DDRGK1 Regulates NF-κB Activity by Modulating IκBα Stability

被引:38
|
作者
Xi, Peng [1 ,2 ]
Ding, Deqiang [1 ,2 ]
Zhou, Junzhi [1 ,2 ]
Wang, Miao [2 ]
Cong, Yu-Sheng [2 ]
机构
[1] Beijing Normal Univ, Coll Life Sci, Key Lab Cell Proliferat & Regulat Biol, Minist Educ,Inst Cell Biol, Beijing 100875, Peoples R China
[2] Hangzhou Normal Univ, Sch Med, Inst Aging Res, Hangzhou, Zhejiang, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 05期
基金
中国国家自然科学基金;
关键词
PROTEIN; COMPLEX; TRANSLOCATION; LEUKEMIA; CANCER; LZAP;
D O I
10.1371/journal.pone.0064231
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
NF-kappa B is a ubiquitously expressed transcription factor that regulates a large number of genes in response to diverse physiological and pathological stimuli. The regulation of the transcriptional activity of NF-kappa B is often dependent on its interaction with I kappa B alpha. Proteins that bind to I kappa B alpha are critical regulators of NF-kappa B activity. DDRGK1 is a member of the DDRGK domain-containing protein family with unknown function. In this study, we showed that the depletion of DDRGK1 inhibits cell proliferation and invasion. Microarray analysis indicated that the expression of NF-kappa B target genes showed the most significant decrease after depleting of DDRGK1, suggesting that DDRGK1 may play an important role in the NF-kappa B signaling pathway. We further demonstrated that DDRGK1 interacts with I kappa B alpha and regulates its stability, thereby regulates the NF-kappa B transcriptional activity. Our findings identify DDRGK1 as an important regulator of the NF-kappa B pathway.
引用
收藏
页数:9
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