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Decoding the Complex Functional Landscape of the ykkC Riboswitches
Kathryn M Barth1,2, David A Hiller1,2, Gabriel Belem de Andrade3
1Institute of Biomolecular Design and Discovery, Yale University, West Haven, Connecticut 06516, United States.
The ykkC riboswitch class demonstrates high ligand specificity through fine-tuned terminator hairpins. Mutational analysis reveals a new subclass binding XMP and GMP, crucial for de novo GMP synthesis.
Area of Science:
- Molecular Biology
- Biochemistry
- Genetics
Background:
- The ykkC riboswitch class exhibits remarkable diversity in ligand recognition despite minor sequence and structural variations.
- Previous structural studies elucidated sequence-structure relationships but lacked functional insights into riboswitch specificity.
Purpose of the Study:
- To investigate the functional role of the ppGpp riboswitch variant in transcriptional control using extensive mutational analysis.
- To define the requirements for functional riboswitch specificity and explore ligand-binding variations within the ykkC class.
Main Methods:
- Extensive mutational analysis of the ppGpp riboswitch.
- Disruption of the terminator hairpin at a single base pair.
- Phylogenetic analysis of natural ykkC riboswitches.
Main Results:
- Disrupting a single base pair in the terminator hairpin abolished nearly all riboswitch function, indicating critical fine-tuning.
- Mutational analysis indicated that G93 is not exclusively linked to PRPP-driven function.
- Phylogenetic analysis identified a novel ykkC subclass binding both XMP and GMP, associated with de novo GMP synthesis genes.
Conclusions:
- Riboswitch fine-tuning, particularly of the terminator hairpin, is essential for function and suggests broad tunability across riboswitches.
- The discovery of a new ykkC subclass binding XMP and GMP provides evidence that small sequence changes can significantly alter ligand specificity.
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