中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Arginine methylation of hnRNP K enhances p53 transcriptional activity

文献类型:期刊论文

作者Chen, YB; Zhou, XY; Liu, N; Wang, CC; Zhang, L; Mo, W; Hu, G
刊名FEBS LETTERS
出版日期2008
卷号582期号:12页码:1761-1765
关键词hnRNP K UV radiation arginine methylation p53 transcriptional regulation
通讯作者Hu, G (reprint author), Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, State Key Lab Mol Biol, Shanghai 200031, Peoples R China.,hgxgene@sunm.shcnc.ac.cn
英文摘要Previous studies have illustrated that hnRNP K, which could be methylated at arginine residues, plays a key role in coordinating transcriptional responses to DNA damage as a cofactor for p53. In this study, we observed that hnRNP K was markedly arginine methylated in response to UV radiation. Furthermore, arginine methylation of hnRNP K enhanced its affinity with p53. Inhibition of methylation in hnRNP K attenuated the recruitment of p53 to p21 promoter, and reduced p53 transcriptional activity. These data suggested that arginine methylation of hnRNP K is a key element for p53 transcriptional activity. (C) 2008 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
学科主题Biochemistry & Molecular Biology ; Biophysics ; Cell Biology
类目[WOS]Biochemistry & Molecular Biology ; Biophysics ; Cell Biology
关键词[WOS]NUCLEAR-RIBONUCLEOPROTEIN-K ; DNA-DAMAGE ; TUMOR-SUPPRESSOR ; ACTIVATES P53 ; C-SRC ; PROTEIN ; COACTIVATOR ; PHOSPHORYLATION ; PATHWAYS ; TARGET
收录类别SCI
语种英语
WOS记录号WOS:000258110600022
版本出版稿
源URL[http://202.127.25.143/handle/331003/1464]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
推荐引用方式
GB/T 7714
Chen, YB,Zhou, XY,Liu, N,et al. Arginine methylation of hnRNP K enhances p53 transcriptional activity[J]. FEBS LETTERS,2008,582(12):1761-1765.
APA Chen, YB.,Zhou, XY.,Liu, N.,Wang, CC.,Zhang, L.,...&Hu, G.(2008).Arginine methylation of hnRNP K enhances p53 transcriptional activity.FEBS LETTERS,582(12),1761-1765.
MLA Chen, YB,et al."Arginine methylation of hnRNP K enhances p53 transcriptional activity".FEBS LETTERS 582.12(2008):1761-1765.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。