中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Involvement of transcription factor XBP1s in the resistance of HDAC6 inhibitor Tubastatin A to superoxidation via acetylation-mediated proteasomal degradation

文献类型:期刊论文

作者Zhang, Yue1,2; Liu, Chang-mei1,2; Cao, Xian-cao1,2; Zang, Yi2; Zhou, Yu-bo2; Li, Jia1,2
刊名BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
出版日期2014-07-18
卷号450期号:1页码:433-439
关键词Tubastatin A HDAC6 XBP1s Oxidative stress Transcription regulation
ISSN号0006-291X
DOI10.1016/j.bbrc.2014.05.134
文献子类Article
英文摘要HDAC6 is a major cytoplasmic deacetylase. XBP1s is a basic-region leucine zipper (bZIP) transcriptional factor. Despite their mutual involvement in the anti-oxidative process, there are no reports about their inter-protein interactions so far. Here we identified a direct link between HDAC6 inhibition and XBP1s transcription activity in anti-oxidative damage. We showed that the specific HDAC6 inhibitor Tubastatin A could up-regulate XBP1s transcriptional activity, thereby increasing anti-oxidative genes expression. Moreover, knock down of XBP1s could significantly abolish the cell growth protection afforded by Tubastatin A. We hypothesize that Tubastatin A acts to increase XBP1s protein levels that are dependent on its HDAC6 deacetylase inhibition via a mechanism involving acetylation-mediated proteasomal degradation, providing novel mechanistic insight into the anti-oxidative effects of HDAC6 inhibition. (C) 2014 Elsevier Inc. All rights reserved.
WOS关键词UNFOLDED PROTEIN RESPONSE ; HISTONE DEACETYLASE ; LYSINE ACETYLATION ; OXIDATIVE STRESS ; RECEPTOR ; DIFFERENTIATION ; ACTIVATION ; STABILITY ; APOPTOSIS ; MOTILITY
资助项目National Natural Science Foundation of China[91029716] ; National Natural Science Foundation of China[81125023] ; National Natural Science Foundation of China[81173033] ; National Natural Science Foundation of China[81270942] ; National Major Scientific and Technological Special Project for "significant new drugs creation"[2012ZX09301001-004]
WOS研究方向Biochemistry & Molecular Biology ; Biophysics
语种英语
WOS记录号WOS:000343641000071
出版者ACADEMIC PRESS INC ELSEVIER SCIENCE
源URL[http://119.78.100.183/handle/2S10ELR8/276984]  
专题国家新药筛选中心
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Zhou, Yu-bo
作者单位1.E China Normal Univ, Sch Life Sci, Shanghai 200062, Peoples R China;
2.Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Natl Ctr Drug Screening, Shanghai 201203, Peoples R China
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GB/T 7714
Zhang, Yue,Liu, Chang-mei,Cao, Xian-cao,et al. Involvement of transcription factor XBP1s in the resistance of HDAC6 inhibitor Tubastatin A to superoxidation via acetylation-mediated proteasomal degradation[J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,2014,450(1):433-439.
APA Zhang, Yue,Liu, Chang-mei,Cao, Xian-cao,Zang, Yi,Zhou, Yu-bo,&Li, Jia.(2014).Involvement of transcription factor XBP1s in the resistance of HDAC6 inhibitor Tubastatin A to superoxidation via acetylation-mediated proteasomal degradation.BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS,450(1),433-439.
MLA Zhang, Yue,et al."Involvement of transcription factor XBP1s in the resistance of HDAC6 inhibitor Tubastatin A to superoxidation via acetylation-mediated proteasomal degradation".BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 450.1(2014):433-439.

入库方式: OAI收割

来源:上海药物研究所

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