白血病中的染色体易位。为了阐明CBFβ的功能,构建了Cbfb基因座发生突变的小鼠。纯合突变胚胎在胚胎第11.5至13.5天之间死亡,原因是中枢神经系统出血。突变胚胎在卵黄囊中具有原始红细胞生成,但在胎儿肝脏中缺乏确定性造血。在突变胚胎的卵黄囊中,未检测到确定性造血来源的红系或髓系祖细胞,并且缺乏确定性造血早期前体细胞的标记基因flk-2/flt-3的表达。这些数据表明,Cbfb对于肝脏中的确定性造血至关重要,尤其是对于早期造血前体细胞的定向分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e11f/37996/9641cd91fe9b/pnas01526-0318-a.jpg

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