INTRODUCTION

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Transcription of eukaryotic organellar genomes depends on RNA polymerases (RNAPs) distinct from the nuclear enzymes. Although the multisubunit chloroplast core RNAP is clearly related to the nuclear, eubacterial, and archaeal RNAPs, the single-subunit mitochondrial and chloroplast core RNAPs are homologous to the single-subunit RNAPs found in bacteriophages T7 and T3 (reviewed in references 6 and 9). The evolutionary relationship of the single-subunit RNAPs to the multisubunit RNAPs is uncertain, although the two classes of polymerases share many mechanistic similarities (49). The single-subunit RNAPs are actually more similar to the family of DNA polymerases and reverse transcriptases. In fact, single mutations can convert T7 RNAP to an enzyme using deoxyribonucleotide substrates (50), and conversely, a point mutation in a reverse transcriptase converts the enzyme to an RNAP (15).

For the most part, the genes that encode the single-subunit organellar RNAPs are found in the nucleus. However, in what may be a clue as to the evolutionary origin of these unusual enzymes, a single-subunit phage-like RNAP is encoded in the mitochondrial genome of a primitive brown alga (44), and genes encoding a multisubunit bacterial-like RNAP are found in the mitochondrion of an ancestral eukaryotic protozoon (29). It is therefore probable that a multisubunit bacterial-like core RNAP was replaced by a single-subunit phage-like core early in the evolution of the eukaryotic mitochondrion.

The yeast mitochondrial core RNAP, Rpo41p, is a single polypeptide of 145 kDa with striking similarity to bacteriophage RNAPs in the C-terminal two-thirds of the protein (33). Nine conserved regions of amino acids have been defined, including positions known to be required for structure and function of the catalytic domain (12, 25), which demonstrate especially high levels of identity. However, the N-terminal third of Rpo41p is not obviously similar to the phage RNAPs or to other proteins in the database. Although this portion of the protein is essential for function (10, 55), its role in transcription has not been elucidated.

Unlike the phage RNAPs, which function independently to recognize and bind to their promoters, open DNA at the transcription start site, and initiate transcription, Rpo41p requires a specificity factor, Mtf1p, functionally similar to bacterial sigma factors (24). Mtf1p acts like a sigma factor in that it allows the polymerase to recognize and bind to promoter DNA, and is required for proper initiation, but is then released after a short transcript has been synthesized (32). Despite these similar functions, Mtf1p has limited amino acid identity with sigma factors, although many of the shared amino acids are critical for Mtf1p function (46). In particular, we have shown that two regions of Mtf1p with similarity to sigma factors also share a functional role, contributing to interaction with the core polymerase (10). These findings suggest a structural as well as functional similarity between Mtf1p and sigma factors.

Many recent reports have focused on identifying regions and specific amino acids of sigma and sigma-like factors required for interaction with their core RNAPs (10, 26, 27, 30, 36, 47, 48, 52). From these studies it has become clear that amino acids along much of the length of sigma factor are required for core RNAP interaction. In contrast, much less is known about the regions of core RNAPs that interact with various initiation factors. Recent studies have used protein cross-linking and protein-protein interaction studies to determine interactions between sigma and the alpha, beta, and beta' subunits of the bacterial core RNAP (1, 11, 19, 37, 38). However, specific interaction domains are still poorly defined, due in part to the large size and complexity of the multisubunit RNAPs. The recent report of the three-dimensional structure of a bacterial core RNAP (57) in combination with the partial structure of a sigma factor (31) will certainly aid the elucidation of how all three subunits of the core RNAP interact with sigma factors.

The yeast mitochondrial core RNAP is a more tractable system for studying subunit interactions due to its modest size and polypeptide composition. Additionally, recent structural data for the T7 RNAP in the absence and presence of template (7, 25) provide an important starting point for modeling and evaluating sites of interaction identified on Rpo41p. In this work we used previously identified Mtf1p mutants defective for Rpo41p interaction to select for suppressing mutations in the core RNAP. Using the structure of T7 RNAP as a model, we have identified a surface of the mitochondrial RNAP that appears to be critical for subunit interactions. Intriguingly, the potential interaction sites on Rpo41p correspond to regions of T7 RNAP with known roles in promoter interaction. These results indicate a possible reallocation of functions from the core RNAP to the sigma-like specificity factor during the evolution of the mitochondrial RNAP.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Media and genetic methods. Standard media such as YP medium containing 2% glucose (YPD) or 2% each glycerol, ethanol, and lactate (YPGEL), synthetic complete (SC) medium lacking the appropriate amino acid(s) and sporulation medium were prepared as described by Guthrie and Fink (20). 5-Fluoro-orotic acid (5-FOA) was added to SC medium to a final concentration of 500 mg/liter (20). Saccharomyces cerevisiae cells were transformed by the lithium acetate method (23). Molecular cloning techniques were as described by Sambrook et al. (45).

Two-hybrid plasmid constructs and assays. MTF1 and RPO41 two-hybrid clones and -galactosidase assays were as described previously (10). Two-hybrid plasmid pVP16 was modified to facilitate cloning RPO41 fragments for suppressor analysis and identification of subfragments responsible for suppression of mtf1 mutants. Plasmid pVP16S (pJJ1135) was made by digesting pVP16 with BamHI and ligating the SalI linker GATCTGTCGACA (SalI site underlined) into the overhangs. Plasmid pVP16E (pJJ1112) was made by digesting pVP16 with EcoRI, filling in the overhangs with Klenow fragment, and religating. Plasmid pVP16N (pJJ1113) was made by digesting pVP16 with NsiI, followed by treatment with T4 DNA polymerase to remove 3' overhangs and then religation. Full-length RPO41 was cloned into the NotI site of the modified vectors and shown to be fully functional in the two-hybrid assay (data not shown). The polylinker of pVP16S was sequenced to confirm proper insertion of the SalI linker.

Plasmid and strain construction for the RPO41 plasmid shuffle. A kanamycin cassette was used to disrupt RPO41 as previously described (54). Yeast haploid strain yJH58a (MATa his4309 ura3-52 ino1-13 leu2-3,112) was transformed with pJJ1148 (YCplac33 [17]) containing a 5.7-kb RPO41 fragment and then subsequently transformed with the kanamycin knockout PCR product. G418-resistant transformants were first tested by PCR to check for integration of the disruption construct in the RPO41 gene. Properly integrated transformants were further tested to confirm that integration was in the chromosomal copy of RPO41. Cells were plated on 5-FOA plates to select for loss of the RPO41-containing plasmid. After 5-FOA treatment, the cells were plated onto YPGEL plates to determine if the cells were petite and thus disrupted for RPO41. A positive rpo41 transformant containing pJJ1148 was designated yJJ1095.

PCR mutagenesis of RPO41 for suppression analysis. To create a library of RPO41 mutants, full-length RPO41 was amplified by PCR using 20 mM Tris-HCl (pH 8.4), 50 mM KCl, 1.5 mM MgCl₂, 50 ng of template, 30 µM primers, 200 µM deoxynucleoside triphosphates (dNTPs), and 5 U of Taq DNA polymerase per 100-µl reaction. pJJ1137 was used as the template with primers pVP16 (5'-TGCCCTTGGAATTGACGAGTACG-3') and RPO41-3' (5'-GGATCCGGCGGCCGCGTTTGTAGTTCACGGCTCACGAG-3').

Construction of site-directed mutations in RPO41. RPO41 mutants F1066I, E1124K, and K1273R identified by the suppressor analysis were recreated to separate the individual mutations and confirm that the single mutations were responsible for suppression. Additionally, we created new RPO41 mutants using overlap extension PCR (53). Overlapping oligonucleotides containing the mutations were designed and used in separate PCRs with oligonucleotides directed to either the 5' or 3' end of RPO41. The oligonucleotides used are listed in Table 1. The products of the separate reactions were purified using a Qiagen PCR purification column and were then fused. The fused products were diluted 1:100 and amplified by further rounds of PCR. Cloned constructs were confirmed by digestion with the appropriate restriction enzyme.

Two-hybrid suppressor screen. RPO41 library DNA was transformed into yeast strain L40 containing two-hybrid MTF1 constructs in plasmid pBTM116. Cells were plated onto SC medium lacking tryptophan, uracil, leucine, and histidine (SC-THUL) supplemented with 5 mM 3-aminotriazole. The plates were incubated at either 30°C or room temperature to identify His⁺ cells. Transformants of mtf1 mutant V135A were first plated at 37°C for 24 h and then transferred to 30°C to eliminate background growth on the minimal medium plates. His⁺ cells were rechecked by streaking the cells onto SC-THUL plates with 5 mM 3-aminotriazole. Plasmid DNA was isolated from the His⁺ cells and transformed into E. coli HB101 cells. The transformed cells were plated onto M9 plates containing 100 µg each of ampicillin and proline per ml. Since the HB101 cells are Leu, only cells complementing this defect with the yeast LEU2 gene on the pVP16 vector can grow on this medium. Isolated plasmids were retransformed into L40 containing the MTF1 mutant. The transformants were restreaked onto SC-THUL medium containing 3-aminotriazole to confirm that the RPO41 plasmids were responsible for suppression.

GST-Mtf1p affinity chromatography. Interaction studies with glutathione S-transferase (GST)-Mtf1p constructs were performed as previously described (10), using morpholinepropanesulfonic acid (MOPS) buffer at pH 7.3. F3 cell extracts (56) were made from yeast strains used for in vivo testing of the RPO41 alleles. Cells (300 ml) were grown overnight to mid-log phase in SC-Leu medium to maintain the RPO41 plasmid. The cells were then diluted 1:10 in YPD medium and grown for an additional 8 to 10 h before harvesting of cells and preparation of extracts. The F3 extracts were twice dialyzed against 2 liters of M(50) (30 mM MOPS [pH 7.3], 5% glycerol, 1 mM EDTA, 10 mM MgCl₂, 50 mM KCl) for 2 h. The conductance of the extracts was less than 50 µs cm¹. Column fractions were analyzed by Western blotting as described previously (10).

Nonspecific RNAP assays. Assays were performed as described previously (56). F3 extracts were prepared as above except that the ammonium sulfate pellet was resuspended in D(0) buffer until conductance was below that of a 60 mM solution of ammonium sulfate. The amount of extract corresponding to about 1 g of yeast cells was passed over a 1-ml DEAE-cellulose (DE-52; Whatman) column. Flowthrough fractions were assayed for activity using calf thymus DNA (Sigma) as a template to determine levels of nuclear polymerase in the fractions. The fractions were then reassayed for activity on a poly(d[AT]) (Sigma) template to measure the activity of the mitochondrial polymerase.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

Isolation of RPO41 suppressors. We have previously studied interaction between Mtf1p and Rpo41p. Using two-hybrid and biochemical assays, we identified specific mutations in Mtf1p defining three distinct regions required for interaction (10) (Fig. 1A). To identify regions of Rpo41p required for interaction with Mtf1p, we applied a two-hybrid suppressor screen to select for mutations that would allow Rpo41p to interact with a defective Mtf1p mutant. A library of two-hybrid RPO41 variants fused to the VP16 transcriptional activation domain was prepared by PCR amplification (see Materials and Methods) and screened for interaction with the interaction-defective mtf1 mutant V135A (Fig. 1A), fused to the LexA DNA-binding domain. The V135A mutation reduces interaction with wild-type Rpo41p over 10-fold and is not functional for transcription inside the yeast mitochondrion (10). A yeast strain containing the V135A mtf1 mutant was transformed with the RPO41 library and plated onto His-deficient medium containing 3-aminotriazole to select for expression of the HIS3 reporter construct. Approximately 10⁶ transformants were screened; His⁺ cells were identified and rechecked for growth on the selective medium. The RPO41 plasmids were isolated and retransformed into the V135A mtf1 two-hybrid strain to confirm suppression. Three suppressors of V135A were identified and initially designated I30, I12, and V1. Quantitative assays for the -galactosidase reporter indicated that each suppressor was capable of interaction with the V135A mutation at a level about 50% of that seen between wild-type subunits (Fig. 2).

View larger version (38K): [in this window] [in a new window]   FIG. 1.   Features of Mtf1p and Rpo41p. (A) Comparison of Mtf1p to sigma factors and location of Mtf1p mutations that affect interactions with Rpo41p. Mtf1p mutant V135A is highlighted. Regions with sequence similarity to sigma factors are shaded (24). aas, amino acids. (B) Comparison of Rpo41p to T7 RNAP. Regions with high levels of identity are shaded. Locations of mutations in Rpo41p suppressors I30, I12, and V1 and convenient restriction enzyme sites used for subcloning the mutations are indicated. Fragments capable of converting the wild-type sequence to a suppressor are depicted as thicker lines. Mutations responsible for suppression are in boldface.

View larger version (45K): [in this window] [in a new window]   FIG. 2.   Three Rpo41p constructs suppress the core-binding defect of Mtf1p mutant V135A. -Galactosidase activity is shown for wild-type (WT) Rpo41p and the suppressor constructs interacting with Mtf1p mutant V135A. The wild-type Rpo41p interaction with wild-type Mtf1p is shown as a reference. The activity is shown for cells grown at 23°C. -Galactosidase activity is expressed as Miller units (34).

Single-point mutations confer suppression. DNA sequencing, subcloning, and site-directed mutagenesis were used to identify the mutations in RPO41 responsible for the suppression of the V135A mtf1 core binding mutation. Each suppressor contained multiple point mutations resulting in missense, but not nonsense, changes in the sequence (Fig. 1B), consistent with our earlier conclusions that the whole folded structure of Rpo41p is required for interaction (10). The salient mutations were identified by cloning individual DNA fragments from the suppressors back into the wild-type background (Materials and Methods) and reassaying for suppression. Subfragments determined to be responsible for suppression were resequenced to confirm that no other mutations were present.

Allele specificity of the RPO41 suppressors. Since the three suppressors of the V135A mutation were located in three different regions of the Rpo41p sequence (Fig. 1B), it seemed unlikely that all three were identifying residues in direct contact with Mtf1p. Rather, one mutation could be in direct contact, but others could be altering the overall structure to increase binding to any MTF1 allele. We therefore tested the interaction of the suppressors with wild-type and mutant forms of Mtf1p. -Galactosidase assays indicated that interaction of the K1273R suppressor with wild-type Mtf1p was unchanged from that of wild-type Rpo41p (Fig. 3A). Therefore, the K1273R suppressor has neither increased nor decreased its affinity for wild-type Mtf1p but has simply changed in a way that selectively increases its interaction with the V135A mutation. In contrast, the A631V and E1124K suppressors both reduce interaction with wild-type Mtf1p (Fig. 3A), by 50 and 30%, respectively. These suppressors have therefore altered sites important for interaction with wild-type Mtf1p.

View larger version (37K): [in this window] [in a new window]   FIG. 3.   Interaction of V135A suppressors with wild-type (WT) Mtf1p (A) and Mtf1p mutant K157E (B). Cells were grown at 30°C. -Galactosidase activity is expressed as Miller units (34).

Functional testing of Rpo41p mutations in vivo. The positive selection of the two-hybrid suppressor screen ensures that the folded structures of the Rpo41p suppressors are still very similar to that of the wild-type protein. Two additional points argue that the suppressors remain functional as core RNAPs. First, as outlined above, all of the mutants still have appreciable interactions with wild-type Mtf1p. Second, none of the suppressor mutations affects any of the amino acids predicted, based on similarities with T7 RNAP, to be involved in catalysis. To confirm that the suppressors could still support mitochondrial transcription in vivo, we replaced the wild-type copy of the gene in yeast with the various mutant alleles. Since functional Rpo41p is required for the propagation of the mitochondrial genome (18), we constructed an rpo41 deletion strain complemented by RPO41 on a URA3-selectable vector for a plasmid shuffle replacement (Materials and Methods). LEU2-selectable plasmids containing the suppressor mutations were transformed into this strain, and then the cells were treated with 5-FOA to select for loss of the wild-type RPO41 URA3 plasmid. The resulting strains were then assessed for possible defects (petite phenotype) by testing their ability to grow on a nonfermentable carbon source (glycerol-ethanol-lactate).

Biochemical interaction studies. To confirm the interaction of the Rpo41p suppressors with the V135A Mtf1p mutant, we used a biochemical assay independent of the two-hybrid fusion constructs. Using affinity chromatography, we previously demonstrated that a GST fusion construct of mtf1 allele V135A is defective for binding wild-type Rpo41p from a yeast whole-cell transcription extract (10). To measure the ability of the Rpo41p suppressors to bind to the noninteracting V135A mutation, we prepared DNA-free transcription extracts from yeast cells expressing only the mutant forms of Rpo41p (see above). We confirmed that the V135A mtf1 mutation was not capable of binding to wild-type Rpo41p in the transcription extract (Fig. 4). However, each of the suppressor mutations was capable of binding to the V135A fusion construct, confirming the two-hybrid results.

View larger version (48K): [in this window] [in a new window]   FIG. 4.   Biochemical confirmation of interactions between the suppressors and Mtf1p mutant V135A. Whole-cell yeast extracts were prepared as described in Materials and Methods from cells expressing only wild-type (WT) or mutant forms of Rpo41p. The extracts were passed over a column of purified GST-Mtf1p that contained the V135A mutation. The columns were washed to eliminate nonspecific binding and then step eluted to release Rpo41p bound to the column. Rpo41p from input (IP), flowthrough (FT), wash, and elution fractions was detected by Western blot analysis using anti-Rpo41p antibody. The arrowheads on the left indicate a cross-reacting band (see also Fig. 7).

Site-specific mutagenesis of RPO41. As shown in Fig. 1B, the three suppressor mutations are located in three different regions of the Rpo41p amino acid sequence. Based on comparisons of Rpo41p to the crystal structure of the T7 RNAP (7, 25), all three suppressors should be located in unstructured or loop regions poorly conserved with the phage RNAPs. However, the A631V and E1124K suppressors are both very close to amino acids used by the phage RNAP for interactions with DNA. To confirm that these regions of the mitochondrial RNAP were in fact important for protein-protein interactions with the specificity factor, we created additional point mutations in Rpo41p near each of the suppressor mutations. The locations of the suppressor mutations in the context of predicted structural features are schematized in Fig. 5, and the site-specific mutations in these regions are described further below.

View larger version (45K): [in this window] [in a new window]   FIG. 5.   Structural and amino acid sequence features near the RPO41 suppressor mutations. Each panel includes a schematic of structural elements flanking a suppressor mutation (position indicated by the asterisk). Cylinders and arrows denote helices and beta sheets, respectively, from the structure of T7 RNAP (25). Below each schematic is an amino acid alignment comparing the core RNAP from S. cerevisiae (Sc; accession no. M17539) to sequences from N. crassa (Nc; L25087), S. pombe (Sp; P13433), and Homo sapiens (Hs; 4826926). The boxed amino acids indicate the original suppressor; boldface indicates positions and identities of site-directed mutations described in the text. (A and B) The consensus below the mitochondrial RNAP alignments uses an uppercase letter for a four-of-four match, lowercase for a three-of-four match, and + for similar amino acids. Below the mitochondrial RNAPs is the relevant sequence from T7 RNAP (M38308) and a consensus derived from this sequence and those of phage T3 (X02981), K11 (X53238), and SP6 (Y00105). Highlighted in boldface are T7 RNAP positions involved in promoter melting or stabilization of single-stranded DNA (filled circles) and amino acids important for promoter recognition (arrowheads) as described in the text. (C) The consensus for the two fungal sequences uses uppercase for identity and + for similarity.

Mutations near A631V. To improve the alignment of Rpo41p to T7 RNAP in the region of the A631V suppressor, we compared it to several putative mitochondrial RNAPs and to several phage RNAPs (Fig. 5A). In this region the mitochondrial RNAPs have a somewhat conserved insertion of 16 to 20 amino acids relative to the phage RNAPs just C terminal to the sequences shown in Fig. 5A. Based on positions that appear to be conserved within the class of mitochondrial RNAPs, we created three mutations near the A631V suppressor as shown in Fig. 5A. The conserved amino acids were changed to alanine, except in one case where a conserved alanine was substituted with a tyrosine. Each mutation was tested in two-hybrid constructs and in the plasmid shuffle assay for in vivo function as described above. The A633Y and H636A mutations are in positions conserved in the different mitochondrial RNAPs but not in the phage RNAPs (Fig. 5A). Consistent with the fact that the A633Y mutation was completely defective for interaction with wild-type Mtf1p in the two-hybrid assay, it also resulted in a petite phenotype in vivo (Fig. 6). In contrast, the H636A mutation reduced the two-hybrid interaction by only 30% and was still functional in vivo.

View larger version (37K): [in this window] [in a new window]   FIG. 6.   Analysis of site-directed Rpo41p mutations by two-hybrid and plasmid shuffle assays. Mutations were cloned into two-hybrid and yeast expression vectors as described in Materials and Methods. Two-hybrid interactions were measured for cells grown at 30°C; -galactosidase activity is expressed as Miller units (34). The ability of the mutations to sustain growth on a nonfermentable carbon source (glycerol-ethanol-lactate) is indicated in the boxes below the bar graph. WT, wild type.

Mutations near E1124K. The E1124K suppressor aligns with the first amino acid of T7 RNAP in the pinky specificity loop, known to be important for interactions with the T7 RNAP promoter (42, 43). This region of the phage and mitochondrial RNAPs can be more clearly aligned than the region around the A631V suppressor, although there are significant differences between the two classes of enzymes as shown in Fig. 5B. We created three mutations in this region at sites conserved within the mitochondrial RNAPs or between the two classes of RNAPs. The Y1122A mutation lies N terminal to the specificity loop at the end of a beta sheet conserved in many polymerases, including DNA polymerases of the polymerase I family (25). Since the conserved beta sheet is probably required for structural integrity of the RNAP, we predicted that this mutation would result in a nonfunctional protein. Consistent with this prediction, the Y1122A mutation results in an interaction defect in the two-hybrid assay and loss of in vivo function (Fig. 6).

Mutations near K1273R. We also created a double mutation near the K1273R suppressor (Fig. 5C). This region of Rpo41p represents an insertion of amino acids relative to the phage RNAPs and all of the known mitochondrial RNAPs except that from the relatively closely related fungus Neurospora crassa (8). This mutation, RQ1275AA, changes two amino acids shared by Rpo41p and the Neurospora homologue. The double mutant reduces interaction with Mtf1p nearly fivefold (Fig. 6), supporting the idea that this insertion plays a role in subunit interaction. However, the defect is not severe enough to abrogate function since the double mutant was functional in vivo (Fig. 6).

Core RNAP assays of interaction-defective mutants. The Rpo41p suppressor mutants are clearly functional in vivo with wild-type Mtf1p as described above. In addition, some of the site-directed mutants with reduced two-hybrid interactions were found to be functional as core RNAPs in vivo (H636A, K1127A, and RQ1275AA). In contrast, site-directed mutants A633Y, Y1122A, and K1127A each reduced interaction in the two-hybrid assay and failed to support mitochondrial function in vivo. To determine if the lack of function was due strictly to a failure to interact or instead to a more serious defect precluding catalytic activity, we tested the mutant constructs in a nonselective transcription assay. Transcription extracts were prepared from the yeast strains described above expressing the mutant polymerases from a plasmid (see Materials and Methods). As shown in Fig. 7A, the wild-type and mutant proteins were present at comparable levels in all of the extracts. The extracts first were passed over a DEAE-cellulose column to remove the nuclear RNAPs (56). The DEAE-adsorbed fractions were then assayed for RNAP activity using a nonselective poly(d[AT]) template which does not require Mtf1p. Using the rpo41 deletion strain as a control, we confirmed that essentially all of the nuclear RNAPs are removed by the DEAE column (Fig. 7B). Although the catalytic activity of the A633Y and the K1127A mutants was somewhat reduced, they still had significant transcriptional activity and are therefore correctly folded functional RNAPs. In contrast, the extract from Rpo41p mutant Y1122A, predicted to disrupt a conserved beta sheet, had no detectable catalytic activity.

View larger version (34K): [in this window] [in a new window]   FIG. 7.   Core RNAP activity of noninteracting Rpo41p mutants. As described in Materials and Methods, transcription extracts were made from yeast cells expressing wild-type (WT) Rpo41p or the indicated Rpo41p mutants. (A) Western blot of the transcription extracts with anti-Rpo41p antibody. The arrow on the left indicates the position of Rpo41p; the arrowhead on the right indicates a cross-reacting band. (B) The extracts were passed over a DEAE-cellulose column to remove nuclear RNAPs. The adsorbed fractions were assayed to determine relative amounts of mitochondrial RNAP, using poly(d[AT]) as a nonspecific template.

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

Using a powerful two-hybrid suppressor screen, we have identified three regions of the yeast mitochondrial RNAP, Rpo41p, important for interactions with its sigma-like specificity factor, Mtf1p. These multiple sites, distant from each other on the linear map of the protein (Fig. 1B), support our earlier observations that essentially the entire length of the 145-kDa core RNAP is required for this interaction (10). These results are therefore consistent with the idea that the interaction surface between core RNA polymerases and initiation/specificity factors is complex. Recent work by Sharp et al. has underscored this complexity; as many as six conserved regions of bacterial sigma factors (some of which are shared with Mtf1p) are involved in interactions with the core RNAP (47). Because the structure of only a portion of sigma has been solved (31), no information on the three-dimensional arrangement of these different sites is available. The absence of a three-dimensional structure of Rpo41p precludes determination of whether the three sites we have identified are adjacent in the folded protein. However, we can use the known structure of the very similar T7 RNAP to create a working model as shown in Fig. 8.

View larger version (46K): [in this window] [in a new window]   FIG. 8.   Rpo41p suppressor mutations modeled on the T7 RNAP structure. Coordinates are from reference 7. The domain colors are similar to the scheme of Jeruzalmi and Steitz (25): N-terminal domain, yellow; thumb, green; palm, red; palm insertion, orange; fingers, blue; pinky specificity loop, light blue; and extended foot, magenta. The approximate locations of the suppressor mutations (as predicted by the alignments shown in Fig. 5) are shown as starred circles on the RNAP structure and are indicated by arrows.

Each of the suppressor substitutions is found in a loop region of the RNAP (Fig. 5); in some cases the mutations are in or near insertions relative to the phage RNAP. The approximate position of the suppressing amino acids shown in Fig. 8 predicts that all of the mutations may lie on one face of the RNAP (Fig. 8). This surface of the mitochondrial RNAP may therefore have diverged significantly from the phage RNAPs in both structure and function. Although all three suppressors were found to restore interaction with a single noninteracting Mtf1p mutation, it is unlikely that each of the positions indicated in Fig. 8 makes direct contact with this single amino acid. Below we present arguments for which suppressor may directly contact the V135A Mtf1p mutation and discuss the possible role of the other positions.

A631V. The A631V suppressor increases interaction with the noninteracting Mtf1p mutation V135A more than fourfold (Fig. 2). This suppressor is also highly allele specific; it reduces interaction with the wild type and does not increase interaction with other Mtf1p mutations (Fig. 3). In addition, the nearby site-directed mutation A633Y abolishes interaction with wild-type Mtf1p in the two-hybrid assay and is nonfunctional in vivo (Fig. 6), although the RNAP retains catalytic activity (Fig. 7). The predicted location of the A631V and A633Y mutations in the structure of T7 RNAP is very intriguing. As shown in Fig. 5A and 8, these residues are in a loop near the thumb domain (25). Part of this loop was unresolved in the crystal structure, but the authors speculated that it was in position to make contacts with DNA, a speculation based in part on the observation that mutations within this region abolish promoter-specific transcription without loss of catalytic activity (39, 51). This model was confirmed in the structure of T7 RNAP bound to promoter DNA (7); the loop now forms a  hairpin with valine 237 stacking on the 4 base of the template strand stabilizing the melted DNA. V237 is highlighted in the alignment shown in Fig. 5A and marked with a symbol to indicate its role in interacting with the melted DNA. Although this position is not conserved even among other phage RNAPs, the adjacent position, G238, is found in all the known phage RNAPs. Note in Fig. 5A that the sequences of the mitochondrial RNAPs differ substantially from those of the phage RNAPs in this region, indicating potentially different structures and functions. In addition to the fact that the loop is 16 to 20 amino acids longer in the mitochondrial RNA polymerases (not shown), different consensus sequences can be derived for the two classes of RNAPs. The conserved glycine at T7 position 238 is absent from the mitochondrial RNAPs; other amino acids conserved within the phage RNAPs (R231 and T244) are also missing.

E1124K. The E1124K suppressor increases interaction with the V135A Mtf1p mutation over fourfold, with only a slight reduction in the ability to interact with wild-type Mtf1p (Fig. 2 and 3A). E1124K also increases interaction with the noninteracting Mtf1p mutant K157E threefold (Fig. 3B). Supporting the idea that this region is important for core-factor interactions, the nearby site-directed mutation K1127A reduces interaction with wild-type Mtf1p dramatically in the two-hybrid assay (Fig. 6). Therefore suppression by E1124K is not allele specific, and although defects were detected in the two-hybrid assay, they are not severe enough to affect in vivo function (Fig. 6).

K1273R. The K1273R suppressor, like the E1124K suppressor, increases interaction with the V135A Mtf1p mutation nearly fourfold (Fig. 2). It does not significantly disrupt interaction with wild-type Mtf1p in the two-hybrid assay (Fig. 3A), although it does confer a ts petite phenotype in vivo. This suppressor increases interaction with the nearby K157E Mtf1p mutation two- to threefold (Fig. 3B). K1273R is located within the extended foot of the RNAP, which is an insertion relative to DNA polymerases and includes C-terminal amino acids that interact with promoter DNA and incoming rNTPs (16, 35). In Rpo41p and the Neurospora homologue the foot is much larger, with nearly 90 extra amino acids relative to the phage RNAPs. As shown in Fig. 5C, the region around the K1273R suppressor is quite similar between the yeast and Neurospora RNAPs. The site-directed double mutant RQ1275AA changes two of these shared positions and dramatically reduces interaction in the two-hybrid assay. However, the double mutant is still functional in vivo (Fig. 6), indicating that this region has a less important role in interaction than the region near the A631V suppressor.

A complex interaction surface. The suppressor screen described in this work was not exhaustive since we did not recover multiple isolates of the three identified suppressors. In addition, we previously tested a truncated form of Rpo41p lacking the N terminus, but containing all of the suppressor sites, in a two-hybrid assay and found that it was not competent for interaction (10). These facts mean that it is very likely that other regions of the Rpo41p core RNAP are also important for factor interaction. In particular, these studies do not resolve the role of the significant N-terminal extension found in the mitochondrial RNAPs relative to the phage RNAPs (Fig. 1B). Since this portion of the protein is required for interaction, either it is involved in direct contacts with the specificity factor or, like region 1 of sigma factor (13), it may be present to mask functional domains of the core RNAP made accessible after interaction.