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Most Extracytoplasmic Function Sigma Factors Control Accessory Functions

Overview
Journal mSphere
Date 2018 Oct 12
PMID 30305320
Citations 11
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Abstract

Bacteria must sense alterations in their environment and respond with changes in function and/or structure in order to cope. Extracytoplasmic function sigma factors (ECF σs) modulate transcription in response to cellular and environmental signals. The symbiotic nitrogen-fixing alphaproteobacterium carries genes for 11 ECF-like σs (RpoE1 to -E10 and FecI). We hypothesized that some of these play a role in mediating the interaction between the bacterium and its plant symbiotic partner. The bacterium senses changes in its immediate environment as it establishes contact with the plant root, initiates invasion of the plant as the root nodule is formed, traverses several root cell layers, and enters plant cortical cells via endocytosis. We used genetics, transcriptomics, and functionality to characterize the entire cohort of ECF σs. We discovered new targets for individual σs, confirmed others by overexpressing individual ECF σs, and identified or confirmed putative promoter motifs for nine of them. We constructed precise deletions of each ECF σ gene and its demonstrated or putative anti-σ gene and also a strain in which all 11 ECF σ and anti-σ genes were deleted. This all-ECF σ deletion strain showed no major defects in free-living growth, in Biolog Phenotype MicroArray assays, or in response to multiple stresses. None of the ECF σs were required for symbiosis on the host plants and : the strain deleted for all ECF σ and anti-σ genes was symbiotically normal. Fixed (reduced) soil nitrogen plays a critical role in soil fertility and successful food growth. Much soil fertility relies on symbiotic nitrogen fixation: the bacterial partner infects the host plant roots and reduces atmospheric dinitrogen in exchange for host metabolic fuel, a process that involves complex interactions between the partners mediated by changes in gene expression in each partner. Here we test the roles of a family of 11 extracytoplasmic function (ECF) gene regulatory proteins (sigma factors [σs]) that interact with RNA polymerase to determine if they play a significant role in establishing a nitrogen-fixing symbiosis or in responding to various stresses, including cell envelope stress. We discovered that symbiotic nitrogen fixation occurs even when all 11 of these regulatory genes are deleted, that most ECF sigma factors control accessory functions, and that none of the ECF sigma factors are required to survive envelope stress.

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References
1.
Gruber T, Gross C . Multiple sigma subunits and the partitioning of bacterial transcription space. Annu Rev Microbiol. 2003; 57:441-66. DOI: 10.1146/annurev.micro.57.030502.090913. View

2.
Tu N, Lima A, Bandeali Z, Anderson B . Characterization of the general stress response in Bartonella henselae. Microb Pathog. 2016; 92:1-10. PMC: 4769946. DOI: 10.1016/j.micpath.2015.12.010. View

3.
Low L, Ryan Kilmartin J, Paul V B, Ulrike K . How are "Atypical" Sulfite Dehydrogenases Linked to Cell Metabolism? Interactions between the SorT Sulfite Dehydrogenase and Small Redox Proteins. Front Microbiol. 2011; 2:58. PMC: 3153034. DOI: 10.3389/fmicb.2011.00058. View

4.
Pinto D, Vecchione S, Wu H, Mauri M, Mascher T, Fritz G . Engineering orthogonal synthetic timer circuits based on extracytoplasmic function σ factors. Nucleic Acids Res. 2018; 46(14):7450-7464. PMC: 6101570. DOI: 10.1093/nar/gky614. View

5.
Jones K, Kobayashi H, Davies B, Taga M, Walker G . How rhizobial symbionts invade plants: the Sinorhizobium-Medicago model. Nat Rev Microbiol. 2007; 5(8):619-33. PMC: 2766523. DOI: 10.1038/nrmicro1705. View