Crosstalk between guanosine nucleotides regulates cellular heterogeneity in protein synthesis during nutrient limitation
| Autor: | Molly Hydorn, Abigail Whalen, Simon Diez, Jonathan Dworkin |
|---|---|
| Rok vydání: | 2022 |
| Předmět: |
chemistry.chemical_classification
Cancer Research Low protein Guanosine biology Nucleotides Chemistry Gene Expression Regulation Bacterial Nutrients Bacillus subtilis biology.organism_classification Cell biology chemistry.chemical_compound Crosstalk (biology) Sasa Protein biosynthesis Genetics Phosphorylation Nucleotide Molecular Biology Genetics (clinical) Ecology Evolution Behavior and Systematics |
| Zdroj: | PLOS Genetics. 18:e1009957 |
| ISSN: | 1553-7404 |
| DOI: | 10.1371/journal.pgen.1009957 |
| Popis: | Phenotypic heterogeneity of microbial populations can facilitate survival in dynamic environments by generating sub-populations of cells that may have differential fitness in a future environment. Bacillus subtilis cultures experiencing nutrient limitation contain distinct sub-populations of cells exhibiting either comparatively high or low protein synthesis activity. This heterogeneity requires the production of phosphorylated guanosine nucleotides (pp)ppGpp by three synthases: SasA, SasB, and RelA. Here we show that these enzymes differentially affect this bimodality: RelA and SasB are necessary to generate the sub-population of cells exhibiting low protein synthesis whereas SasA is necessary to generate cells exhibiting comparatively higher protein synthesis. The RelA product (pppGpp) allosterically activates SasB and we find, in contrast, that the SasA product (pGpp) competitively inhibits this activation. Finally, we provide in vivo evidence that this antagonistic interaction mediates the observed heterogeneity in protein synthesis. This work therefore identifies the mechanism underlying phenotypic heterogeneity in the central physiological process of protein synthesis.Author SummaryUpon encountering conditions that are unfavorable to growth, such as nutrient limitation, bacteria enter into a quiescent phenotype that is mediated by group of guanosine nucleotides collectively known as (pp)pGpp. These nucleotides direct the down-regulation of energy intensive processes and are essential for a striking heterogeneity in protein synthesis observed during exit from rapid growth. Here, we show that a network of (pp)pGpp synthases is responsible for this heterogeneity and describe a mechanism that allows for the integration of multiple signals into the decision to down regulate the most energy intensive process in a cell. |
| Databáze: | OpenAIRE |
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