Tunable Signal Processing through a Kinase Control Cycle: the IKK Signaling Node

被引:24
作者
Behar, Marcelo [1 ,2 ]
Hoffmann, Alexander [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, Signaling Syst Lab, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, San Diego Ctr Syst Biol, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
STAT TRANSCRIPTION FACTORS; KAPPA-B ACTIVATION; TEMPORAL CONTROL; MATHEMATICAL-MODELS; GENE-EXPRESSION; SPECIFICITY; TRANSDUCTION; INFORMATION; TRANSIENT; DYNAMICS;
D O I
10.1016/j.bpj.2013.05.013
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
The transcription factor NF kappa B, a key component of the immune system, shows intricate stimulus-specific temporal dynamics. Those dynamics are thought to play a role in controlling the physiological response to cytokines and pathogens. Biochemical evidence suggests that the NF kappa B inducing kinase, IKK, a signaling hub onto which many signaling pathways converge, is regulated via a regulatory cycle comprising a poised, an active, and an inactive state. We hypothesize that it operates as a modulator of signal dynamics, actively reshaping the signals generated at the receptor proximal level. Here we show that a regulatory cycle can function in at least three dynamical regimes, tunable by regulating a single kinetic parameter. In particular, the simplest three-state regulatory cycle can generate signals with two well-defined phases, each with distinct coding capabilities in terms of the information they can carry about the stimulus. We also demonstrate that such a kinase cycle can function as a signal categorizer classifying diverse incoming signals into outputs with a limited set of temporal activity profiles. Finally, we discuss the extension of the results to other regulatory motifs that could be understood in terms of the regimes of the three-state cycle.
引用
收藏
页码:231 / 241
页数:11
相关论文
共 42 条
[1]
[Anonymous], 2006, Elements of Information Theory
[2]
Pulsatile Stimulation Determines Timing and Specificity of NF-κB-Dependent Transcription [J].
Ashall, Louise ;
Horton, Caroline A. ;
Nelson, David E. ;
Paszek, Pawel ;
Harper, Claire V. ;
Sillitoe, Kate ;
Ryan, Sheila ;
Spiller, David G. ;
Unitt, John F. ;
Broomhead, David S. ;
Kell, Douglas B. ;
Rand, David A. ;
See, Violaine ;
White, Michael R. H. .
SCIENCE, 2009, 324 (5924) :242-246
[3]
Mathematical models of specifcity in cell signaling [J].
Bardwell, Lee ;
Zou, Xiufen ;
Nie, Qing ;
Komarova, Natalia L. .
BIOPHYSICAL JOURNAL, 2007, 92 (10) :3425-3441
[4]
Kinetic insulation as an effective mechanism for achieving pathway specificity in intracellular signaling networks [J].
Behar, Marcelo ;
Dohlman, Henrik G. ;
Elston, Timothy C. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (41) :16146-16151
[5]
Mathematical and computational analysis of adaptation via feedback inhibition in signal transduction pathways [J].
Behar, Marcelo ;
Hao, Nan ;
Dohlman, Henrik G. ;
Elston, Timothy C. .
BIOPHYSICAL JOURNAL, 2007, 93 (03) :806-821
[6]
Requirement of Hsp90 activity for IκB kinase (IKK) biosynthesis and for constitutive and inducible IKK and NF-κB activation [J].
Broemer, M ;
Krappmann, D ;
Scheidereit, C .
ONCOGENE, 2004, 23 (31) :5378-5386
[7]
Transient IκB kinase activity mediates temporal NF-κB dynamics in response to a wide range of tumor necrosis factor-αdoses [J].
Cheong, R ;
Bergmann, A ;
Werner, SL ;
Regal, J ;
Hoffmann, A ;
Levchenko, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (05) :2945-2950
[8]
Information Transduction Capacity of Noisy Biochemical Signaling Networks [J].
Cheong, Raymond ;
Rhee, Alex ;
Wang, Chiaochun Joanne ;
Nemenman, Ilya ;
Levchenko, Andre .
SCIENCE, 2011, 334 (6054) :354-358
[9]
Positive and negative regulation of IκB kinase activity through IKKβ subunit phosphorylation [J].
Delhase, M ;
Hayakawa, M ;
Chen, Y ;
Karin, M .
SCIENCE, 1999, 284 (5412) :309-313
[10]
RGS proteins and signaling by heterotrimeric G proteins [J].
Dohlman, HG ;
Thorner, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (07) :3871-3874