{"title":"揭示RNA聚合酶的空间相互作用对基因表达噪声的影响:新生和成熟RNA数量的分析分布","authors":"Juraj Szavits-Nossan, Ramon Grima","doi":"arxiv-2304.05304","DOIUrl":null,"url":null,"abstract":"The telegraph model is the standard model of stochastic gene expression,\nwhich can be solved exactly to obtain the distribution of mature RNA numbers\nper cell. A modification of this model also leads to an analytical distribution\nof the nascent RNA numbers. These solutions are routinely used for the analysis\nof single-cell data, including the inference of transcriptional parameters.\nHowever, these models neglect important mechanistic features of transcription\nelongation, such as the stochastic movement of RNA polymerases and their steric\ninteractions. Here we construct a model of gene expression describing promoter\nswitching between inactive and active states, binding of RNA polymerases in the\nactive state, their stochastic movement including steric interactions along the\ngene, and their unbinding leading to a mature transcript that subsequently\ndecays. We derive the steady-state distributions of the nascent and mature RNA\nnumbers in two important limiting cases: constitutive expression and slow\npromoter switching. We show that RNA fluctuations are suppressed by steric\ninteractions between RNA polymerases, and that this suppression can even lead\nto sub-Poissonian fluctuations; these effects are most pronounced for nascent\nRNA and less prominent for mature RNA, since the latter is not a direct sensor\nof transcription. We find a relationship between the parameters of our\nmicroscopic mechanistic model and those of the standard models that ensures\nexcellent consistency in their prediction of the first and second RNA number\nmoments over vast regions of parameter space, encompassing slow, intermediate,\nand rapid promoter switching, provided the RNA number distributions are\nPoissonian or super-Poissonian. Furthermore, we identify the limitations of\ninference from mature RNA data, specifically showing that it cannot\ndifferentiate between highly distinct RNA polymerase traffic patterns on a\ngene.","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"85 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Uncovering the effect of RNA polymerase steric interactions on gene expression noise: analytical distributions of nascent and mature RNA numbers\",\"authors\":\"Juraj Szavits-Nossan, Ramon Grima\",\"doi\":\"arxiv-2304.05304\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The telegraph model is the standard model of stochastic gene expression,\\nwhich can be solved exactly to obtain the distribution of mature RNA numbers\\nper cell. A modification of this model also leads to an analytical distribution\\nof the nascent RNA numbers. These solutions are routinely used for the analysis\\nof single-cell data, including the inference of transcriptional parameters.\\nHowever, these models neglect important mechanistic features of transcription\\nelongation, such as the stochastic movement of RNA polymerases and their steric\\ninteractions. Here we construct a model of gene expression describing promoter\\nswitching between inactive and active states, binding of RNA polymerases in the\\nactive state, their stochastic movement including steric interactions along the\\ngene, and their unbinding leading to a mature transcript that subsequently\\ndecays. We derive the steady-state distributions of the nascent and mature RNA\\nnumbers in two important limiting cases: constitutive expression and slow\\npromoter switching. We show that RNA fluctuations are suppressed by steric\\ninteractions between RNA polymerases, and that this suppression can even lead\\nto sub-Poissonian fluctuations; these effects are most pronounced for nascent\\nRNA and less prominent for mature RNA, since the latter is not a direct sensor\\nof transcription. We find a relationship between the parameters of our\\nmicroscopic mechanistic model and those of the standard models that ensures\\nexcellent consistency in their prediction of the first and second RNA number\\nmoments over vast regions of parameter space, encompassing slow, intermediate,\\nand rapid promoter switching, provided the RNA number distributions are\\nPoissonian or super-Poissonian. Furthermore, we identify the limitations of\\ninference from mature RNA data, specifically showing that it cannot\\ndifferentiate between highly distinct RNA polymerase traffic patterns on a\\ngene.\",\"PeriodicalId\":501170,\"journal\":{\"name\":\"arXiv - QuanBio - Subcellular Processes\",\"volume\":\"85 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-04-11\",\"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-2304.05304\",\"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-2304.05304","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Uncovering the effect of RNA polymerase steric interactions on gene expression noise: analytical distributions of nascent and mature RNA numbers
The telegraph model is the standard model of stochastic gene expression,
which can be solved exactly to obtain the distribution of mature RNA numbers
per cell. A modification of this model also leads to an analytical distribution
of the nascent RNA numbers. These solutions are routinely used for the analysis
of single-cell data, including the inference of transcriptional parameters.
However, these models neglect important mechanistic features of transcription
elongation, such as the stochastic movement of RNA polymerases and their steric
interactions. Here we construct a model of gene expression describing promoter
switching between inactive and active states, binding of RNA polymerases in the
active state, their stochastic movement including steric interactions along the
gene, and their unbinding leading to a mature transcript that subsequently
decays. We derive the steady-state distributions of the nascent and mature RNA
numbers in two important limiting cases: constitutive expression and slow
promoter switching. We show that RNA fluctuations are suppressed by steric
interactions between RNA polymerases, and that this suppression can even lead
to sub-Poissonian fluctuations; these effects are most pronounced for nascent
RNA and less prominent for mature RNA, since the latter is not a direct sensor
of transcription. We find a relationship between the parameters of our
microscopic mechanistic model and those of the standard models that ensures
excellent consistency in their prediction of the first and second RNA number
moments over vast regions of parameter space, encompassing slow, intermediate,
and rapid promoter switching, provided the RNA number distributions are
Poissonian or super-Poissonian. Furthermore, we identify the limitations of
inference from mature RNA data, specifically showing that it cannot
differentiate between highly distinct RNA polymerase traffic patterns on a
gene.