Stochasticity Triggers Activation of the S-phase Checkpoint Pathway in Budding Yeast

In a complex and ever-changing environment, various signal transduction pathways mediate outside signals and stress to a living cell and its intracellular responses. Eukaryotic cells utilize the DNA synthesis phase (S-phase) checkpoint to respond to DNA damage and replication stress, and the activat...

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Main Authors: Peijie Zhou, Xin Gao, Xiaoli Li, Linxi Li, Caoyuan Niu, Qi Ouyang, Huiqiang Lou, Tiejun Li, Fangting Li
Format: Article
Language:English
Published: American Physical Society 2021-01-01
Series:Physical Review X
Online Access:http://doi.org/10.1103/PhysRevX.11.011004
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spelling doaj-be6024750869433f98eae86303ca5f732021-02-12T00:12:27ZengAmerican Physical SocietyPhysical Review X2160-33082021-01-0111101100410.1103/PhysRevX.11.011004Stochasticity Triggers Activation of the S-phase Checkpoint Pathway in Budding YeastPeijie ZhouXin GaoXiaoli LiLinxi LiCaoyuan NiuQi OuyangHuiqiang LouTiejun LiFangting LiIn a complex and ever-changing environment, various signal transduction pathways mediate outside signals and stress to a living cell and its intracellular responses. Eukaryotic cells utilize the DNA synthesis phase (S-phase) checkpoint to respond to DNA damage and replication stress, and the activation of the S-phase checkpoint defers the routine progression in the S phase. Through the analysis of microfluidic single-cell measurements, we find that the behavior of yeast cells exhibits bimodal distribution in the activation of the S-phase checkpoint, and the nonactivated portion of cells obeys the exponential decay law over time, the rate of which is dictated by HU dosage. Mathematical modeling and further experimental evidence from different mutant strains support the idea that the activation of the yeast S-phase checkpoint is a stochastic barrier-crossing process in a double-well system, where the barrier height is determined by both DNA replication stress and autophosphorylation of the key effector kinase Rad53. Our approach, as a novel methodology, is generally applicable to quantitative analysis of the signal transduction pathways at the single-cell level.http://doi.org/10.1103/PhysRevX.11.011004
collection DOAJ
language English
format Article
sources DOAJ
author Peijie Zhou
Xin Gao
Xiaoli Li
Linxi Li
Caoyuan Niu
Qi Ouyang
Huiqiang Lou
Tiejun Li
Fangting Li
spellingShingle Peijie Zhou
Xin Gao
Xiaoli Li
Linxi Li
Caoyuan Niu
Qi Ouyang
Huiqiang Lou
Tiejun Li
Fangting Li
Stochasticity Triggers Activation of the S-phase Checkpoint Pathway in Budding Yeast
Physical Review X
author_facet Peijie Zhou
Xin Gao
Xiaoli Li
Linxi Li
Caoyuan Niu
Qi Ouyang
Huiqiang Lou
Tiejun Li
Fangting Li
author_sort Peijie Zhou
title Stochasticity Triggers Activation of the S-phase Checkpoint Pathway in Budding Yeast
title_short Stochasticity Triggers Activation of the S-phase Checkpoint Pathway in Budding Yeast
title_full Stochasticity Triggers Activation of the S-phase Checkpoint Pathway in Budding Yeast
title_fullStr Stochasticity Triggers Activation of the S-phase Checkpoint Pathway in Budding Yeast
title_full_unstemmed Stochasticity Triggers Activation of the S-phase Checkpoint Pathway in Budding Yeast
title_sort stochasticity triggers activation of the s-phase checkpoint pathway in budding yeast
publisher American Physical Society
series Physical Review X
issn 2160-3308
publishDate 2021-01-01
description In a complex and ever-changing environment, various signal transduction pathways mediate outside signals and stress to a living cell and its intracellular responses. Eukaryotic cells utilize the DNA synthesis phase (S-phase) checkpoint to respond to DNA damage and replication stress, and the activation of the S-phase checkpoint defers the routine progression in the S phase. Through the analysis of microfluidic single-cell measurements, we find that the behavior of yeast cells exhibits bimodal distribution in the activation of the S-phase checkpoint, and the nonactivated portion of cells obeys the exponential decay law over time, the rate of which is dictated by HU dosage. Mathematical modeling and further experimental evidence from different mutant strains support the idea that the activation of the yeast S-phase checkpoint is a stochastic barrier-crossing process in a double-well system, where the barrier height is determined by both DNA replication stress and autophosphorylation of the key effector kinase Rad53. Our approach, as a novel methodology, is generally applicable to quantitative analysis of the signal transduction pathways at the single-cell level.
url http://doi.org/10.1103/PhysRevX.11.011004
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