DDRGK1 Regulates NF-κB Activity by Modulating IκBα Stability

被引:43
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
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
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页数:9
相关论文
共 18 条
[1]   Matrix metalloproteinases: roles in cancer and metastasis [J].
Fingleton, B .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2006, 11 :479-491
[2]   Signaling to NF-κB [J].
Hayden, MS ;
Ghosh, S .
GENES & DEVELOPMENT, 2004, 18 (18) :2195-2224
[3]   The PCI domain: a common theme in three multiprotein complexes [J].
Hofmann, K ;
Bucher, P .
TRENDS IN BIOCHEMICAL SCIENCES, 1998, 23 (06) :204-205
[4]   Structure of an IκBα/NF-κB complex [J].
Jacobs, MD ;
Harrison, SC .
CELL, 1998, 95 (06) :749-758
[5]   Nuclear factor-κB in cancer development and progression [J].
Karin, Michael .
NATURE, 2006, 441 (7092) :431-436
[6]   PCI complexes: pretty complex interactions in diverse signaling pathways [J].
Kim, TH ;
Hofmann, K ;
von Arnim, AG ;
Chamovitz, DA .
TRENDS IN PLANT SCIENCE, 2001, 6 (08) :379-386
[7]   A novel protein-conjugating system for Ufm1, a ubiquitin-fold modifier [J].
Komatsu, M ;
Chiba, T ;
Tatsumi, K ;
Iemura, S ;
Tanida, I ;
Okazaki, N ;
Ueno, T ;
Kominami, E ;
Natsume, T ;
Tanaka, K .
EMBO JOURNAL, 2004, 23 (09) :1977-1986
[8]   A Novel LZAP-binding Protein, NLBP, Inhibits Cell Invasion [J].
Kwon, Junhye ;
Cho, Hyun Jung ;
Han, Seung Hun ;
No, Jin Gu ;
Kwon, Jae Young ;
Kim, Hongtae .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (16) :12232-12240
[9]   Ubiquitin Fold Modifier 1 (UFM1) and Its Target UFBP1 Protect Pancreatic Beta Cells from ER Stress-Induced Apoptosis [J].
Lemaire, Katleen ;
Moura, Rodrigo F. ;
Granvik, Mikaela ;
Igoillo-Esteve, Mariana ;
Hohmeier, Hans E. ;
Hendrickx, Nico ;
Newgard, Christopher B. ;
Waelkens, Etienne ;
Cnop, Miriam ;
Schuit, Frans .
PLOS ONE, 2011, 6 (04)
[10]   Oscillations in NF-κB signaling control the dynamics of gene expression [J].
Nelson, DE ;
Ihekwaba, AEC ;
Elliott, M ;
Johnson, JR ;
Gibney, CA ;
Foreman, BE ;
Nelson, G ;
See, V ;
Horton, CA ;
Spiller, DG ;
Edwards, SW ;
McDowell, HP ;
Unitt, JF ;
Sullivan, E ;
Grimley, R ;
Benson, N ;
Broomhead, D ;
Kell, DB ;
White, MRH .
SCIENCE, 2004, 306 (5696) :704-708