[1]王京伟.泛素结合结构域与泛素化信号的识别[J].现代检验医学杂志,2015,30(02):99-104.[doi:10.3969/j.issn.1671-7414.2015.02.031]
 WANG Jing-wei.Recognition of Ubiquitination Signal with Ubiquitin-binding Domains[J].Journal of Modern Laboratory Medicine,2015,30(02):99-104.[doi:10.3969/j.issn.1671-7414.2015.02.031]
点击复制

泛素结合结构域与泛素化信号的识别()
分享到:

《现代检验医学杂志》[ISSN:/CN:]

卷:
第30卷
期数:
2015年02期
页码:
99-104
栏目:
综述
出版日期:
2015-03-20

文章信息/Info

Title:
Recognition of Ubiquitination Signal with Ubiquitin-binding Domains
作者:
王京伟
武汉大学人民医院检验科,武汉 430060
Author(s):
WANG Jing-wei
Department of Clinical Laboratory,Renmin Hospital of Wuhan University,Wuhan 430060,China
关键词:
泛素 泛素结合结构域 识别 调节机制
分类号:
R446
DOI:
10.3969/j.issn.1671-7414.2015.02.031
文献标志码:
A
摘要:
泛素化(Ubiquitylation,UB)是目前最为复杂最为多元的翻译后修饰,几乎参与胞内所有的生物学过程。其通过改变底物的分子景观(landscape)、三维结构、位置、活性、影响底物蛋白与其他蛋白的相互作用等方法,从时间和空间上调节底物所参与的生物学过程。而泛素化底物功能的发挥依赖于特异性的泛素结合结构域(Ubiquitin binding domains,UBDs)。UBDs的表面功能基团特异性识别具有不同修饰类型的泛素化底物,并决定其功能的特异性。已知的20多种UBDs超家族对泛素化信号网络的有序调节是人们开启泛素化网络的一把钥匙,同时了解UBD-ubiquitin的特异性识别是认识泛素化蛋白质组学“ubiquitome”的基础。
Abstract:
Ubiquitylation is a highly versatile post-translation modification that controls virtually all types of cellular events by changing the molecular landscape,the three-dimensional structure,the location oractivity of the substrate,influencing the interactions of substrate with otherproteins.Many cellular activities of ubiquitin and its functions are decipheredby specific ubiquitin binding domains(UBDs).UBD interacts with the differenttype of Ubiquitylation with a variety of lengths and linkage patterns based on the specific functional surfaces.So far over twenty distinct UBD families have been identified,and the known members of this group have expanded rapidly.The UBD families,the decoder of ubiquitylation network,are building a foundation for in-depth understanding the ubiquitination proteomics “ubiquitome”.

参考文献/References:

[1] Woelk T,Sigismund S,Penengo L,et al.The ubiquitination code:a signalling problem[J].Cell Division,2007,2(1):11.
[2] Suryadinata R,Roesley SN,Yang G,et al.Mechanisms of generating polyubiquitin chains of different topology[J].Cells(Basel,Switzerland),2014,3(3):674-689.
[3] Hicke L,Schubert HL,Hill CP.Ubiquitin-binding domains[J].Nature Reviews Molecular Cell Biology,2005,6(8):610-621.
[4] Hurley JH,Lee S,Prag G.Ubiquitin-binding domains[J].Biochemical Journal,2006,399(3):361-372.
[5] Ikeda F,Crosetto N,Dikic I.What determines the specificity and outcomes of ubiquitin signaling?[J].Cell,2010,143(5):677-681.
[6] Song AX,Zhou CJ,Peng Y,et al.Structural transformation of the tandemubiquitin-interacting motifs in ataxin-3 and their cooperative interactions with ubiquitin chains[J].PLoS One,2010,5(10):e13202.
[7] Tyrrell A,Flick K,Kleiger G,et al.Physiologically relevant and portable tandem ubiquitin-binding domain stabilizes polyubiquitylated proteins[J].Proceedings of the National Academy of Sciences of the United States of America,2010,107(46):19796-19801.
[8] Winget JM,Mayor T.The diversity of ubiquitin recognition:hot spots andvaried specificity[J].Molecular Cell,2010,38(5):627-635.
[9] Dikic I,Wakatsuki S,Walters KJ.Ubiquitin-binding domains-from structures to functions[J].Nature Reviews Molecular Cell Biology,2009,10(10):659-671.
[10] Komander D,Rape M.The ubiquitin code[J].Annu Rev Biochem,2012(81):203-229.
[11] Rahighi S,Ikeda F,Kawasaki M,et al.Specific recognition of linear ubiquitin chains by NEMO is important for NF-kappa B activation[J].Cell,2009,136(6):1098-1109.
[12] Bomar MG,D'souza S,Bienko M,et al.Unconventional ubiquitin recognition by the ubiquitin-binding motif within the Y family DNA polymerases iota andRev1[J].Molecular Cell,2010,37(3):408-417.
[13] Zhang DN,Chen T,Ziu I,et al.Together,Rpn10 and Dsk2 can serve as apolyubiquitin chain-length sensor[J].Molecular Cell,2009,36(6):1018-1033.
[14] Fushman D,Walker O.Exploring the linkage dependence of polyubiquitin conformations using molecular modeling[J].Journal of Molecular Biology,2010,395(4):803-814.
[15] Rahighi S,Ikeda F,Kawasaki M,et al.Specific recognition of linear ubiquitin chains by NEMO is important for NF-kappa B activation[J].Cell,2009,136(6):1098-1109.
[16] Komander D,Reyes-turcu F,Licchesi JD,et al.Molecular discriminationof structurally equivalent Lys 63-linked and linear polyubiquitin chains[J].EMBO Reports,2009,10(5):466-473.
[17] Budhidarmo R,Day CL.The ubiquitin-associated domain of cellular inhibitor of apoptosis proteins facilitates ubiquitylation[J].Journal of Biological Chemistry,2014,289(37):25721-25736.
[18] Ortega Roldan JL,Casares S,Ringkjobing Jensen M,et al.Distinct ubiquitin binding modes exhibited by SH3 domains:molecular determinants and functional implications[J].PLoS One,2013,8(9):e73018.
[19] Liu J,Shaik S,Dai X,et al.Targeting the ubiquitin pathway for cancertreatment[J].Biochimicaet Biophysica Acta,2015,1855(1):50-60.
[20] Hoeller D,Dikic I.Targeting the ubiquitin system in cancer therapy[J].Nature,2009,458(7237):438-444.

备注/Memo

备注/Memo:
基金项目:国家自然基金面上项目:低密度脂蛋白主动氧化的识别机制及其氧化环境的建立,编号:81170273。 作者简介:王京伟(1986-),女,博士,医师,主要从事分子生物和泛素化蛋白质组学研究,E-mail:sophia wang03@hotmail.com。
更新日期/Last Update: 2015-03-20