Long-range pseudoknot interactions dictate the regulatory response in the tetrahydrofolate riboswitch Journal Article


Authors: Huang, L.; Ishibe-Murakami, S.; Patel, D. J.; Serganov, A.
Article Title: Long-range pseudoknot interactions dictate the regulatory response in the tetrahydrofolate riboswitch
Abstract: Tetrahydrofolate (THF), a biologically active form of the vitamin folate (B9), is an essential cofactor in one-carbon transfer reactions. In bacteria, expression of folate-related genes is controlled by feedback modulation in response to specific binding of THF and related compounds to a riboswitch. Here, we present the X-ray structures of the THF-sensing domain from the Eubacterium siraeum riboswitch in the ligand-bound and unbound states. The structure reveals an "inverted" three-way junctional architecture, most unusual for riboswitches, with the junction located far from the regulatory helix P1 and not directly participating in helix P1 formation. Instead, the three-way junction, stabilized by binding to the ligand, aligns the riboswitch stems for long-range tertiary pseudoknot interactions that contribute to the organization of helix P1 and therefore stipulate the regulatory response of the riboswitch. The pterin moiety of the ligand docks in a semiopen pocket adjacent to the junction, where it forms specific hydrogen bonds with two moderately conserved pyrimidines. The aminobenzoate moiety stacks on a guanine base, whereas the glutamate moiety does not appear to make strong interactions with the RNA. In contrast to other riboswitches, these findings demonstrate that the THF riboswitch uses a limited number of available determinants for ligand recognition. Given that modern antibiotics target folate metabolism, the THF riboswitch structure provides insights on mechanistic aspects of riboswitch function and may help in manipulating THF levels in pathogenic bacteria.
Keywords: nonhuman; protein binding; protein interaction; structure-activity relationship; guanine; hydrogen bond; crystallography, x-ray; folic acid; nucleic acid conformation; rna structure; pyrimidine; riboswitch; coenzyme; rna, bacterial; 4 aminobenzoic acid; eubacterium; tetrahydrobiopterin; vitamin b9; folate metabolism; tetrahydrofolates; pterin; tetrahydrofolic acid; eubacterium siraeum
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 108
Issue: 36
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2011-09-01
Start Page: 14801
End Page: 14806
Language: English
DOI: 10.1073/pnas.1111701108
PROVIDER: scopus
PMCID: PMC3169164
PUBMED: 21873197
DOI/URL:
Notes: --- - "Export Date: 3 October 2011" - "CODEN: PNASA" - "Source: Scopus"
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  1. Dinshaw J Patel
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  2. Lili Huang
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