<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Laman Trip DS</submitter><funding>European Research Council</funding><funding>Dutch Research Council (NWO)</funding><pagination>7518</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9726825</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>Determining whether life can progress arbitrarily slowly may reveal fundamental barriers to staying out of thermal equilibrium for living systems. By monitoring budding yeast's slowed-down life at frigid temperatures and with modeling, we establish that Reactive Oxygen Species (ROS) and a global gene-expression speed quantitatively determine yeast's pace of life and impose temperature-dependent speed limits - shortest and longest possible cell-doubling times. Increasing cells' ROS concentration increases their doubling time by elongating the cell-growth (G1-phase) duration that precedes the cell-replication (S-G2-M) phase. Gene-expression speed constrains cells' ROS-reducing rate and sets the shortest possible doubling-time. To replicate, cells require below-threshold concentrations of ROS. Thus, cells with sufficiently abundant ROS remain in G1, become unsustainably large and, consequently, burst. Therefore, at a given temperature, yeast's replicative life cannot progress arbitrarily slowly and cells with the lowest ROS-levels replicate most rapidly. Fundamental barriers may constrain the thermal slowing of other organisms' lives.</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Slowest possible replicative life at frigid temperatures for yeast.</pubmed_title><pmcid>PMC9726825</pmcid><funding_grant_id>680-47-544</funding_grant_id><funding_grant_id>677972</funding_grant_id><pubmed_authors>Youk H</pubmed_authors><pubmed_authors>Laman Trip DS</pubmed_authors><pubmed_authors>Maire T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Slowest possible replicative life at frigid temperatures for yeast.</name><description>Determining whether life can progress arbitrarily slowly may reveal fundamental barriers to staying out of thermal equilibrium for living systems. By monitoring budding yeast's slowed-down life at frigid temperatures and with modeling, we establish that Reactive Oxygen Species (ROS) and a global gene-expression speed quantitatively determine yeast's pace of life and impose temperature-dependent speed limits - shortest and longest possible cell-doubling times. Increasing cells' ROS concentration increases their doubling time by elongating the cell-growth (G1-phase) duration that precedes the cell-replication (S-G2-M) phase. Gene-expression speed constrains cells' ROS-reducing rate and sets the shortest possible doubling-time. To replicate, cells require below-threshold concentrations of ROS. Thus, cells with sufficiently abundant ROS remain in G1, become unsustainably large and, consequently, burst. Therefore, at a given temperature, yeast's replicative life cannot progress arbitrarily slowly and cells with the lowest ROS-levels replicate most rapidly. Fundamental barriers may constrain the thermal slowing of other organisms' lives.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-22T08:44:23.871Z</modification><creation>2024-10-17T21:45:57.55Z</creation></dates><accession>S-EPMC9726825</accession><cross_references><pubmed>36473846</pubmed><doi>10.1038/s41467-022-35151-2</doi></cross_references></HashMap>