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Unified bursting strategies in ectopic and endogenous even-skipped expression patterns

Transcription often occurs in bursts as gene promoters switch stochastically between active and inactive states. Enhancers can dictate transcriptional activity in animal development through the modulation of burst frequency, duration, or amplitude. Previous studies observed that different enhancers...

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Autores principales: Berrocal, Augusto, Lammers, Nicholas C, Garcia, Hernan G, Eisen, Michael B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934701/
https://www.ncbi.nlm.nih.gov/pubmed/36798351
http://dx.doi.org/10.1101/2023.02.09.527927
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author Berrocal, Augusto
Lammers, Nicholas C
Garcia, Hernan G
Eisen, Michael B
author_facet Berrocal, Augusto
Lammers, Nicholas C
Garcia, Hernan G
Eisen, Michael B
author_sort Berrocal, Augusto
collection PubMed
description Transcription often occurs in bursts as gene promoters switch stochastically between active and inactive states. Enhancers can dictate transcriptional activity in animal development through the modulation of burst frequency, duration, or amplitude. Previous studies observed that different enhancers can achieve a wide range of transcriptional outputs through the same strategies of bursting control. For example, despite responding to different transcription factors, all even-skipped enhancers increase transcription by upregulating burst frequency and amplitude while burst duration remains largely constant. These shared bursting strategies suggest that a unified molecular mechanism constraints how enhancers modulate transcriptional output. Alternatively, different enhancers could have converged on the same bursting control strategy because of natural selection favoring one of these particular strategies. To distinguish between these two scenarios, we compared transcriptional bursting between endogenous and ectopic gene expression patterns. Because enhancers act under different regulatory inputs in ectopic patterns, dissimilar bursting control strategies between endogenous and ectopic patterns would suggest that enhancers adapted their bursting strategies to their trans-regulatory environment. Here, we generated ectopic even-skipped transcription patterns in fruit fly embryos and discovered that bursting strategies remain consistent in endogenous and ectopic even-skipped expression. These results provide evidence for a unified molecular mechanism shaping even-skipped bursting strategies and serve as a starting point to uncover the realm of strategies employed by other enhancers.
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spelling pubmed-99347012023-02-17 Unified bursting strategies in ectopic and endogenous even-skipped expression patterns Berrocal, Augusto Lammers, Nicholas C Garcia, Hernan G Eisen, Michael B bioRxiv Article Transcription often occurs in bursts as gene promoters switch stochastically between active and inactive states. Enhancers can dictate transcriptional activity in animal development through the modulation of burst frequency, duration, or amplitude. Previous studies observed that different enhancers can achieve a wide range of transcriptional outputs through the same strategies of bursting control. For example, despite responding to different transcription factors, all even-skipped enhancers increase transcription by upregulating burst frequency and amplitude while burst duration remains largely constant. These shared bursting strategies suggest that a unified molecular mechanism constraints how enhancers modulate transcriptional output. Alternatively, different enhancers could have converged on the same bursting control strategy because of natural selection favoring one of these particular strategies. To distinguish between these two scenarios, we compared transcriptional bursting between endogenous and ectopic gene expression patterns. Because enhancers act under different regulatory inputs in ectopic patterns, dissimilar bursting control strategies between endogenous and ectopic patterns would suggest that enhancers adapted their bursting strategies to their trans-regulatory environment. Here, we generated ectopic even-skipped transcription patterns in fruit fly embryos and discovered that bursting strategies remain consistent in endogenous and ectopic even-skipped expression. These results provide evidence for a unified molecular mechanism shaping even-skipped bursting strategies and serve as a starting point to uncover the realm of strategies employed by other enhancers. Cold Spring Harbor Laboratory 2023-02-10 /pmc/articles/PMC9934701/ /pubmed/36798351 http://dx.doi.org/10.1101/2023.02.09.527927 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Berrocal, Augusto
Lammers, Nicholas C
Garcia, Hernan G
Eisen, Michael B
Unified bursting strategies in ectopic and endogenous even-skipped expression patterns
title Unified bursting strategies in ectopic and endogenous even-skipped expression patterns
title_full Unified bursting strategies in ectopic and endogenous even-skipped expression patterns
title_fullStr Unified bursting strategies in ectopic and endogenous even-skipped expression patterns
title_full_unstemmed Unified bursting strategies in ectopic and endogenous even-skipped expression patterns
title_short Unified bursting strategies in ectopic and endogenous even-skipped expression patterns
title_sort unified bursting strategies in ectopic and endogenous even-skipped expression patterns
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934701/
https://www.ncbi.nlm.nih.gov/pubmed/36798351
http://dx.doi.org/10.1101/2023.02.09.527927
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