Translation profiling of stress-induced small proteins reveals a novel link among signaling systems

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Abstract

Signaling networks allow adaptation to stressful environments by activating genes that counteract stressors. Small proteins (≤ 50 amino acids long) are a rising class of stress response regulators. Escherichia coli encodes over 150 small proteins, most of which lack phenotypes and their biological roles remain elusive. Using magnesium limitation as a stressor, we identify stress-induced small proteins using ribosome profiling, RNA sequencing, and transcriptional reporter assays. We uncover 17 small proteins with increased translation initiation, several of them transcriptionally upregulated by the PhoQ-PhoP two-component signaling system, crucial for magnesium homeostasis. Next, we describe small protein-specific deletion and overexpression phenotypes, underscoring their physiological significance in low magnesium stress. Most remarkably, we elucidate an unusual connection via a small membrane protein YoaI, between major signaling networks – PhoR-PhoB and EnvZ-OmpR in E. coli , advancing our understanding of small protein regulators in cellular signaling.

Synopsis

  • Ribo-RET identifies 17 small proteins induced under low magnesium (Mg 2+ ) stress in E. coli

  • Many of these proteins are transcriptionally activated by PhoQP signaling system

  • Half of the stress-induced small proteins localize to the membrane

  • Deletion or overexpression of specific small proteins affects growth under stress

  • Small protein YoaI connects PhoR-PhoB and EnvZ-OmpR signaling networks

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