Mapping the SUMOylated landscape

被引:64
作者
Eifler, Karolin [1 ]
Vertegaal, Alfred C. O. [1 ]
机构
[1] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2333 ZA Leiden, Netherlands
基金
欧洲研究理事会;
关键词
cross-talk; group modification; mass spectrometry; post-translational modification; proteomics; site-specific; small ubiquitin-like modifier; SUMO; ubiquitin; PML NUCLEAR-BODIES; TARGETED UBIQUITIN LIGASE; PROTEIN SUMOYLATION; STRUCTURAL BASIS; SUMO PATHWAY; CHROMOSOME SEGREGATION; MODIFIER CONJUGATION; MASS-SPECTROMETRY; SLX4; COMPLEX; E3; LIGASE;
D O I
10.1111/febs.13378
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SUMOylation is a post-translational modification that regulates a multitude of cellular processes, including replication, cell-cycle progression, protein transport and the DNA damage response. Similar to ubiquitin, SUMO (small ubiquitin-like modifier) is covalently attached to target proteins in a reversible process via an enzymatic cascade. SUMOylation is essential for nearly all eukaryotic organisms, and deregulation of the SUMO system is associated with human diseases such as cancer and neurodegenerative diseases. Therefore, it is of great interest to understand the regulation and dynamics of this post-translational modification. Within the last decade, mass spectrometry analyses of SUMO proteomes have overcome several obstacles, greatly expanding the number of known SUMO target proteins. In this review, we briefly outline the basic concepts of the SUMO system, and discuss the potential of proteomic approaches to decipher SUMOylation patterns in order to understand the role of SUMO in health and disease.
引用
收藏
页码:3669 / 3680
页数:12
相关论文
共 86 条
[1]  
Bawa-Khalfe Tasneem, 2010, Genes Cancer, V1, P748
[2]   Detecting endogenous SUMO targets in mammalian cells and tissues [J].
Becker, Janina ;
Barysch, Sina V. ;
Karaca, Samir ;
Dittner, Claudia ;
Hsiao, He-Hsuan ;
Diaz, Mauricio Berriel ;
Herzig, Stephan ;
Urlaub, Henning ;
Melchior, Frauke .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2013, 20 (04) :525-+
[3]   The ubiquitin- and SUMO-dependent signaling response to DNA double-strand breaks [J].
Bekker-Jensen, Simon ;
Mailand, Niels .
FEBS LETTERS, 2011, 585 (18) :2914-2919
[4]   Structural basis for E2-mediated SUMO conjugation revealed by a complex between ubiquitin-conjugating enzyme Ubc9 and RanGAP1 [J].
Bernier-Villamor, V ;
Sampson, DA ;
Matunis, MJ ;
Lima, CD .
CELL, 2002, 108 (03) :345-356
[5]   Purification and identification of endogenous polySUMO conjugates [J].
Bruderer, Roland ;
Tatham, Michael H. ;
Plechanovova, Anna ;
Matic, Ivan ;
Garg, Amit K. ;
Hay, Ronald T. .
EMBO REPORTS, 2011, 12 (02) :142-148
[6]  
Chen A, 1998, BIOCHEM MOL BIOL INT, V46, P1161
[7]   SUMO: A Multifaceted Modifier of Chromatin Structure and Function [J].
Cubenas-Potts, Caelin ;
Matunis, Michael J. .
DEVELOPMENTAL CELL, 2013, 24 (01) :1-12
[8]   Emerging roles of the SUMO pathway in mitosis [J].
Dasso, Mary .
CELL DIVISION, 2008, 3 (1)
[9]   Resolution of sister centromeres requires RanBP2-mediated SUMOylation of topoisomerase IIα [J].
Dawlaty, Meelad M. ;
Malureanu, Liviu ;
Jeganathan, Karthik B. ;
Kao, Esther ;
Sustmann, Claudio ;
Tahk, Samuel ;
Shuai, Ke ;
Grosschedl, Rudolf ;
van Deursen, Jan M. .
CELL, 2008, 133 (01) :103-115
[10]   A proteomic strategy for gaining insights into protein sumoylation in yeast [J].
Denison, C ;
Rudner, AD ;
Gerber, SA ;
Bakalarski, CE ;
Moazed, D ;
Gygi, SP .
MOLECULAR & CELLULAR PROTEOMICS, 2005, 4 (03) :246-254