Zhang Jian, Chen Suning, Zhang Wei, Zhang Jing, Liu Xinping, Shi Hai, Che Honglei, Wang Weizhong, Li Fuyang, Yao Libo
The Department of Biochemistry and Molecular Biology and The State Key Laboratory of Cancer Biology, The Fourth Military Medical University, Xi'an, 710032, People's Republic of China.
Gene. 2008 Jul 1;417(1-2):5-12. doi: 10.1016/j.gene.2008.03.002. Epub 2008 Mar 12.
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.
N-Myc下游调控基因1(ndrg1)在N-Myc基因敲除的小鼠胚胎中表达上调。人类NDRG家族由4个高度同源的成员组成,其中人类Ndrg1与小鼠ndrg1的同源性约为94%。然而,NDRG1通过Myc抑制的调控机制尚不清楚。我们之前鉴定了人类NDRG2,并证明该基因通过与NDRG2核心启动子区域的Miz-1依赖性相互作用被Myc转录下调。在此,我们提供证据表明人类NDRG1以与NDRG2相似的方式受到Myc的调控。我们发现,在分化细胞中,随着Myc表达下降,Ndrg1表达水平升高,但在Myc诱导后则下调。数据显示,N-Myc和c-Myc均可在转录水平抑制人类NDRG1。我们进一步确定,人类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。然而,蛋白质合成抑制剂放线菌酮的存在可逆转Myc的抑制作用,表明Myc对人类NDRG1的抑制是间接的。此外,我们发现HDACs抑制剂TSA可抑制c-Myc介导的抑制作用,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,人类NDRG1可通过与NDRG1核心启动子相互作用被Myc间接转录下调。