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c-Maf与c-Myb相互作用,在分化过程中调节一个早期髓系基因的转录。

c-Maf interacts with c-Myb to regulate transcription of an early myeloid gene during differentiation.

作者信息

Hedge S P, Kumar A, Kurschner C, Shapiro L H

机构信息

Department of Experimental Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

Mol Cell Biol. 1998 May;18(5):2729-37. doi: 10.1128/MCB.18.5.2729.

Abstract

The MafB transcriptional activator plays a pivotal role in regulating lineage-specific gene expression during hematopoiesis by repressing Ets-1-mediated transcription of key erythroid-specific genes in myeloid cells. To determine the effects of Maf family proteins on the transactivation of myeloid-specific genes in myeloid cells, we tested the ability of c-Maf to influence Ets-1- and c-Myb-dependent CD13/APN transcription. Expression of c-Maf in human immature myeloblastic cells inhibited CD13/APN-driven reporter gene activity (85 to 95% reduction) and required the binding of both c-Myb and Ets, but not Maf, to the promoter fragment. c-Maf's inhibition of CD13/APN expression correlates with its ability to physically associate with c-Myb. While c-Maf mRNA and protein levels remain constant during myeloid differentiation, formation of inhibitory Myb-Maf complexes was developmentally regulated, with their levels being highest in immature myeloid cell lines and markedly decreased in cell lines representing later developmental stages. This pattern matched that of CD13/APN reporter gene expression, indicating that Maf modulation of c-Myb activity may be an important mechanism for the control of gene transcription during hematopoietic cell development.

摘要

MafB转录激活因子通过抑制髓系细胞中关键红系特异性基因的Ets-1介导的转录,在造血过程中调节谱系特异性基因表达方面发挥关键作用。为了确定Maf家族蛋白对髓系细胞中髓系特异性基因反式激活的影响,我们测试了c-Maf影响Ets-1和c-Myb依赖的CD13/氨肽酶N转录的能力。在人未成熟髓母细胞中c-Maf的表达抑制了CD13/氨肽酶N驱动的报告基因活性(降低85%至95%),并且需要c-Myb和Ets两者与启动子片段结合,但不需要Maf。c-Maf对CD13/氨肽酶N表达的抑制与其与c-Myb物理缔合的能力相关。虽然c-Maf mRNA和蛋白水平在髓系分化过程中保持恒定,但抑制性Myb-Maf复合物的形成受到发育调控,其水平在未成熟髓系细胞系中最高,而在代表后期发育阶段的细胞系中明显降低。这种模式与CD13/氨肽酶N报告基因表达的模式相匹配,表明Maf对c-Myb活性的调节可能是造血细胞发育过程中基因转录控制的重要机制。

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