A small RNA that cooperatively senses two stacked metabolites in one pocket for gene control.
Griffin M SchroederChapin E CavenderMaya E BlauJermaine L JenkinsDavid H MathewsJoseph E WedekindPublished in: Nature communications (2022)
Riboswitches are structured non-coding RNAs often located upstream of essential genes in bacterial messenger RNAs. Such RNAs regulate expression of downstream genes by recognizing a specific cellular effector. Although nearly 50 riboswitch classes are known, only a handful recognize multiple effectors. Here, we report the 2.60-Å resolution co-crystal structure of a class I type I preQ 1 -sensing riboswitch that reveals two effectors stacked atop one another in a single binding pocket. These effectors bind with positive cooperativity in vitro and both molecules are necessary for gene regulation in bacterial cells. Stacked effector recognition appears to be a hallmark of the largest subgroup of preQ 1 riboswitches, including those from pathogens such as Neisseria gonorrhoeae. We postulate that binding to stacked effectors arose in the RNA World to closely position two substrates for RNA-mediated catalysis. These findings expand known effector recognition capabilities of riboswitches and have implications for antimicrobial development.
Keyphrases
- type iii
- genome wide
- genome wide identification
- regulatory t cells
- dendritic cells
- induced apoptosis
- poor prognosis
- nucleic acid
- genome wide analysis
- staphylococcus aureus
- dna methylation
- binding protein
- ms ms
- copy number
- cell cycle arrest
- bioinformatics analysis
- clinical trial
- cell proliferation
- signaling pathway
- antimicrobial resistance
- oxidative stress
- gene expression
- dna binding
- pi k akt