DCUN1D3 activates SCFSKP2 ubiquitin E3 ligase activity and cell cycle progression under UV damage

被引:3
|
作者
Zhang, Shuai [1 ]
Huang, Jing [1 ]
Shi, Taiping [1 ,2 ]
Hu, Fanlei [1 ]
Zhang, Li [1 ]
Zhou, Ping-Kun [3 ]
Ma, Dalong [1 ]
Ma, Teng [1 ,3 ]
Qiu, Xiaoyan [1 ]
机构
[1] Peking Univ, Sch Basic Med Sci, Dept Immunol, Beijing, Peoples R China
[2] Chinese Natl Human Genome Ctr, Beijing, Peoples R China
[3] Beijing Inst Radiat Med, Dept Radiat Toxicol & Oncol, Beijing Key Lab Radiobiol BKLRB, Beijing, Peoples R China
关键词
DCUN1D3; CAND1; SCFSKP2; p27; cell cycle; PROTEIN-PROTEIN INTERACTIONS; REGULATES PROTEOLYSIS; NEDD8; MODIFICATION; SCCRO DCUN1D1; MICE LACKING; G(1) PHASE; P27(KIP1); NEDDYLATION; COMPLEX; PATHWAY;
D O I
10.18632/oncotarget.11302
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Our previous study showed that knockdown the endogenous expression of DCUN1D3 (also called SCCRO3 or DCNL3) blocked the S phase progression after UV irradiation. Here, we show that the silence of DCUN1D3 can increase the cyclin-dependent kinase inhibitor p27 protein levels after UV irradiation. Through Co-immunoprecipitation experiments, we found that DCUN1D3 bound to CAND1. And DCUN1D3 knockdown synergized with CAND1 over-expression in arresting the S phase. Given the CAND1's established role in Cullin-1 neddylation, we found Cullin-1 was less neddylated in DCUN1D3 deficient cells. So the silence of DCUN1D3 can inhibit the formation of SCFSKP2 complex by reducing Cullin-1 neddylation. Given that p27 is the primary target of SCFSKP2 complex, the cells lost DCUN1D3 showed a remarkable accumulation of p27 to cause S phase block.
引用
收藏
页码:58483 / 58491
页数:9
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