RT Journal Article SR Electronic T1 Characterization of an ECF56-family sigma factor from Streptomyces venezuelae reveals a highly conserved regulome JF bioRxiv FD Cold Spring Harbor Laboratory SP 2020.01.30.927608 DO 10.1101/2020.01.30.927608 A1 Mitchell G. Thompson A1 Amin Zargar A1 Pablo Cruz-Morales A1 Tristan De Rond A1 Samantha Chang A1 Allison N. Pearson A1 Garima Goyal A1 Jesus F. Barajas A1 Jacquelyn M. Blake-Hedges A1 Ryan M. Phelan A1 Victor Reyes-Umana A1 Amanda C. Hernández A1 Nathan J. Hillson A1 Patrick M. Shih A1 Jay D. Keasling YR 2020 UL http://biorxiv.org/content/early/2020/01/31/2020.01.30.927608.abstract AB 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.