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本文引用的文献

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The myeloid master regulator transcription factor PU.1 is inactivated by AML1-ETO in t(8;21) myeloid leukemia.在t(8;21)髓系白血病中,髓系主要调节转录因子PU.1被AML1-ETO失活。
Blood. 2003 Jan 1;101(1):270-7. doi: 10.1182/blood-2002-04-1288. Epub 2002 Aug 29.
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Granulocyte inducer C/EBPalpha inactivates the myeloid master regulator PU.1: possible role in lineage commitment decisions.粒细胞诱导因子C/EBPα使髓系主调节因子PU.1失活:在谱系定向决定中的可能作用。
Blood. 2002 Jul 15;100(2):483-90. doi: 10.1182/blood.v100.2.483.
3
Ras signaling enhances the activity of C/EBP alpha to induce granulocytic differentiation by phosphorylation of serine 248.Ras信号传导通过丝氨酸248的磷酸化增强C/EBPα的活性以诱导粒细胞分化。
J Biol Chem. 2002 Jul 19;277(29):26293-9. doi: 10.1074/jbc.M202301200. Epub 2002 Apr 26.
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Mutations in the gene encoding the transcription factor CCAAT/enhancer binding protein alpha in myelodysplastic syndromes and acute myeloid leukemias.骨髓增生异常综合征和急性髓系白血病中编码转录因子CCAAT/增强子结合蛋白α的基因突变。
Blood. 2002 Feb 15;99(4):1332-40. doi: 10.1182/blood.v99.4.1332.
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Dichotomy of AML1-ETO functions: growth arrest versus block of differentiation.AML1-ETO功能二分法:生长停滞与分化阻滞
Mol Cell Biol. 2001 Aug;21(16):5577-90. doi: 10.1128/MCB.21.16.5577-5590.2001.
6
AML1-ETO downregulates the granulocytic differentiation factor C/EBPalpha in t(8;21) myeloid leukemia.AML1-ETO在t(8;21)髓系白血病中下调粒细胞分化因子C/EBPα。
Nat Med. 2001 Apr;7(4):444-51. doi: 10.1038/86515.
7
Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia.急性髓系白血病中编码CCAAT/增强子结合蛋白α(C/EBPα)的CEBPA的显性负性突变
Nat Genet. 2001 Mar;27(3):263-70. doi: 10.1038/85820.
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Differential regulation of macrophage CCAAT-enhancer binding protein isoforms by lipopolysaccharide and cytokines.脂多糖和细胞因子对巨噬细胞CCAAT增强子结合蛋白异构体的差异调节
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9
Phosphoacetylation of histone H3 on c-fos- and c-jun-associated nucleosomes upon gene activation.基因激活时,c-fos和c-jun相关核小体上组蛋白H3的磷酸乙酰化作用。
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10
Accurate and rapid analysis of residual disease in patients with CML using specific fluorescent hybridization probes for real time quantitative RT-PCR.使用特异性荧光杂交探针进行实时定量逆转录聚合酶链反应,对慢性粒细胞白血病患者的残留疾病进行准确快速分析。
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转录因子C/EBPα对c-Jun表达的下调对于粒细胞谱系定向分化至关重要。

Downregulation of c-Jun expression by transcription factor C/EBPalpha is critical for granulocytic lineage commitment.

作者信息

Rangatia Janki, Vangala Rajani Kanth, Treiber Nicolai, Zhang Pu, Radomska Hanna, Tenen Daniel G, Hiddemann Wolfgang, Behre Gerhard

机构信息

Department of Medicine III, Ludwig Maximilians University Munich, and GSF-National Research Center, Munich, Germany.

出版信息

Mol Cell Biol. 2002 Dec;22(24):8681-94. doi: 10.1128/MCB.22.24.8681-8694.2002.

DOI:10.1128/MCB.22.24.8681-8694.2002
PMID:12446786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC139872/
Abstract

The transcription factor C/EBPalpha is crucial for the differentiation of granulocytes. Conditional expression of C/EBPalpha triggers neutrophilic differentiation, and C/EBPalpha can block 12-O-tetradecanoylphorbol-13-acetate-induced monocytic differentiation of bipotential myeloid cells. In C/EBPalpha knockout mice, no mature granulocytes are present. A dramatic increase of c-Jun mRNA in C/EBPalpha knockout mouse fetal liver was observed. c-Jun, a component of the AP-1 transcription factor complex and a coactivator of the transcription factor PU.1, is important for monocytic differentiation. Here we report that C/EBPalpha downregulates c-Jun expression to drive granulocytic differentiation. An ectopic increase of C/EBPalpha expression decreases the c-Jun mRNA level, and the human c-Jun promoter activity is downregulated eightfold in the presence of C/EBPalpha. C/EBPalpha and c-Jun interact through their leucine zipper domains, and this interaction prevents c-Jun from binding to DNA. This results in downregulation of c-Jun's capacity to autoregulate its own promoter through the proximal AP-1 site. Overexpression of c-Jun prevents C/EBPalpha-induced granulocytic differentiation. Thus, we propose a model in which C/EBPalpha needs to downregulate c-Jun expression and transactivation capacity for promoting granulocytic differentiation.

摘要

转录因子C/EBPα对粒细胞的分化至关重要。C/EBPα的条件性表达可触发嗜中性粒细胞分化,且C/EBPα能阻断12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯诱导的双能髓系细胞的单核细胞分化。在C/EBPα基因敲除小鼠中,不存在成熟的粒细胞。在C/EBPα基因敲除小鼠的胎肝中观察到c - Jun mRNA显著增加。c - Jun是AP - 1转录因子复合物的一个组分以及转录因子PU.1的共激活因子,对单核细胞分化很重要。在此我们报道,C/EBPα下调c - Jun表达以驱动粒细胞分化。C/EBPα表达的异位增加会降低c - Jun mRNA水平,并且在有C/EBPα存在的情况下,人c - Jun启动子活性下调8倍。C/EBPα和c - Jun通过它们的亮氨酸拉链结构域相互作用,这种相互作用阻止c - Jun与DNA结合。这导致c - Jun通过近端AP - 1位点自动调节其自身启动子的能力下调。c - Jun的过表达会阻止C/EBPα诱导的粒细胞分化。因此,我们提出一个模型,其中C/EBPα需要下调c - Jun表达和反式激活能力以促进粒细胞分化。