The Escherichia coli transcription system is the best characterized from a biochemical and genetic point of view and has served as a model system. Nevertheless, a molecular understanding of the details of E. coli transcription and its regulation, and therefore its full exploitation as a model system, has been hampered by the absence of high-resolution structural information on E. coli RNA polymerase (RNAP). We use a combination of approaches, including high-resolution X-ray crystallography, ab initio structural prediction, homology modeling, and single-particle cryo-electron microscopy, to generate complete atomic models of E. coli core RNAP and an E. coli RNAP ternary elongation complex. The detailed and comprehensive structural descriptions can be used to help interpret previous biochemical and genetic data in a new light and provide a structural framework for designing experiments to understand the function of the E. coli lineage-specific insertions and their role in the E. coli transcription program.
Transcription, or the synthesis of RNA from DNA, is one of the most important processes in the cell. The central enzyme of transcription is the DNA-dependent RNA polymerase (RNAP), a large, macromolecular assembly consisting of at least five subunits. Historically, much of our fundamental information on the process of transcription has come from genetic and biochemical studies of RNAP from the model bacterium Escherichia coli. More recently, major breakthroughs in our understanding of the mechanism of action of RNAP have come from high resolution crystal structures of various bacterial, archaebacterial, and eukaryotic enzymes. However, all of our high-resolution bacterial RNAP structures are of enzymes from the thermophiles Thermus aquaticus or T. thermophilus, organisms with poorly characterized transcription systems. It has thus far proven impossible to obtain a high-resolution structure of E. coli RNAP, which has made it difficult to relate the large collection of genetic and biochemical data on RNAP function directly to the available structural information. Here, we used a combination of approaches—high-resolution X-ray crystallography of E. coli RNAP fragments, ab initio structure prediction, homology modeling, and single-particle cryo-electron microscopy—to generate complete atomic models of E. coli RNAP. Our detailed and comprehensive structural models provide the heretofore missing structural framework for understanding the function of the highly characterized E. coli RNAP.
Citation: Opalka N, Brown J, Lane WJ, Twist K-AF, Landick R, Asturias FJ, et al. (2010) Complete Structural Model of Escherichia coli RNA Polymerase from a Hybrid Approach. PLoS Biol 8(9): e1000483. https://doi.org/10.1371/journal.pbio.1000483
Academic Editor: Leemor Joshua-Tor, Cold Spring Harbor Laboratory, United States of America
Received: March 2, 2010; Accepted: August 4, 2010; Published: September 14, 2010
Copyright: © 2010 Opalka et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The use of the Rigaku/MSC microMax 007HF in the RU-SBRC was made possible by grant number 1S10RR022321-01 from the National Center for Research Resources of the National Institutes of Health (NIH). SAD is a member of the NYSBC, a STAR center supported by the New York State Office of Science, Technology, and Academic Research. This work was supported by NIH grants GM038660 to RL, GM073829 to FJA and SAD, and GM061898 and GM053759 to SAD. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: Abbreviations BBM1, β-β' module 1; BBM2, β-β' module 2; BH, bridge-helix; Cryo-EM, cryo-electron microscopy; Eco, Escherichia coli; hEM, helical cryo-electron microscopy; MccJ25, microcin J25; NSLS, National Synchrotron Light Source; NYSBC, New York Structural Biology Center; paf, prevent Alc function; RNAP, RNA polymerase; RU-SBRC, The Rockefeller University Structural Biology Resource Center; SBHM, sandwich-barrel hybrid motif; spEM, single-particle cryo-electron microscopy; TEC, ternary elongation complex; Taq, Thermus aquaticus; TL, trigger-loop; TLH1, trigger-loop helix 1; TLH2, trigger-loop helix 2; Tth, Thermus thermophilus; us-DNA, upstream DNA
RNA in all cellular organisms is synthesized by a complex molecular machine, the DNA-dependent RNA polymerase (RNAP). In bacteria, the catalytically competent core RNAP (subunit composition α2ββ'ω) has a molecular mass of ∼400 kDa. Evolutionary relationships for each of the bacterial core subunits have been identified between all organisms from bacteria to man –. These relationships are particularly strong between the two largest subunits, β' and β, which contain colinearly arranged segments of conserved sequence (Figure 1) . These conserved segments are separated by relatively nonconserved spacer regions in which large, lineage-specific gaps or insertions can occur ,. The functional significance of these lineage-specific differences is poorly understood due to a lack of correlated biochemical and structural information. The bulk of our biochemical and genetic knowledge on bacterial RNAP comes from studies of Escherichia coli (Eco) RNAP but all of our high-resolution structural information comes form Thermus RNAPs – as Eco RNAP has not been amenable to X-ray crystallography analysis. The Eco and Thermus β and β' subunits harbor large sequence insertions (>40 amino acids) that are not present in the other species and are not shared across bacterial species (Figure 1) . For example, the Eco β' subunit contains β'-insert-6 (or β'i6, using the lineage-specific insert nomenclature of Lane et al. ), a 188-residue insertion in the middle of the highly conserved “trigger loop.” On the other hand, the Thermus β' subunit lacks β'i6 but contains β'i2 (283 residues). High-resolution structures of both of these lineage-specific inserts reveal that they comprise repeats of a previously characterized fold, the sandwich-barrel hybrid motif (SBHM) ,. Similarly, the Eco β subunit harbors three large insertions missing in Thermus, βi4 (119 residues), βi9 (99 residues), and βi11 (54 residues), whereas the Thermus β subunit harbors βi12 (43 residues).
The vertical bars represent the primary sequence of the bacterial RNAP β (top, light cyan) and β' (bottom, light pink) subunits.The white boxes indicate sequence regions common to all bacterial RNAPs, as defined by Lane et al. . Important structural features are labeled above the bars . Lineage-specific insertions (labeled according to the nomenclature of Lane et al.  are shown below the bars. The color-coding for the large subunits and the lineage-specific insertions shown here is used throughout this article.
In some respects, the high-resolution Thermus RNAP structures have served as good models to interpret the functional literature obtained from biochemical, biophysical, and genetic studies of Eco RNAP ,. Nevertheless, a complete molecular model of Eco core RNAP has not been available due to the absence of high-resolution structural information on the Eco β subunit lineage-specific inserts. The most detailed structural studies of Eco RNAP have come from cryo-electron microscopy (cryo-EM) analysis of helical crystals at about 15 Å-resolution . This cryo-EM reconstruction of Eco core RNAP could be interpreted in detail by fitting the Taq core RNAP X-ray structure, revealing a large distortion of the structure (opening of the active site channel by more than 20 Å) due to intermolecular contacts in the helical crystals. Strong electron density for Eco βi9 was present in the cryo-EM reconstruction, but weak density for Eco βi4 and Eco β'i6 indicated these domains were flexible in the context of the helical crystals . Most previous EM reconstructions of various forms of Eco RNAP have not revealed information concerning the lineage-specific inserts (for instance, see ). A recent 20 Å-resolution, negative-stain EM reconstruction of an activator-dependent transcription initiation complex containing Eco RNAP  allowed the positioning of the Eco β'i6 crystal structure , but the lack of structural information on the other Eco lineage-specific inserts prevented the detailed interpretation of additional densities present in the reconstruction .
In this study, we used a combination of structural approaches to generate a complete molecular model of Eco core RNAP. We determined two new high-resolution X-ray crystal structures of Eco RNAP β subunit fragments that include Eco βi4 and βi9 and used an ab initio method to predict the structure of the small Eco βi11 . The three available X-ray crystal structures of Eco RNAP fragments (the two structures determined herein and the structure of Eco β'i6 ) and the predicted structure of Eco βi11 were incorporated into a homology model of Eco core RNAP. Finally, we used cryo-EM imaging combined with single-particle image analysis to obtain a low-resolution structure of the solution conformation of Eco core RNAP in which densities corresponding to lineage-specific insertions could be clearly identified. Flexible-fitting of the Eco RNAP homology model into cryo-EM densities generated a complete molecular model of Eco core RNAP and an Eco RNAP ternary elongation complex (TEC).
Crystal Structure of Eco RNAP β2-βi4
The lineage-specific insert βi4 (previously named β dispensable region 1, or βDR1, or SI1 in the literature ,,), located between bacterial shared regions βb6 and βb7 (using the bacterial RNAP common region nomenclature of Lane et al. ) in the β2 domain (Figure 1) ,, was predicted to comprise from one to six tandem repeats of a structural motif termed the β-β' module 2 (BBM2) . The βi4 of Acidobacteria, Mollicutes, and Proteobacteria (including Eco) was predicted to comprise two tandem BBM2 repeats . Eco βi4 comprises β residues 225–343 (Figure 2A).
(A) Sequence alignment comparing Eco RNAP β2-βi4 with the corresponding region of Taq (which lacks βi4). Shaded residues are identical between the two sequences. The secondary structures are indicated directly above (for Eco) and below (for Taq) the sequences; filled rectangles denote α-helices, open rectangles denote β-strands, the dashed lines denote disordered regions. The number scale above the Eco secondary structure corresponds to the Eco β subunit sequence. Above the number scale, black lines denote the sequence regions common to all bacterial RNAPs . The yellow and orange lines denote the two BBM2 motifs . The extent of the common β2 domain (thick cyan line) and the lineage-specific insert βi4 (thick green line) is indicated at the top. (B) Ribbon diagram of Eco β2-βi4 (β2 domain, cyan; βi4, green). A disordered loop (Eco β 161–169) is denoted by small spheres. The view corresponds to the reference view of Taq core RNAP (lower left, β-side view), shown as a backbone worm and color-coded as follows: αI, αII, ω, gray; β', light pink; β, light cyan, except the β2 domain is colored cyan and labeled. (C) Ribbon diagram of Eco βi4 (same view as B). The tandem BBM2 motifs predicted by Iyer et al.  are color-coded as in (A) (BBM2a, yellow; BBM2b, orange).
We prepared a construct comprising the Eco β2 domain including βi4 inserted within it (Eco β residues 152–443, hereafter called Eco β2-βi4). After reductive methylation , the protein formed crystals that diffracted X-rays to 1.6 Å-resolution (Table 1). The structure was solved by single-anomalous dispersion using a dataset collected from crystals of selenomethionyl-substituted protein  and refined to an R/Rfree of 0.209/0.229 at 1.6 Å-resolution (Table 1, Figures 2, S1).
As expected, the Eco β2 (Eco β residues 151–224 and 344–445) and the Thermus β2 (Taq or Tth β residues 138–325) domains have similar overall structures (Figure S2). A superimposition of the two domains over 100 residues (excluding flexible loops connecting secondary structural elements) yields a root-mean-square deviation in α-carbon positions of 1.68 Å. Significant differences in the structures include: (i) the loop connecting the first two β-strands of the β2 domain, where Eco has a 5-residue insertion (Eco β residues 164–168, disordered in our structure), and (ii) the loop connecting the last two α-helices of the β2 domain, which includes a 7-residue insertion present in Taq β (Taq β residues 293–299; Figures 2A, S2).
The βi4 domain is inserted at the surface of the β2 domain distal to the connection with the RNAP (Figure 2B). A 3-residue segment of Taq β (Taq β 212–214) is replaced by the 119-residue Eco βi4 (Figure 2A). The Eco βi4 folds into a compact, cylinder-shaped domain about 22 Å in diameter and about 50 Å in length (Figures 2B, 2C). The compact domain is connected to the β2 domain by two short connector loops (Eco β 225–226 and 337–345). The βi4 domain packs against β2, resulting in the burial of a modest 618 Å2 of surface area. As predicted , the Eco βi4 includes two tandem BBM2 motifs (Figure 2A, 2C).
Crystal Structure of Eco RNAP βflap-βi9
The lineage-specific insert βi9 (previously named β dispensable region 2, or βDR2, or SI2 in the literature ,,,) is located between bacterial shared regions βb13 and βb14  at the base of the flap domain (Figure 1) ,. The βi9 is found in Acidobacteria, Aquificae, Bacteriodetes, Chlamydiae, Chlorobi, Planctomycetes, Proteobacteria (including Eco), and Nitrospirae . Eco βi9 comprises β residues 938–1042 (Figure 3A).
(A) Sequence alignment comparing the sequence context of Eco RNAP βi9 with the corresponding region of Taq (which lacks βi9). Shaded residues are identical between the two sequences. The secondary structure for Eco is indicated directly above the sequence; filled rectangles denote α-helices, open rectangles denote β-strands. The number scale above the Eco secondary structure corresponds to the Eco β subunit sequence. Above the number scale, black lines denote the sequence regions common to all bacterial RNAPs . Gaps in the βi9 sequence with numbers above denote the location and residue length of insertions in an alignment of 307 non-redundant βi9 sequences (see Supporting Information). The extent of the common βflap domain (thick cyan line) and the lineage-specific insert βi9 (thick orange line) is indicated at the top. (B) Two orthogonal views of Eco βflap-βi9 (βflap, cyan; βi9, orange). The views correspond to the reference views of Taq core RNAP (left, bottom view; right, front view), shown as a backbone worm and color-coded as follows: αI, αII, ω, gray; β', light pink; β, light cyan, except the βflap domain is colored cyan and labeled.
A construct comprising the Eco flap domain (Eco β 831–1057), including βi9, was crystallized as a complex with bacteriophage T4 gp33 (K.-A.F.T., P. Deighan, S. Nechaev, A. Hochschild, E.P. Geiduschek, S.A.D., in preparation). The structure was solved by a combination of molecular replacement (using the Taq flap domain as a search model) and single-anomalous dispersion using data collected from selenomethionyl-substituted protein (Table S1, Figure S3) . The complete structure was refined to an R/Rfree of 0.264/0.291 at 3.0 Å-resolution. T4 gp33 interacts primarily with the flap-tip and does not make any interactions with βi9. These and further details of the complex with T4 gp33 will be described elsewhere (K.-A.F.T., P. Deighan, S. Nechaev, A. Hochschild, E.P. Geiduschek, S.A.D., in preparation).
The βi9 domain is inserted at the base of the flap domain, near the C-terminal connection of the flap with the rest of the RNAP and distal to the flap-tip (Figure 3B). A 6-residue segment of Taq β (Taq β 809–814) is replaced by the 105-residue Eco βi9 (Figure 3A). The Eco βi9 comprises two long, parallel α-helices of 38 and 32 residues (Eco β 943–980 and 1006–1037, respectively) with a short, hook-like connecting segment (residues 981–1005) at the end distal to the flap (Figure 3B), forming an apparently rigid structure reminiscent of a hook-and-ladder that extends nearly 65 Å out from the flap domain. The βi9 is connected to the flap domain by two connector loops (Eco β 938–942 and 1038–142) but makes minimal interactions with the flap itself. The structure does not appear to conform to the β-β' module 1 motif (BBM1, similar to the BBM2 motif, Figure 2C) predicted for βi9 . The 105-residue Eco βi9 is at the lower end of the size range for βi9 sequences, which ranges from 105 residues in some Proteobacteria to 143 residues in some Bacteriodetes. An alignment of 307 non-redundant βi9 sequences (see Dataset S1) reveals that the two long, ladder α-helices do not harbor insertions; all of the insertions occur in the hook-like connector at the distal end of βi9 (Figure 3A). Therefore, we conclude that βi9 has a conserved core structure with the two ladder α-helices of conserved length.
Cryo-EM Reconstruction of Eco RNAP
We generated a single-particle cryo-EM (spEM) reconstruction of Eco RNAP by analyzing ∼42,000 images of Eco RNAP particles preserved in vitreous ice (Figures 4A, S4–S6). Initial image orientation parameters were determined using a 35 Å-resolution RNAP model based on the Taq core RNAP X-ray structure . Final refinement of image orientation parameters by projection matching yielded a structure of Eco RNAP with a 0.5 Fourier-shell cutoff resolution of ∼11.2 Å (Figure S4). Nevertheless, information beyond about 14 Å resolution was very weak, and so the figures and analysis described herein were performed on a low-pass Fourier-filtered map ,. Although the cryo-EM grids were prepared with samples of Eco RNAP holoenzyme (core RNAP plus the promoter-specificity σ70 subunit), the σ70 subunit apparently dissociated during grid preparation as density corresponding to σ70 was completely absent. Dissociation during cryo-EM sample preparation has been noted for other macromolecular complexes  and is also consistent with reports of dissociation constants for the σ70/core RNAP complex as high as 200–300 nM (the RNAP concentration used here was about 200 nM). The spEM reconstruction showed Eco core RNAP in a conformation similar to that observed in Thermus X-ray structures but with clear density corresponding to βi4, βi11, and β'i6 (Figures 4A, S5, S6).
(A) Three views of the spEM density map and corresponding fit of the Eco RNAP homology model (excluding ω, the C-terminal 41 residues of β', and βi9). For each view (β-side, top, and channel views), the left image shows the spEM density map (grey surface, contoured at 2.5 σ), and the right image shows the spEM density map (grey transparent surface) with the fitted Eco RNAP homology model superimposed. The Eco RNAP homology model is shown as a backbone worm, color-coded as shown in the key (lower left). (B) View of the hEM density map and corresponding fit of the Taq core RNAP crystal structure . The small view (left, which corresponds roughly to the bottom view) shows the entire structure (weak density due to βi4 is noted). The boxed region is magnified on the right, where the Eco βflap-βi9 structure (βflap, cyan; βi9, light orange) is superimposed via the flap domain (excluding the flap-tip). The resulting position of βi9 (light orange) was adjusted to fit into the hEM density (βi9', orange). The red dot denotes the position of a positive difference peak from a hEM reconstruction of a mutant RNAP harboring a 234-residue insertion in βi9 between residues 998 and 999 .
Molecular Model of the Complete Eco Core RNAP
In order to interpret the spEM map of Eco core RNAP, we generated a homology model of Eco core RNAP using the core component of the T. thermophilus (Tth) RNAP holoenzyme structure (PDB ID 1IW7)  as a template. The locations of the Eco lineage-specific insertions βi4, βi9, βi11, and β'i6 (absent in Thermus) were left as gaps in the Eco sequences. Thermus-specific inserts βi12 and β'i2 (Figure 1) were also removed from the structural template. The crystal structures of Eco β2-βi4 (Figure 2B) and βflap-βi9 (Figure 3B) were spliced into the resulting homology model by superimposition of the overlapping β2 and βflap domains, respectively. At this stage, the Eco RNAP model was readily fit manually into the spEM map. The spEM map contained clear density corresponding to βi4, but density for βi9 was absent. Density for the ω subunit as well as the C-terminal helix of β' were also absent. In addition, extra density not accounted for by the homology model was present for βi11 and β'i6. An ab initio predicted structure of the short βi11 (see below) was placed into the corresponding density to fill in the gap in the Eco β sequence between 1121 and 1181. The crystal structure of Eco β'i6 (PDB ID 2AUK)  was readily fit manually into excess density in the vicinity of its insertion point in β'. Two criteria were used to determine the orientation of β'i6 with respect to the rest of the RNAP. First, although β'i6 comprises a tandem repeat of two SBHM domains, the C-terminal SBHM domain (SBHMb)  harbors larger insertions between the core SBHM β-strands, making β'i6 asymmetric in shape. The asymmetry is clearly seen in the spEM density as well (see Figure 4A, top view). Moreover, only one orientation of β'i6 allows connection to the gap in the Eco β' sequence (between residues 940 and 1132) without severe distortion. The positioned β'i6 was readily connected to the open (unfolded) trigger-loop (TL) conformation of the model.
Flexible-fitting of the final Eco RNAP model (excluding ω, the C-terminal 41 residues of β', and βi9) into the spEM map was performed using YUP.SCX , resulting in a superb fit of the conserved RNAP as well as of the lineage-specific inserts (excluding βi9; Figures 4A, S5, S6). In order to position βi9 in the context of the entire RNAP structure, we used our previously determined helical cryo-EM map of Eco core RNAP (hEM) and fit of the Taq core RNAP X-ray crystal structure  since the hEM map contains strong density for βi9. The βflap portion (excluding the flexible flap-tip) of the Eco βflap-βi9 crystal structure (Figure 3B) was superimposed on the Taq βflap domain in the context of the Taq RNAP fit into the hEM density. The resulting position of βi9 did not correspond to the hEM density (light orange, βi9 in Figure 4B) but was fit into the density by a rotation of about 35° (orange, βi9' in Figure 4B). This positioning of βi9 is consistent with the location of positive difference density observed in the context of the helical crystals due to a 234-residue insertion between Eco β residues 998 and 999 (red dot, Figure 4B). The Eco core RNAP model was completed by adding back the C-terminal segment of β' as well as ω (in accordance with the Thermus RNAP structures).
The Eco core RNAP model was then used as the basis for generating a homology model of an Eco TEC, using the Tth TEC crystal structure (open TL conformation, PDB ID 2O5I) . For both models, the lineage-specific inserts (βi4, βi9, βi11, β'i6 for Eco; β'i2 and β'i12 for Tth) were removed. The nucleic acids present in the Tth crystal structure were fixed during the modeling. The Eco lineage-specific inserts were added back to the resulting TEC model (according to their positions in the Eco core RNAP model), and missing portions of the nucleic acids (the upstream double-stranded DNA, and the nontemplate strand of the DNA within the transcription bubble) were modeled according to Korzheva et al. .
In this work, two new X-ray crystal structures (Eco β2-βi4, Figure 2; Eco βflap-βi9, Figure 3) and an ab initio predicted structure (Eco βi11, see below), combined with a previously determined X-ray crystal structure of Eco β'i6 , provide high-resolution structural descriptions of each of the lineage-specific sequence insertions found in the highly biochemically and genetically characterized Eco RNAP . In addition, a new 15 Å-resolution cryo-EM single-particle reconstruction of Eco RNAP (Figures 4A, S4–S6) reveals clear electron density for βi4, βi11, and β'i6, while a previously determined cryo-EM reconstruction of Eco core RNAP from helical crystals contains strong electron density for βi9 ,. The combination of these structural data provides the basis for a detailed and complete atomic model of Eco RNAP and an Eco core RNAP TEC.
The large β and β' subunits comprise regions of sequence shared among all bacterial RNAPs . These shared regions, which make up 63% of the Eco β and 67% of the Eco β' sequence, are expected to have nearly identical structure among all bacterial RNAPs. The α subunits are also highly homologous ,. Thus, most of the Eco RNAP structure is expected to be highly similar, if not identical, to the Thermus RNAP structures. The unique contribution of this work is the high-resolution structural information on the Eco lineage-specific inserts βi4, βi9, and βi11, as well as the detailed structural model of all the lineage-specific inserts in the context of the entire RNAP and a TEC. The following discussion therefore focuses on the Eco lineage-specific inserts and insights into their role in RNAP function provided by our new structural information.
RNAPs harboring deletions or insertions within βi4 support cell growth and retain basic in vitro transcription function, leading to its designation as “dispensable region I” of the β subunit . Nevertheless, careful studies of a nearly precise βi4 deletion (deletion of Eco β 226–350) revealed defects . The purified Δβi4-RNAP showed only very mild defects, or no defects at all, in a number of in vitro tests ,. In vivo, however, the Δβi4-RNAP was unable to support cell growth at 42°C and could only support slow growth at 30°C.
In our model of the Eco TEC, βi4 extends out from the β2 domain roughly in the direction of the downstream double-stranded DNA (Figure 5). However, βi4 is unlikely to interact directly with the downstream DNA to form part of an extended DNA binding channel since βi4 tilts away from the DNA, creating a roughly 15 Å gap between itself and the DNA. Moreover, the solvent-exposed surface of βi4, including the entire surface facing the DNA, is highly acidic (Figure 5, front view), except for a “neutral patch” that arises from three conserved residues, Eco β R268, R272, and R275 (Figure 5, top view). These positions are conserved as basic residues (either R or K) in 98%, 91%, and 91% of the sequences, respectively, in an alignment of 316 non-redundant βi4 sequences (containing only “Eco-like” βi4 sequences comprising two BBM2 domains; see Dataset S2) and may comprise an interaction determinant for an as yet unidentified regulatory factor.
In each view, the RNAP is shown as a molecular surface, and the nucleic acids are shown as phosphate backbone worms (DNA template strand, dark green; DNA nontemplate strand, light green; RNA transcript, gold). Channel view (left): The RNAP is color coded as follows: αI, αII, ω, grey; β, cyan, except βi4 is green, βi9 is orange, and βi11 is magenta; β', pink, except β'i6 is red. The positions of two paf mutants (βR368 and βP372) , are colored blue. β'T1068 (within β'i6), which is phosphorylated by bacteriophage T7 Gp0.7 , is shown in yellow. The thick black arrow points in the downstream direction. Front view (middle): The RNAP molecular surface is colored according to the solvent-exposed electrostatic surface distribution , scaled from –10 kT (red) to +10 kT (blue). The locations of the paf mutants βR368 and βP372, and β'T1068, are denoted. The upstream DNA (us-DNA) is labeled. Top view (right): The RNAP molecular surface is colored according to the solvent-exposed electrostatic surface distribution , scaled from −10 kT (red) to +10 kT (blue). The locations of highly conserved basic residues in βi4 (βR268, R272, and R275) are denoted. In this view, the nucleic acids are fortuitously hidden from view.
The bacteriophage T4 Alc protein interacts with the host Eco RNAP  and causes premature transcription termination on Eco DNA while allowing Eco RNAP-mediated transcription of phage DNA containing 5-hydroxymethylcytosine . Eco paf mutants (prevent Alc function) have been mapped to the rpoB gene encoding the RNAP β subunit ,. Eco β mutants R368H, R368C, and a double mutant (P345S/P372L) display the paf phenotype, possibly by directly preventing Alc interaction with RNAP . These mutations lie within a region of the β subunit that could be deleted without disrupting basic transcription function  but are not, in fact, contained within βi4 (Figure 2A). Two of the mutated positions (368 and 372) lie within βb7, a region shared among all bacterial RNAPs (Figure 2A) . In our structural model of the Eco RNAP TEC, βR368 and βP372 lie within a structural feature that sits at the entrance of the main RNAP active site channel, inside the “V” formed by the upstream and downstream DNA of the TEC (Figure 5, channel and front views). These residues are not near any nucleic acids in the TEC (the closest approach is for the backbone carbonyl of βP372, which is 15 Å away from the nontemplate DNA phosphate backbone at the -10 position) but could comprise part of an Alc binding determinant on the RNAP . The 19 kDa Alc protein bound in this vicinity (Figure 5, channel and front views) would be well positioned to distinguish the presence of cytosine or 5-hydroxymethylcytosine in either the downstream double-stranded DNA (where the 5-hydroxymethyl moiety would be exposed in the major groove) or the single-stranded non-template DNA in the transcription bubble.
RNAPs harboring deletions or insertions within βi9 support cell growth and retain in vitro transcription function, leading to its designation as “dispensable region II” of the β subunit ,,,. Nevertheless, careful studies of a precise βi9 deletion (deletion of Eco β 938–1040) revealed defects . The purified Δβi9-RNAP showed only very mild defects, or no defects at all, in a number of in vitro tests . The βi9 contains the epitope for the PYN-6 monoclonal antibody and, consistent with in vitro tests showing little effect of deleting βi9 on normal RNAP function, RNAP can be immobilized using the PYN-6 antibody but remains active for in vitro transcription . In vivo, however, the Δβi9-RNAP was unable to support cell growth in minimal media .
Our crystal structure of the Eco βflap-βi9 suggests that βi9 is attached to the flap via flexible linkers and does not make a significant, stable interaction with the flap (Figure 3B), suggesting that βi9 is highly flexible in its orientation with respect to the flap. Indeed, the position of βi9 in the βflap-βi9 crystal structure appears to be determined by packing interactions with neighboring, symmetry-related molecules. In keeping with this, there is no density for βi9 in the spEM reconstruction (Figures 4A, S5, S6). However, in our previous hEM reconstruction of Eco RNAP, strong density consistent with βi9 was observed, and this density was shown to correspond to βi9 through a helical reconstruction of a mutant RNAP harboring a large insertion between positions 998 and 999 . In the helical crystals, the packing of a neighboring, symmetry-related RNAP molecule restricts the range of positions available to βi9, allowing its visualization (Figure 4B). Fitting βi9 into the corresponding density in the hEM reconstruction required a large change in the position of βi9 with respect to the flap, but the final model fits very well into the density and is also consistent with the EM localization results , which were not used as a constraint in the fitting (Figure 4B). This model for the position of βi9 in the context of the entire RNAP is presented as an example of a particular orientation that is possible for βi9 (since it was observed in the helical crystals), but the evidence indicates that βi9 does not adopt a particular conformation with respect to the RNAP but can access a wide range of positions (Figure 6).
Bottom view of the Eco RNAP model. The RNAP is shown as a molecular surface (αI, αII, ω, grey; β, light cyan, except βi4 is green and βi11 is magenta; β', light pink) except for βi9, which is shown as a backbone worm. The modeled position of βi9 (see Figure 4B) is colored orange. Selected alternative orientations accessible to βi9 are colored light orange. The potential reach of βi9 maps out roughly a hemisphere with a radius of 65 Å.
The modeled position of βi9 is not near any nucleic acids in the TEC or in the open promoter complex . Moreover, the solvent-exposed surface of βi9 is primarily acidic (Figure S7). Interestingly, an alignment of 307 non-redundant βi9 sequences (see Dataset S1) reveals that conserved, solvent-exposed residues are all displayed on the back face of the “ladder,” opposite the “hook” (Figure S7). Conserved features of this face comprise charged residues D959 (conserved as D or E in 97% of the sequences), E962 (D/E, 95%), R974 (K/R, 89%), K1032 (K/R, 95%), and K1035 (K/R, 94%), and one conserved hydrophobic residue, I966. These features suggest that this face of the ladder may serve as an interaction determinant for as yet unidentified regulatory factors. D959 and K1032 participate in an apparently conserved salt bridge. Predictably, a number of conserved hydrophobic residues participate in the hydrophobic core of the domain, either between the ladder and the hook (L979, L989) or in the packing interface between the two ladder helices (L1029, I1036).
The lineage-specific insert βi11 is located between bacterial shared regions βb14 and βb15 (Figures 1, 7A) . The βi11 is found in Acidobacteriaceae, Aquificae, and Proteobacteria (including Eco) . In each bacterial species where it is found, βi11 has a length ranging from 54–69 residues. Comparing Taq with Eco, a 5-residue segment of Taq β (Taq β 895–899) is replaced by the 59-residue Eco βi11, comprising Eco β residues 1122–1180 (Figure 7A).
(A) Sequence alignment comparing the sequence context of Eco RNAP βi11 with the corresponding region of Taq (which lacks βi11 but harbors βi12) . Shaded residues are identical between the two sequences. The experimentally determined secondary structure for Taq is indicated directly below the sequence; filled rectangles denote α-helices, open rectangles denote β-strands. The number scale above the Eco secondary structure corresponds to the Eco β subunit sequence. Above the number scale, black lines denote the sequence regions common to all bacterial RNAPs . The extent of Eco βi11 and Taq βi12 are denoted by the thick magenta line (above) and the thick blue line (below). (B) A portion of the spEM map (contoured at 2.5 σ) is shown (transparent grey surface) with the superimposed Taq core RNAP structure (left, with βi12 colored blue) and the fitted Eco RNAP model (right, with βi11 colored magenta). The view corresponds roughly to the reference view of the Eco RNAP model (top view), shown as a backbone worm and color-coded as follows: αI, αII, ω, gray; β', light pink, except β'i6 is red; β, light cyan, except βi4 is green, βi9 is orange, and βi11 is magenta.
Although a construct corresponding to Eco RNAP βi11 overexpressed and was well behaved, we were unable to obtain crystals suitable for X-ray analysis. The Robetta server (http://robetta.bakerlab.org/) provided an ab initio predicted structure of this short, 59-residue fragment (Figure S8) that is consistent with a number of observations from our structural and sequence analyses:
- The overall predicted structure of βi11 fits well into the corresponding spEM density (Figure 7B, right).
- The termini of the predicted βi11 structure could be readily connected to the corresponding gap in the Eco RNAP β structure with only minor modifications.
- In an alignment of 310 non-redundant βi11 sequences (see Dataset S3), insertions and gaps occur in locations consistent with the predicted structure (i.e. in loops connecting secondary structural elements and away from the RNAP; Figure S8).
- Analysis of the βi11 sequence alignment reveals that most of the conserved residues are hydrophobic in nature and are buried in the hydrophobic core of the βi11 fold (Figure S8C). Two conserved, solvent-accessible polar residues (R1142 and D1166) form an apparently conserved salt-bridge that may stabilize the structure (Figure S8C).
The βi11 was only recently recognized as a distinct, lineage-specific insertion ,. To our knowledge, no information on the effects of deletions or mutations in this region is available. Inspection of the spEM map and the aligned X-ray structure of Taq core RNAP in the region of the β subunit between shared regions βb14 and βb16 revealed a clear discrepancy that corresponds to Taq βi12 (Figure 7B). In our Eco RNAP model, the Taq βi12 was removed and the resulting gap was connected by the loop corresponding to Eco β residues 1200–1207. The predicted structure of Eco βi11 (Figure S8) was then spliced between Eco β residues 1121 and 1181 and oriented to fit into the EM density, resulting in a good fit. The resulting location of Eco βi11 clashed with the position of the β-subunit N-terminus, which was redirected to relieve the clash (Figure 7B).
While the large Eco lineage-specific insertions βi4 and βi9 appear to play only peripheral roles in RNAP function, and the complete deletion of either one results in relatively minor growth defects , β'i6 plays a more important role in Eco RNAP function. Complete deletion, or even partial deletion, of β'i6 is not viable ,. Complete deletion causes a severe defect in RNAP assembly, both in vivo and in vitro ,, but the in vivo–assembled Δβ'i6-RNAP can be obtained from cells simultaneously overexpressing the other RNAP subunits , and partial deletions of β'i6 can be assembled in vitro . Biochemical studies of enzymes with complete or partial β'i6 deletions reveal a number of severe defects. The Δβ'i6-RNAP forms dramatically destabilized open promoter complexes . RNAPs harboring partial deletions in β'i6 are defective in transcript cleavage and have a dramatically reduced transcript elongation rate at subsaturating NTP concentrations . Antibody binding to epitopes within β'i6 inhibit transcription as well as intrinsic transcript cleavage ,.
The β'i6 plays a central role in the pausing/termination behavior of elongating Eco RNAP ,. Full or partial deletions in β'i6 result in RNAPs with dramatically altered pausing behavior ,. A genetic screen for termination-altering mutants in Eco RNAP uncovered 10 positions scattered throughout β'i6 .
These profound effects of β'i6 on Eco RNAP function are likely due to its insertion in the middle of a critical and highly conserved structural feature of the RNAP, the so-called “trigger-loop” (TL), which connects two highly conserved α-helices (TL-helices 1 and 2, TLH1 and TLH2; Figures 1, 8). The TLHs, in turn, interact with another central structural element, the bridge-helix (BH; Figure 8B). The TL tends to be unstructured (open) in RNAP and in the substrate-free TEC but is found in a structured conformation (closed) where it makes many direct contacts with the incoming NTP substrate in the TEC ,. The TL has been proposed to cycle between open and closed conformations at each nucleotide addition step to promote rNTP substrate recognition, enzyme fidelity, and possibly catalysis –.
(A) β-side view of the Eco RNAP TEC model. The RNAP is shown as a backbone worm (αI, αII, grey; β, cyan, except βi4 is green, βi9 is orange, βi11 is magenta; β', pink, except β'i6 is red). β'T1068 (within β'i6), which is phosphorylated by bacteriophage T7 Gp0.7 , is shown as yellow CPK atoms. The nucleic acids are shown as phosphate backbone worms (DNA template strand, dark green; DNA nontemplate strand, light green; RNA transcript, gold). The thick black arrow points in the downstream direction. The boxed region is magnified in (B). (B) Magnified view of boxed region from (A). The obscuring portion of the β subunit has been removed to reveal the inside surface of the RNAP active site channel. Color-coding is the same as (A) but the BH, TLH1, TLH2, the β'-jaw, and β'i6 are highlighted. The active-site Mg2+-ion is shown as a yellow sphere.
Microcin J25 (MccJ25) is a bactericidal 21-residue peptide that inhibits transcription by binding bacterial RNAP within the secondary channel –. Based on saturation mutagenesis of Eco rpoC (the gene encoding the RNAP β' subunit), MccJ25 does not contact β'i6; most amino acid substitutions that yield strong resistance against MccJ25 lie in the BH and the TL ,,. Nevertheless, a deletion of β'i6 perturbs the effects of MccJ25 , likely through the effects of the β'i6 deletion on the TL conformation.
Our positioning of β'i6 in the spEM density (Figures 4, S5, S6) and its connections with the open TL conformation (Figure 8B) are similar to the results of Hudson et al. . The β'i6 sits outside the RNAP active site channel and makes extensive interactions with the β'-jaw (Figure 8B). The N-terminal SBHM domain of β'i6 (SBHMa) faces the secondary channel, consistent with the results of crosslinks mapped from backtracked TECs (in which the 3′-end of the RNA transcript is extruded out the secondary channel) between analogs incorporated into the RNA 3′-end and the N-terminal region of β'i6 . SBHMb faces the downstream double-stranded DNA-binding channel (Figures 5, 8) but does not contact the DNA; the closest approach between the DNA and β'i6 is 16 Å (between β'D1073 and the nontemplate strand backbone phosphate at +14). Moreover, β'i6 is highly acidic over its entire solvent-exposed surface, including the region facing the downstream double-stranded DNA (Figure 5, front view).
Although β'i6 connects readily to the open conformation of the TL via extended linkers (Figure 8B), modeling suggests it would not be able to connect with the closed TL conformation in the modeled position, a conclusion also reached by Hudson et al. . Since the folding of the TL is required for interactions between highly conserved TL-residues and the incoming nucleotide substrate ,,, it is likely that the position of β'i6 must change to accommodate the folded TL conformation at each nucleotide addition step of the transcription cycle.
During bacteriophage T7 infection, the Eco RNAP β' subunit is phosphorylated by the phage-encoded kinase Gp0.7 , and the site of phosphorylation has been identified as a single amino acid in β'i6, T1068 (Figures 5, 8) . Phosphorylation at this site appears to affect pausing, as well as ρ-dependent termination behavior, of Eco RNAP . This site is in the β'i6 loop that makes the closest approach to the downstream DNA, but as discussed above, this region is nevertheless not in close contact with the DNA. The surface is already overall acidic (Figure 5, front view), so it seems unlikely that phosphorylation at this site affects RNAP function by affecting interactions with the downstream DNA.
An understanding of the basic principles of transcription and its regulation has been garnered largely through detailed study of the transcription system of one organism, Eco, which has served as a model for understanding transcription at the molecular and cellular level for more than four decades. The detailed and comprehensive structural description of Eco core RNAP and an Eco RNAP TEC presented here sheds new light on the interpretation of previous biochemical and genetic data. Moreover, the molecular models provide a structural framework for designing future experiments to investigate the function of the Eco RNAP lineage-specific insertions and their role in the Eco transcription program, allowing a fuller exploitation of Eco as a model transcription system.
Materials and Methods
Crystallization and Structure Determination of Eco RNAP β2-βi4
Eco β2-βi4 was amplified by the polymerase chain reaction from the Eco rpoB expression plasmid pRL706  and cloned between the NdeI and BamHI sites of a pET28a-based expression plasmid, creating pSKB2(10-His)Ecoβ2-βi4, encoding Eco β2-βi4 with an N-terminal PreScission protease (GE Healthcare) cleavable His10-tag. The pSKB2(10-His)Ecoβ2-βi4 was transformed into Eco BL21 (DE3) cells. After growing transformed cells in LB medium with kanamycin (50 µg/ml) at 37 °C to an A600 nm = 0.6, isopropyl β-D-1-thiogalactopyranoside was added to a final concentration of 1 mM and cells were grown for an additional 3 h at 37 °C. Cells were harvested by centrifugation, resuspended in lysis buffer (20 mM Tris-HCl, 0.5 M NaCl, 0.5 mM β-mercaptoethanol, 5% v/v glycerol, 0.5 mM phenylmethanesulphonylfluoride), lysed in a continuous-flow French press (Avestin), and clarified by centrifugation. The protein was purified by HiTrap Ni2+-chelating affinity chromatography (GE Healthcare) and the His10-tag was removed using PreScission protease (GE Healthcare). The sample was further purified by a second, subtractive HiTrap Ni2+-chelating affinity chromatography step to remove uncleaved His10-tagged protein and the His10-tag released from the cleaved product, and gel filtration chromatography (Superdex 75, GE Healthcare). The purified protein was concentrated to 17 mg/ml by centrifugal filtration (VivaScience) and exchanged into storage buffer (10 mM Tris-HCl, pH 8.0, 0.15 M NaCl, 1 mM DTT), and stored at –80 °C. Selenomethionyl-substituted protein was prepared by suppression of methionine biosynthesis  and purified by using similar procedures. Reductive methylation of lysine residues was performed as described .
Crystals were grown at 22°C in sitting drops using vapor diffusion by mixing equal volumes of protein solution (0.5 µl at 6 mg/ml in storage buffer) and crystallization solution (0.2 M potassium-sodium tartrate, 20% PEG3350). Crystals (irregular plates) appeared after a few days and grew to a maximum size of about 200×100×50 µm in 1 wk. Crystals were prepared for cryo-crystallography by a quick soak in cryo-solution (0.2 M potassium-sodium tartrate, 35% PEG3350), then flash frozen and stored in liquid nitrogen. Diffraction data were collected at beamline X3A at the National Synchrotron Light Source (NSLS, Brookhaven, NY) and processed using HKL2000 . Six of seven possible Se sites were located within the asymmetric unit using the anomalous signal from the Se1 dataset (Table 1) using SHELX . Heavy atom refinement, phasing, and density modification calculations were performed with SHARP  using the single-wavelength anomalous dispersion data to 1.9 Å-resolution from the Se1 dataset, as well as the 1.6 Å-resolution Se2 dataset (Table 1), yielding an excellent map that allowed automatic building of almost the entire structure using ARP/wARP . Iterative cycles of refinement and model building were carried out using Coot  and RefMac5 . The final model was refined to an R/Rfree of 0.209/229 at 1.6 Å-resolution (Rfree was calculated using 5% random data omitted from the refinement). 97.5% of residues fall in the most favored regions of the Ramachandran plot, while no residues are in disallowed regions.
Crystallization and Structure Determination of Eco RNAP βflap-βi9
The Eco βflap-βi9 (Eco β residues 831–1057) was co-expressed with bacteriophage T4 gp33  as a single operon from a modified pET29a vector  and the complex was purified using standard procedures (K.-A.F.T., P. Deighan, S. Nechaev, A. Hochschild, E.P. Geiduschek, S.A.D., in preparation). Selenomethionyl-substituted complex was produced by suppression of methionine biosynthesis .
Crystals of the complex were grown at 22°C in sitting drops using vapor diffusion by mixing equal volumes of protein solution (1 µl at 7.5–12 mg/ml in 10 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% v/v glycerol, 1 mM β-mercaptoethanol, 1 mM DTT) and crystallization solution (0.2 M tri-potassium citrate, 20% w/v PEG3350). Crystals were prepared for cryo-crystallography by slow exchange into cryo-solution (0.2 M tri-potassium citrate, 20% w/v PEG3350, 20% v/v ethylene glycol), then flash frozen and stored in liquid nitrogen. Diffraction data were collected at beamline X3A at the NSLS (Brookhaven, NY) and processed using HKL2000 (Table S1) . A molecular replacement solution was obtained using the Native amplitudes (Table S1) with a search model consisting of a homology model of the Eco βflap based on the Taq βflap generated using MODELLER (the search model excluded the flexible flap-tip) . The molecular replacement phases were used to locate four Se sites from the anomalous signal of the Se dataset (Table S1). Heavy atom refinement, phasing, and density modification calculations were performed with SHARP  using the single-wavelength anomalous dispersion data from the Se dataset (Table S1) yielding an interpretable map (Figure S3). Iterative cycles of refinement and model building were carried out using Coot  and RefMac5 . The final model was refined to an R/Rfree of 0.265/0.291 at 3.0 Å-resolution (Rfree was calculated using 5% random data omitted from the refinement). 95.25% of residues fall in the most favored regions of the Ramachandran plot, while no residues are in disallowed regions.
Cryo-EM Reconstruction of Eco RNAP by Single-Particle Averaging
Purification of Eco core RNAP from an overexpression system was performed as described . This results in highly pure Eco RNAP core enzyme, which is deficient in the ω subunit. Eco RNAP holoenzyme was prepared by incubating core RNAP (3 mg/ml in 10 mM Tris-HCl, pH 8, 0.2 M NaCl, 0.1 mM EDTA, 5 mM DTT) with a 5-fold molar excess of σ70 for 30 min at room temperature. For cryo-EM, a 5 µl sample (0.1 mg/ml in the same buffer) was applied to a Quantifoil grid coated with holey carbon film previously made hydrophilic by glow-discharge. The grid was blotted with filter paper and then immediately plunged into liquid ethane slush. The sample was imaged at 50,000× magnification with a Tecnai F20 transmission electron microscope operating at 200 kV. Micrographs displaying minimal astigmatism were digitized at a 14 µm interval (corresponding to 2.8 Å on the image) using a Zeiss SCAI flat-bed densitometer (ZI/Carl Zeiss). Individual particles were selected by eye and windowed in 90×90 pixel images. Defocus values were estimated from digitized micrographs using ctfit (EMAN) .
We generated a spEM reconstruction of Eco RNAP by analyzing ∼42,000 cryo-images of Eco RNAP particles (Figures 4A, S4–S6). Particle image orientation parameters were approximately determined using reference projections of a volume generated by low-pass filtration of the Taq core RNAP X-ray structure  to 35 Å-resolution. We used a previously devised protocol in which image orientation parameters are iteratively refined by cycling through sets comprising relatively small numbers of reference projections . After a large number of iterations (130) using the SPIDER software package , we obtained a structure in which well-defined densities not present in the original model volume were apparent. Further refinement of image orientation parameters by projection matching  using the SPARX software package  yielded a structure of Eco core RNAP with a 0.5 Fourier-shell cutoff resolution of about 11.2 Å (Figure S4). For further analysis, the map was Fourier filtered using an ahyperbolic tangent low-pass filter  as implemented in the SPARX software package  with a stop-band frequency of 0.28 and a fall-off of 0.45.
Alignments for the Eco lineage-specific insertions (see Datasets S1–S3) were created using the bacterial lineage-specific insertions alignments from Lane et al.  as a starting point. The final alignments were created by iterative cycles in which sequences that did not match the Eco domains were removed, followed by re-alignment with MUSCLE  or PCMA .
Electron Microscopy Data Bank: The single-particle cryoEM reconstruction volume has been deposited under ID code EMD-5169. Protein Data Bank: Atomic coordinates and structure factors for Eco RNAP β2-βi4 have been deposited under accession code 3LTI. The EM-fitted coordinate model of Eco core RNAP has been deposited under accession code 3LU0. The coordinates of the Eco RNAP TEC model are available in the Supporting Information (Dataset S4).
beta-i9_blast_to_fas_to_aln_man4_cull.msf – Sequence alignment (msf format) containing 307 non-redundant βi9 sequences.
(0.07 MB TDS)
beta-i4_blast_to_fas_to_aln_man5_cull.msf – Sequence alignment (msf format) containing 316 non-redundant βi4 sequences (only Eco-like βi4 sequences comprising two BBM2 domains).
(0.12 MB TDS)
beta-i11_blast_to_fas_to_aln_man4_cull.msf – Sequence alignment (msf format) containing 310 non-redundant βi11 sequences.
(0.07 MB TDS)
Eco_TEC_model.pdb – Coordinates (PDB format) of the Eco TEC model.
(2.22 MB TXT)
Eco β2-βi4 electron density map. Stereo view of the 1.6 Å-resolution 2|Fo|–|Fc| map, contoured at 1.5 σ. The model is shown as sticks, with nitrogen atoms colored blue, oxygen atoms red, and carbon atoms colored according to Figure 2B. Water molecules are represented as red spheres. Shown is the region surrounding dimethylated  K324.
(2.07 MB TIF)
Comparison of Taq β2 and Eco β2-βi4. The two structures were superimposed over 100 α-carbon positions (excluding flexible loops connecting secondary structural elements), yielding a root-mean-square-deviation of 1.68 Å. Other than the insertion of βi4 in Eco, significant differences in the β2 structures include: (i) the loop connecting the first two β-strands of the β2 domain, where Eco has a 5-residue insertion (Eco β residues 164–168, disordered in the structure), and (ii) the loop connecting the last two α-helices of the β2 domain, which includes a 7-residue insertion present in Taq β (Taq β residues 293–299; Figure 2A).
(5.47 MB TIF)
Eco βflap-βi9 electron density map. Stereo view of the 3.0 Å-resolution 2|Fo|–|Fc| map, contoured at 1.0 σ. The model is shown as sticks, with nitrogen atoms colored blue, oxygen atoms red, and carbon atoms colored according to Figure 3B. Shown is a region of the βi9 ladder helices.
(2.90 MB TIF)
Image analysis. (A) Unprocessed electron micrograph of a field of Eco RNAP molecules preserved in vitreous ice. Selected particles are circled. (B) Distribution of image orientations, plotted as a polar-angle diagram, viewed along the θ = 0° axis. (C) Fourier shell correlation , as a function of spatial frequency.
(1.54 MB TIF)
Back, bottom, channel, and front views of spEM density and fit of Eco RNAP model. For each view, the left image shows the spEM density map (grey surface, contoured at 2.5 σ), and the right image shows the spEM density map (grey transparent surface) with the fitted Eco RNAP homology model superimposed (excluding ω, the C-terminal 41 residues of β', and βi9). The Eco RNAP homology model is shown as a backbone worm, color-coded as in Figure 4.
(7.72 MB TIF)
β'-side, bottom, β-side, and top views of spEM density and fit of Eco RNAP model. For each view, the left image shows the spEM density map (grey surface, contoured at 2.5 σ), and the right image shows the spEM density map (grey transparent surface) with the fitted Eco RNAP homology model superimposed (excluding ω, the C-terminal 41 residues of β', and βi9). The Eco RNAP homology model is shown as a backbone worm, color-coded as in Figure 4.
(8.62 MB TIF)
Structural features of Eco βi9. Two views of Eco βi9 are shown: The left column shows the “front” view (the side facing the “hook”), and the right column shows the “back” view (the side away from the “hook”). The top row shows the backbone ribbon. The middle row shows the structure (with transparent molecular surface) colored in a gradient according to the Blosum 62 information score (as determined by the program PFAAT ) calculated from an alignment of 307 non-redundant βi9 sequences (see Supporting Information). The color gradient covers scores from 0 to 1 (0, white; 0.5, yellow; 1.0, red). Individual residues with score ≥0.75 are labeled. Underlined residues denote residues with significant solvent accessibility. The bottom row shows the molecular surface colored according to the electrostatic surface distribution of the solvent-accessible surface in units of kT (−5, red; 0, white; +5, blue), as calculated by APBS .
(6.13 MB TIF)
Details of ab initio-predicted Eco βi11 structure. (A) Sequence context of Eco RNAP βi11. The secondary structure for the predicted Eco βi11 structure (determined using the Robetta server (http://robetta.bakerlab.org/)) is indicated directly below the sequence (filled rectangles denote α-helices). Above the number scale, black lines denote the sequence regions common to all bacterial RNAPs . Gaps in the βi11 sequence with numbers above denote the location and residue length of insertions in an alignment of 310 non-redundant βi11 sequences (see Supporting Information). The insertions all occur in loops connecting the helices. The extent of Eco βi11 is denoted by the thick magenta line (above). (B) Backbone ribbon of the predicted Eco βi11 structure. The grey spheres mark α-carbon positions surrounding the insertions from the sequence alignment. The numbers pointing to each insertion point denote the insertion length. (C) The predicted Eco βi11 structure is colored in a gradient according to the Blosum 62 information score (as determined by the program PFAAT ) calculated from the alignment of 310 non-redundant βi11 sequences (see Supporting Information). The color gradient covers scores from 0 to 1 (0, white; 0.5, yellow; 1.0, red). Individual residues with score ≥0.75 are labeled. Nearly all of the conserved hydrophobic residues are buried in the hydrophobic core of the structure. Two solvent-accessible polar residues (R1142 and D1166) form an apparently conserved salt-bridge that may stabilize the structure.
(3.18 MB TIF)
We thank Deena Oren of The Rockefeller University Structural Biology Resource Center (RU-SBRC) for expert assistance. We thank Wuxian Shi at the National Synchrotron Light Source beamline X3A for assistance with data collection. We thank K.D. Derr, Bill Rice, and Ruben Diaz-Avalos from the New York Structural Biology Center (NYSBC) for helpful technical support in using the Tecnai F20 electron microscope.
The author(s) have made the following declarations about their contributions: Conceived and designed the experiments: NJO KAFT RL FJA SAD. Performed the experiments: NJO JB KAFT RL FJA SAD. Analyzed the data: NJO JB WJL KAFT RL FJA SAD. Contributed reagents/materials/analysis tools: FJA. Wrote the paper: FJA SAD.
- 1. Jokerst R. S, Weeks J. R, Zehring W. A, Greenleaf A. L (1989) Analysis of the gene encoding the largest subunit of RNA polymerase II in Drosophila. Mol Gen Genet 215: 266–275.
- 2. Sweetser D, Nonet M, Young R. A (1987) Prokaryotic and eukaryotic RNA polymerases have homologous core subunits. Proc Natl Acad Sci U S A 84: 1192–1196.
- 3. Lane W. J, Darst S. A (2009) Molecular evolution of multi-subunit RNA polymerases: sequence analysis. J Mol Biol 395: 671–685.
- 4. Iyer L. M, Koonin E. V, Aravind L (2004) Evolution of bacterial RNA polymerase: implications for large-scale bacterial phylogeny, domain accretion, and horizontal gene transfer. Gene 335: 73–88.
- 5. Zhang G, Campbell E. A, Minakhin L, Richter C, Severinov K, et al. (1999) Crystal structure of Thermus aquaticus core RNA polymerase at 3.3 Å resolution. Cell 98: 811–824.
- 6. Murakami K, Masuda S, Darst S. A (2002) Structural basis of transcription initiation: RNA polymerase holoenzyme at 4 Å resolution. Science 296: 1280–1284.
- 7. Vassylyev D. G, Sekine S, Laptenko O, Lee J, Vassylyeva M. N, et al. (2002) Crystal structure of a bacterial RNA polymerase holoenzyme at 2.6 Å resolution. Nature 417: 712–719.
- 8. Vassylyev D. G, Vassylyeva M. N, Perederina A, Tahirov T. H, Artsimovitch I (2007) Structural basis for transcription elongation by bacterial RNA polymerase. Nature 448: 157–162.
- 9. Iyer L. M, Koonin E. V, Aravind L (2003) Evolutionary connection between the catalytic subunits of DNA-dependent RNA polymerases and eukaryotic RNA-dependent RNA polymerases and the origin of RNA polymerases. BMC Struct Biol 3: 1–23.
- 10. Chlenov M, Masuda S, Murakami K. S, Nikiforov V, Darst S. A, et al. (2005) Structure and function of lineage-specific sequence insertions in the bacterial RNA polymerase b' subunit. J Mol Biol 353: 138–154.
- 11. Gross C. A, Chan C. L, Lonetto M. A (1996) A structure/function analysis of Escherichia coli RNA polymerase. Philos Trans R Soc London, B, Biol Sci 351: 475–482.
- 12. Mooney R. A, Artsimovitch I, Landick R (1998) Information processing by RNA polymerase: recognition of regulatory signals during RNA chain elongation. J Bacteriol 180: 3265–3275.
- 13. Darst S. A, Opalka N, Chacon P, Polyakov A, Richter C, et al. (2002) Conformational flexibility of bacterial RNA polymerase. Proc Natl Acad Sci U S A 99: 4296–4301.
- 14. Bose D, Pape T, Burrows P. C, Rappas M, Wigneshweraraj S, et al. (2008) Organization of an activator-bound RNA polymerase holoenzyme. Mol Cell 32: 337–346.
- 15. Hudson B, Quispe J, Lara-Gonzalez S, Kim Y, Berman H, et al. (2009) Three-dimensional EM structure of an intact activator-dependent transcription initiation complex. Proc Natl Acad Sci U S A 106: 19830–19835.
- 16. Kim D. E, Chivian D, Baker D (2004) Protein structure prediction and analysis using the Robetta server. Nucleic Acids Res 32: Suppl 2W526–W531.
- 17. Severinov K, Kashlev M, Severinova E, Bass I, McWilliams K, et al. (1994) A non-essential domain of E. coli RNA polymerase required for the action of the termination factor Alc. J Biol Chem 269: 14254–14259.
- 18. Artsimovitch I, Svetlov V, Murakami K. S, Landick R (2003) Co-overexpression of Escherichia coli RNA polymerase subunits allows isolation and analysis of mutant enzymes lacking lineage-specific sequence insertions. J Biol Chem 278: 12344–12355.
- 19. Lane W. J, Darst S. A (2009) Molecular evolution of multi-subunit RNA polymerases: structural analysis. J Mol Biol 395: 686–704.
- 20. Rayment I (1997) Reductive alkylation of lysine residues to alter crystallization properties of proteins. Methods Enzymol 276: 171–179.
- 21. Hendrickson W, Norton J. R, LeMaster D. M (1990) Selenomethionyl proteins produced for analysis by multiwavelength anomalous diffraction (MAD). EMBO J 9: 1665–1672.
- 22. Borukhov S, Severinov K, Kashlev M, Lebedev A, Bass I, et al. (1991) Mapping of trypsin cleavage and antibody-binding sites and delineation of a dispensable domain in the ß subunit of Escherichia coli RNA polymerase. J Biol Chem 266: 23921–23926.
- 23. Opalka N, Mooney R. A, Richter C, Severinov K, Landick R, et al. (1999) Direct localization of a b subunit domain on the three-dimensional structure of Escherichia coli RNA polymerase. Proc Natl Acad Sci USA 97: 617–622.
- 24. Basokur A. T (1998) Digital filter design using the hyperbolic tangent functions. J Balkan Geophys Soc 1: 14–18.
- 25. Hohn M, Tang G, Goodyear G, Baldwin P. R, Huang Z, et al. (2007) SPARX, a new environment for cryo-EM image processing. J Structural Biol 157: 47–55.
- 26. Kastner B, Fischer N, Golas M. M, Sander B, Dube P, et al. (2008) GraFix: sample preparation for single-particle electron cryomicroscopy. Nature Meth 5: 53–55.
- 27. Tan R. K-Z, Devkota B, Harvey S. C (2008) YUP.SCX: coaxing atomic models into medium resolution electron density maps. J Structural Biol 163: 163–174.
- 28. Korzheva N, Mustaev A, Kozlov M, Malhotra A, Nikiforov V, et al. (2000) A structural model of transcription elongation. Science 289: 619–625.
- 29. Zhang G, Darst S. A (1998) Structure of the Escherichia coli RNA polymerase a subunit amino-terminal domain. Science 281: 262–266.
- 30. Westblade L. F, Minakhin L, Kuznedelov K, Tackett A. J, Chang E, et al. (2008) Rapid isolation and identification of bacteriophage T4-encoded modifications of Escherichia coli RNA polymerase: a generic method to study bacteriophage/host interactions. J Proteome Res 7: 1244–1250.
- 31. Snyder L, Gold L, Kutter E (1976) A gene of bacteriophage T4 whose product prevents true late transcription on cytosine-containing T4 DNA. Proc Natl Acad Sci U S A 73: 3098–3102.
- 32. Snyder L, Jorissen L (1988) Escherichia coli mutations that prevent the action of the T4 unf/alc protein map in an RNA polymerase gene. Genetics 118: 173–180.
- 33. Nene V, Glass R (1984) Genetic studies on the b subunit of Escherichia coli RNA polyerase VI. A redundant region in the b polypeptide. Mol Gen Genet 196: 64–67.
- 34. Murakami K, Masuda S, Campbell E. A, Muzzin O, Darst S. A (2002) Structural basis of transcription initiation: an RNA polymerase holoenzyme/DNA complex. Science 296: 1285–1290.
- 35. Zakharova N, Bass I, Arsenieva E, Nikiforov V, Severinov K (1998) Mutations in and monoclonal antibody binding to evolutionary hypervariable region of E. coli RNA polymerase b' subunit inhibit transcript cleavage and transcript elongation. J Biol Chem 273: 19371–19374.
- 36. Luo J, Krakow J. S (1992) Characterization and epitope mapping of monoclonal antibodies directed against the beta' subunit of the Escherichia coli RNA polymerase. J Biol Chem 267: 18175–18181.
- 37. Weilbacher R. G, Hebron C, Feng G, Landick R (1994) Termination-altering amino acid substitutions in the beta' subunit of Escherichia coli RNA polymerase identify regions involved in RNA chain elongation. Genes & Development 8: 2913–2927.
- 38. Wang D, Bushnell D. A, Westover K. D, Kaplan C. D, Kornberg R. D (2006) Structural basis of transcription: role of the trigger loop in substrate specificity and catalysis. Cell 127: 941–954.
- 39. Vassylyev D. G, Vassylyeva M. N, Zhang J, Palangat M, Artsimovitch I, et al. (2007) Structural basis for substrate loading in bacterial RNA polymerase. Nature 448: 163–168.
- 40. Kaplan C. D, Larsson K-M, Kornberg R. D (2008) The RNA polymerase II trigger loop functions in substrate selection and is directly targeted by alpha-amanitin. Mol Cell 30: 547–556.
- 41. Kireeva M. L, Nedialkov Y. A, Cremona G. H, Purtov Y. A, Lubkowska L, et al. (2008) Transient reversal of RNA polymerase II active site closing controls fidelity of transcription elongation. Mol Cell 30: 557–566.
- 42. Bar-Nahum G, Epshtein V, Ruckenstein A. E, Rafikov R, Mustaev A, et al. (2005) A ratchet mechanism of transcription elongation and its control. Cell 120: 183–193.
- 43. Delgado M. A, Rintoul M. R, Farias R. N, Salomon R. A (2001) Escherichia coli RNA polymerase is the target of the cyclopeptide antibiotic microcin J25. J Bacteriol 183: 4543–4550.
- 44. Mukhopadhyay J, Sineva E, Knight J, Levy R. M, Ebright R. H (2004) Antibacterial peptide microcin J25 inhibits transcription by binding within and obstructing the RNA polymerase secondary channel. Mol Cell 14: 739–751.
- 45. Salomon R. A, Farias R. N (1992) Microcin-25, a novel antimicrobial peptide produced by Escherichia-coli. J Bacteriol 174: 7428–7435.
- 46. Yuzenkova J, Delgado M. A, Nechaev S, Savalia D, Epshtein V, et al. (2002) Mutations of bacterial RNA polymerase leading to resistance to microcin J25. J Biol Chem 277: 50867–50875.
- 47. Zillig W, Fujiki H, Blum W, Janekovi D, Schweig M, et al. (1975) In vivo and in vitro phosphorylation of DNA-dependent RNA polymerase of Escherichia coli by bacteriophage-T7-induced protein kinase. Proc Natl Acad Sci U S A 72: 2506–2510.
- 48. Severinova E, Severinov K (2006) Localization of the Escherichia coli RNA polymerase beta' subunit residue phosphorylated by bacteriophage T7 kinase Gp0.7. J Bacteriol 188: 3470–3476.
- 49. Severinov K, Mooney R, Darst S. A, Landick R (1997) Tethering of the large subunits of Escherichia coli RNA polymerase. J Biol Chem 272: 24137–24140.
- 50. Doublie S (1997) Preparation of selenomethionyl proteins for phase determination. Methods Enzymol 276: 523–530.
- 51. Otwinowski Z, Minor W (1997) Processing of X-ray diffraction data collected in oscillation mode. Methods Enzymol 276: 307–326.
- 52. Sheldrick G. M (2008) A short history of SHELX. Acta Crystallogr A 64: 112–122.
- 53. de La Fortelle E, Irwin J. J, Bricogne G (1997) SHARP: a maximum-likelihood heavy-atom parameter refinement and phasing program for the MIR and MAD methods. In: Bourne P, Watenpaugh K, editors. Crystallographic computing. Boston: Kluwer Academic Publishers. pp. 1–9.
- 54. Langer G, Cohen S. X, Lamzin V. S, Perrakis A (2008) Automated macromolecular model building for X-ray crystallography using ARP/wARP version 7. Nature Protocols 3: 1171–1179.
- 55. Emsley P, Cowtan K (2004) Coot: model-building tools for molecular graphics. Acta Crystallogr D Biol Crystallogr 60: 2126–2132.
- 56. Murshudov G. N, Vagin A. A, Dodson E. J (1997) Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallogr D Biol Crystallogr D53: 240–255.
- 57. Nechaev S, Kamali-Moghaddam M, Andre E, Leonetti J-P, Geiduschek E. P (2004) The bacteriophage T4 late-transcription coactivator gp33 binds the flap domain of Escherichia coli RNA polymerase. Proc Natl Acad Sci U S A 101: 17365–17370.
- 58. Campbell E. A, Darst S. A (2000) The anti-s factor SpoIIAB forms a 2:1 complex with sF, contacting multiple conserved regions of the s factor. J Mol Biol 300: 17–28.
- 59. Sali A, Potterton L, Yuan F, van-Vlijmen H, Karplus M (1995) Evaluation of comparative protein modeling by MODELLER. Proteins 23: 318–326.
- 60. Opalka N, Chlenov M, Chacon P, Rice W. J, Wriggers W, et al. (2003) Structure and function of the transcription elongation factor GreB bound to bacterial RNA polymerase. Cell 114: 335–345.
- 61. Ludtke S. J, Baldwin P. R, Chiu W (1999) EMAN: semi-automated software for high resolution single particle reconstructions. J Structural Biol 128: 82–97.
- 62. Craighead J. L, Chang W. H, Asturias F. J (2002) Structure of yeast RNA polymerase II in solution: implications for enzyme regulation and interaction with promoter DNA. Structure (Camb) 10: 1117–1125.
- 63. Frank J, Radermacher M, Penczek P, Zhu J, Li Y, et al. (1996) SPIDER and WEB: processing and visualization of images in 3D electron microscopy and related fields. J Struct Biol 116: 190–199.
- 64. Penczek P, Grassucci R. A, Frank J (1994) The ribosome at improved resolution: new techniques for merging and orientation refinement in 3D cryo-electron microscopy of biological particles. Ultramicroscopy 53: 251–270.
- 65. Edgar R. C (2004) MUSCLE: a multiple sequence alignment method with reduced time and space complexity. BMC Bioinformat 5: 113.
- 66. Pei J, Sadreyev R, Grishin N. V (2003) PCMA: fast and accurate multiple sequence alignment based on profile consistency. Bioinformatics 19: 427–428.
- 67. Saxton W. O, Baumeister W (1982) The correlation averaging of a regularly arranged bacterial-cell envelope protein. J Microsc 127: 127–138.
- 68. Harauz G, van Heel M (1986) Exact filters for general geometry three-dimensional reconstruction. Optik 73: 146–156.
- 69. Baker N. A, Sept D, Joseph S, Holst M. J, McCammon J. A (2001) Electrostatics of nanosystems: application to microtubules and the ribosome. Proc Natl Acad Sci U S A 98: 10037–10041.
- 70. Caffrey D. R, Dana P. H, Mathur V, Ocano M, Hong E-J, et al. (2007) PFAAT version 2.0: a tool for editing, annotating, and analyzing multiple sequence alignments. BMC Bioinformat 8: 381.