TY - JOUR
T1 - Human differentiation-related gene NDRG1 is a Myc downstream-regulated gene that is repressed by Myc on the core promoter region
AU - Zhang, Jian
AU - Chen, Suning
AU - Zhang, Wei
AU - Zhang, Jing
AU - Liu, Xinping
AU - Shi, Hai
AU - Che, Honglei
AU - Wang, Weizhong
AU - Li, Fuyang
AU - Yao, Libo
N1 - Funding Information:
This work was supported by grants from the National Key Basic Research & Development Program of China (No. 2002CB513007), the National High Technology Research and Development Program of China (863 Program) (No. 2006AA02Z194), the Program for Scholars and Innovative Research Team in University (PCSIRT0459) and the National Natural Science Foundation of China (No. 30700416, No. 30700918, No. 30670452, No. 30600161, No. 30570676 and No. 06G092).
PY - 2008/7/1
Y1 - 2008/7/1
N2 - 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.
AB - 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.
KW - Cancer
KW - Differentiation
KW - Myc
KW - NDRG1
KW - Transcriptional repression
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U2 - 10.1016/j.gene.2008.03.002
DO - 10.1016/j.gene.2008.03.002
M3 - Article
C2 - 18455888
AN - SCOPUS:44449136357
SN - 0378-1119
VL - 417
SP - 5
EP - 12
JO - Gene
JF - Gene
IS - 1-2
ER -