The intense periodic calcium activity experimentally observed in the Xenopus embryo at the Mid Blastula Transition stage is closely related to the competence of the embryonic cells of the marginal zone to respond to the posterior-mesodermal inducting signals from the Fibroblast Growth Factor (FGF). In this work we do a stability analysis and study numerically an extension of a mathematical model previously introduced by us [Diaz, J., Baier, G., Martinez-Mekler, G., Pastor, N., 2002. Interaction of the IP(3)-Ca(2+) and the FGF-MAPK signaling pathways in the Xenopus laevis embryo: a qualitative approach to the mesodermal induction problem. Biophys. Chem. 97, 55-72] for the interaction of the Inositol 1,4,5-triphosphate-Calcium (IP(3)-Ca(2+)) and the Mitogen-Activated Protein Kinase (MAPK) signaling pathways at the Mid Blastula Transition stage or stage 8 of development. This allows us to consider the effect of the oscillatory calcium dynamics on the FGF input signal carried by the MAP kinase (ERK) into the nucleus. We find that this interaction of the pathways induces a limit cycle behavior for ERK with frequency-encoding characteristics. We believe that this periodic increase of the ERK levels in the nucleus is related to the ability of the cell to express posteriorizing mesodermal features induced by the FGF signal at stage 8.
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http://dx.doi.org/10.1016/j.bulm.2004.08.002 | DOI Listing |
Front Biosci (Landmark Ed)
June 2013
State Key Laboratory of Genetic Engineering, Institute of Genetics, School of Life Sciences, Fudan University, Shanghai 200433, PR China.
ITPKC, a susceptibility gene of Kawasaki disease, encodes a kinase that negatively regulates intracellular Ca2+ level and inhibits calcineurin-dependent activation of NFAT by phosphorylating IP3. In this study, we identified a novel ITPKC-interacting protein, namely PPP3CC, using yeast two-hybrid. This interaction was further confirmed by GST pull-down and co-immunoprecipitation assays, and fluorescent microscopy showed co-localization of both proteins in the cell cytoplasm.
View Article and Find Full Text PDFBiochim Biophys Acta
August 2012
Department of Zoology, University of Cambridge, Cambridge, UK.
Background: The nematode, Caenorhabditis elegans is an established model system that is particularly well suited to genetic analysis. C. elegans is easily manipulated and we have an in depth knowledge of many aspects of its biology.
View Article and Find Full Text PDFLab Invest
February 2012
Department of Internal Medicine, Scott and White Digestive Disease Research Center, Scott and White Hospital and Texas A&M Health Science Center, College of Medicine, Temple, TX, USA.
Although large cholangiocytes exert their functions by activation of cyclic adenosine 3',5'-monophosphate (cAMP), Ca(2+)-dependent signaling regulates the function of small cholangiocytes. Histamine interacts with four receptors, H1-H4HRs. H1HR acts by Gαq activating IP(3)/Ca(2+), whereas H2HR activates Gα(s) stimulating cAMP.
View Article and Find Full Text PDFBiochim Biophys Acta
August 2012
Department of Pharmacology, Cambridge, UK.
Background: Inositol 1,4,5-trisphosphate receptors (IP3R) are expressed in almost all animal cells. Three mammalian genes encode closely related IP3R subunits, which assemble into homo- or hetero-tetramers to form intracellular Ca2+ channels.
Scope Of The Review: In this brief review, we first consider a variety of complementary methods that allow the links between IP3 binding and channel gating to be defined.
Chem Senses
February 2010
Sensory and Cognitive Food Sciences, National Food Research Institute, 2-1-12 Kannondai, Tsukuba-shi, Ibaraki 305-8642, Japan.
Inositol 1,4,5-triphosphate-mediated calcium (IP3-Ca2+) signal cascade is an essential process in sweet, bitter, and umami taste signal transduction. Although the main components of this cascade have been identified, the candidate regulators of them in taste tissues are still unclear. In an effort to identify genes involved in taste signal transduction, we found that a gene encoding lymphoid-restricted membrane protein (Lrmp/Jaw1) was expressed in mouse taste tissues.
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