中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
The Ubiquitin Ligase RNF220 Enhances Canonical Wnt Signaling through USP7-Mediated Deubiquitination of beta-Catenin

文献类型:期刊论文

作者Ma, Pengcheng1; Yang, Xiangcai1,2; Kong, Qinghua1; Li, Chaocui1; Yang, Shuangjuan3; Li, Yan4; Mao, Bingyu1
刊名MOLECULAR AND CELLULAR BIOLOGY
出版日期2014-12-01
卷号34期号:23页码:4355-4366
关键词STEM-CELL FATE SHOOT APICAL MERISTEM ARABIDOPSIS SHOOT CRABS-CLAW NECTARY DEVELOPMENT EXPRESSION THALIANA FAMILY LOOP POLARITY IaYABBY2 Ad-abaxial polarity Incarvillea arguta Arabidopsis thaliana
ISSN号0270-7306
产权排序第一
通讯作者Mao,BY (reprint author),Kunming Inst Zool,State Key Lab Genet Resources & Evolut,Kunming,Peoples R China. ; mao@mail.kiz.ac.cn
英文摘要Wnt/beta-catenin signaling plays critical roles in embryonic development and disease. Here, we identify RNF220, a RING domain E3 ubiquitin ligase, as a new regulator of beta-catenin. RNF220 physically interacts with beta-catenin, but instead of promoting its ubiquitination and proteasomal degradation, it stabilizes beta-catenin and promotes canonical Wnt signaling. Our analysis showed that RNF220 interacts with USP7, a ubiquitin-specific peptidase, which is required for RNF220 to stabilize beta-catenin. The RNF220/USP7 complex deubiquitinates beta-catenin and enhances canonical Wnt signaling. Interestingly, the stability of RNF220 itself is negatively regulated by Gsk3 beta, which is a key component of the beta-catenin destruction complex and is inhibited upon Wnt stimulation. Accordingly, the RNF220/USP7 complex works as a positive feedback regulator of beta-catenin signaling. In colon cancer cells with stimulated Wnt signaling, knockdown of RNF220 or USP7 impairs Wnt signaling and expression of Wnt target genes, suggesting a potentially novel role of RNF220 in Wnt-related tumorigenesis.
学科主题Biochemistry & Molecular Biology;Cell Biology
类目[WOS]Biochemistry & Molecular Biology ; Cell Biology
研究领域[WOS]Biochemistry & Molecular Biology ; Cell Biology
关键词[WOS]NEGATIVE REGULATOR ; XENOPUS EMBRYOS ; C-CBL ; PATHWAY ; PROTEIN ; P53 ; KINASE ; DEGRADATION ; DISEASE ; MECHANISMS
收录类别SCI
资助信息National Natural Science Foundation of China [90813004, 2009312311024]; 973 Program [2009CB522300]
语种英语
WOS记录号WOS:000344631500011
公开日期2015-01-20
源URL[http://ir.kib.ac.cn/handle/151853/18482]  
专题昆明植物研究所_植物化学与西部植物资源持续利用国家重点实验室
作者单位1.Kunming Inst Zool, State Key Lab Genet Resources & Evolut, Kunming, Peoples R China
2.Univ Chinese Acad Sci, Kunming Coll Life Sci, Kunming, Peoples R China
3.Kunming Inst Zool, Kunming Biol Divers Reg Ctr Large Apparat & Equip, Kunming, Peoples R China
4.Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming, Peoples R China
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Ma, Pengcheng,Yang, Xiangcai,Kong, Qinghua,et al. The Ubiquitin Ligase RNF220 Enhances Canonical Wnt Signaling through USP7-Mediated Deubiquitination of beta-Catenin[J]. MOLECULAR AND CELLULAR BIOLOGY,2014,34(23):4355-4366.
APA Ma, Pengcheng.,Yang, Xiangcai.,Kong, Qinghua.,Li, Chaocui.,Yang, Shuangjuan.,...&Mao, Bingyu.(2014).The Ubiquitin Ligase RNF220 Enhances Canonical Wnt Signaling through USP7-Mediated Deubiquitination of beta-Catenin.MOLECULAR AND CELLULAR BIOLOGY,34(23),4355-4366.
MLA Ma, Pengcheng,et al."The Ubiquitin Ligase RNF220 Enhances Canonical Wnt Signaling through USP7-Mediated Deubiquitination of beta-Catenin".MOLECULAR AND CELLULAR BIOLOGY 34.23(2014):4355-4366.

入库方式: OAI收割

来源:昆明植物研究所

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