131 Subunit of Yeast Transcription Factor IIIC (TFIIIC) in TFIIIB Assembly
Joël Acker, Rosalia Arrebola, André Sentenac, and Christian Marck*
Service de Biochimie et de Génétique Moléculaire, CEA/Saclay, F-91191 Gif-sur-Yvette Cedex, France
Received 22 June 2001/ Returned for modification 3 August 2001/ Accepted 5 October 2001
| ABSTRACT |
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131, is thought to initiate TFIIIB assembly by interacting with Brf1/TFIIIB70. In this work, we have analyzed a TFIIIC mutant (
131-
TPR2) harboring a deletion in
131 removing the second of its 11 tetratricopeptide repeats. Remarkably, this thermosensitive mutation was selectively suppressed in vivo by overexpression of B"/TFIIIB90, but not Brf1 or TATA-binding protein. In vitro, the mutant factor preincubated at restrictive temperature bound DNA efficiently but lost transcription factor activity. The in vitro transcription defect was abolished at high concentrations of B" but not Brf1. Copurification experiments of baculovirus-expressed proteins confirmed a direct physical interaction between
131 and B".
131, therefore, appears to be involved in the recruitment of both Brf1 and B". | INTRODUCTION |
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Saccharomyces cerevisiae TFIIIB comprises three components: the TATA binding protein (TBP), Brf1/TFIIIB70, which is evolutionarily related to the class II factor TFIIB (9, 14, 27, 37), and B"/TFIIIB90 (28, 50, 51). The Pol III transcription system can use alternative pathways to build the TFIIIB-DNA complex. TFIIIB needs TFIIIC to bind to TATA-less Pol III genes like most tDNAs, but it can assemble by itself, at least in vitro, onto the TATA element of the SNR6 gene (24, 40, 41), although TFIIIC enhances the transcription efficiency (18). In vivo, the transcription of the SNR6 snRNA gene requires TFIIIC to direct TFIIIB binding and probably to overcome the repressive effect of chromatin (10, 20). Some tRNA genes that harbor a TATA-like element can also be transcribed, in vitro, without TFIIIC (17).
Yeast TFIIIC factor, also called
, is a multiprotein complex comprising six subunits,
138,
131,
95,
91,
60, and
55 (5, 19, 46), each of which is essential for cell viability. Mutagenesis (3, 34, 45, 56) and protein-DNA and protein-protein interaction studies (12, 16, 30, 38) have provided a global view of TFIIIC-DNA complex formation and shed light on the role of TFIIIC subunits. Five subunits of TFIIIC could be photocross-linked to chemical probes specifically located within or immediately flanking the SUP4 tRNA and the 5S RNA genes (5, 8). This elegant approach has allowed their positioning within the factor-DNA complex. Subunits
138 and
91 interact around the B block and ensure the primary binding of TFIIIC to the B block of tDNA (3, 34).
95 and
55 interact physically with each other (38) and bind on the vicinity of the A block on opposite sides of the DNA helix (5).
60 could not be cross-linked to DNA, but this polypeptide is located in
B, at least in part, together with
138 and
91 (16). Finally, in the TFIIIC-tDNA complex,
131 is the only subunit cross-linked upstream of the transcription start site, in a region occupied by TFIIIB, and it also extends downstream between the A and B blocks (5, 6).
The mechanism by which TFIIIC recruits TFIIIB onto TATA-less class III genes appears to involve a stepwise series of intricate protein-protein interactions and conformational changes the submolecular details of which are poorly understood. In vitro experiments have shown that TFIIIB assembly starts with the recruitment of Brf1 by the TFIIIC-tDNA complex, through its interaction with
131 (6, 12, 27, 30, 42, 57). A region of
131 responsible for this interaction has been mapped in two-hybrid experiments to the first 168 residues (12). Entry of TBP in the complex, mediated by Brf1 (27, 36) and by
60 (16), stabilizes the binding of TFIIIC to the DNA and dramatically increases the cross-linking of
131 to upstream DNA (6). Addition of B" leads to further drastic changes in complex conformation and stability: (i) the TFIIIB-DNA complex becomes resistant to high salt or polyanions concentrations (29), and (ii) cross-linking of
131 to upstream DNA is greatly reduced (6, 31). The change in cross-linking efficiency of
131 during the TFIIIB assembly underscores the flexibility of this polypeptide within the complex. Upon binding to tDNA genes harboring long introns or long extra arms (or both as in some Leu or Ser tRNA genes), TFIIIC is able to stretch out between the A and B blocks, as seen by electron microscopy (54). The fact that TFIIIB could be assembled by TFIIIC at various distances from the A block further suggested that
131 itself is able to stretch out along DNA, possibly due to its peculiar structure rich in tetratricopeptide repeat (TPR) motifs (23, 39, 49). Although the in vitro experiments are strongly suggestive of a multistep assembly pathway, it is not clear whether the in vivo recruitment of Brf1 and B" components of TFIIIB involves a one-step or two-step mechanism.
In this work, we have pursued the characterization of the
131 subunit by investigating the effect of the deletion of its second TPR motif (
TPR2). We present biochemical and genetic evidence that this mutation causes a defective recruitment of the B" subunit. The transcription defect can be rescued by overdosage of B" both in vivo and in vitro. A direct interaction between
131 and B" could be demonstrated. The results suggest that
131 directs the recruitment of TFIIIB by interacting with both Brf1 and B".
| MATERIALS AND METHODS |
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Yeast strains are as follows: SC55 (a/
ura3 to 52/ura3-52 trp1-
1/trp1-
1 his3-
200/his3-
200 ade2-101/ade2-101 lys2-801/lys2-801 leu2-
1/+ cans/canR) (13), YCK107 (a ura3-52 trp1-
1 his3-
200 ade2-101 lys2-801 tfc4::HIS3 +pCK17) (39), YHD3 (a ura3-52 trp1-
1 his3-
200 ade2-101 lys2-801 tfc4-
::HIS3 +pCK17) (this work), YHD7 (a ura3-52 trp1-
1 his3-
200 ade2-101 lys2-801 tfc4-
::HIS3 +pUN45-
131-
TPR2) (this work). All deletion mutants of
131 used in this work have been described previously:
131-
N1,
131-
N2,
131-
TPR1,
131-
TPR2,
131-
TPR3,
131-
TPR4,
131-
TPR5,
131-
TPR6,
131-
TPR7,
131-
TPR8,
131-
TPR9,
131-
basic1,
131-
basic2,
131-
H1,
131-
loop,
131-
loop1,
131-
loop2,
131-
H2,
131-
zipper,
131-
TPR10,
131-
TPR11 (12). The plasmids used for the in vivo suppression studies (pLR30, pL1, and pJR38, overexpressing Brf1, TBP, and B", respectively) have been described by Lefebvre et al. (34) and Rüth et al. (51), except pFL
TPR2, which was constructed by cloning the SalI-BamHI fragment of pNC14 (12) into pFL44L.
Deletion of TFC4 ORF.
The whole TFC4 open reading frame (ORF) (YGR047c) coding for
131 was deleted using the direct deletion method (7). Two 40-mer oligonucleotides were used to amplify by PCR a DNA fragment containing the HIS3 gene flanked by the sequences upstream and downstream of TFC4. The PCR-amplified fragment was directly used to transform yeast strain SC55. The structure of the diploid His3+ transformants was checked by PCR analysis on genomic DNA, and these cells were transformed with plasmid pCK17 (39), which contains a wild-type copy of TFC4. After sporulation and dissection, a His3+ spore containing pCK17 was chosen to yield strain YHD3. Plasmids harboring mutant alleles of TFC4 were substituted to wild-type TFC4 in YHD3 by shuffling out the wild-type copy on plates containing 5-fluoro-orotic acid. Strain YHD7, which harbored a mutant TFC4 gene lacking the second TPR unit, was built in this way. Viable strains isolated at 30°C were also tested for growth at 37 and 16°C.
Cloning of the Kluyveromyces lactis
131 ortholog.
The gene coding for the K. lactis ortholog of
131 was cloned by genomic PCR using degenerate oligonucleotides targeted to sequences presumably conserved inside the TPR units. Two direct and two reverse oligonucleotides were devised, and one of the four PCR experiments yielded a PCR fragment of the predicted length. In the positive experiment, the sequence of the direct oligonucleotide was TGGGARTTYTGGAARATHGT, targeted at the start of TPR3 (peptide sequence WEFWKIV), and the sequence of the antiparallel oligonucleotide was GGNGTRAARAARTCDATNGC (antiparallel to peptide sequence AIDFFTP), targeted at position 20 of TPR7 (alanine at position 20 is the best-conserved residue in the TPR motif). A K. lactis genomic library in vector KEp6 (a gift from M. Weslowski-Louvel, Université Claude Bernard Lyon 1, Lyon, France) (58) was screened with this PCR fragment, and one clone was isolated that contained a whole ORF (3,087 bases). The resulting protein showed a strong homology to the
131 sequence of S. cerevisiae. Sequencing on both strands by oligonucleotide walking was performed with an ABI 377 Sequencer.
Sequences of other
131 orthologs.
The sequences of
131 Schizosaccharomyces pombe ortholog (accession no. CAA20753), Caenorhabditis elegans (accession no. CAA94857, hypothetical protein ZK856.9), and Drosophila melanogaster (accession no. AAF57909) were identified with the NCBI Blast server (http://www.ncbi.nlm.nih.gov/blast/blast.cgi?Jform = 1) by running BlastP 2.1.2, using the S. cerevisiae sequence as entry. The sequence data from S. pombe were determined by the S. pombe Sequencing Group at the Sanger Centre and can be obtained from ftp://ftp.sanger.ac.uk/pub/yeast/sequences/pombe/. The three sequences have been already annotated as homolog to yeast TFC4 gene. Only amino acids 543 to 1491 of the C. elegans protein were retained, as it appeared that the CAA94857 protein was a fusion of two proteins ortholog to YHR040w and YGR047c (coding for
131). The sequence of the
131 Candida albicans ortholog was identified in the unpublished sequence named con6-2367 using the NCBI Blast server http://www.ncbi.nlm.nih.gov/Microb_blast/unfinishedgenome.html. Sequence data for C. albicans was obtained from the Stanford DNA Sequencing and Technology Center website at http://www-sequence.stanford.edu/group/candida. Sequencing of C. albicans was accomplished with the support of the NIDR and the Burroughs Wellcome Fund.
Purification of wild-type and mutant TFIIIC.
TFIIIC was purified starting from about 14 g of S. cerevisiae cells using fast protein liquid chromatography grade resins. Cells were harvested in the exponential phase, and crude extracts were prepared as described by Huet et al. (22). The extracts were first diluted to 0.25 M ammonium sulfate (AS) with buffer I (20 mM Tris-HCl [pH 8.0], 0.5 mM EDTA, 10 mM ß-mercaptoethanol, 10% [vol/vol] glycerol), then they were loaded at 2.5 ml/min onto a 25-ml heparin Hyper-D (BioSepra) column previously equilibrated with buffer I (0.25 M AS). The resin was then washed at 5 ml/min with 250 ml of buffer I (0.35 M AS). A linear gradient of AS from 0.35 to 0.70 M in 180 ml of buffer I was then applied at 2.5 ml/min. Fractions (2 ml) were collected and assayed for TFIIIC-DNA binding activity (see below). TFIIIC-containing fractions (0.45 to 0.55 M AS) were pooled and dialyzed against buffer I (0.07 M AS). Proteins were then loaded at 0.5 ml/min on a 1-ml Mono Q column (Amersham Pharmacia Biotech) previously equilibrated with buffer I (0.07 M AS). The column was then washed at 0.5 ml/min with 20 ml of buffer I (0.07 M AS). A linear gradient of AS from 0.07 to 0.4 M in 15 ml of buffer I was then applied at 0.5 ml/min. Fractions (200 µl) containing TFIIIC-DNA binding activity were eluted between 0.24 and 0.30 M AS. Based on Western blotting experiments using anti-
55 and anti-
60 polyclonal antibodies, the TFIIIC preparation from wild-type cells was found to contain fivefold more factor than the TFIIC-
TPR2 preparation.
DNA binding and in vitro transcription assays. TFIIIC-tDNA interactions were monitored by gel retardation analysis as described previously (22, 34). Mono Q-purified TFIIIC fractions (100 ng of protein) were incubated with 32P-labeled DNA fragment (3 to 10 fmol; 4,000 to 10,000 cpm) carrying the tRNA3Leu (327 bp) or tRNA3Glu (198 bp) genes for 15 min at 25°C in a 15-µl reaction mixture containing 10 mM Tris-HCl (pH 8.0), 10% (vol/vol) glycerol, 180 mM monovalent cations (K+ and NH4+), 10 µg of bovine serum albumin, and 200 ng of competitor DNA (pBluescript-SK). Transcription mixtures (40 µl) contained standard transcription buffer (20 mM HEPES [pH 8.0], 5 mM MgCl2, 1 mM dithiothreitol, 0.1 mM EDTA), 5% (vol/vol) glycerol, 8 units of RNasin (Amersham Pharmacia Biotech), 0.6 mM concentrations each of ATP, GTP, and CTP, 0.03 mM UTP and 10 µCi of [32P]UTP, recombinant TBP (250 ng), recombinant Brf1 (1.2 µg), and partially purified B" fraction (1.8 µg), RNA Pol III (50 ng), and TFIIIC (Mono Q fraction, 100 ng of protein). The concentration of monovalent cations was 110 mM. Protein fractions were prepared according to the method of Huet et al. (22). After 10 min of preincubation at 25°C, the transcription reaction was started by addition of 130 ng of plasmid pRS316-SUP4, containing the yeast SUP4 tRNATyr gene (a gift from B. D. Hall), and allowed to proceed for 45 min at 25°C. Transcripts were analyzed by electrophoresis on an 8 M urea gel (6% polyacrylamide) and revealed by autoradiography. Single-round transcription experiments were performed by incubating the reaction mixture in the absence of GTP (29). Addition of heparin and GTP (300-µg/ml and 0.6 mM final concentrations, respectively) allowed to pursue transcription for 10 min at 25°C. The artificially engineered tRNA Leu genes, displaying various A block-B block distances, have already been described (4).
Preparation of recombinant B" protein. The vector expressing TFC5 gene (coding for B") has been described previously (51). This construct was transformed into Escherichia coli strain BL21(LysS) for expression of recombinant B" (rB") protein fused at its N terminus to six histidines and the T7-Tag (Novagen) epitope; cultures were grown at 37°C up to an optical density of 0.4 at 600 nm before adding isopropylthio-ß-d-galactoside (IPTG) at 2 mM. After a further 2-h growth at 30°C, cells were harvested and proteins were purified by Ni2+ batch column, essentially as described by Chaussivert et al. (12). Western analysis was performed to monitor rB" purification with T7-Tag antibodies.
Production of recombinant baculoviruses.
PCR-mediated mutagenesis was used to insert unique restriction sites at the boundaries of the ORFs coding for
131, B", and TBP. The NheI/
131/SpeI or NheI/Gea1/NotI (48) restriction endonuclease fragments were subcloned into the XbaI site of the PVLGST vector (1). The NheI/B"/NotI restriction endonuclease fragment was subcloned into the NheI/NotI sites of a modified PVL1393 (PharMingen) containing an octa-histidine tag. The NheI/TBP/NotI restriction endonuclease fragment was subcloned into the NheI/NotI sites of a modified PVL1393 (PharMingen) containing a calmodulin binding peptide (PCR amplified from vector pCAL-n; Stratagene, La Jolla, Calif.). The resulting transfer vectors were recombined with baculovirus DNA (Bac3000; Novagen) in High Five cells (Invitrogen). The High Five cells were grown in the express five medium complemented with L-glutamine (Life Technologies) at 28°C. The recombinant viruses were plaque purified; stocks were prepared by three-step growth amplification as described by OReilly et al. (44).
Coexpression and copurification of
131 and B".
High Five cells (typically 2 x 108 cells) were coinfected with pairs of the appropriate baculovirus (B" + GST-
131 or TBP + GST-
131). Multiplicities of infection (between 2 and 10 PFU/cell) were adjusted so as to balance the amount of recombinant proteins simultaneously expressed from each virus. The cells were collected 72 h postinfection, washed in phosphate-buffered saline, and lysed by three cycles of freeze-thawing followed by sonication in buffer A (50 mM Tris [pH 7.5], 100 mM NaCl, 20% glycerol, 1% NP-40, 5 mM ß-mercaptoethanol, and 1x protease inhibitor cocktail). The extract was then clarified by ultracentrifugation (30,000 x g, 1 h) at 4°C and loaded continuously overnight onto 2 ml of GSH-Fast Flow resin (Pharmacia) at 0.4 ml/min. The column was washed at 1 ml/min with 20 column volumes of buffer A and then washed with buffer B (50 mM Tris [pH 7.5], 100 mM NaCl, 20% glycerol, 5 mM ß-mercaptoethanol). Elution was performed at 0.5 ml/min using five column volumes of buffer C (buffer B + 20 mM glutathione with pH adjusted to 8). The protein fractions were concentrated with StrataClean resin (Stratagene) and eluted in electrophoresis sample buffer (100 µl). Proteins retained were analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) (8% acrylamide) followed by either Coomassie blue staining or Western blotting using anti-histidine (QIAGEN) antibody.
Nucleotide sequence accession number. The sequence determined in this study has been deposited in GenBank under accession no. AF229182.
| RESULTS. |
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131 are conserved from yeasts to higher eukaryotes.
The sequence of the
131 subunit is characterized by the presence of 11 TPR motifs and a bHLH-zipper motif (39). On the basis of sequence conservation within the TPR we have cloned the ortholog gene from K. lactis (GenBank accession no. AF229182). With the complete sequencing of several eukaryotic genomes, the sequences of four other orthologs have been found in S. pombe, C. albicans, C. elegans, and D. melanogaster. The human ortholog has been isolated through cDNA cloning by Roeder and coworkers (21). TPR motifs were identified in these ortholog sequences using a TPR consensus sequence derived from 200 TPR motifs of S. cerevisiae (H. Dumay-Odelot and C. Marck, unpublished data). All seven sequences retained the same typical 5-4-1-1 grouping of the 11 TPR motifs (Fig. 1A). This feature was used to sector the sequence of
131 and its orthologs into six regions termed A to F. Outside the TPR regions, the sequences clearly segregated into two phylogenetic groups, the yeasts and higher eukaryotes. Regions C and E were the most divergent between the two groups, while regions F1 and F2, which flanked the last TPR unit, were more highly conserved. The conservation of this global structural organization, with an alternation of high- and low-homology regions, suggested that these proteins were built on a common TPR scaffold. Figure 1B presents the sequence of TPR2 in the seven orthologs: this TPR departed from the usual 34-residue consensus in S. pombe (addition of 4 residues) and D. melanogaster (deletion of 1 residue).
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131 contained a bHLH-zipper motif (39). From the analysis of S. cerevisiae
131 and six of its orthologs, it appeared that most of the residues that defined the bHLH-zipper motif were not conserved, even in the closest ortholog, K. lactis (data not shown). For this reason, we have decided to consider the bHLH-zipper motif of
131 as spurious. However, for the sake of clarity, we have continued using in this work the bHLH-zipper-related names already given to some mutants (e.g.,
Loop,
Zipper, etc.) (12).
Not all TPR motifs are essential for growth.
In a previous deletion analysis of
131, most of the TPR motifs, when deleted individually, were found to be essential (12). However, in the strain YCK107 used for these experiments, the chromosomal copy of the wild-type TFC4 gene had not been fully deleted but simply inactivated by replacing the central part of the gene (residues 169 to 840, representing 65% of the protein) with a HIS3 cassette (39). This gene disruption perhaps resulted in the expression of a truncated form of
131 containing the 168 first amino acids of the protein. Later, it was found that
131 interacted, in the two-hybrid system, with Brf1 and that this interaction could be restricted to
131 (residues 1 to 168) (12). Therefore, there was the possibility that the phenotype of the deletion mutants was altered by the presence of this putative truncated form of the wild-type protein, inasmuch as the N-terminal half of
131 (residues 1 to 580) was found to inhibit, in vitro, the formation of Brf1-TFIIIC-tDNA complex (42). We thus performed the complete deletion of TFC4 (in strain SC55, yielding strain YHD3) and reexamined the phenotype of the
131 deletion mutants (Fig. 2). Indeed, the phenotypes of deletions in the first TPR block (region B in Fig. 1A) changed from lethal to thermosensitive (deletions
TPR2,
TPR3, or
TPR4). On the other hand, the phenotypes of TPR deletions within region D (except for
TPR9) or region F remained unchanged. Deletions within regions B and E induced strain-dependent growth phenotypes. The thermosensitive and recessive phenotype of the
131-
TPR2 mutation in strain YHD3 (previously determined as lethal in YCK107) is illustrated in Fig. 3A. The mutant cells grew slower than the wild type at permissive temperature (generation time, 2.5 instead of 2 h at 30°C) and stopped growing at 37°C. Overexpressing
131-
TPR2 in a wild-type context showed that the phenotype of this mutation was not dominant negative (Fig. 3B). The loss of the wild-type copy of TFC4 was lethal at 30°C, showing that the wild-type copy was responsible for cell viability at permissive temperature (not shown). The conditional phenotype of the
TPR2 mutation prompted us to examine the properties of the mutant factor.
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TPR2 mutation (TFIIIC-
TPR2) was purified from YHD7 strain (tfc4-
;::HIS3 + pUN-
131-
TPR2) and from a strain expressing a hemagglutinin-tagged version of
138, the largest subunit of TFIIIC, to provide a control (33). Mutant and wild-type TFIIIC factors were partially purified, based on a tDNA binding assay, and compared for their ability to direct specific transcription of various tRNA genes in vitro. The same and limiting amount of both TFIIIC preparations, calibrated by Western blot analysis with anti-
55 and anti-
60 polyclonal antibodies, was used in transcription assays in the presence of reconstituted TFIIIB and purified Pol III. As shown in Fig. 4A, the transcriptional activity of the mutant TFIIIC was similar to that of the wild-type factor with several versions of the tRNA3Leu gene harboring different deletions in the region separating the A and B blocks (4). Remarkably, the deletion of TPR2 did not detectably affect the start site position, whatever the distance and the relative helical phasing of the A and B blocks. However, the mutant factor exhibited a marked thermosensitivity: in contrast to the wild-type factor, the mutant factor lost all its transcriptional activity in single-round or multiple-round transcription of the SUP4 tRNA gene, after 10 min of preincubation at 40°C (Fig. 4B). These results suggested that the heat treatment caused or enhanced a conformational change in the mutant factor, incompatible with proper initiation complex formation.
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TPR2 factor.
We first investigated whether the
TPR2 mutation affected the binding of mutant TFIIIC to tDNA using tRNA3Leu and tRNA3Glu genes as a probe. When the same amount of wild-type and mutant TFIIIC factors were used in gel-shift assays, the TFIIIC-
TPR2-DNA complex was formed as efficiently, but it displayed a sensitivity to salt concentration different from that of the wild-type factor (Fig. 5A). The optimum monovalent cation concentration for complex formation was 150 to 180 mM for the wild type and 200 to 230 mM for the mutant factor. This difference in salt concentration optima between wild-type and mutant factors remained unchanged at a twofold higher or lower concentration of competitor DNA (results not shown). In the following experiment, we selected the average monovalent cation concentration of 180 mM to examine the temperature sensitivity of factor-tDNA binding. Incubation at various temperatures, ranging from 25 to 45°C, was done prior to the formation of factor-tDNA complexes, under the same conditions as for transcription assays (Fig. 4). The mutant and wild-type factors showed the same thermosensitivity: DNA binding activities of the mutant and wild-type factors were only moderately affected after a 10-min preincubation at 40°C (Fig. 5B), in sharp contrast with the total loss of transcription activity (Fig. 4B). This observation suggested that the main transcriptional defect occurred after DNA binding, during or after TFIIIB assembly.
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TPR2 mutation affected TFIIIB assembly rather than a later step of transcription like TFIIIC displacement from the transcriptional start site.
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TPR2 is corrected by overdosage of the B" subunit of TFIIIB in vivo and in vitro.
In order to determine the critical step of TFIIIB assembly that mutant TFIIIC-
TPR2 failed to correctly accomplish, we tested whether the overexpression of the components of TFIIIB, TBP, Brf1, or B" was able to suppress the
131-
TPR2 mutation in vivo. TFIIIC-
TPR2 mutant cells were transformed with high-copy-number plasmids harboring the genes of TFIIIB components. A series of cell dilutions of YHD7 was plated on yeast extract-peptone-dextrose medium and incubated at permissive or nonpermissive temperature. Among the three genes coding for the components of TFIIIB, only TFC5 (encoding B") was able to restore growth at 37°C (Fig. 7). This suppression had some allele specificity as other TPR deletions in
131 that confer a thermosensitive phenotype could not be suppressed at nonpermissive temperature by overexpression of B" (
TPR3 and
TPR8) or were only partially suppressed (
TPR4) (data not shown).
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131 in the recruitment of B" on a biochemical basis, we performed multiple-round transcription experiments with the SUP4 tRNA gene as a template at various concentrations of B". Wild-type and mutant TFIIIC were preincubated at 40°C, and monovalent cation concentration was kept constant at 110 mM (Fig. 8A). The dosage-dependent effects of B" on transcriptional efficiency were clearly different for wild-type and mutant TFIIIC. Transcription with the wild-type factor displayed an optimum at B" concentrations around 60 ng/µl; an optimum concentration for B" has been previously observed (16). In contrast, with mutant TFIIIC, the transcription efficiency increased with B" concentration to reach the wild-type level at 120 ng/µl. On the other hand, increasing the concentration of rBrf1 did not correct the transcription defect of mutant TFIIIC (Fig. 8B). This result confirmed that the incorporation of B", and not that of Brf1, into TFIIIB was the critical step of TFIIIB assembly directed by mutant TFIIIC on SUP4 tDNA. These results suggested that the assembly of B" by TFIIIC-
TPR2 factor was the main defective step of the preinitiation complex formation.
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131 and B" proteins interact physically.
A direct interaction between
131 (TFIIICs subunit) and B" (TFIIIBs subunit) was suggested by previous two-hybrid experiments (51) and by the above multicopy suppression experiment. We therefore set out to determine whether
131 could interact directly with B" in the absence of all the other components of TFIIIC and TFIIIB and DNA. To obtain full-length recombinant proteins, we used the baculovirus expression system. To facilitate the identification of the proteins and the purification of the protein complexes, tagged proteins were expressed (GST-
131 and 8His-B"). As revealed by immunoblot analysis, cell crude extracts contained a majority of full-length recombinant proteins (data not shown). High Five insect cells were coinfected with three different pairs of recombinant baculoviruses, GST-
131 and 8His-B", GST-
131 and calmodulin-TBP, or GST-Gea1 and 8His-B". GST-
131 or the GST-Gea1 control was purified from crude extracts on GSH-columns, and glutathione-eluted protein fractions were analyzed by SDS-PAGE followed by Coomassie blue staining and immunoblot analysis. As shown in Fig. 9A, a polypeptide of about 90 kDa specifically copurified with GST-
131 from extracts of cells coexpressing GST-
131 and 8His-B" but not from controls coexpressing GST-Gea1 and 8His-B" or GST-
131 and TBP (Fig. 9A, compare lane 2 to lanes 3 and 4). On the other hand, in the same type of experiment, there was no detectable interaction between the tagged versions of
131 and TBP. Immunoblotting experiments using anti-B" antibodies confirmed the specific copurification of B" with GST-
131 (Fig. 9B, lane 4). No trace of B" was detected in the control experiment using GST-Gea1 instead of GST-
131 (lane 5). Calmodulin-tagged TPB did not copurify with GST-
131 (lane 6). These results showed that
131 interacted directly and specifically with B". A reverse experiment gave the same result: the GST-
131 subunit was found to copurify with 8His-B" after immobilized metal ion affinity chromatography (IMAC) purification performed on extracts coexpressing GST-
131 + 8His-B" (data not shown).
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| DISCUSSION |
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131, the TPR-containing and most upstream subunit of yeast TFIIIC, participates in the recruitment of B" on class III genes. The
131 subunit of TFIIIC and the B" component of TFIIIB are two major actors of preinitiation complex assembly.
131 extends from downstream of block A to within the TFIIIB binding site (5, 6), interacts with Brf1 (12, 30), and undergoes profound and successive conformational changes upon TFIIIB assembly onto DNA as evidenced by the altered pattern of
131-DNA cross-linking during complex assembly and by the variable placement of TFIIIB on templates with altered 5' sequences (23, 25, 27). While the interaction between Brf1 and
131 is the limiting step for transcription complex assembly in vitro (27, 42, 43, 55), it is the recruitment of B" that confers the characteristic of fully assembled TFIIIB-DNA complex: much increased resistance to heparin and high-salt treatments, further DNA bending, accessibility of the transcription start site to DNase I, and rearrangement of
131, Brf1, and TBP in the complex (26, 27, 31, 47). Of prime interest, therefore, is the mechanism of B" recruitment by TFIIIC. Deletion studies have shown that B" can be extensively truncated on either end and still retain TFIIIC-independent transcription activity on the TATA-containing SNR6 gene, but not TFIIIC-dependent activity on a tRNA gene (31). This striking observation suggested complex interactions of B" with TFIIIC components, likely the
131 subunit (31).
We focused on a specific deletion mutant of
131 removing precisely the TPR2 for several reasons. First, an attractive model of TFIIIB assembly suggested that
131, with its many TPR motifs, provides the elasticity that allows variable placement of TFIIIB by the TFIIIC-DNA complex (23, 39). The deletion of the TPR motif vicinal to the N-terminal part of
131 involved in Brf1 recruitment was expected to alter the geometric requisites of this interaction. However, we noted no qualitative defect in transcription accuracy of different templates (Fig. 4A and data not shown). Second, previous genetic studies had pointed to TPR2 as the central target of mutations enhancing transcription of tRNA gene bearing a defective A block by facilitating Brf1 recruitment (43, 49). Unexpectedly, however, the thermosensitive phenotype of the
TPR2 mutant was selectively suppressed by overexpression of B" and not by that of Brf1 or TBP. The TFIIIC-
TPR2 transcriptional defect was also suppressed in vitro by increasing the concentration of B", not that of Brf1 (Fig. 9). These results suggested that TFIIIC-
TPR2 was primarily affected at the level of B" recruitment. Two-hybrid experiments between each of the six subunits of TFIIIC and B" gave a positive interaction signal with the
131-B" pair only, and
131-
TPR2 was even more efficient than wild-type
131 (51). While quantitative two-hybrid responses are difficult to interpret in the absence of protein expression data, these observations suggested that
131 is likely involved in B" binding and that the interaction does not require the TPR2 motif. The
131-B" interaction domain remains to be identified. In vitro competition experiments did not disclose any interaction between B" and the N-terminal half of
131 (
131 residues 1 to 580) encompassing TPR 1 to 9, which, however, interacted detectably with Brf1 in solution (42). Two-hybrid experiments using
131 (residues 1 to 579) were similarly negative with B" (51) but positive with Brf1 (12).
To investigate a possible direct interaction between
131 and B", we therefore turned to the baculovirus and insect cell system to coexpress the full-length proteins. Under these conditions, the formation of a
131-B" complex was demonstrated by the selective copurification of the two proteins (Fig. 9).
131 appears, therefore, to play a central role in TFIIIB assembly since it is the only TFIIIC subunit to detectably interact with both Brf1 and B". Remarkably, no interaction between
131 and TBP could be detected by the coexpression-copurification assay. As previously reported, the recruitment of TBP is directed by Brf1 (27, 30, 35) probably together with
60 (16). It is notable that the mutant factor has modified DNA binding properties, which suggests an additional role for
131 in TFIIIC-DNA binding. However, no evidence for DNA binding by recombinant
131 was found (J. Acker, unpublished results); these results are much like those of Moir et al., who used recombinant
131 (residues 1 to 580) (42).
How to rationalize the effect of the
TPR2 mutation on the function of
131 within TFIIIC? TPR2 does not provide a critical interaction site for TFIIIB or TFIIIC components, since the mutant cells are viable at permissive temperature. However, TPR2 could be involved in the conformation changes that occur during the TFIIIB assembly. Hence, the mutations in or in close vicinity of TPR2 could facilitate the Brf1 recruitment by favoring the conformation of
131 required for that specific step (42). In the process of Brf1 loading,
131 appears to undergo structural changes important for allowing the entry of B" into the preinitiation complex (27, 29, 31). The deletion of TPR2, in changing the geometry of
131, could interfere with this dynamic process, for instance by stabilizing a transient conformation state favorable for Brf1 recruitment but unfavorable for B" assembly. This interpretation is in favor of a two-step assembly pathway for Brf1 and B". The fact that multicopy expression of B" suppresses the
TPR2 phenotype also suggests the existence of a specific incorporation step for B". If there are two predominant steps for TFIIIB assembly in vivo (B' and then B"), then
131 does get involved in both steps.
Based on the structures of two TPR proteins (15, 53), adjacent TPR motifs are tightly packed to form a superhelical structure that forms a concave surface used, in some case, in ligand binding (53). The deletion of TPR2 could mimic a reordering of the interactions within the TPR1-to-TPR5 block, with TPR1 and TPR3 interacting directly and TPR2 being flipped out of the TPR superhelix. The structure of the TPR motif calls for the presence of small hydrophobic residues at positions 8, 20, and 27 (32, 53), and we have noted that, in TPR2, residue 20 is not A as is usually found in the other TPR of
131 (C in the four yeasts or F in D. melanogaster [Fig. 1B]). Four intervening residues are also found in the S. pombe ortholog, and one deletion occurs in the D. melanogaster ortholog. These deviations in the sequence of TPR2 suggest a special role for this motif. We were initially surprised to find that the deletion of TPR2 did not affect the transcription accuracy (i.e., TFIIIB placement). In fact, the N terminus of
131 would be shortened by only 8.5 Å due to the tilting of the TPR
-helices with respect to the axis of the TPR superhelix (15). Further insights into such a complex trancription factor will require a structural analysis of
131, isolated or reassembled into the
A complex.
| ACKNOWLEDGMENTS |
|---|
H.D.-O. acknowledges fellowships from the French Ministère de lÉducation Nationale, de la Recherche et de la Technologie, and from the Association pour la Recherche contre le Cancer.
| FOOTNOTES |
|---|
Present address: CNRS, UMR 8532, LBPA, École Normale Supérieure de Cachan, F-94235 Cachan Cedex, France. ![]()
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