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The transcriptional regulator EarA and intergenic terminator sequences modulate archaellation in Pyrococcus furiosus

The regulation of archaellation, the formation of archaeal-specific cell appendages called archaella, is crucial for the motility, adhesion, and survival of archaeal organisms. Although the heavily archaellated and highly motile Pyrococcus furiosus is a key model organism for understanding the produ...

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Autores principales: Stöckl, Richard, Nißl, Laura, Reichelt, Robert, Rachel, Reinhard, Grohmann, Dina, Grünberger, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665913/
https://www.ncbi.nlm.nih.gov/pubmed/38029142
http://dx.doi.org/10.3389/fmicb.2023.1241399
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author Stöckl, Richard
Nißl, Laura
Reichelt, Robert
Rachel, Reinhard
Grohmann, Dina
Grünberger, Felix
author_facet Stöckl, Richard
Nißl, Laura
Reichelt, Robert
Rachel, Reinhard
Grohmann, Dina
Grünberger, Felix
author_sort Stöckl, Richard
collection PubMed
description The regulation of archaellation, the formation of archaeal-specific cell appendages called archaella, is crucial for the motility, adhesion, and survival of archaeal organisms. Although the heavily archaellated and highly motile Pyrococcus furiosus is a key model organism for understanding the production and function of archaella in Euryarchaea, the transcriptional regulation of archaellum assembly is so far unknown. Here we show that the transcription factor EarA is the master regulator of the archaellum (arl) operon transcription, which is further modulated by intergenic transcription termination signals. EarA deletion or overexpression strains demonstrate that EarA is essential for archaellation in P. furiosus and governs the degree of archaellation. Providing a single-molecule update on the transcriptional landscape of the arl operon in P. furiosus, we identify sequence motifs for EarA binding upstream of the arl operon and intergenic terminator sequences as critical elements for fine-tuning the expression of the multicistronic arl cluster. Furthermore, transcriptome re-analysis across different Thermococcales species demonstrated a heterogeneous production of major archaellins, suggesting a more diverse composition of archaella than previously recognized. Overall, our study provides novel insights into the transcriptional regulation of archaellation and highlights the essential role of EarA in Pyrococcus furiosus. These findings advance our understanding of the mechanisms governing archaellation and have implications for the functional diversity of archaella.
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spelling pubmed-106659132023-11-09 The transcriptional regulator EarA and intergenic terminator sequences modulate archaellation in Pyrococcus furiosus Stöckl, Richard Nißl, Laura Reichelt, Robert Rachel, Reinhard Grohmann, Dina Grünberger, Felix Front Microbiol Microbiology The regulation of archaellation, the formation of archaeal-specific cell appendages called archaella, is crucial for the motility, adhesion, and survival of archaeal organisms. Although the heavily archaellated and highly motile Pyrococcus furiosus is a key model organism for understanding the production and function of archaella in Euryarchaea, the transcriptional regulation of archaellum assembly is so far unknown. Here we show that the transcription factor EarA is the master regulator of the archaellum (arl) operon transcription, which is further modulated by intergenic transcription termination signals. EarA deletion or overexpression strains demonstrate that EarA is essential for archaellation in P. furiosus and governs the degree of archaellation. Providing a single-molecule update on the transcriptional landscape of the arl operon in P. furiosus, we identify sequence motifs for EarA binding upstream of the arl operon and intergenic terminator sequences as critical elements for fine-tuning the expression of the multicistronic arl cluster. Furthermore, transcriptome re-analysis across different Thermococcales species demonstrated a heterogeneous production of major archaellins, suggesting a more diverse composition of archaella than previously recognized. Overall, our study provides novel insights into the transcriptional regulation of archaellation and highlights the essential role of EarA in Pyrococcus furiosus. These findings advance our understanding of the mechanisms governing archaellation and have implications for the functional diversity of archaella. Frontiers Media S.A. 2023-11-09 /pmc/articles/PMC10665913/ /pubmed/38029142 http://dx.doi.org/10.3389/fmicb.2023.1241399 Text en Copyright © 2023 Stöckl, Nißl, Reichelt, Rachel, Grohmann and Grünberger. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Stöckl, Richard
Nißl, Laura
Reichelt, Robert
Rachel, Reinhard
Grohmann, Dina
Grünberger, Felix
The transcriptional regulator EarA and intergenic terminator sequences modulate archaellation in Pyrococcus furiosus
title The transcriptional regulator EarA and intergenic terminator sequences modulate archaellation in Pyrococcus furiosus
title_full The transcriptional regulator EarA and intergenic terminator sequences modulate archaellation in Pyrococcus furiosus
title_fullStr The transcriptional regulator EarA and intergenic terminator sequences modulate archaellation in Pyrococcus furiosus
title_full_unstemmed The transcriptional regulator EarA and intergenic terminator sequences modulate archaellation in Pyrococcus furiosus
title_short The transcriptional regulator EarA and intergenic terminator sequences modulate archaellation in Pyrococcus furiosus
title_sort transcriptional regulator eara and intergenic terminator sequences modulate archaellation in pyrococcus furiosus
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665913/
https://www.ncbi.nlm.nih.gov/pubmed/38029142
http://dx.doi.org/10.3389/fmicb.2023.1241399
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