Cancer-testis antigen HCA587/MAGE-C2 interacts with BS69 and promotes its degradation in the ubiquitin-proteasome pathway

被引:12
作者
Hao, Jiaqing [1 ]
Shen, Rui [1 ]
Li, Yan [1 ]
Zhang, Yu [1 ]
Yin, Yanhui [1 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Minist Hlth, Dept Immunol,Sch Basic Med Sci,Key Lab Med Immuno, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
Cancer-testis antigen; HCA587; BS69; Ubiquitination; ADENOVIRUS E1A-ASSOCIATED PROTEIN; CYTOLYTIC T-LYMPHOCYTES; KAPPA-B ACTIVATION; HEPATOCELLULAR-CARCINOMA; BREAST-CANCER; C-MYB; MAGE-C2; CELLS; IDENTIFICATION; TRANSCRIPTION;
D O I
10.1016/j.bbrc.2014.05.078
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
HCA587, also known as MAGE-C2, belonging to the MAGE gene family which is characterized by a conserved MAGE Homology Domain, is active in various types of tumors and silent in normal tissues except in male germ-line cells. The biological function of HCA587 is largely unknown. To analyze it, we attempted to identify protein partners of HCA587. We immunopurified HCA587-containing complex from HEK293 cells and identified BS69, a potential tumor suppressor, as an associated protein by mass spectrometry, and the following Immunoprecipitation and GST pull-down assays confirmed HCA587 interaction with BS69. Interestingly, overexpression of HCA587 promoted ubiquitination and the proteasomal degradation of BS69 whereas knockdown of endogenous HCA587 increased the protein level of BS69. Consistent with a functional role for BS69 in negatively regulating LMP1-induced NF-kappa B activation, overexpression of HCA587 resulted in a significant enhancement of LMP1-induced IL-6 production. These data indicate that HCA587 is a new negative regulator of BS69. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:386 / 391
页数:6
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