首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Human differentiation-related gene NDRG1 is a Myc downstream-regulated gene that is repressed by Myc on the core promoter region.
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Human differentiation-related gene NDRG1 is a Myc downstream-regulated gene that is repressed by Myc on the core promoter region.

机译:人类分化相关基因NDRG1是Myc下游调控的基因,在核心启动子区域受Myc抑制。

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N-Myc downstream-regulated gene 1 (ndrg1) is up-regulated in N-Myc knockout mouse embryos. The human NDRG family consists of 4 highly homologous members and human Ndrg1 exhibits approximately 94% homology with mouse ndrg1. However, the regulatory mechanism of NDRG1 via Myc repression is as yet unknown. We previously identified human NDRG2 and demonstrated that this gene is transcriptionally down-regulated by Myc via Miz-1-dependent interaction with the core promoter region of NDRG2. Here, we provide evidence that human NDRG1 is regulated by Myc in a manner similar to NDRG2. We found that Ndrg1 expression levels were enhanced as Myc expression declined in differentiated cells, but were down-regulated following Myc induction. The data revealed that both N-Myc and c-Myc can repress human NDRG1 at the transcriptional level. We further determined that the core promoter region of human NDRG1 is required for Myc repression, and verified the interaction of Myc with the core promoter region. However, the presence of the protein synthesis inhibitor cycloheximide could reverse the repression of Myc, indicating the indirect repression of human NDRG1 by Myc. Moreover, we found that c-Myc-mediated repression can be inhibited by TSA, an HDACs inhibitor, which suggests the involvement of HDACs in the repression process. Taken together, our results demonstrate that, in common with NDRG2, human NDRG1 can be indirectly transcriptionally down-regulated by Myc via interaction with the NDRG1 core promoter.
机译:N-Myc下游调节基因1(ndrg1)在N-Myc敲除小鼠胚胎中上调。人类NDRG家族由4个高度同源的成员组成,人类Ndrg1与小鼠ndrg1的同源性约为94%。但是,通过Myc抑制NDRG1的调控机制尚不清楚。我们之前鉴定了人NDRG2,并证明了Myc通过与NDRG2核心启动子区域的Miz-1依赖性相互作用而被Myc转录下调。在这里,我们提供证据表明Myc对人NDRG1的调控方式与NDRG2类似。我们发现,随着Myc表达在分化细胞中下降,Ndrg1表达水平增强,但在Myc诱导后被下调。数据显示,N-Myc和c-Myc均可在转录水平上抑制人NDRG1。我们进一步确定了人NDRG1的核心启动子区域是Myc抑制所必需的,并验证了Myc与核心启动子区域的相互作用。但是,蛋白质合成抑制剂环己酰亚胺的存在可以逆转Myc的阻遏,表明Myc对人NDRG1的间接阻遏。此外,我们发现c-Myc介导的抑制作用可以被TDAC(一种HDACs抑制剂)抑制,这表明HDACs参与了抑制过程。综上所述,我们的结果表明,与NDRG2一样,人NDRG1可以通过Myc通过与NDRG1核心启动子相互作用而间接转录下调。

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