Mapping of Trypsin Cleavage and Antibody-binding Sites and Delineation of a Dispensable Domain in the #I Subunit of Escherichia coli RNA Polymerase*

We have mapped principal sites in the Escherichia coli RNA polymerase molecule that are exposed to attack by trypsin under limited proteolysis conditions. The 1342-amino acid-long fi subunit is alternatively cleaved at Argeo3 or Lyseos. The cleavage occurs adja- cer,t to a dispensable domain (residues 940-1040) that is absent in the homologous RNA polymerase subunits from chloroplasts, eukaryotes, and archaebacteria. In E. coli, this region can be disrupted with genetic dele- tions and insertions without the loss of RNA polymerase function. Insertion of 127 amino acids into this region introduces a new highly labile site for trypsin proteolysis. The dispensable domain carries the epitope for monoclonal antibody PYN-6 (near residue lOOO), which can be used for anchoring the catalytically ac- tive enzyme on a solid support. We also report the identification of a secondary trypsin cleavage at Ar8‘ of the B’ subunit within a putative zinc-binding domain that is conserved in prokaryotes Trypsin Proteolysis of RNA Polymerase-RNA polymerase core enzyme was isolated as described (23) with modifications to be reported elsewhere. The wild-type enzyme was obtained from E. coli C600, and the enzyme carrying the elongated Bin. subunit from E. coli MKDC747 (QT988). The u subunit was prepared from the overex- pression strain as described (24). Type XI11 L-1-tosylamido-2-phen-ylethyl chloromethyl ketone-treated trypsin was purchased from Sigma. The 2 0 4 standard digestion mixture contained 5 pg of RNA polymerase holoenzyme in 40 mM Tris-HC1, pH 7.9,40 mM KCl, 5% (v/v) glycerol, and either 50 or 5 ng of trypsin in the case of the wild-type or QT988 RNA polymerase, respectively. The samples were incubated for 30 min at 32 “C; and the reactions were terminated by adding phenylmethylsulfonyl fluoride to a final concentration of 5 mM, followed by electrophoresis on sodium dodecyl sulfate-10 and -5% polyacrylamide gels (25). N-terminal Sequencing of Trypsin Cleavage Products-The bands were excised from the gel and electroeluted using a Bio-Rad electroe-luter. The eluted material (-100 pl) was precipitated with 2 volumes of cold acetone; and the pellets were washed with 70% acetone, dissolved in lop1 of 50% formic acid, and precipitated by adding 100 pl of 10% trichloroacetic acid. The precipitates were washed twice with 70% acetone, and their N-terminal sequences were analyzed in 20 cycles of Edman degradation using an Applied Biosystems Protein Sequencer at the Columbia University Core Protein Facility.

from each other only by protein denaturation (7). The localities in the linear sequence of the core subunits that participate in RNA polymerase basic function can be deduced from the mapping of derivatization sites of affinity probes (8)(9)(10) and analysis of lethal mutations (11,12) as well as from homology alignments with evolutionarily distant organisms (see Fig. lA) (13,14).
The focus of this report is a region in the subunit shown in Fig. lA that is located between two highly conserved sections of the linear sequence. Our interest in this region stems from the presumed functional cooperation between the flanking domains that harbor the sites of lethal mutations E813K (Glua13 + Lys) (15), K1065R (LYS''~~ + Arg) (111, and H1237A (His'237 + Ala) (lo), which disrupt the catalytic function of RNA polymerase. The sequence region between them that is centered around residue 1000 is present only in eubacteria, where it is highly variable. In other major groups of organisms including closely related chloroplasts, this region is missing, which results in an -100-residue-long gap in the sequence alignment. On this basis, it can be suggested that the nonconserved region is looped out in the three-dimensional structure of RNA polymerase, whereas the flanking domains interact to perform the enzyme's catalytic function.
The notion of an exposed loop in this general area seemed to agree with the early observations that, upon limited trypsin proteolysis of RNA polymerase, the p subunit is cleaved once approximately one third along its length (16,17). In a previous study from one of our laboratories, it was reported that the larger and smaller trypsin fragments of the p subunit represent its amino-and carboxyl-terminal sections, respectively, placing the cleavage site in the general vicinity of the nonconserved region (17). We also found that monoclonal antibodies PYN-2 and PYN-6 selectively reacted with the larger and smaller trypsin fragments of the subunit, respectively. However, the reported localization of the trypsin cleavage and antibody-binding sites based on indirect data was not precise.
The notion that a significant section of the p subunit in this area may be dispensable for biological function was first put forward by one of us (18, 19) on the basis of the isolation of a viable deletion mutant of rpoB missing -50 amino acids. However, the location of this deletion based on indirect data was reported in a more distal region of the 6 subunit (18) that turned out to be highly conserved when sequence comparison became possible. Thus, when this work was initiated, the available data on homology alignment, proteolytic cleavage, and genetic mapping lacked the sequence level resolution and were in disagreement with each other. We report here the 23921 Trypsin Cleavage and Epitope Mapping in RNA Polymerase precise localization of the trypsin cleavage and PYN-6 antibody-binding sites on the amino acid sequence level and in relation to the previously reported (18-20) and newly constructed insertions and deletions in this area.

MATERIALS AND METHODS
Bacterial Strains and Plosmids-The map positions of the rpoB deletions and insertions used in this work are indicated in Fig. IA. The E. coli strains used were C600 (wild type), W31107 rpoBA1570- A(967-1028)) (18), and MKDC747 (92'988) (20). The principal 0 subunit expression plasmid used was pMKA92 (II), which carries a rifampicin-resistant allele of the rpoB gene under the control of the inducible lac promoter.

(
rpoB Deletions and Insertions-The sequence of rpoBA1570-I (originally obtained as a chromosomal mutation) was determined by cloning it on a plasmid using thepolA(Ts) technique (21), subcloning into the pTZ18/19 vectors, and sequencing on both strands from the polylinker. The deletion occurred between two 9-base pair direct repeats (effectively removing one of them) and removed 186 base pairs (62 codons) encoding amino acid residues 967-1028 inclusive. The deletion is therefore referred to as A(967-1028).
QT988 is a fortuitous duplication of 127 codons of the subunit (Asp434-Ile661) inserted in-frame in the TaqI site between codons 988 A. and 989. It was isolated in the course of in vitro manipulations with cloned rpoB involving TaqI restriction and ligations. The insertion was transferred into the chromosome, where it could function as the sole rpoB allele in the cell (20). The map position of Q2'988 originally inferred from restriction analysis of DNA has now been confirmed by sequencing. rpoB deletions and insertions originating from TaqI restriction sites were constructed in the pMKA92 plasmid as follows. In the first step, the plasmid DNA was linearized by random cuts at TaqI sites, and its termini were filled in using Klenow DNA polymerase. The DNA was ligated with the EcoRI fragment (with termini filled in using Klenow DNA polymerase) from phage mpl7Km carrying the kanamycin resistance gene. Kanamycin-resistant transformants were selected and screened for the appearance of inducible truncated fragments of the 0 polypeptide that were visualized by gel electrophoresis. The size of these fragments corresponded to the known positions of TaqI restriction sites within the rpoB gene and to the location of kanamycin inserts determined in each case by restriction mapping. In the next step, the kanamycin cassette was excised from individually isolated plasmids with the inserts using BamHI, followed by religation. This procedure was expected to generate insertions of a 22-base pair BamHI linker between the flushed termini of the original TaqI site, thus restoring the rpoB reading frame. The transformants were screened for the restoration of the rpoB reading frame manifested by   (26) is aligned with corresponding segments of homologous RNA polymerase subunits from (top to bottom) P. putida (P. p.) (47); chloroplasts from spinach ( S ) (38), tobacco ( T ) (48), and liverwort ( L ) (49); and Saccharomyces cerevisiae (14), Drosophila mebnogaster (50); and Sulfolobus acidocaldarim (51). The dots symbolize identity to the E. coli sequence, and the hyphens represent gaps. The horizontal bars over the sequence represent deletions, and the arrows indicate insertion and substitution mutations. All mutations have viable phenotypes unless indicated otherwise. Note that the large insertion QT988 (127 amino acids) is not drawn to scale. B, the alignment is shown of the two bacterial p' subunit sequences (27,47) in the area of the putative zinc-binding domain with the corresponding segments from chloroplasts (38,48,49).
the disappearance of the truncated B fragments and the reappearance of inducible normal-sized / 3 fragments visualized as a major overexpressed protein by gel electrophoresis. In the third step, deletions around the introduced linker were generated by opening the plasmids with BamHI, limited digestion with the Bal-31 nuclease, religation, and screening for the maintenance of the reading frame (see above). The complete collection of these mutations will be described elsewhere. Here we present the insertion Q952 and three associated deletions (A(952-964), A(947-967), and A(937-983)) (see Fig. 1). Their map location was verified by DNA sequencing, The three mutations originating from the AluI site at codon 1010 (insertions MIOIO-fs and MI010 and deletion AAIOIO) were obtained previously (20). Their breakpoints have not been verified by DNA sequencing and are therefore tentative. A A I O I O removes -15 amino acids judging by a shift in the electrophoretic mobility of the p subunit (20).
Plasmid-borne mutants were tested for biological function by monitoring their ability to confer isopropyl-l-thio-/3-D-galactopyranosideinducible rifampicin resistance on a rifampicin-sensitive host as described previously (11).
Monoclonal Antibodies-The isolation and initial characterization of the anti$ subunit mAbs' PYN-2 and PYN-6 and the protocols of Western blots with separated subunits and their fragments have been reported (17). The dot blot activity assay of immobilized polymerase was performed essentially as described (22) using 1 pg of ascites fluid protein/dot. It should be noted that immobilized RNA polymerase apparently used as template the endogenous E. coli DNA present in the extracts since the addition of exogenous DNA to the assay did not have any effect. The activity that was observed in this assay could be completely inhibited by rifampicin, as expected.
Limited Trypsin Proteolysis of RNA Polymerase-RNA polymerase core enzyme was isolated as described (23) with modifications to be reported elsewhere. The wild-type enzyme was obtained from E. coli C600, and the enzyme carrying the elongated Bin. subunit from E. coli MKDC747 (QT988). The u subunit was prepared from the overexpression strain as described (24). Type XI11 L-1-tosylamido-2-phenylethyl chloromethyl ketone-treated trypsin was purchased from Sigma. The 2 0 4 standard digestion mixture contained 5 pg of RNA polymerase holoenzyme in 40 mM Tris-HC1, pH 7.9,40 mM KCl, 5% (v/v) glycerol, and either 50 or 5 ng of trypsin in the case of the wildtype or QT988 RNA polymerase, respectively. The samples were incubated for 30 min at 32 "C; and the reactions were terminated by adding phenylmethylsulfonyl fluoride to a final concentration of 5 mM, followed by electrophoresis on sodium dodecyl sulfate-10 and -5% polyacrylamide gels (25).

N-terminal Sequencing of Trypsin Cleavage Products-The bands
were excised from the gel and electroeluted using a Bio-Rad electroeluter. The eluted material (-100 pl) was precipitated with 2 volumes of cold acetone; and the pellets were washed with 70% acetone, dissolved in lop1 of 50% formic acid, and precipitated by adding 100 pl of 10% trichloroacetic acid. The precipitates were washed twice with 70% acetone, and their N-terminal sequences were analyzed in 20 cycles of Edman degradation using an Applied Biosystems Protein Sequencer at the Columbia University Core Protein Facility.

Mapping of Trypsin Cleavage Sites in p' and @ Subunits-
When RNA polymerase is treated with trypsin, a pattern of distinct fragments is generated, which can be visualized by combining the resolution of a 10% (Fig. 2 A ) , and a 5% (Fig.  2B) polyacrylamide gel. Three principal products can be seen after limited trypsin digestion of the wild-type holoenzyme ( Fig. 2 A , lane 2): bands bl, bz, and s, with apparent M, values of about 105,000,50,000, and 43,000, respectively. Under these conditions, 30-50% of the p and p' (Fig. 2B, lane 2 ) and a ( Fig. 2 A , lane 2 ) subunits remain intact, whereas the u subunit is cleaved completely. Of the three major products, band s is likely to be the fragment of the u subunit that has been observed by others (6) because it is not found among the products of the core enzyme digestion (Fig. 2A, lane 3 ) . The cleavage products bl and b2 apparently correspond, respectively, to the longer and shorter fragments of the p subunit The abbreviation used is: mAbs, monoclonal antibodies. observed earlier (see Introduction). The addition of sonicated denatured calf thymus DNA causes a noteworthy qualitative change of the cleavage pattern (Fig. 2B, lane 4 ) . Under these conditions, the p' subunit is completely cleaved, giving rise to a new products, band c (Mr -145,000), with a mobility close to that of the p and p' subunits.
Bands bl, b2, and c were isolated from the gel, and their Nterminal sequences were determined in 20 consecutive cycles of Edman degradation. The comparison of the results with the known sequences of RNA polymerase subunits (26,27) clearly showed that band c contained homogeneous material with the N terminus corresponding to Glf2 of the p' subunit.
The analysis of band bl revealed a 2:l mixture of two overlapping sequences starting with Met' and Val2 of the j3 polypeptide. This result agrees with the report that, in purified E. coli RNA polymerase, -30% of the subunits have lost their Nterminal methionine (26). Band b2 turned out to contain two components that yielded two overlapping sequences. About 75% of this material carried, on the N terminus, Alaw4, and the rest, Ala9" of the p polypeptide. The cleavage sites deduced from these data should have, on their C-terminal sides, Arg81 in the 6' subunit and Arg903 and Lysm in the p subunit, in accord with the known trypsin preference for positively charged amino acids. The genetic context of the trypsin cleavages in the 0 and p' subunits is presented in Fig. 1 ( A and B, respectively) and is reviewed under "Discussion."

Insertion into Nonconserved Region Introduces New Labile Site for
Proteolysis-The in-frame insertion QT988 (see Fig.   1) of 127 amino acids between codons 988 and 989 leads to a perfectly functional p subunit (Pins) that can substitute for the wild-type p subunit in vivo (20). During electrophoresis, the elongated subunit migrates slightly above the 0' subunit (Fig.   2B, lane 5 ) . As can be seen in Fig. 2B (lanes 5-8), the insertion renders the @ins subunit extremely sensitive to proteolysis since all of it is degraded after exposure to a trypsin concentration 10 times lower than that in lanes 1-4. Under these conditions, most of the u and p' subunits remain intact, and the normal products of p subunit cleavage (bands bl and bz) are not seen (Fig. 2, A and B, compare lanes 6 and 2). Instead, a new product, band d (MI -115,000), appears, which represents the N-terminal fragment of the pin. subunit, as was verified by its reactivity with monoclonal antibody PYN-2 (data not shown). In fact, band d is seen in fresh preparations of pins subunit-carrying RNA polymerase not treated with Trypsin Cleavage and Epitope Mapping in RNA Polymerase trypsin, which apparently results from the action by cellular proteases. Judging by its size, band d is generated by cleavage within the inserted amino acid sequence. No C-terminal fragment of the Pins subunit could be found in this experiment, suggesting that the cleavage within the insertion leads to rapid degradation of the distal sequences. Finally, the exposure of the core RNA polymerase with the Pins subunit to denatured calf thymus DNA leads to the reappearance of a fragment co-migrating with N-terminal band bl (Fig. 2, A and  B, lanes 7). The nature of this fragment has not been investigated.
Trypsin Cleavage in / 3 Subunit Occurs on Border of Vital and Dispensable Domains-We report here a corrected sequence position of the large nonlethal deletion mutant originally isolated by Nene and Glass (19). The deletion, A(967-1028), occurred between codons 966 and 1029 (Fig. LA), demonstrating that a substantial portion of the nonconserved region is dispensable. To determine how far the dispensable region extends in the upstream direction, we generated a series of deletions expanding bidirectionally from a linker insertion (Q952) after codon 952 (see Fig. 1). Insertion Q952 and deletions A(952-964), A(947-967), and A(937-983) were engineered in a rifampicin-resistant allele of rpoB carried on the inducible expression plasmid pMKA92 under the control of the lacUV5 promoter (11). All of these alleles conferred an isopropyl-l-thio-/3-D-galactopyranoside-inducible rifampicinresistant phenotype on a rifampicin-sensitive host strain. It should be noted that, in the case of all four mutations, the efficiency of plating and the growth rate in the presence of rifampicin as well as the maximum concentration of rifampicin tolerated were somewhat lower (by a factor of 2-4) than in the case of the parent plasmid pMKA92. This deficiency probably reflects the lability of the mutant p subunit to cellular proteases and will be analyzed elsewhere. However, the ability of these strains to grow in the presence of rifampicin clearly demonstrated the functionality of the plasmidencoded / 3 subunit, which extends the upstream boundary of the nonessential region to codon 936, i.e. just beyond the point where the alignment with chloroplasts reveals a gap. We note that a viable insertion of three amino acids, Xho-29, was recently mapped in this area (12). In conclusion, trypsin cleavage appears to occur immediately upstream from a long nonconserved and dispensable stretch of the p polypeptide and, at the same time, immediately downstream from a highly conserved region that is the site of the dominant lethal mutation Xho-19 (12).
Mapping of Epitope for mAb As was reported previously from one of our laboratories, the shorter trypsingenerated fragment of the p subunit reacted with anti-P subunit mAb PYN-6 (17). The location of the PYN-6 epitope can now be identified using the deletions and insertions shown in Fig. 1. To locate the distal boundary of the epitope, we used the previously described deletion and insertion mutations originated from the AluI restriction site at codon 1010 ( Fig. 1) (20). Each of these mutants was available on an rpoB expression plasmid. As the host strain for the plasmids, E. coli MKDC747 specifying elongated Pina subunit (QT988) was used, which permits clear distinction between the plasmidand chromosome-encoded p subunits by gel electrophoresis.
The Western blots of Fig. 3 show the analysis of strains carrying the wild-type (lane 4 ) or different mutant (lanes [1][2][3] plasmids. It can be seen that, under these conditions, the chromosome-encoded pin. subunit reacted well with the control PYN-2 mAb (Fig. 3A), but not with the PYN-6 mAb (Fig. 3B) The two anti-RNA polymerase mAbs were blotted as dots on nitrocellulose strips and exposed to crude RNA polymerase preparations, followed by incubation under RNA polymerase assay conditions, fixation with trichloroacetic acid, and autoradiography (see "Materials and Methods"). Lane 1, wild-type cells (E. coli C600); lane 2, cells with shortened subunits that have lost the PYN-6 epitope due to deletion A(967-1028) (E. coli W3110).
with PYN-6, whereas the 4-amino acid insertion, Q A l O l O (lane 2 ) did. Lane 3 represents the frameshifting insertion QA1010-fs, which leads to the formation of a prematurely terminated fragment of the p subunit. Clearly, this fragment reacts with mAb PYN-6. These results place the distal border of the PYN-6 epitope upstream from residue 1010.
To map the proximal boundary of the PYNB epitope, we used deletions A (952-964), A(947-967), and A(937-983) described above. As can be seen from Fig. 4, the p subunits with the two shorter deletions readily reacted with the antibody (lanes 1 and 2, respectively), whereas the longer deletion completely abolished the binding of PYN-6 (lane 3). Thus, the proximal boundary of the PYN-6 epitope maps between residues 967 and 983.
Solid-state Transcription-We were interested whether the PYN-6 mAb could be employed to immobilize active RNA polymerase on solid support, a procedure that would have several applications in the transcription field. The experiment of Fig. 5 documents the successful development of such technology. The nitrocellulose strips were each dot-blotted with the PYNB mAb as well as the control PYN-5 mAb, which interacts with the a subunit? The strips were incubated with crude extracts of the bacterial strains carrying either the wildtype rpoB gene (Fig. 5 , lane 1 ) or the rpoB1570-1 deletion allele (A(967-1028)) (see Fig. 1A) that removes the PYN-6 epitope ( l a n e 2). The strips were washed and then incubated with in vitro transcription mixture as described under "Materials and Methods." After the reaction was completed, the strips were developed with trichloroacetic acid, washed, and autoradiographed to detect the incorporation of [(u-~'P]UTP into acid-insoluble fractions. Clearly, the PYN-6 dot was able to attract enough wild-type RNA polymerase to generate a massive locus of solid-state transcription (Fig. 5 , lane 21, whereas the deletion control displayed no activity (lane 2). Moreover, the antibody was able to selectively anchor RNA polymerase carrying the epitope from a mixture with an excess of the enzyme that has lost it. Reconstitution experiments (data not shown) demonstrate that as little as 3% of the RNA polymerase with full-sized p subunits can be detected in this way in the presence of an excess of A(967-1028) RNA polymerase.

Genetic Context of Trypsin Cleavage Site in fi Subunit-
Since the pioneering paper of Khesin et al. (28), limited trypsin proteolysis has been used by many authors for structural and functional studies of RNA polymerase (16,17,(29)(30)(31)(32), leading in many cases to conflicting conclusions about the location of cleavage sites and identities of the products. Our present results unequivocally identify a single principal site of trypsin attack on the core RNA polymerase that is located in the p subunit. The cleavage occurs immediately downstream from a highly conserved region, the disruption of which by the mutation Xho-19 leads to a dominant lethal phenotype (12). The X h -1 9 substitution destroys the phosphate loop part of the bipartite motif Asn-X-X-Asps14 . . . G I~-X -X -X -X -G I~-L~S~, which is found in many GTP-binding proteins (33). Recently, we reported that the dominant lethal substitution GIu"~ * Lys (E813K), which destroys the upstream part of this motif, affects the catalytic function of RNA polymerase (15). On this basis, it was suggested that the domain located immediately upstream from the trypsin cleavage site participates in the RNA polymerase activity center.
The region on the downstream side of the trypsin cleavage harbors many mutations that do not affect cell viability when the mutant allele is the sole source of the 6 subunit. These data together with the low level of sequence conservation between E. coli and Pseudomonas putida and the gap in the sequence alignment with chloroplasts, eukaryotes, and archaebacteria (Fig. I A ) indicate that the trypsin cut in E. coli is located precisely at the border between a large dispensable sequence section and an upstream domain presumed to be involved in the catalytic function. The next highly conserved region downstream in the fi subunit sequence includes L Y S "~~, which has also been shown to participate in catalytic function by genetic and affinity labeling experiments (9)(10)(11).
Our data show that, in the wild-type RNA polymerase, the dispensable region is structured enough to make it resistant to proteolysis under conditions where trypsin cleaves the borderline site. This structure must protrude away from the functionally important domains for a distance long enough to accommodate drastic changes caused by deletions and insertions and to permit anchoring to the PYN-6 antibody without loss of RNA polymerase catalytic function. The apparent structural and functional autonomy of the dispensable region A. Lebedev and V. Nikiforov, unpublished data. justifies categorizing it as a distinct domain in the folded RNA polymerase molecule.
The reason why eubacteria keep an apparently nonessential domain in their RNA polymerase remains obscure. Several eubacteria such as Rickettsia prowazeki (34), Clostridium acetobutylicum (35), Thermus thermophilus (36), and Thermotoga maritima (37) have been shown to possess RNA polymerase p subunits -10 kDa shorter than the E. coli p subunit. One can anticipate that these species may contain deletions of the nonconserved domain. Our results do not address the possibility that this domain may be important for some fine nonvital aspect of RNA polymerase function. In this connection, we should note the change of in vitro promoter selectivity observed previously with deletions in this area (18).
Cleavage Site in ( 3 ' Subunit-In the wild-type RNA polymerase, the p' subunit is relatively resistant to limited proteolysis by trypsin. However, if the core enzyme is exposed to denatured DNA, a site in the 6' subunit that is located in the middle of the putative zinc-binding domain becomes susceptible to trypsin cleavage. The zinc-binding motif is conserved in all prokaryotic and chloroplast RNA polymerases (38) and may be functionally important. It should be noted that the RNA polymerase molecule is known to contain two Zn2+ cations, one in the p subunit and the other in the p' subunit (39)(40)(41). Each of them can be individually removed by reconstituting RNA polymerase from subunits obtained under appropriate ionic conditions (42). Thus, it would be interesting to determine whether the removal of the p' subunit Zn2+ will affect the kinetics of trypsin cleavage of the p' subunit.

Technical Implications for RNA Polymerase Studies-Our
results present several technical advances that will find applications in the field of RNA polymerase structure/function analysis. The characterization of the p subunit with slower electrophoretic mobility (pina) and of the cleavage products of the two large subunits (bands bl, bz, c, and d) (Fig. 2) and the mapping of the PYN-6 epitope will facilitate the analysis of derivatized RNA polymerase labeled with affinity reagents. For example, the use of RNA polymerase with the elongated Pins subunit helped us to map the sites cross-linked to the 5' (10) and 3' (8) substrate derivatives.
The elongated p subunit and the PYN-6 mAb can be employed as tags for orienting RNA polymerase image in twodimensional crystals (43) or neutron scattering analysis (44). The product of trypsin treatment of RNA polymerase with the pins subunit (Fig. 2, A and B, lanes 6 ) presents an interesting model for study: this material seems to have completely lost the C-terminal domains of the p subunit, whereas the Nterminal section as well as the rest of the subunits are still present. Is the u factor association affected by the loss of the distal domains of the / 3 subunit? Can this preparation interact with promoters? These questions are currently under investigation. Finally, the anchoring reaction in the format of Fig. 5 constitutes an easy and highly selective way for assessing one type of RNA polymerase (carrying the PYN-6 epitope) in the presence of another (lacking the epitope). Such an assay can be useful for massive biochemical screening of mutations engineered in the cloned rpoB gene, which is the main focus of our current research.