Abstract
The exquisite specificity of the adenine-responsive riboswitch toward its cognate metabolite has been shown to arise from the formation of a Watson-Crick interaction between the adenine ligand and residue U65. A recent crystal structure of a U65C adenine aptamer variant has provided a rationale for the phylogenetic conservation observed at position 39 for purine aptamers. The G39-C65 variant adopts a compact ligand-free structure in which G39 is accommodated by the ligand binding site and is base-paired to the cytosine at position 65. Here, we demonstrate using a combination of biochemical and biophysical techniques that the G39-C65 base pair not only severely impairs ligand binding but also disrupts the functioning of the riboswitch in vivo by constitutively activating gene expression. Folding studies using single-molecule FRET revealed that the G39-C65 variant displays a low level of dynamic heterogeneity, a feature reminiscent of ligand-bound wild-type complexes. A restricted conformational freedom together with an ability to significantly fold in monovalent ions are exclusive to the G39-C65 variant. This work provides a mechanistic framework to rationalize the evolutionary exclusion of certain nucleotide combinations in favor of sequences that preserve ligand binding and gene regulation functionalities.
Original language | English |
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Pages (from-to) | 27406-27415 |
Number of pages | 10 |
Journal | Journal of Biological Chemistry |
Volume | 286 |
Issue number | 31 |
DOIs | |
Publication status | Published - 5 Aug 2011 |
Keywords
- RESONANCE ENERGY-TRANSFER
- 4-WAY DNA JUNCTION
- SAM-I RIBOSWITCH
- APTAMER DOMAIN
- PURINE RIBOSWITCH
- BACILLUS-SUBTILIS
- RNA STRUCTURE
- ADENINE RIBOSWITCH
- STRUCTURAL BASIS
- GENE-EXPRESSION