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The free-energy cost of interaction between DNA loops

From the viewpoint of thermodynamics, the formation of DNA loops and the interaction between them, which are all non-equilibrium processes, result in the change of free energy, affecting gene expression and further cell-to-cell variability as observed experimentally. However, how these processes dis...

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Autores principales: Huang, Lifang, Liu, Peijiang, Yuan, Zhanjiang, Zhou, Tianshou, Yu, Jianshe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626758/
https://www.ncbi.nlm.nih.gov/pubmed/28974770
http://dx.doi.org/10.1038/s41598-017-12765-x
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author Huang, Lifang
Liu, Peijiang
Yuan, Zhanjiang
Zhou, Tianshou
Yu, Jianshe
author_facet Huang, Lifang
Liu, Peijiang
Yuan, Zhanjiang
Zhou, Tianshou
Yu, Jianshe
author_sort Huang, Lifang
collection PubMed
description From the viewpoint of thermodynamics, the formation of DNA loops and the interaction between them, which are all non-equilibrium processes, result in the change of free energy, affecting gene expression and further cell-to-cell variability as observed experimentally. However, how these processes dissipate free energy remains largely unclear. Here, by analyzing a mechanic model that maps three fundamental topologies of two interacting DNA loops into a 4-state model of gene transcription, we first show that a longer DNA loop needs more mean free energy consumption. Then, independent of the type of interacting two DNA loops (nested, side-by-side or alternating), the promotion between them always consumes less mean free energy whereas the suppression dissipates more mean free energy. More interestingly, we find that in contrast to the mechanism of direct looping between promoter and enhancer, the facilitated-tracking mechanism dissipates less mean free energy but enhances the mean mRNA expression, justifying the facilitated-tracking hypothesis, a long-standing debate in biology. Based on minimal energy principle, we thus speculate that organisms would utilize the mechanisms of loop-loop promotion and facilitated tracking to survive in complex environments. Our studies provide insights into the understanding of gene expression regulation mechanism from the view of energy consumption.
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spelling pubmed-56267582017-10-12 The free-energy cost of interaction between DNA loops Huang, Lifang Liu, Peijiang Yuan, Zhanjiang Zhou, Tianshou Yu, Jianshe Sci Rep Article From the viewpoint of thermodynamics, the formation of DNA loops and the interaction between them, which are all non-equilibrium processes, result in the change of free energy, affecting gene expression and further cell-to-cell variability as observed experimentally. However, how these processes dissipate free energy remains largely unclear. Here, by analyzing a mechanic model that maps three fundamental topologies of two interacting DNA loops into a 4-state model of gene transcription, we first show that a longer DNA loop needs more mean free energy consumption. Then, independent of the type of interacting two DNA loops (nested, side-by-side or alternating), the promotion between them always consumes less mean free energy whereas the suppression dissipates more mean free energy. More interestingly, we find that in contrast to the mechanism of direct looping between promoter and enhancer, the facilitated-tracking mechanism dissipates less mean free energy but enhances the mean mRNA expression, justifying the facilitated-tracking hypothesis, a long-standing debate in biology. Based on minimal energy principle, we thus speculate that organisms would utilize the mechanisms of loop-loop promotion and facilitated tracking to survive in complex environments. Our studies provide insights into the understanding of gene expression regulation mechanism from the view of energy consumption. Nature Publishing Group UK 2017-10-03 /pmc/articles/PMC5626758/ /pubmed/28974770 http://dx.doi.org/10.1038/s41598-017-12765-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Huang, Lifang
Liu, Peijiang
Yuan, Zhanjiang
Zhou, Tianshou
Yu, Jianshe
The free-energy cost of interaction between DNA loops
title The free-energy cost of interaction between DNA loops
title_full The free-energy cost of interaction between DNA loops
title_fullStr The free-energy cost of interaction between DNA loops
title_full_unstemmed The free-energy cost of interaction between DNA loops
title_short The free-energy cost of interaction between DNA loops
title_sort free-energy cost of interaction between dna loops
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626758/
https://www.ncbi.nlm.nih.gov/pubmed/28974770
http://dx.doi.org/10.1038/s41598-017-12765-x
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