Prospects for Riboswitch Discovery and Analysis Ronald R. Breaker  Molecular Cell  Volume 43, Issue 6, Pages 867-879 (September 2011) DOI: 10.1016/j.molcel.2011.08.024 Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 1 Riboswitch Ligands and Mechanisms (A) Top: List of the riboswitch ligands with biochemical and or genetic validation. Bottom: Demonstrated mechanisms for riboswitch-mediated gene control. (B) Schematic representation of the most common form of riboswitch-mediated gene regulation: transcription termination. Image depicts RNA polymerase (RNAP) in the act of transcribing the U-rich portion of an intrinsic transcription terminator stem in “state 1,” wherein ligand has been bound by the aptamer and transcription will terminate. Alternatively, in “state 2” (not shown), the absence of ligand allows nucleotides from the aptamer to form a competing antiterminator stem that allows transcription to pass beyond the U-rich termination site. Other riboswitch mechanisms are described elsewhere (Breaker, 2011). Molecular Cell 2011 43, 867-879DOI: (10.1016/j.molcel.2011.08.024) Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 2 The Collection of Riboswitch Classes that Sense SAM and/or SAH Depicted are the consensus sequence and structural models for four major families of riboswitches that respond to SAM. The SAM-I family is comprised of representatives classified as SAM-I (or S box), SAM-IV, and SAM-I/IV riboswitches. Note that nucleotides shaded in turquoise are identical in these three consensus models, and these nucleotides are intimately involved in forming the SAM-binding site (Montange and Batey, 2006). Similarly, the SAM-II family is comprised of SAM-II and SAM-V riboswitches that share nucleotides that form the ligand-binding pocket. The remaining two families are represented by SAM-III (or SMK box) and SAM-SAH riboswitch classes. A fifth riboswitch class that rejects SAM and selectively binds its metabolic derivative S-adenosylhomocysteine (SAH) (Wang et al., 2008) is not shown. P1 and related notations indicate base paired substructures. Molecular Cell 2011 43, 867-879DOI: (10.1016/j.molcel.2011.08.024) Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 3 Purine Riboswitch Variants and Their Ligand Specificities Depicted are the consensus sequence and secondary structure models for riboswitch aptamers that selectively respond to guanine, adenine or 2′-deoxyguanosine. Red nucleotides are present in greater than 90% of the guanine riboswitch representatives. Blue nucleotides in the adenine and 2′-deoxyguanosine aptamers differ from the guanine consensus. Other annotations are as described in the legend to Figure 2. Molecular Cell 2011 43, 867-879DOI: (10.1016/j.molcel.2011.08.024) Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 4 The Most Abundant Orphan Riboswitch Classes The consensus sequences and secondary structure models are depicted for the four most common classes of candidate riboswitch aptamers (Block et al., 2010; Meyer et al., 2011). (A) The yybP/ykoK motif RNAs are frequently associated with genes whose protein products mediate pH stress responses. (B) The ydaO/yuaA motif RNAs are frequently associated with genes involved in osmotic stress responses. (C) The pfl motif RNAs control genes centered on folate metabolism. (D) The ykkC/ykkD motif RNAs are associated with genes for transporters and for purine metabolism. Molecular Cell 2011 43, 867-879DOI: (10.1016/j.molcel.2011.08.024) Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 5 Architectures of Riboswitches and Their Effects on Ligand-Mediated Gene Control The expression platforms can be conventional systems as listed in Figure 1, or can be self-processing ribozymes. R designates the fraction of gene regulation, Y designates the fraction of aptamer bound by ligand, [L] designates ligand concentration, and KD designates apparent dissociation constant. For all riboswitch architectures other than cooperative systems, values for Y are determined with the equation for a simple riboswitch. Molecular Cell 2011 43, 867-879DOI: (10.1016/j.molcel.2011.08.024) Copyright © 2011 Elsevier Inc. Terms and Conditions

Figure 6 Allosteric Control Mechanism of a Group I Self-Splicing Ribozyme by a c-di-GMP Riboswitch Aptamer Sequence and secondary structure model for the allosteric ribozyme from the bacterium C. difficile (Lee et al., 2010). A class II c-di-GMP riboswitch aptamer, formed by three conventional base-paired regions (P1 through P3) and one pseudoknot, resides only 6 nucleotides upstream of the initial structured portion (shaded P1) of a group I ribozyme. The 5′ splice site (red “5′ SS” between nucleotides 101 and 102) is a target for GTP attack (“GTP1”) when c-di-GMP is bound by the aptamer. After this first step of splicing, the second step promotes attack by G101 of the 5′ exon at the 3′ splice site (red “3′ SS” between nucleotides 667 and 668) to yield spliced exons. In the absence of c-di-GMP binding, alternative base pairing (blue “anti-5′ SS stem”) occurs between aptamer and ribozyme nucleotides. This anti-5′ SS stem displaces the ribozyme P1 stem, which precludes normal splicing. In contrast, an “alternative ribozyme P1 stem” (green) forms and promotes GTP attack (GTP2) after nucleotide 670. The products of normal splicing, promoted by c-di-GMP, are efficiently translated because they carry a typical ribosome binding site located the proper distance upstream of the unusual UUG start codon. The products of alternative splicing, which occurs when c-di-GMP is low in concentration, lack a ribosome binding site and therefore are not translated. Molecular Cell 2011 43, 867-879DOI: (10.1016/j.molcel.2011.08.024) Copyright © 2011 Elsevier Inc. Terms and Conditions