<HashMap><database>BioModels</database><scores/><additional><submitter>Quentin Thommen</submitter><curationStatus>Non-curated</curationStatus><modellingApproach>differential equation model</modellingApproach><levelVersion>L3V2</levelVersion><full_dataset_link>https://www.ebi.ac.uk/biomodels/MODEL2608180002</full_dataset_link><isPrivate>false</isPrivate><repository>BioModels</repository><modelFormat>SBML</modelFormat><omics_type>Models</omics_type><tokenised_name>Ostreococcus tauri forced clock   code faithful unnormalised parameterization</tokenised_name><publication_year>2015</publication_year><submissionId>MODEL2608180002</submissionId><publication_authors>Thommen Q, Benjamin Pfeuty, Philippe Schatt, Amandine Bijoux, François-Yves Bouget, Marc Lefranc</publication_authors><first_author>Thommen Q</first_author><publication>10.3389/fgene.2015.00065,
                            Most organisms anticipate daily environmental variations and orchestrate cellular functions thanks to a circadian clock which entrains robustly to the day/night cycle, despite fluctuations in light intensity due to weather or seasonal variations. Marine organisms are also subjected to fluctuations in light spectral composition as their depth varies, due to differential absorption of different wavelengths by sea water. Studying how light input pathways contribute to circadian clock robustness is therefore important. Ostreococcus tauri, a unicellular picoplanktonic marine green alga with low genomic complexity and simple cellular organization, has become a promising model organism for systems biology. Functional and modeling approaches have shown that a core circadian oscillator based on orthologs of Arabidopsis TOC1 and CCA1 clock genes accounts for most experimental data acquired under a wide range of conditions. Some evidence points at putative light input pathway(s) consisting of a two-component signaling system (TCS) controlled by the only two histidine kinases (HK) of O. tauri. LOV-HK is a blue light photoreceptor under circadian control, that is required for circadian clock function. An involvement of Rhodopsin-HK (Rhod-HK) is also conceivable since rhodopsin photoreceptors mediate blue to green light input in animal circadian clocks. Here, we probe the role of LOV-HK and Rhod-HK in mediating light input to the TOC1-CCA1 oscillator using a mathematical model incorporating the TCS hypothesis. This model agrees with clock gene expression time series representative of multiple environmental conditions in blue or green light, characterizing entrainment by light/dark cycles, free-running in constant light, and resetting. Experimental and theoretical results indicate that both blue and green light can reset O. tauri circadian clock. Moreover, our mathematical analysis suggests that Rhod-HK is a blue-green light receptor and drives the clock together with LOV-HK.. null, 6.
                            Laboratoire de Physique, Lasers, Atomes, Molécules, Université Lille 1 Sciences et Technologies, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8523 Villeneuve d'Ascq, France.</publication><submitter_mail>quentin.thommen@univ-lille.fr</submitter_mail><publication_doi>10.3389/fgene.2015.00065</publication_doi><submitter_affiliation>Univ. Lille</submitter_affiliation></additional><is_claimable>false</is_claimable><name>Ostreococcus tauri forced clock - code-faithful unnormalised parameterization</name><description>This model describes light entrainment of the Ostreococcus tauri circadian clock through a minimal network combining the TOC1–CCA1 core oscillator with the putative photoreceptors LOV-HK and Rhod-HK. The model contains ten ordinary differential equations describing mRNA and protein dynamics for CCA1, TOC1, LOV-HK, Rhod-HK and an intermediate regulator X. Light input controls the phosphorylation state of TOC1 through LOV-HK and Rhod-HK, thereby modulating TOC1 stability and its transcriptional activity on CCA1. The parameter values correspond to the corrected values published in  Thommen et al. (2015).</description><dates><last_modification>2026-08-18</last_modification><publication>2026-09-02</publication><submission>2026-08-18</submission></dates><accession>MODEL2608180002</accession><cross_references><doi>10.3389/fgene.2015.00065</doi></cross_references></HashMap>