Redefining the BH3 Death Domain as a 'Short Linear Motif'

被引:51
作者
Aouacheria, Abdel [1 ]
Combet, Christophe [2 ,3 ]
Tompa, Peter [4 ,5 ]
Hardwick, J. Marie [6 ]
机构
[1] Ecole Normale Super Lyon, Mol Cell Biol Lab, UMR 5239, CNRS,UCBL, F-69364 Lyon 07, France
[2] Univ Lyon 1, Bases Mol & Struct Syst Infect, UMR 5086, CNRS, F-69367 Lyon 07, France
[3] Univ Lyon 1, Ctr Rech Cancerol Lyon, UMR INSERM U1052, CNRS 5286,Ctr Leon Berard, F-69424 Lyon 03, France
[4] Hungarian Acad Sci, Inst Enzymol, Res Ctr Nat Sci, H-1117 Budapest, Hungary
[5] Vrije Univ Brussel, VIB Struct Biol Res Ctr SBRC, B-1050 Brussels, Belgium
[6] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, W Harry Feinstone Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
INTRINSICALLY DISORDERED REGIONS; BCL-2 FAMILY PROTEINS; MITOCHONDRIAL APOPTOSIS; BH3-ONLY PROTEIN; PROAPOPTOTIC BAX; INDUCE APOPTOSIS; BINDING MOTIF; CELL-DEATH; HOMOLOGY; MCL-1;
D O I
10.1016/j.tibs.2015.09.007
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
B cell lymphoma-2 (BCL-2)-related proteins control programmed cell death through a complex network of protein-protein interactions mediated by BCL-2 homology 3 (BH3) domains. Given their roles as dynamic linchpins, the discovery of novel BH3-containing proteins has attracted considerable attention. However, without a clearly defined BH3 signature sequence the BCL-2 family has expanded to include a nebulous group of nonhomologous BH3-only proteins, now justified by an intriguing twist. We present evidence that BH3s from both ordered and disordered proteins represent a new class of short linear motifs (SLiMs) or molecular recognition features (MoRFs) and are diverse in their evolutionary histories. The implied corollaries are that BH3s have a broad phylogenetic distribution and could potentially bind to non-BCL-2-like structural domains with distinct functions.
引用
收藏
页码:736 / 748
页数:13
相关论文
共 92 条
[1]   A Dynamic View of Domain-Motif Interactions [J].
Akiva, Eyal ;
Friedlander, Gilgi ;
Itzhaki, Zohar ;
Margalit, Hanah .
PLOS COMPUTATIONAL BIOLOGY, 2012, 8 (01)
[2]   Phylogenomics of life-or-death switches in multicellular animals: Bcl-2, BH3-only, and BNip families of apoptotic regulators [J].
Aouacheria, A ;
Brunet, F ;
Gouy, M .
MOLECULAR BIOLOGY AND EVOLUTION, 2005, 22 (12) :2395-2416
[3]   Evolution of Bcl-2 homology motifs: homology versus homoplasy [J].
Aouacheria, Abdel ;
de Laval, Valentine Rech ;
Combet, Christophe ;
Hardwick, J. Marie .
TRENDS IN CELL BIOLOGY, 2013, 23 (03) :103-111
[4]   Proteome-Wide Discovery of Evolutionary Conserved Sequences in Disordered Regions [J].
Ba, Alex N. Nguyen ;
Yeh, Brian J. ;
van Dyk, Dewald ;
Davidson, Alan R. ;
Andrews, Brenda J. ;
Weiss, Eric L. ;
Moses, Alan M. .
SCIENCE SIGNALING, 2012, 5 (215)
[5]   Minimotif Miner: a tool for investigating protein function [J].
Balla, S ;
Thapar, V ;
Verma, S ;
Luong, T ;
Faghri, T ;
Huang, CH ;
Rajasekaran, S ;
del Campo, JJ ;
Shinn, JH ;
Mohler, WA ;
Maciejewski, MW ;
Gryk, MR ;
Piccirillo, B ;
Schiller, SR ;
Schiller, MR .
NATURE METHODS, 2006, 3 (03) :175-177
[6]   Intrinsic Order and Disorder in the Bcl-2 Member Harakiri: Insights into Its Proapoptotic Activity [J].
Barrera-Vilarmau, Susana ;
Obregon, Patricia ;
de Alba, Eva .
PLOS ONE, 2011, 6 (06)
[7]   Control of mitochondrial apoptosis by the Bcl-2 family [J].
Brunelle, Joslyn K. ;
Letai, Anthony .
JOURNAL OF CELL SCIENCE, 2009, 122 (04) :437-441
[8]   Differential targeting of prosurvival Bcl-2 proteins by their BH3-only ligands allows complementary apoptotic function [J].
Chen, L ;
Willis, SN ;
Wei, A ;
Smith, BJ ;
Fletcher, JI ;
Hinds, MG ;
Colman, PM ;
Day, CL ;
Adams, JM ;
Huang, DCS .
MOLECULAR CELL, 2005, 17 (03) :393-403
[9]   Rational drug design via intrinsically disordered protein [J].
Cheng, Yugong ;
LeGall, Tanguy ;
Oldfield, Christopher J. ;
Mueller, James P. ;
Van, Ya-Yue J. ;
Romero, Pedro ;
Cortese, Marc S. ;
Uversky, Vladimir N. ;
Dunker, A. Keith .
TRENDS IN BIOTECHNOLOGY, 2006, 24 (10) :435-442
[10]   NOXA, a sensor of proteasome integrity, is degraded by 26S proteasomes by an ubiquitin-independent pathway that is blocked by MCL-1 [J].
Craxton, A. ;
Butterworth, M. ;
Harper, N. ;
Fairall, L. ;
Schwabe, J. ;
Ciechanover, A. ;
Cohen, G. M. .
CELL DEATH AND DIFFERENTIATION, 2012, 19 (09) :1424-1434