A model explaining mRNA level fluctuations based on activity demands and RNA age.

Cellular RNA levels typically fluctuate and are influenced by different transcription rates and RNA degradation rates. However, the understanding of the fundamental relationships between RNA abundance, environmental stimuli, RNA activities, and RNA age distributions is incomplete. Furthermore, the r...

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Main Authors: Zhongneng Xu, Shuichi Asakawa
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-07-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1009188
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spelling doaj-c9cb1a2817914924884c78e9c2a4fba32021-08-08T04:32:23ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582021-07-01177e100918810.1371/journal.pcbi.1009188A model explaining mRNA level fluctuations based on activity demands and RNA age.Zhongneng XuShuichi AsakawaCellular RNA levels typically fluctuate and are influenced by different transcription rates and RNA degradation rates. However, the understanding of the fundamental relationships between RNA abundance, environmental stimuli, RNA activities, and RNA age distributions is incomplete. Furthermore, the rates of RNA degradation and transcription are difficult to measure in transcriptomic experiments in living organisms, especially in studies involving humans. A model based on activity demands and RNA age was developed to explore the mechanisms of RNA level fluctuations. Using single-cell time-series gene expression experimental data, we assessed the transcription rates, RNA degradation rates, RNA life spans, RNA demand, accumulated transcription levels, and accumulated RNA degradation levels. This model could also predict RNA levels under simulation backgrounds, such as stimuli that induce regular oscillations in RNA abundance, stable RNA levels over time that result from long-term shortage of total RNA activity or from uncontrollable transcription, and relationships between RNA/protein levels and metabolic rates. This information contributes to existing knowledge.https://doi.org/10.1371/journal.pcbi.1009188
collection DOAJ
language English
format Article
sources DOAJ
author Zhongneng Xu
Shuichi Asakawa
spellingShingle Zhongneng Xu
Shuichi Asakawa
A model explaining mRNA level fluctuations based on activity demands and RNA age.
PLoS Computational Biology
author_facet Zhongneng Xu
Shuichi Asakawa
author_sort Zhongneng Xu
title A model explaining mRNA level fluctuations based on activity demands and RNA age.
title_short A model explaining mRNA level fluctuations based on activity demands and RNA age.
title_full A model explaining mRNA level fluctuations based on activity demands and RNA age.
title_fullStr A model explaining mRNA level fluctuations based on activity demands and RNA age.
title_full_unstemmed A model explaining mRNA level fluctuations based on activity demands and RNA age.
title_sort model explaining mrna level fluctuations based on activity demands and rna age.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2021-07-01
description Cellular RNA levels typically fluctuate and are influenced by different transcription rates and RNA degradation rates. However, the understanding of the fundamental relationships between RNA abundance, environmental stimuli, RNA activities, and RNA age distributions is incomplete. Furthermore, the rates of RNA degradation and transcription are difficult to measure in transcriptomic experiments in living organisms, especially in studies involving humans. A model based on activity demands and RNA age was developed to explore the mechanisms of RNA level fluctuations. Using single-cell time-series gene expression experimental data, we assessed the transcription rates, RNA degradation rates, RNA life spans, RNA demand, accumulated transcription levels, and accumulated RNA degradation levels. This model could also predict RNA levels under simulation backgrounds, such as stimuli that induce regular oscillations in RNA abundance, stable RNA levels over time that result from long-term shortage of total RNA activity or from uncontrollable transcription, and relationships between RNA/protein levels and metabolic rates. This information contributes to existing knowledge.
url https://doi.org/10.1371/journal.pcbi.1009188
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