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Gene Activity as the Predictive Indicator for Transcriptional Bursting Dynamics

Transcription commonly occurs in bursts, with alternating productive (ON) and quiescent (OFF) periods, governing mRNA production rates. Yet, how transcription is regulated through bursting dynamics remains unresolved. In this study, we conduct real-time measurements of endogenous transcriptional bur...

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Autores principales: Chen, Po-Ta, Zoller, Benjamin, Levo, Michal, Gregor, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cornell University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153294/
https://www.ncbi.nlm.nih.gov/pubmed/37131882
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author Chen, Po-Ta
Zoller, Benjamin
Levo, Michal
Gregor, Thomas
author_facet Chen, Po-Ta
Zoller, Benjamin
Levo, Michal
Gregor, Thomas
author_sort Chen, Po-Ta
collection PubMed
description Transcription commonly occurs in bursts, with alternating productive (ON) and quiescent (OFF) periods, governing mRNA production rates. Yet, how transcription is regulated through bursting dynamics remains unresolved. In this study, we conduct real-time measurements of endogenous transcriptional bursting with single-mRNA sensitivity. Leveraging the diverse transcriptional activities in early fly embryos, we uncover stringent relationships between bursting parameters. Specifically, we find that the durations of ON and OFF periods are linked. Regardless of the developmental stage or body-axis position, gene activity levels predict the average ON and OFF periods of individual alleles. Lowly transcribing alleles predominantly modulate OFF durations (burst frequency), while highly transcribing alleles primarily tune ON durations (burst size). Importantly, these relationships persist even under perturbation of cis-regulatory elements or trans-factors. This suggests a novel mechanistic constraint governing bursting dynamics rather than a modular control of distinct parameters by distinct regulatory processes. Our study provides a foundation for future investigations into the molecular mechanisms underpinning spatiotemporal transcriptional control.
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spelling pubmed-101532942023-05-03 Gene Activity as the Predictive Indicator for Transcriptional Bursting Dynamics Chen, Po-Ta Zoller, Benjamin Levo, Michal Gregor, Thomas ArXiv Article Transcription commonly occurs in bursts, with alternating productive (ON) and quiescent (OFF) periods, governing mRNA production rates. Yet, how transcription is regulated through bursting dynamics remains unresolved. In this study, we conduct real-time measurements of endogenous transcriptional bursting with single-mRNA sensitivity. Leveraging the diverse transcriptional activities in early fly embryos, we uncover stringent relationships between bursting parameters. Specifically, we find that the durations of ON and OFF periods are linked. Regardless of the developmental stage or body-axis position, gene activity levels predict the average ON and OFF periods of individual alleles. Lowly transcribing alleles predominantly modulate OFF durations (burst frequency), while highly transcribing alleles primarily tune ON durations (burst size). Importantly, these relationships persist even under perturbation of cis-regulatory elements or trans-factors. This suggests a novel mechanistic constraint governing bursting dynamics rather than a modular control of distinct parameters by distinct regulatory processes. Our study provides a foundation for future investigations into the molecular mechanisms underpinning spatiotemporal transcriptional control. Cornell University 2023-10-02 /pmc/articles/PMC10153294/ /pubmed/37131882 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Chen, Po-Ta
Zoller, Benjamin
Levo, Michal
Gregor, Thomas
Gene Activity as the Predictive Indicator for Transcriptional Bursting Dynamics
title Gene Activity as the Predictive Indicator for Transcriptional Bursting Dynamics
title_full Gene Activity as the Predictive Indicator for Transcriptional Bursting Dynamics
title_fullStr Gene Activity as the Predictive Indicator for Transcriptional Bursting Dynamics
title_full_unstemmed Gene Activity as the Predictive Indicator for Transcriptional Bursting Dynamics
title_short Gene Activity as the Predictive Indicator for Transcriptional Bursting Dynamics
title_sort gene activity as the predictive indicator for transcriptional bursting dynamics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153294/
https://www.ncbi.nlm.nih.gov/pubmed/37131882
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