7D82

Crystal Structure of the Domain2 of NAD+ Riboswitch with nicotinamide adenine dinucleotide (NAD+), soaked in Mn2+

Summary for 7D82

• Entry DOI: 10.2210/pdb7d82/pdb
• Descriptor: 832GAAA (50-MER), MANGANESE (II) ION, NICOTINAMIDE-ADENINE-DINUCLEOTIDE, ... (5 entities in total)
• Functional Keywords: riboswitch, rna structure, rna folding, rna-ligand interactions, rna crystallography, rna
• Biological source: Acidobacteriaceae bacterium KBS 83
• Total number of polymer chains: 1
• Total formula weight: 17321.73

Authors

Chen, H.,Ren, A.M. (deposition date: 2020-10-06, release date: 2020-11-25, Last modification date: 2023-11-29)

Primary citation

Chen, H.,Egger, M.,Xu, X.,Flemmich, L.,Krasheninina, O.,Sun, A.,Micura, R.,Ren, A.
Structural distinctions between NAD+ riboswitch domains 1 and 2 determine differential folding and ligand binding.
Nucleic Acids Res., 48:12394-12406, 2020

PubMed Abstract: Riboswitches are important gene regulatory elements frequently encountered in bacterial mRNAs. The recently discovered nadA riboswitch contains two similar, tandemly arrayed aptamer domains, with the first domain possessing high affinity for nicotinamide adenine dinucleotide (NAD+). The second domain which comprises the ribosomal binding site in a putative regulatory helix, however, has withdrawn from detection of ligand-induced structural modulation thus far, and therefore, the identity of the cognate ligand and the regulation mechanism have remained unclear. Here, we report crystal structures of both riboswitch domains, each bound to NAD+. Furthermore, we demonstrate that ligand binding to domain 2 requires significantly higher concentrations of NAD+ (or ADP retaining analogs) compared to domain 1. Using a fluorescence spectroscopic approach, we further shed light on the structural features which are responsible for the different ligand affinities, and describe the Mg2+-dependent, distinct folding and pre-organization of their binding pockets. Finally, we speculate about possible scenarios for nadA RNA gene regulation as a putative two-concentration sensor module for a time-controlled signal that is primed and stalled by the gene regulation machinery at low ligand concentrations (domain 1), and finally triggers repression of translation as soon as high ligand concentrations are reached in the cell (domain 2).

PubMed: 33170270
DOI: 10.1093/nar/gkaa1029

Experimental method

X-RAY DIFFRACTION (2.489 Å)