{"title":"Temperature Compensation through Kinetic Regulation in Biochemical Oscillators","authors":"Haochen Fu, Chenyi Fei, Qi Ouyang, Yuhai Tu","doi":"arxiv-2401.13960","DOIUrl":null,"url":null,"abstract":"Nearly all circadian clocks maintain a period that is insensitive to\ntemperature changes, a phenomenon known as temperature compensation (TC). Yet,\nit is unclear whether there is any common feature among different systems that\nexhibit TC. From a general timescale invariance, we show that TC relies on\nexistence of certain period-lengthening reactions wherein the period of the\nsystem increases strongly with the rates in these reactions. By studying\nseveral generic oscillator models, we show that this counter-intuitive\ndependence is nonetheless a common feature of oscillators in the nonlinear\n(far-from-onset) regime where the oscillation can be separated into fast and\nslow phases. The increase of the period with the period-lengthening reaction\nrates occurs when the amplitude of the slow phase in the oscillation increases\nwith these rates while the progression-speed in the slow phase is controlled by\nother rates of the system. The positive dependence of the period on the\nperiod-lengthening rates balances its inverse dependence on other kinetic rates\nin the system, which gives rise to robust TC in a wide range of parameters. We\ndemonstrate the existence of such period-lengthening reactions and their\nrelevance for TC in all four model systems we considered. Theoretical results\nfor a model of the Kai system are supported by experimental data. A study of\nthe energy dissipation also shows that better TC performance requires higher\nenergy consumption. Our study unveils a general mechanism by which a\nbiochemical oscillator achieves TC by operating at regimes far from the onset\nwhere period-lengthening reactions exist.","PeriodicalId":501325,"journal":{"name":"arXiv - QuanBio - Molecular Networks","volume":"156 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Molecular Networks","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2401.13960","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Nearly all circadian clocks maintain a period that is insensitive to
temperature changes, a phenomenon known as temperature compensation (TC). Yet,
it is unclear whether there is any common feature among different systems that
exhibit TC. From a general timescale invariance, we show that TC relies on
existence of certain period-lengthening reactions wherein the period of the
system increases strongly with the rates in these reactions. By studying
several generic oscillator models, we show that this counter-intuitive
dependence is nonetheless a common feature of oscillators in the nonlinear
(far-from-onset) regime where the oscillation can be separated into fast and
slow phases. The increase of the period with the period-lengthening reaction
rates occurs when the amplitude of the slow phase in the oscillation increases
with these rates while the progression-speed in the slow phase is controlled by
other rates of the system. The positive dependence of the period on the
period-lengthening rates balances its inverse dependence on other kinetic rates
in the system, which gives rise to robust TC in a wide range of parameters. We
demonstrate the existence of such period-lengthening reactions and their
relevance for TC in all four model systems we considered. Theoretical results
for a model of the Kai system are supported by experimental data. A study of
the energy dissipation also shows that better TC performance requires higher
energy consumption. Our study unveils a general mechanism by which a
biochemical oscillator achieves TC by operating at regimes far from the onset
where period-lengthening reactions exist.