Crystal structures reveal the distinct features of the 2′-dG-III riboswitch in the purine riboswitch family
Purine riboswitches, located in the 5'-untranslated regions of bacterial messenger RNA, regulate gene expression by sensing purines and their derivatives. A class of the guanine-I riboswitch variants was recently reported to be the third class of 2'-deoxyguanosine (2'-dG) riboswitch termed 2'-dG-III riboswitch. Here we present the crystal structures of the 2'-dG-III riboswitch bound with 2'-dG, guanosine, or guanine. Despite similarities in secondary and overall structures to other purine riboswitches, the 2'-dG-III riboswitch exhibits unique features in its loop-loop interaction, three-way junction, and ligand binding. The 2'-dG-III riboswitch exhibits a tuning fork-like structure with a unique six-tiered interaction within the three-way junction. The second, third, and fourth tiers form the ligand-binding pocket, with a consistent binding mode for the guanine moiety of all three ligands. Structural and biochemical analyses reveal detailed interactions between the 2'-dG-III riboswitch and different ligands, providing insights into its regulatory mechanisms in purine metabolism.
Authors
- Wenjian Liao (ORCID: https://orcid.org/0000-0001-9823-9949)
- Zhizhong Lu (ORCID: https://orcid.org/0000-0003-1461-9093)
- Lin Huang (ORCID: https://orcid.org/0000-0002-2121-365X)
- Xuemei Peng (ORCID: https://orcid.org/0000-0002-5363-3085)
- Jiali Wang (ORCID: https://orcid.org/0000-0002-0780-5624)
- Ke Chen (ORCID: https://orcid.org/0009-0005-5702-9597)
- Yuan Ren
- Jia Wang (ORCID: https://orcid.org/0000-0002-2330-8505)
Institutions
- Sun Yat-sen University (CN)
- Guangdong Pharmaceutical University (CN)
- Sun Yat-sen Memorial Hospital (CN)
- Shenzhen Technology University (CN)
Publication Details
- Journal
- Nucleic Acids Research
- Published
- 2025-07-14
- DOI
- https://doi.org/10.1093/nar/gkaf702
- Primary Topic
- RNA and protein synthesis mechanisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China