Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Periodic Signaling Controlled by an Oscillatory Circuit That Includes Protein Kinases ERK2 and PKA
Mineko Maeda,1Sijie Lu,2*Gad Shaulsky,3Yuji Miyazaki,1Hidekazu Kuwayama,4Yoshimasa Tanaka,4Adam Kuspa,2,3William F. Loomis5
Self-regulating systems often use robust oscillatory circuits.One such system controls the chemotactic signaling mechanismof Dictyostelium, where pulses of adenosine 3',5'-monophosphate(cAMP) are generated with a periodicity of 7 minutes. We haveobserved spontaneous oscillations in activation of the mitogen-activatedprotein (MAP) kinase ERK2 that occur in phase with peaks ofcAMP, and we show that ERK2 modulates cAMP levels through thephosphodiesterase RegA. Computer modeling and simulations ofthe underlying circuit faithfully account for the ability ofthe cells to spontaneously generate periodic pulses during specificstages of development. Similar oscillatory processes may occurin cells of many different species.
1 Department of Biology, Graduate School of Science, Osaka University, Machikaneyama-cho 1-16, Toyonaka, Osaka 560-0043, Japan. 2 Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston TX 77030, USA. 3 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston TX 77030, USA. 4 Institute of Biological Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8572, Japan. 5 Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
* Present address: Department of Blood and Marrow Transplantation,M. D. Anderson Cancer Center, Houston, TX 77030, USA.
To whom correspondence should be addressed. E-mail: wloomis{at}ucsd.edu
Systematic analysis of synchronized oscillatory neuronal networks reveals an enrichment for coupled direct and indirect feedback motifs.
C.-Y. Dong, J. Lim, Y. Nam, and K.-H. Cho (2009)
Bioinformatics
25, 1680-1685
|Abstract »|Full Text »|PDF »
MPL1, a Novel Phosphatase with Leucine-Rich Repeats, Is Essential for Proper ERK2 Phosphorylation and Cell Motility.
M. Rodriguez, B. Kim, N.-S. Lee, S. Veeranki, and L. Kim (2008)
Eukaryot. Cell
7, 958-966
|Abstract »|Full Text »|PDF »
Regulation of cAMP dynamics by Ca2+ and G protein-coupled receptors in the pancreatic -cell: a computational approach.
L. E. Fridlyand, M. C. Harbeck, M. W. Roe, and L. H. Philipson (2007)
Am J Physiol Cell Physiol
293, C1924-C1933
|Abstract »|Full Text »|PDF »
ATP Release Guides Neutrophil Chemotaxis via P2Y2 and A3 Receptors.
Y. Chen, R. Corriden, Y. Inoue, L. Yip, N. Hashiguchi, A. Zinkernagel, V. Nizet, P. A. Insel, and W. G. Junger (2006)
Science
314, 1792-1795
|Abstract »|Full Text »|PDF »
Nonadaptive Regulation of ERK2 in Dictyostelium: Implications for Mechanisms of cAMP Relay.
Microarray phenotyping in Dictyostelium reveals a regulon of chemotaxis genes.
E. O. Booth, N. V. Driessche, O. Zhuchenko, A. Kuspa, and G. Shaulsky (2005)
Bioinformatics
21, 4371-4377
|Abstract »|Full Text »|PDF »
Oscillatory ROP GTPase Activation Leads the Oscillatory Polarized Growth of Pollen Tubes.
J.-U. Hwang, Y. Gu, Y.-J. Lee, and Z. Yang (2005)
Mol. Biol. Cell
16, 5385-5399
|Abstract »|Full Text »|PDF »
Interplay of Ca2+ and cAMP Signaling in the Insulin-secreting MIN6 {beta}-Cell Line.
L. R. Landa Jr., M. Harbeck, K. Kaihara, O. Chepurny, K. Kitiphongspattana, O. Graf, V. O. Nikolaev, M. J. Lohse, G. G. Holz, and M. W. Roe (2005)
J. Biol. Chem.
280, 31294-31302
|Abstract »|Full Text »|PDF »
Loss of SMEK, a Novel, Conserved Protein, Suppresses mek1 Null Cell Polarity, Chemotaxis, and Gene Expression Defects.
M. C. Mendoza, F. Du, N. Iranfar, N. Tang, H. Ma, W. F. Loomis, and R. A. Firtel (2005)
Mol. Cell. Biol.
25, 7839-7853
|Abstract »|Full Text »|PDF »
A chemical waveform synthesizer.
J. Olofsson, H. Bridle, J. Sinclair, D. Granfeldt, E. Sahlin, and O. Orwar (2005)
PNAS
102, 8097-8102
|Abstract »|Full Text »|PDF »
Intracellular Role of Adenylyl Cyclase in Regulation of Lateral Pseudopod Formation during Dictyostelium Chemotaxis.
V. Stepanovic, D. Wessels, K. Daniels, W. F. Loomis, and D. R. Soll (2005)
Eukaryot. Cell
4, 775-786
|Abstract »|Full Text »|PDF »
Constitutively Active G Protein-coupled Receptor Mutants Block Dictyostelium Development.