How the ends signal the end: Regulation by E3 ubiquitin ligases recognizing protein termini

被引:68
作者
Sherpa, Dawafuti [1 ]
Chrustowicz, Jakub [1 ]
Schulman, Brenda A. [1 ]
机构
[1] Max Planck Inst Biochem, Dept Mol Machines & Signaling, Martinsried, Germany
基金
欧盟地平线“2020”;
关键词
RULE PATHWAY; STRUCTURAL BASIS; MOLECULAR-BASIS; RECOGNITION COMPONENT; SUBSTRATE RECOGNITION; CELLULAR-PROTEINS; COHESIN SUBUNIT; GID COMPLEX; N-DEGRON; UBR BOX;
D O I
10.1016/j.molcel.2022.02.004
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
Specificity of eukaryotic protein degradation is determined by E3 ubiquitin ligases and their selective binding to protein motifs, termed ???degrons,???in substrates for ubiquitin-mediated proteolysis. From the discovery of the first substrate degron and the corresponding E3 to a flurry of recent studies enabled by modern systems and structural methods, it is clear that many regulatory pathways depend on E3s recognizing protein termini. Here, we review the structural basis for recognition of protein termini by E3s and how this recognition underlies biological regulation. Diverse E3s evolved to harness a substrate???s N and/or C terminus (and often adjacent residues as well) in a sequence-specific manner. Regulation is achieved through selective activation of E3s and also through generation of degrons at ribosomes or by posttranslational means. Collectively, many E3 interactions with protein N and C termini enable intricate control of protein quality and responses to cellular signals.
引用
收藏
页码:1424 / 1438
页数:15
相关论文
共 100 条
[1]   First Things First: Vital Protein Varks by N-Terminal Acetyltransferases [J].
Aksnes, Henriette ;
Drazic, Adrian ;
Marie, Michael ;
Arnesen, Thomas .
TRENDS IN BIOCHEMICAL SCIENCES, 2016, 41 (09) :746-760
[2]   INVIVO HALF-LIFE OF A PROTEIN IS A FUNCTION OF ITS AMINO-TERMINAL RESIDUE [J].
BACHMAIR, A ;
FINLEY, D ;
VARSHAVSKY, A .
SCIENCE, 1986, 234 (4773) :179-186
[3]   NEDD8 nucleates a multivalent cullin-RING-UBE2D ubiquitin ligation assembly [J].
Baek, Kheewoong ;
Krist, David T. ;
Prabu, J. Rajan ;
Hill, Spencer ;
Kluegel, Maren ;
Neumaier, Lisa-Marie ;
von Gronau, Susanne ;
Kleiger, Gary ;
Schulman, Brenda A. .
NATURE, 2020, 578 (7795) :461-+
[4]   INHIBITION OF THE N-END RULE PATHWAY IN LIVING CELLS [J].
BAKER, RT ;
VARSHAVSKY, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (04) :1090-1094
[5]   THE RECOGNITION COMPONENT OF THE N-END RULE PATHWAY [J].
BARTEL, B ;
WUNNING, I ;
VARSHAVSKY, A .
EMBO JOURNAL, 1990, 9 (10) :3179-3189
[6]   The many blades of the β-propeller proteins: conserved but versatile [J].
Chen, Cammy K. -M. ;
Chan, Nei-Li ;
Wang, Andrew H. -J. .
TRENDS IN BIOCHEMICAL SCIENCES, 2011, 36 (10) :553-561
[7]  
Chen SJ, 2021, P NATL ACAD SCI USA, V118, DOI [10.1073/pnas.2115430118, 10.1073/pnas.2115430118j1of7]
[8]   An N-end rule pathway that recognizes proline and destroys gluconeogenic enzymes [J].
Chen, Shun-Jia ;
Wu, Xia ;
Wadas, Brandon ;
Oh, Jang-Hyun ;
Varshavsky, Alexander .
SCIENCE, 2017, 355 (6323)
[9]   Molecular basis for arginine C-terminal degron recognition by Cul2FEM1 E3 ligase [J].
Chen, Xinyan ;
Liao, Shanhui ;
Makaros, Yaara ;
Guo, Qiong ;
Zhu, Zhongliang ;
Krizelman, Rina ;
Dahan, Karin ;
Tu, Xiaoming ;
Yao, Xuebiao ;
Koren, Itay ;
Xu, Chao .
NATURE CHEMICAL BIOLOGY, 2021, 17 (03) :254-+
[10]   Structural basis for the recognition of N-end rule substrates by the UBR box of ubiquitin ligases [J].
Choi, Woo Suk ;
Jeong, Byung-Cheon ;
Joo, Yoo Jin ;
Lee, Myeong-Ryeol ;
Kim, Joon ;
Eck, Michael J. ;
Song, Hyun Kyu .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2010, 17 (10) :1175-+