共 50 条
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:
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
相关论文