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A global search for novel transcription factors impacting the Neurospora crassa circadian clock

Eukaryotic circadian oscillators share a common circuit architecture, a negative feedback loop in which a positive element activates the transcription of a negative one that then represses the action of the former, inhibiting its own expression. While studies in mammals and insects have revealed add...

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Autores principales: Muñoz-Guzmán, Felipe, Caballero, Valeria, Larrondo, Luis F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495738/
https://www.ncbi.nlm.nih.gov/pubmed/33792687
http://dx.doi.org/10.1093/g3journal/jkab100
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author Muñoz-Guzmán, Felipe
Caballero, Valeria
Larrondo, Luis F
author_facet Muñoz-Guzmán, Felipe
Caballero, Valeria
Larrondo, Luis F
author_sort Muñoz-Guzmán, Felipe
collection PubMed
description Eukaryotic circadian oscillators share a common circuit architecture, a negative feedback loop in which a positive element activates the transcription of a negative one that then represses the action of the former, inhibiting its own expression. While studies in mammals and insects have revealed additional transcriptional inputs modulating the expression of core clock components, this has been less characterized in the model Neurospora crassa, where the participation of other transcriptional components impacting circadian clock dynamics remains rather unexplored. Thus, we sought to identify additional transcriptional regulators modulating the N. crassa clock, following a reverse genetic screen based on luminescent circadian reporters and a collection of transcription factors (TFs) knockouts, successfully covering close to 60% of them. Besides the canonical core clock components WC-1 and -2, none of the tested transcriptional regulators proved to be essential for rhythmicity. Nevertheless, we identified a set of 23 TFs that when absent lead to discrete, but significant, changes in circadian period. While the current level of analysis does not provide mechanistic information about how these new players modulate circadian parameters, the results of this screen reveal that an important number of light and clock-regulated TFs, involved in a plethora of processes, are capable of modulating the clockworks. This partial reverse genetic clock screen also exemplifies how the N. crassa knockout collection continues to serve as an expedite platform to address broad biological questions.
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spelling pubmed-84957382021-10-07 A global search for novel transcription factors impacting the Neurospora crassa circadian clock Muñoz-Guzmán, Felipe Caballero, Valeria Larrondo, Luis F G3 (Bethesda) Mutant Screen Report Eukaryotic circadian oscillators share a common circuit architecture, a negative feedback loop in which a positive element activates the transcription of a negative one that then represses the action of the former, inhibiting its own expression. While studies in mammals and insects have revealed additional transcriptional inputs modulating the expression of core clock components, this has been less characterized in the model Neurospora crassa, where the participation of other transcriptional components impacting circadian clock dynamics remains rather unexplored. Thus, we sought to identify additional transcriptional regulators modulating the N. crassa clock, following a reverse genetic screen based on luminescent circadian reporters and a collection of transcription factors (TFs) knockouts, successfully covering close to 60% of them. Besides the canonical core clock components WC-1 and -2, none of the tested transcriptional regulators proved to be essential for rhythmicity. Nevertheless, we identified a set of 23 TFs that when absent lead to discrete, but significant, changes in circadian period. While the current level of analysis does not provide mechanistic information about how these new players modulate circadian parameters, the results of this screen reveal that an important number of light and clock-regulated TFs, involved in a plethora of processes, are capable of modulating the clockworks. This partial reverse genetic clock screen also exemplifies how the N. crassa knockout collection continues to serve as an expedite platform to address broad biological questions. Oxford University Press 2021-04-19 /pmc/articles/PMC8495738/ /pubmed/33792687 http://dx.doi.org/10.1093/g3journal/jkab100 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Mutant Screen Report
Muñoz-Guzmán, Felipe
Caballero, Valeria
Larrondo, Luis F
A global search for novel transcription factors impacting the Neurospora crassa circadian clock
title A global search for novel transcription factors impacting the Neurospora crassa circadian clock
title_full A global search for novel transcription factors impacting the Neurospora crassa circadian clock
title_fullStr A global search for novel transcription factors impacting the Neurospora crassa circadian clock
title_full_unstemmed A global search for novel transcription factors impacting the Neurospora crassa circadian clock
title_short A global search for novel transcription factors impacting the Neurospora crassa circadian clock
title_sort global search for novel transcription factors impacting the neurospora crassa circadian clock
topic Mutant Screen Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495738/
https://www.ncbi.nlm.nih.gov/pubmed/33792687
http://dx.doi.org/10.1093/g3journal/jkab100
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