{"title":"转录猝发效应对基因调控网络动态的高效近似值","authors":"Jochen Kursawe, Antoine Moneyron, Tobias Galla","doi":"arxiv-2406.19109","DOIUrl":null,"url":null,"abstract":"Mathematical models of gene regulatory networks are widely used to study cell\nfate changes and transcriptional regulation. When designing such models, it is\nimportant to accurately account for sources of stochasticity. However, doing so\ncan be computationally expensive and analytically untractable, posing limits on\nthe extent of our explorations and on parameter inference. Here, we explore\nthis challenge using the example of a simple auto-negative feedback motif, in\nwhich we incorporate stochastic variation due to transcriptional bursting and\nnoise from finite copy numbers. We find that transcriptional bursting may\nchange the qualitative dynamics of the system by inducing oscillations when\nthey would not otherwise be present, or by magnifying existing oscillations. We\ndescribe multiple levels of approximation for the model in the form of\ndifferential equations, piecewise deterministic processes, and stochastic\ndifferential equations. Importantly, we derive how the classical chemical\nLangevin equation can be extended to include a noise term representing\ntranscriptional bursting. This approximation drastically decreases computation\ntimes and allows us to analytically calculate properties of the dynamics, such\nas their power spectrum. We explore when these approximations break down and\nprovide recommendations for their use. Our analysis illustrates the importance\nof accounting for transcriptional bursting when simulating gene regulatory\nnetwork dynamics and provides recommendations to do so with computationally\nefficient methods.","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficient approximations of transcriptional bursting effects on the dynamics of a gene regulatory network\",\"authors\":\"Jochen Kursawe, Antoine Moneyron, Tobias Galla\",\"doi\":\"arxiv-2406.19109\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Mathematical models of gene regulatory networks are widely used to study cell\\nfate changes and transcriptional regulation. When designing such models, it is\\nimportant to accurately account for sources of stochasticity. However, doing so\\ncan be computationally expensive and analytically untractable, posing limits on\\nthe extent of our explorations and on parameter inference. Here, we explore\\nthis challenge using the example of a simple auto-negative feedback motif, in\\nwhich we incorporate stochastic variation due to transcriptional bursting and\\nnoise from finite copy numbers. We find that transcriptional bursting may\\nchange the qualitative dynamics of the system by inducing oscillations when\\nthey would not otherwise be present, or by magnifying existing oscillations. We\\ndescribe multiple levels of approximation for the model in the form of\\ndifferential equations, piecewise deterministic processes, and stochastic\\ndifferential equations. Importantly, we derive how the classical chemical\\nLangevin equation can be extended to include a noise term representing\\ntranscriptional bursting. This approximation drastically decreases computation\\ntimes and allows us to analytically calculate properties of the dynamics, such\\nas their power spectrum. We explore when these approximations break down and\\nprovide recommendations for their use. Our analysis illustrates the importance\\nof accounting for transcriptional bursting when simulating gene regulatory\\nnetwork dynamics and provides recommendations to do so with computationally\\nefficient methods.\",\"PeriodicalId\":501170,\"journal\":{\"name\":\"arXiv - QuanBio - Subcellular Processes\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - QuanBio - Subcellular Processes\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2406.19109\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Subcellular Processes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2406.19109","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Efficient approximations of transcriptional bursting effects on the dynamics of a gene regulatory network
Mathematical models of gene regulatory networks are widely used to study cell
fate changes and transcriptional regulation. When designing such models, it is
important to accurately account for sources of stochasticity. However, doing so
can be computationally expensive and analytically untractable, posing limits on
the extent of our explorations and on parameter inference. Here, we explore
this challenge using the example of a simple auto-negative feedback motif, in
which we incorporate stochastic variation due to transcriptional bursting and
noise from finite copy numbers. We find that transcriptional bursting may
change the qualitative dynamics of the system by inducing oscillations when
they would not otherwise be present, or by magnifying existing oscillations. We
describe multiple levels of approximation for the model in the form of
differential equations, piecewise deterministic processes, and stochastic
differential equations. Importantly, we derive how the classical chemical
Langevin equation can be extended to include a noise term representing
transcriptional bursting. This approximation drastically decreases computation
times and allows us to analytically calculate properties of the dynamics, such
as their power spectrum. We explore when these approximations break down and
provide recommendations for their use. Our analysis illustrates the importance
of accounting for transcriptional bursting when simulating gene regulatory
network dynamics and provides recommendations to do so with computationally
efficient methods.