The CCAAT box-binding transcription factor NF-Y regulates basal expression of human proteasome genes

被引:36
|
作者
Xu, Haiming [1 ]
Fu, Jiejun [1 ,2 ]
Ha, Seung-Wook [1 ,2 ]
Ju, Donghong [1 ,2 ]
Zheng, Jianpu [3 ]
Li, Li [3 ]
Xie, Youming [1 ,2 ]
机构
[1] Wayne State Univ, Sch Med, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Dept Oncol, Detroit, MI 48201 USA
[3] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI 48201 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2012年 / 1823卷 / 04期
基金
美国国家科学基金会;
关键词
Proteasome; Protein degradation; NF-Y transcription factor; CCAAT box; Rpn4; Cancer therapy; CELL-CYCLE REGULATION; 26S PROTEASOME; SACCHAROMYCES-CEREVISIAE; DOWN-REGULATION; UBIQUITIN; CANCER; DEGRADATION; INHIBITION; DROSOPHILA; VIABILITY;
D O I
10.1016/j.bbamcr.2012.01.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein degradation by the proteasome plays an important role in all major cellular pathways. Aberrant proteasome activity is associated with numerous human diseases including cancer and neurological disorders, but the underlying mechanism is virtually unclear. At least part of the reason for this is due to lack of understanding of the regulation of human proteasome genes. In this study, we found that a large set of human proteasome genes carry the CCAAT box in their promoters. We further demonstrated that the basal expression of these CCAAT box-containing proteasome genes is regulated by the transcription factor NF-Y. Knockdown of NF-YA, an essential subunit of NF-Y, reduced proteasome gene expression and compromised the cellular proteasome activity. In addition, we showed that knockdown of NF-YA sensitized breast cancer cells to the proteasome inhibitor MG132. This study unveils a new role for NF-Y in the regulation of human proteasome genes and suggests that NF-Y may be a potential target for cancer therapy. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:818 / 825
页数:8
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