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DNA 环相互作用的自由能成本。

The free-energy cost of interaction between DNA loops.

机构信息

Research Centre of Applied Mathematics, Guangzhou University, Guangzhou, 510006, P.R. China.

School of Statistics and Mathematics, Guangdong University of Finance & Economics, Guangzhou, 510275, P.R. China.

出版信息

Sci Rep. 2017 Oct 3;7(1):12610. doi: 10.1038/s41598-017-12765-x.

DOI:10.1038/s41598-017-12765-x
PMID:28974770
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5626758/
Abstract

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.

摘要

从热力学的角度来看,DNA 环的形成以及它们之间的相互作用都是非平衡过程,这会导致自由能的变化,从而影响基因表达,并进一步导致实验观察到的细胞间变异性。然而,这些过程如何耗散自由能在很大程度上仍不清楚。在这里,通过分析一个力学模型,该模型将两个相互作用的 DNA 环的三个基本拓扑结构映射到基因转录的 4 状态模型中,我们首先表明,较长的 DNA 环需要更多的平均自由能消耗。然后,无论相互作用的两个 DNA 环的类型(嵌套、并排或交替)如何,它们之间的促进作用总是消耗较少的平均自由能,而抑制作用则消耗较多的平均自由能。更有趣的是,我们发现,与启动子和增强子之间的直接环化机制相反,促进跟踪机制消耗较少的平均自由能,但增强了平均 mRNA 表达,这验证了促进跟踪假说,这是生物学中一个长期存在的争论。基于最小能量原理,我们因此推测,生物体将利用环环促进和促进跟踪的机制来在复杂的环境中生存。我们的研究从能量消耗的角度为理解基因表达调控机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/4aca37fbca09/41598_2017_12765_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/05c41b709dc9/41598_2017_12765_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/c3b5504da90d/41598_2017_12765_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/786b7c98027f/41598_2017_12765_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/4aca37fbca09/41598_2017_12765_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/05c41b709dc9/41598_2017_12765_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/c3b5504da90d/41598_2017_12765_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/786b7c98027f/41598_2017_12765_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28b0/5626758/4aca37fbca09/41598_2017_12765_Fig7_HTML.jpg

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