Drosophila Mitochondrial Transcription Factor B1 Modulates Mitochondrial Translation but Not Transcription or DNA Copy Number in Schneider Cells*

We report the cloning and molecular analysis of Drosophila mitochondrial transcription factor (d-mtTF) B1. An RNA interference (RNAi) construct was designed that reduces expression of d-mtTFB1 to 5% of its normal level in Schneider cells. In striking contrast with our previous study on d-mtTFB2, we found that RNAi knock-down of d-mtTFB1 does not change the abundance of specific mitochondrial RNA transcripts, nor does it affect the copy number of mitochondrial DNA. In a corollary manner, overexpression of d-mtTFB1 did not increase either the abundance of mitochondrial RNA transcripts or mitochondrial DNA copy number. Our data suggest that, unlike d-mtTFB2, d-mtTFB1 does not have a critical role in either transcription or regulation of the copy number of mitochondrial DNA. Instead, because we found that RNAi knockdown of d-mtTFB1 reduces mitochondrial protein synthesis, we propose that it serves its primary role in modulating translation. Our work represents the first study to document the role of mtTFB1 in vivo and establishes clearly functional differences between mtTFB1 and mtTFB2.

Mitochondrial number and DNA content vary widely depending on cellular energy requirements, which are met in large part by ATP production by the oxidative phosphorylation pathway. Expression of the 13 polypeptides involved in oxidative phosphorylation that are encoded in the mtDNA 1 genome is essential for this process. Transcription in animal mitochondria is thought to involve mitochondrial RNA polymerase and three distinct transcription factors (1,2). Mitochondrial transcription factor A (formerly referred to as mtTFA) contains two HMG boxes and was shown in organello to bind nonspecifically at regularly phased intervals to the control region of human mtDNA (3) and to package mtDNA in nucleoids (4,5). Human mitochondrial transcription factor A was also shown to be required for specific initiation at mitochondrial promoters in vitro (6 -9). Two additional human transcription factors, mtTFB1/TFB1M and mtTFB2/TFB2M, have also been shown to activate transcription from mitochondrial promoters in the presence of mitochondrial transcription factor A and mitochondrial RNA polymerase in vitro, and h-mtTFB2 is more active in promoting transcription than h-mtTFB1 (6,10). Recent studies show that h-mtTFB1 has rRNA adenine dimethyltransferase activity when expressed in bacteria (11) and that its in vitro transcriptional activation and methylase activities can be inactivated differentially by mutation (12).
Although in vitro studies show that both mtTFB1 and mtTFB2 support transcription from human mitochondrial promoters (6), their relative importance and specific physiological roles are not well understood. In a recent study (13), we showed that RNAi knockdown of d-mtTFB2 reduces the abundance of specific mitochondrial RNA transcripts and decreases the copy number of mtDNA in Drosophila cultured cells. This finding suggests that endogenous d-mtTFB1 cannot complement a deficiency in d-mtTFB2 and thus is not functionally redundant with d-mtTFB2, pointing to specialized roles for the two transcription factors in vivo. Here, we report the cloning and overexpression of Drosophila mtTFB1 and the knockdown phenotype of Drosophila Schneider cells treated with d-mtTFB1targeted RNAi. Our results do not support an important role for mtTFB1 in either efficient mitochondrial transcription or maintenance of mtDNA. Rather, we found that mtTFB1 modulates mitochondrial translation.

EXPERIMENTAL PROCEDURES
Identification and Sequence Analysis of d-mtTFB1 cDNA-The amino acid sequence of d-mtTFB1 was used to search the Berkeley Drosophila Genome Project Data Base. One sequence (CG7319) was identified that has a high level of homology to d-mtTFB1. Full-length cDNA was prepared using the SMART RACE cDNA amplification kit (Clontech), total RNA from Drosophila Schneider S2 cells, and the following primers; 5Ј-TTACCCAACTTGCTACTCTTGGTGG-3Ј and 5Ј-GGGCTCGAGGCACCTTGGCTATGAATTTGTGCTC-3Ј for 5Ј-RACE, and 5Ј-CAAAATGGACGGTGGTTCCAGG-3Ј and 5Ј-GGGGAATTCCT-TCAAGCACTTGATCAACTCC-3Ј for 3Ј-RACE. RACE products were purified from an agarose gel and sequenced, and sequence analysis was performed using MacDNASIS version 3.7 (Hitachi Software). Similarity searches against the non-redundant GenBank TM data base were performed using BLAST (14). The deduced amino acid sequence was checked for targeting signal peptides using iPSORT (15) and MITPROT (16). Multiple sequence alignments were performed with ClustalW (17).
Bacterial Overexpression of d-mtTFB1 and Preparation of d-mtTFB1 Antibody-To express d-mtTFB1 in Escherichia coli, a PCR fragment of d-mtTFB1 cDNA encoding amino acid residues Gly-12 to Leu-330 was cloned into pET-28a (Novagen) cleaved with EcoRI and XhoI. Bacterial cells harboring the plasmid were grown in LB medium containing 100 g/ml kanamycin, and expression was induced with 1 mM isopropylthiogalactoside. The C-terminal His 6 tag was utilized for nickel-nitrilotriacetic acid affinity purification of recombinant d-mtTFB1 according to the manufacturer's instructions (Qiagen). Rabbits were immunized by injection of column-purified d-mtTFB1 in Freund's complete adjuvant, followed by secondary immunization in Freund's incomplete adjuvant. To prepare affinity-purified antiserum, purified d-mtTFB1 (100 g) was bound to a polyvinylidene difluoride membrane, and the filter was preincubated for 1 h with 5% skim milk in PBS, incubated for 1 h with crude antiserum (1 ml in 5 ml of PBS containing 0.1% Tween 20), washed four times with PBS containing 0.1% Tween 20, and eluted with 0.2 M glycine-HCl (pH 2.4) (ϳ5 ml). The eluted antibody was neutralized with 1 M Tris base.
Preparation of Inducible Plasmids Expressing d-mtTFB1 and d-mtTFB1-targeted RNAi-The plasmid pMt/B1/Hy, in which d-mtTFB1 cDNA is regulated by the metallothionein promoter, was constructed as follows: a fragment of d-mtTFB1 cDNA was amplified by PCR using 5Ј-GGGCTCGAGGAAGTCGTTGCACAACAG-3Ј as 5Јprimer and 5Ј-GCGCACTAGTCAGGAGTGAAATCGTTGC-3Ј as 3Јprimer. The PCR fragment was cleaved by XhoI and SpeI and subcloned. The plasmid pMt/invB1/Hy carries an inverted repeat of a nucleotide sequence from d-mtTFB1 cDNA that is transcribed from the metallothionein promoter. The insert in pMt/invB1/Hy was generated from two PCR-amplified fragments of d-mtTFB1 cDNA. One fragment has terminal XhoI and EcoRI sites and was prepared using the following pair of primers: 5Ј-CGCCTCGAGACTAGTACGGACAAGAT-AGTCAAGTCG-3Ј (forward) and 5Ј-CGCGAATTCGGGATCGATTAGC-TTCTCAGCAACCTCCTC-3Ј (reverse). A second fragment has terminal SpeI and EcoRI sites and was prepared using the primers 5Ј-CGCCT-CGAGACTAGTACGGACAAGATAGTCAAGTCG-3Ј (forward) and 5Ј-C-GCGAATTCAAAAAGCTTTAGCTTCTCAGCAACCTCCTC-3Ј (reverse). The two PCR products were ligated and cloned into the pMt/Hy vector cleaved with XhoI and SpeI.
Generation and Induction of Stable Cell Lines-Drosophila Schneider S2 cells were cultured at 25°C in Drosophila Schneider Medium (Invitrogen) supplemented with 10% fetal bovine serum. Cells were subcultured to 3 ϫ 10 6 cells/ml every third day. Cells were transfected using Effectene (Qiagen). Hygromycin-resistant cells were selected with 200 g/l hygromycin. Cells were passaged at least five times in hygromycin-containing medium and then cultured in standard medium. The cell lines were grown to a density of 3 ϫ 10 6 cells/ml and then treated with 0.4 mM CuSO 4 to induce high level expression from the metallothionein promoter (18). Overexpression of d-mtTFB1 was effected by growth of the cell culture in the presence of 0.05, 0.1, and 0.4 mMCuSO 4 .
Analysis of Mitochondrial Protein Synthesis-Cell lines were grown in the presence or absence of 0.4 mM CuSO 4 for 10 days. Cells were harvested at room temperature, washed twice with methionine-free Grace's insect culture medium (Invitrogen), and resuspended at 3 ϫ 10 6 cells/ml in methionine-free Grace's insect culture medium supplemented with 10% dialyzed fetal bovine serum, 200 g/ml emetine, and 100 g/ml cycloheximide. Five minutes after cell resuspension, 35 S-Trans-label (ICN) was added to 300 Ci/ml, and the cells were incubated for 2 h at 25°C. After incubation, the cells were diluted with 2 volumes of Schneider Medium and then washed twice with PBS. The cells were lysed in 10 mM Tris-HCl (pH 7.5), 1 mM EDTA, and 1% SDS. Total cellular protein (30 g/lane) was fractionated by 15-20% gradient SDS-PAGE. The gels were stained with Coomassie Brilliant Blue and dried. The gels were autoradiographed by exposure to x-ray film (Kodak) for 3-10 days; the mitochondrial polypeptides indicated at right in Fig. 5 were quantitated from two independent experiments using the Kodak 1D program software.
Immunoblotting-Total cellular protein (20 g/lane) was fractionated by 10.5% SDS-PAGE and transferred to nitrocellulose filters. Filters were preincubated for 1 h with 5% skim milk in PBS, followed by incubation for 1 h with d-mtTFB1 antibody (1:20) in PBS containing 0.1% Tween 20. Filters were washed four times with PBS containing 0.1% Tween 20, incubated for 1 h with horseradish peroxidase-conjugated anti-rabbit IgG (Bio-Rad), and washed with PBS containing 0.1% Tween 20. Protein bands were visualized using ECL Western blotting reagents (Amersham Biosciences). Polyclonal antibody against Drosophila mtTFB2 was prepared and used as described in Ref. 13.
Genomic DNA was purified from Drosophila Schneider S2 cells by standard methods. DNA (5 g/lane) was cleaved with XhoI, fractionated in a 0.8% agarose/TBE gel, and transferred to nylon membrane. Hybridization was performed as described above. Filters were washed three times for 10 min at room temperature with 2ϫ SSC containing 0.1% SDS, washed once for 30 min at 65°C with 0.2ϫ SSC containing 0.1% SDS, and then analyzed with a PhosphorImager. Blots were probed with radiolabeled DNAs for the mitochondrial gene Cytb and the nuclear histone gene cluster. The ratio of the signals for these two genes was used to determine the relative copy number of mtDNA.

RNAi-dependent Knockdown of d-mtTFB1 Does Not Reduce
Mitochondrial Transcription and Does Not Induce mtDNA Depletion in Schneider Cells-The sequence of a putative d-mtTFB1 (10) was used to identify and clone a full-length cDNA by RACE. The cDNA clone obtained is 1530 nucleotides and encodes a predicted polypeptide of 330 amino acids. Rabbit antiserum was raised against a recombinant, truncated form of d-mtTFB1 (Gly-12 to Leu-330). The antibody detects a single polypeptide in mitochondrial extracts from Drosophila Schneider cells with an electrophoretic mobility corresponding to an approximate molecular mass of 38 kDa (Fig. 1A). Immunoblot analysis of subcellular fractions of Drosophila Schneider cells demonstrated that d-mtTFB1 is localized to the mitochondria (data not shown).
Cells stably expressing pMt/invB1/Hy or the control plasmid pMt/Hy were cultured for 10 days in the presence or absence of 0.4 mM CuSO 4 . Immunoblot analysis of copper-treated cells showed an undetectable level of d-mtTFB1 in cells carrying pMt/invB1/Hy (Fig. 1B). Basal, uninduced expression from pMt/invB1/Hy also repressed expression of d-mtTFB1 by 6-fold. In contrast, expression of d-mtTFB2 was unchanged under all experimental conditions. RT-PCR analysis of coppertreated cells showed that cells carrying pMt/invB1/Hy expressed 20-fold less d-mtTFB1 RNA than cells carrying the control vector, and basal, uninduced expression from pMt/ invB1/Hy also suppressed expression of d-mtTFB1 RNA by 7-fold (Fig. 1C). Copper-treated cells carrying pMt/invB1/Hy showed moderate growth retardation, but copper treatment had no adverse effects on growth of control cells (data not shown). This finding contrasts with the poor growth and reduced viability phenotype we observed upon similar reduction of d-mtTFB2 using the RNAi strategy (13).
The biological function of d-mtTFB1 was examined in cells expressing d-mtTFB1-targeted RNAi. Transcription of several mitochondrial genes and mtDNA copy number were measured in cells with no plasmid and cells carrying pMt/Hy or pMt/ invB1/Hy. Northern blots were used to quantitate the relative expression of the Cytb, ND4, and 12S rRNA genes in cells grown for 10 days in the presence or absence of copper. Neither basal nor induced expression of d-mtTFB1-targeted RNAi resulted in reduced transcript levels for 12S rRNA, ND4, or Cytb (Fig. 2); transcript levels were unchanged, both before and after induction, as compared with the level of transcripts from the nuclear gene RP49 used as a control. These results argue that either d-mtTFB1 is not critical for transcription of either strand of Drosophila mtDNA or its endogenous level is markedly higher than that which is required for transcription. With regard to the latter, however, we find that the physiological level of d-mtTFB1 is, at most, severalfold higher than that of d-mtTFB2 (data not shown). RNAi knockdown of d-mtTFB2 (13) but not d-mtTFB1 results in a substantial reduction in mitochondrial transcription. This, combined with the observation that mtTFB2 is apparently 10-fold more effective in stimulating mitochondrial transcription in vitro than mtTFB1 (6), supports our conclusion of the relative lack of physiological importance of mtTFB1 in mitochondrial transcription.
The copy number of mtDNA was also unchanged in cells expressing d-mtTFB1-targeted RNAi. Total cellular DNA was isolated from cells with no plasmid and cells carrying pMt/Hy or pMt/invB1/Hy, cleaved with XhoI, and analyzed by Southern blot. Blots were hybridized sequentially with probes for the nuclear histone gene cluster and for the mitochondrial gene Cytb (Fig. 3A). Relative mtDNA copy number was determined from the ratio of Cytb hybridization to histone cluster hybridization (Fig. 3B). After induction of d-mtTFB1-targeted RNAi for 10 days, relative mtDNA copy number was almost the same as the control. This result suggests that d-mtTFB1 is not critical for maintenance of mtDNA.

Overexpression of d-mtTFB1 Has No Effect on Mitochondrial Transcription or mtDNA Copy Number-d-mtTFB1
was subcloned into the inducible expression vector pMt/Hy under the control of the metallothionein promoter. The resulting expression vector, pMt/mtTFB1/Hy, was introduced into Schneider cells, and stable cell lines harboring this plasmid were cultured in the presence of 0, 0.05, 0.1, and 0.4 mM CuSO 4 . After 10 days of incubation, immunoblot analysis indicated a 2-50-fold increase in d-mtTFB1 relative to that in the uninduced control (Fig. 4A). At the same time, d-mtTFB2 expression was unchanged under all experimental conditions (Fig. 4A). Overexpression had no effect on cell growth or viability (data not shown). The effect of d-mtTFB1 overexpression on mitochondrial transcript abundance was evaluated by Northern blots. Blots were probed for transcripts from the mitochondrial 12S rRNA, ND4, and Cytb genes and for nuclear RP49 gene as a control (Fig. 4B). We found that the levels of all three mitochondrial RNA transcripts were unchanged. Similarly, we found that the relative copy number of mtDNA was also unchanged in cells that overexpress d-mtTFB1 (Fig. 4C).
RNAi-dependent Knockdown of d-mtTFB1 Reduces the Efficiency of Mitochondrial Translation-The apparent lack of mo- FIG. 1. Expression of d-mtTFB1-targeted RNAi in Schneider cells. A, immunoblot analysis of mitochondrial extracts probed with affinity-purified rabbit antiserum against d-mtTFB1. B, Schneider cells with no plasmid (control) or carrying pMt/Hy (vector) or pMt/invB1/Hy (RNAiB1) were cultured for 10 days in the presence or absence of 0.4 mM CuSO 4 . Protein extracts (20 g) were fractionated by 10.5% SDS-PAGE, transferred to nitrocellulose filters, and probed with rabbit antiserum against d-mtTFB1 or d-mtTFB2 as indicated. C, total RNA was extracted from Schneider cells (control) or Schneider cells carrying pMt/Hy (vector) or pMt/invB1/Hy (RNAiB1) after 10 days of culture in the presence or absence of 0.4 mM CuSO 4 . RNAs were analyzed by RT-PCR. PCR products were run on a 1.2% agarose gel and stained with ethidium bromide. The relative abundance of the d-mtTFB1 PCR product was evaluated by densitometric scanning and normalizing its level to that of nuclear RP49 as a control.

FIG. 2. Effects of RNAi on the level of mitochondrial transcription.
A, total RNA (5 g) was extracted from Schneider cells (control) or Schneider cells carrying pMt/Hy (vector) or pMt/invB1/Hy (RNAiB1) after 10 days of culture in the presence or absence of 0.4 mM CuSO 4 . RNA was fractionated in a 1.2% agarose/formaldehyde gel, blotted to nylon membrane, and hybridized with radiolabeled probes for the mitochondrial transcripts 12S rRNA, ND4, and Cytb and the nuclear transcript RP49. B, relative transcription efficiency was quantitated by normalizing mitochondrial transcript abundance to that of RP49.

FIG. 3. Effect of RNAi on the copy number of mtDNA.
A, total DNA (5 g) was isolated from control Schneider cells (control) or Schneider cells carrying pMt/Hy (vector) or pMt/invB1/Hy (RNAiB1) after 10 days of culture in the presence or absence of 0.4 mM CuSO 4 . DNA was digested with XhoI, fractionated in a 0.7% agarose/TBE gel, and blotted to nylon membrane. The membrane was hybridized with radiolabeled probe for the histone gene cluster (control) and then stripped and re-hybridized with radiolabeled probe for Cytb. B, relative mtDNA copy number was quantitated as described under "Experimental Procedures." lecular defects in either mitochondrial transcription or mtDNA replication, upon either RNAi knockdown or overexpression of d-mtTFB1, and recent studies showing that human mtTFB1 catalyzes rRNA adenosine dimethyltransferase activity when expressed in E. coli (11) led us to examine mitochondrial protein synthesis in cells with no plasmid and cells carrying pMt/Hy or pMt/invB1/Hy. The cell lines were cultured for 10 days in the presence or absence of 0.4 mM CuSO 4 . Pulse labeling of mitochondrial translation was then performed for 2 h in the presence of emetine and cycloheximide, specific inhibitors of cytoplasmic protein synthesis, and Fig. 5 shows the mitochondrial protein synthesis pattern obtained. This pattern was eliminated in the presence of 100 g/ml chloramphenicol, a specific inhibitor of mitochondrial protein synthesis (data not shown). We observed no significant effect on mitochondrial translation in either cells carrying no plasmid or cells carrying pMt/Hy in the presence or absence of induction. However, basal expression of d-mtTFB1-targeted RNAi reduced the newly synthesized mitochondrial proteins to 70% of their levels in control cells, and after induction in the presence of copper, mitochondrial protein synthesis was reduced further to 40% of that in control cells. These data show that d-mtTFB1 modulates mitochondrial translation in Schneider cells. The fact that we observed only a modest effect on translation despite a large reduction in mtTFB1 levels suggests endogenous d-mtTFB1 exceeds that required for dimethylation of mitochondrial 12S rRNA. Consistent with that conclusion, we found that a 2-50fold overexpression of d-mtTFB1 has no effect on either the pattern or abundance of mitochondrial proteins (data not shown).

DISCUSSION
Drosophila mtTFB1 shares homology with human mtTFB1, which has been shown to stimulate mitochondrial transcription in vitro (6) and to have rRNA adenine dimethyltransferase activity in bacteria (11). In Drosophila Schneider cells treated with RNAi, d-mtTFB1 is expressed at 5% of the endogenous level. Although abundance of mitochondrial transcripts and mtDNA copy number were unchanged, RNAi treatment reduces the level of mitochondrial protein synthesis. Overexpression of d-mtTFB1 does not stimulate transcription of mitochondrial genes, nor does it increase mtDNA copy number. These data provide the first evidence that animal mtTFB1 plays a significant role in mitochondrial translation but apparently does not serve a critical function in mitochondrial transcription or mtDNA maintenance in vivo.
In an earlier report (13), we demonstrated that the abundance of d-mtTFB2 influences both mitochondrial transcription and the efficiency of mtDNA replication. It is particularly significant that RNAi knockdown of d-mtTFB2 lowers the efficiency of mitochondrial transcription in Drosophila cultured cells because the data suggest strongly that endogenous mtTFB1 cannot complement a deficiency in mtTFB2. In striking contrast, neither RNAi knockdown nor overexpression of mtTFB1 affects the levels of mitochondrial transcripts or mtDNA copy number in Drosophila cultured cells. In vitro studies have shown that both mtTFB1 and mtTFB2 support transcription from human mitochondrial promoters (6), but their relative importance and specific roles are not well understood. Our data argue strongly that either mtTFB1 does not play an important role in mitochondrial transcription in vivo or endogenous mtTFB2 is functionally redundant with the role of mtTFB1 in transcription. In this regard, it has been reported that h-mtTFB1 has rRNA methyltransferase activity (11) and that h-mtTFB2 is at least 1 order of magnitude more active in promoting transcription in vitro than h-mtTFB1 (6).
In composite, our current and previous data (13) document functional differences between mtTFB1 and mtTFB2 in vivo. Both mtTFB1 and mtTFB2 are related in primary sequence to a family of rRNA adenine dimethyltransferases that modify two adjacent adenosine bases near the 3Ј-end of small subunit rRNA to produce N 6 ,N 6 -dimethyladenosine (25), and Shadel and co-workers (11) have shown that h-mtTFB1 can methylate E. coli small rRNA in vivo. Fig. 6 shows an amino acid sequence alignment between bacterial (KsgA and ErmCЈ) and yeast (Dim1) rRNA adenine dimethyltransferases and mtTFBs. KsgA and ErmCЈ are well-studied rRNA adenine dimethyltransferases (26 -29), and the three-dimensional structure of sc-mtTFB (30) is very similar to those of KsgA (31) and ErmCЈ (32). Thus, we aligned KsgA, ErmCЈ, and sc-mtTFB based on their structures, and the mtTFB1s and mtTFB2s are aligned based on sequence homology with KsgA and ErmCЈ. The Nterminal domains of KsgA and ErmCЈ share a negatively charged pocket that corresponds to residues in the canonical S-adenosyl-L-methionine (S-AdoMet)-binding site, and 12 residues in ErmCЈ were shown to interact directly with S- AdoMet   FIG. 4. mtRNA and mtDNA abundance in Schneider cells overexpressing d-mtTFB1. Schneider cells (control, C) or Schneider cells carrying pMt/Hy (vector, V) or pMt/mtTFB1/Hy (oexB1) were grown for 10 days in the presence or absence of CuSO 4 as described under "Experimental Procedures." A, immunoblot analysis of d-mtTFB1 and d-mtTFB2 was carried out as described in the Fig. 1 legend. B, Northern blot analysis using probes for 12S rRNA, ND4, Cytb, and RP49 was carried out as described in the Fig. 3 (33). Most of these residues are well conserved in ErmCЈ, KsgA, Dim1, and mtTFB1s but are poorly conserved in sc-mtTFB and mtTFB2s. Absolutely conserved residues among KsgA family members that are indicated in Fig. 6 are also well conserved in ErmCЈ, Dim1, and mtTFB1s. In contrast, fewer than half are conserved in sc-mtTFB and mtTFB2s. Notably, mutations in these residues have been documented to be poorly tolerated for methyltransferase activity. For example, the activity of the N101A mutant in ErmCЈ is reduced to 10% in vivo and is eliminated in vitro; a Y104A mutation in ErmCЈ was inactive both in vivo and in vitro (27). These 2 residues are not well conserved in sc-mtTFB and mtTFB2. The comparative data suggest strongly that d-mtTFB1 has rRNA adenine dimethyltransferase activity like h-mtTFB1 and that sc-mtTFB and mtTFB2 do not. Modification by dimethylation of two adjacent adenosine bases at the 3Ј-end of the small rRNA is conserved in bacteria and animal mtDNA (25). Indeed, the structure of this entire region is highly conserved. Whereas the functional role of the dimethyladenosine modification in mitochondrial small rRNA is unknown, the importance of this modification has been studied in E. coli using mutants in ksgA. ksgA mutants fail to dimethylate the 16S rRNA and, in consequence, are resistant to kasugamycin, an antibiotic in the aminoglycoside family (29,34,35). The non-dimethylated ribosome is mildly impaired in protein synthesis, mainly at the initiation and elongation steps, and ksgA mutants show a slight decrease in growth (29, 36 -38). Our data show that the abundance of d-mtTFB1 influences the efficiency of mitochondrial translation and is consistent with these observations. Saccharomyces cerevisiae Dim1, an ortholog of KsgA, is an 18S rRNA dimethylase. S. cerevisiae Dim1 is essential for viability, and loss of S. cerevisiae Dim1 activity that eliminates 18S rRNA methylation also results in the inhibition of rRNA processing of the 18S precursor at a step prior to adenosine dimethylation. In contrast, rRNA processing does not occur in animal mitochondria, and in mtTFB1-depleted Drosophila cells, we did not detect any change in either the level or electrophoretic mobility of the mitochondrial small subunit rRNA. Differing from animals, S. cerevisiae has only one mtTFB gene, sc-mtTFB, and mitochondrial 12S rRNA is not methylated on the two adenosine bases (25,39). It is particularly significant that RNAi knockdown of d-mtTFB1 lowers the efficiency of mitochondrial translation in Drosophila cultured cells because the data suggest strongly that endogenous mtTFB2 cannot complement a deficiency in mtTFB1 in its role in translation. These data are consistent with a lack of adenine dimethyltransferase activity in sc-mtTFB and mtTFB2s.
Taken together, our data suggest strongly that the primary roles of mtTFB1 and mtTFB2 differ in vivo; mtTFB1 is an rRNA adenine dimethyltransferase that influences the efficiency of mitochondrial translation, and mtTFB2 is a critical mitochondrial transcription factor.