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Characterization of an ECF56-family sigma factor from Streptomyces venezuelae reveals a highly conserved regulome

View ORCID ProfileMitchell G. Thompson, Amin Zargar, Pablo Cruz-Morales, Tristan De Rond, Samantha Chang, Allison N. Pearson, Garima Goyal, Jesus F. Barajas, Jacquelyn M. Blake-Hedges, Ryan M. Phelan, Victor Reyes-Umana, Amanda C. Hernández, Nathan J. Hillson, Patrick M. Shih, Jay D. Keasling
doi: https://doi.org/10.1101/2020.01.30.927608
Mitchell G. Thompson
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
3Department of Plant and Microbial Biology, University of California-Berkeley, Berkeley, CA, USA
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  • ORCID record for Mitchell G. Thompson
Amin Zargar
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
4QB3 Institute, University of California-Berkeley, 5885 Hollis Street, 4th Floor, Emeryville, CA 94608, United States
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Pablo Cruz-Morales
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
4QB3 Institute, University of California-Berkeley, 5885 Hollis Street, 4th Floor, Emeryville, CA 94608, United States
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Tristan De Rond
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
5Department of Chemistry, University of California-Berkeley, Berkeley, CA, USA
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Samantha Chang
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
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Allison N. Pearson
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
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Garima Goyal
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
6Department of Energy Agile BioFoundry, Emeryville, CA, USA
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Jesus F. Barajas
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
6Department of Energy Agile BioFoundry, Emeryville, CA, USA
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Jacquelyn M. Blake-Hedges
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
5Department of Chemistry, University of California-Berkeley, Berkeley, CA, USA
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Ryan M. Phelan
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
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Victor Reyes-Umana
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
3Department of Plant and Microbial Biology, University of California-Berkeley, Berkeley, CA, USA
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Amanda C. Hernández
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
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Nathan J. Hillson
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
6Department of Energy Agile BioFoundry, Emeryville, CA, USA
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Patrick M. Shih
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
7Department of Plant Biology, University of California-Davis, Davis, CA, USA
8Genome Center, University of California-Davis, Davis, CA, USA
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Jay D. Keasling
1Joint BioEnergy Institute, Emeryville, CA, USA
2Biological Systems & Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
9Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA
10Department of Bioengineering, University of California-Berkeley, Berkeley, CA 94720, USA
11Department of Chemical and Biomolecular Engineering, University of California-Berkeley, Berkeley, CA, USA
12The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Denmark
13Center for Synthetic Biochemistry, Shenzhen Institutes for Advanced Technologies, Shenzhen, China
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  • For correspondence: jdkeasling@lbl.gov
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Abstract

Bacteria often possess alternative sigma factors that initiate the transcription of specific genes under environmental stresses, the largest and most diverse group being the extracytoplasmic function (ECF) sigma factors. The regulation of ECF activity is crucial for ensuring the distinct transcription of stress responsive genes only occurs under the appropriate conditions. While most ECFs are comprised of only the core σ2 and σ4 regions, a unique form of ECF sigma factor regulation also contains a C-terminal extension bearing homology to the NTF2 superfamily of protein domains. While previous work has shown that this NTF2 domain can affect transcriptional activity in vivo in ECF41 and ECF42, its role in the newly classified ECF56 subgroup is unknown. In this work, we show that truncation of the C-terminus of the ECF56 sigma factor SVEN_4562 of Streptomyces venezuelae upregulates its activity in a hybrid assay. Through transcriptomics in S. venezuelae, we found that this truncated ECF56 sigma factor has a highly conserved promoter sequence in vivo. Bioinformatic assays illustrated that deep branches of the Actinobacteria phylum contained putative ECF56 promoter motifs identical to those found in the S. venezuelae ECF56 regulon. We validated these findings through ex situ hybrid assays illustrating that truncated ECF56 sigma factors from phylogenetically diverse Actinobacteria activate transcription from these promoters. Importantly, our work shows that the genetic infrastructure of the ECF56 family of sigma factors is highly conserved and performs important functions yet to be understood in Actinobacteria.

Importance Most ECF sigma-factors rely on anti-sigma factor regulation; in contrast, the unique classes of ECF sigma-factors that contain a C-terminal extension are thought to respond directly to an environmental signal. Here we show that the cis-acting regulatory element of the ECF56 regulon is likely highly conserved in many Actinobacteria, with exact nucleotide level conservation over ~2 billion years of evolution. The high conservation of this genetic architecture, as well as a conserved gene content within the regulon, strongly point to a specialized and important role in Actinobacteria biology.

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Posted January 31, 2020.
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Characterization of an ECF56-family sigma factor from Streptomyces venezuelae reveals a highly conserved regulome
Mitchell G. Thompson, Amin Zargar, Pablo Cruz-Morales, Tristan De Rond, Samantha Chang, Allison N. Pearson, Garima Goyal, Jesus F. Barajas, Jacquelyn M. Blake-Hedges, Ryan M. Phelan, Victor Reyes-Umana, Amanda C. Hernández, Nathan J. Hillson, Patrick M. Shih, Jay D. Keasling
bioRxiv 2020.01.30.927608; doi: https://doi.org/10.1101/2020.01.30.927608
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Characterization of an ECF56-family sigma factor from Streptomyces venezuelae reveals a highly conserved regulome
Mitchell G. Thompson, Amin Zargar, Pablo Cruz-Morales, Tristan De Rond, Samantha Chang, Allison N. Pearson, Garima Goyal, Jesus F. Barajas, Jacquelyn M. Blake-Hedges, Ryan M. Phelan, Victor Reyes-Umana, Amanda C. Hernández, Nathan J. Hillson, Patrick M. Shih, Jay D. Keasling
bioRxiv 2020.01.30.927608; doi: https://doi.org/10.1101/2020.01.30.927608

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