Tribbles in the 21st Century: The Evolving Roles of Tribbles Pseudokinases in Biology and Disease

被引:169
作者
Eyers, Patrick A. [1 ]
Keeshan, Karen [2 ]
Kannan, Natarajan [3 ,4 ]
机构
[1] Univ Liverpool, Inst Integrat Biol, Dept Biochem, Liverpool L69 7ZB, Merseyside, England
[2] Univ Glasgow, Coll Med Vet & Life Sci, Inst Canc Sci, Paul OGorman Leukemia Res Ctr, Glasgow G12 0YN, Lanark, Scotland
[3] Univ Georgia, Inst Bioinformat, Athens, GA 30602 USA
[4] Univ Georgia, Dept Biochem & Mol Biol, Athens, GA 30602 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
C/EBP-ALPHA; GENE-EXPRESSION; FUNCTIONAL DIVERGENCE; MEDIATES DEATH; BREAST-CANCER; KINASE DOMAIN; TAL1; COMPLEX; BETA-TRCP; TRIB2; CLASSIFICATION;
D O I
10.1016/j.tcb.2016.11.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Tribbles (TRIB) pseudokinases control multiple aspects of eukaryotic cell biology and evolved unique features distinguishing them from all other protein kinases. The atypical pseudokinase domain retains a regulated binding platform for substrates, which are ubiquitinated by context-specific E3 ligases. This plastic configuration has also been exploited as a scaffold to support the modulation of canonical MAPK and AKT modules. In this review, we discuss the evolution of TRIBs and their roles in vertebrate cell biology. TRIB2 is the most ancestral member of the family, whereas the emergence of TRIB3 homologs in mammals supports additional biological roles, many of which are currently being dissected. Given their pleiotropic role in diseases, the unusual TRIB pseudokinase conformation provides a highly attractive opportunity for drug design.
引用
收藏
页码:284 / 298
页数:15
相关论文
共 96 条
[1]   Trib3 Is Elevated in Parkinson's Disease and Mediates Death in Parkinson's Disease Models [J].
Aime, Pascaline ;
Sun, Xiaotian ;
Zareen, Neela ;
Rao, Apeksha ;
Berman, Zachary ;
Volpicelli-Daley, Laura ;
Bernd, Paulette ;
Crary, John F. ;
Levy, Oren A. ;
Greene, Lloyd A. .
JOURNAL OF NEUROSCIENCE, 2015, 35 (30) :10731-10749
[2]   Linkage of Meis1 leukemogenic activity to multiple downstream effectors including Trib2 and Ccl3 [J].
Argiropoulos, Bob ;
Palmqvist, Lars ;
Yung, Eric ;
Kuchenbauer, Florian ;
Heuser, Michael ;
Sly, Laura M. ;
Wan, Adrian ;
Krystal, Gerald ;
Humphries, R. Keith .
EXPERIMENTAL HEMATOLOGY, 2008, 36 (07) :845-859
[3]   Essential roles for ankyrin repeat and transactivation domains in induction of T-cell leukemia by Notch1 [J].
Aster, JC ;
Xu, LW ;
Karnell, FG ;
Patriub, V ;
Pui, JC ;
Pear, WS .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (20) :7505-7515
[4]   The Tribbles 2 (TRB2) pseudokinase binds to ATP and autophosphorylates in a metal-independent manner [J].
Bailey, Fiona P. ;
Byrne, Dominic P. ;
Oruganty, Krishnadev ;
Eyers, Claire E. ;
Novotny, Christopher J. ;
Shokat, Kevan M. ;
Kannan, Natarajan ;
Eyers, Patrick A. .
BIOCHEMICAL JOURNAL, 2015, 467 :47-62
[5]   Going for broke: targeting the human cancer pseudokinome [J].
Bailey, Fiona P. ;
Byrne, Dominic P. ;
McSkimming, Daniel ;
Kannan, Natarajan ;
Eyers, Patrick A. .
BIOCHEMICAL JOURNAL, 2015, 465 :195-211
[6]   EphB6 Receptor Modulates Micro RNA Profile of Breast Carcinoma Cells [J].
Bhushan, Lokesh ;
Kandpal, Raj P. .
PLOS ONE, 2011, 6 (07)
[7]   Emerging roles of pseudokinases [J].
Boudeau, Jerome ;
Miranda-Saavedra, Diego ;
Barton, Geoffrey J. ;
Alessi, Dario R. .
TRENDS IN CELL BIOLOGY, 2006, 16 (09) :443-452
[8]   Structure of the PAN3 Pseudokinase Reveals the Basis for Interactions with the PAN2 Deadenylase and the GW182 Proteins [J].
Christie, Mary ;
Boland, Andreas ;
Huntzinger, Eric ;
Weichenrieder, Oliver ;
Izaurralde, Elisa .
MOLECULAR CELL, 2013, 51 (03) :360-373
[9]   Will the Ubiquitin System Furnish as Many Drug Targets as Protein Kinases? [J].
Cohen, Philip ;
Tcherpakov, Marianna .
CELL, 2010, 143 (05) :686-693
[10]   Drosophila Tribbles Antagonizes Insulin Signaling-Mediated Growth and Metabolism via Interactions with Akt Kinase [J].
Das, Rahul ;
Sebo, Zachary ;
Pence, Laramie ;
Dobens, Leonard L. .
PLOS ONE, 2014, 9 (10)