Domains, motifs, and scaffolds:: The role of modular interactions in the evolution and wiring of cell signaling circuits

被引:354
作者
Bhattacharyya, Roby P. [1 ]
Remenyi, Attila [1 ]
Yeh, Brian J. [1 ]
Lim, Wendell A. [1 ]
机构
[1] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94143 USA
关键词
signal transduction; modularity; evolvability; docking; synthetic biology;
D O I
10.1146/annurev.biochem.75.103004.142710
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Living cells display complex signal processing behaviors, many of which are mediated by networks of proteins specialized for signal transduction. Here we focus on the question of how the remarkably diverse array of eukaryotic signaling circuits may have evolved. Many of the mechanisms that connect signaling proteins into networks are highly modular: The core catalytic activity of a signaling protein is physically and functionally separable from molecular domains or motifs that determine its linkage to both inputs and outputs. This high degree of modularity may make these systems more evolvable-in principle, novel circuits, and therefore highly innovative regulatory behaviors, can arise from relatively simple genetic events such as recombination, deletion, or insertion. In support of this hypothesis, recent studies show that such modular systems can be exploited to engineer normatural signaling proteins and pathways with novel behavior.
引用
收藏
页码:655 / 680
页数:26
相关论文
共 157 条
[1]
Custom zinc-finger nucleases for use in human cells [J].
Alwin, S ;
Gere, MB ;
Guhl, E ;
Effertz, K ;
Barbas, CF III ;
Sega, DJ ;
Weitzman, MD ;
Cathomen, T .
MOLECULAR THERAPY, 2005, 12 (04) :610-617
[2]
Human zinc fingers as building blocks in the construction of artificial transcription factors [J].
Bae, KH ;
Do Kwon, Y ;
Shin, HC ;
Hwang, MS ;
Ryu, EH ;
Park, KS ;
Yang, HY ;
Lee, D ;
Lee, Y ;
Park, J ;
Kwon, HS ;
Kim, HW ;
Yeh, BI ;
Lee, HW ;
Sohn, SH ;
Yoon, J ;
Seol, W ;
Kim, JS .
NATURE BIOTECHNOLOGY, 2003, 21 (03) :275-280
[3]
A conserved docking site in MEKs mediates high-affinity binding to MAP kinases and cooperates with a scaffold protein to enhance signal transmission [J].
Bardwell, AJ ;
Flatauer, LJ ;
Matsukuma, K ;
Thorner, J ;
Bardwell, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (13) :10374-10386
[4]
A conserved motif at the amino termini of MEKs might mediate high-affinity interaction with the cognate MAPKs [J].
Bardwell, L ;
Thorner, J .
TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (10) :373-374
[5]
Bardwell L, 1996, MOL CELL BIOL, V16, P3637
[6]
Specificity determinants in MAPK signaling to transcription factors [J].
Barsyte-Lovejoy, D ;
Galanis, A ;
Sharrocks, AD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (12) :9896-9903
[7]
The structure of phosphorylated GSK-3β complexed with a peptide, FRATtide, that inhibits β-catenin phosphorylation [J].
Bax, B ;
Carter, PS ;
Lewis, C ;
Guy, AR ;
Bridges, A ;
Tanner, R ;
Pettman, G ;
Mannix, C ;
Culbert, AA ;
Brown, MJB ;
Smith, DG ;
Reith, AD .
STRUCTURE, 2001, 9 (12) :1143-1152
[8]
Toward controlling gene expression at will:: Specific regulation of the erbB-2/HER-2 promoter by using polydactyl zinc finger proteins constructed from modular building blocks [J].
Beerli, RR ;
Segal, DJ ;
Dreier, B ;
Barbas, CF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14628-14633
[9]
Positive and negative regulation of endogenous genes by designed transcription factors [J].
Beerli, RR ;
Dreier, B ;
Barbas, CF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1495-1500
[10]
The C2 domain of PKCδ is a phosphotyrosine binding domain [J].
Benes, CH ;
Wu, N ;
Elia, AEH ;
Dharia, T ;
Cantley, LC ;
Soltoff, SP .
CELL, 2005, 121 (02) :271-280