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Nucleic Acids Res. Jun 2011; 39(11): 4866–4874.
Published online Feb 14, 2011. doi:  10.1093/nar/gkr073
PMCID: PMC3113583
An unusual tRNAThr derived from tRNAHis reassigns in yeast mitochondria the CUN codons to threonine
Dan Su,1 Allyson Lieberman,1 B. Franz Lang,2 Miljan Simonović,3 Dieter Söll,1,4* and Jiqiang Ling1*
1Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06520-8114, USA, 2Département de Biochimie, Robert Cedergren Centre, Université de Montréal, Montréal, Québec, Canada, 3Department of Biochemistry and Molecular Genetics, University of Illinois, 900 S. Ashland Avenue, MBRB 1170, Chicago, IL 60607 and 4Department of Chemistry, Yale University, New Haven, CT 06520-8114, USA
*To whom correspondence should be addressed. Tel: Phone: +1 203 432 6205; Fax: +1 203 432 6202; Email: jiqiang.ling/at/yale.edu
Correspondence may also be addressed to Dieter Söll. Tel: Phone: +1 203 432 6200; Fax: +1 203 432 6202; Email: dieter.soll/at/yale.edu
Received January 4, 2011; Revised January 27, 2011; Accepted January 28, 2011.
The standard genetic code is used by most living organisms, yet deviations have been observed in many genomes, suggesting that the genetic code has been evolving. In certain yeast mitochondria, CUN codons are reassigned from leucine to threonine, which requires an unusual tRNAThr with an enlarged 8-nt anticodon loop (An external file that holds a picture, illustration, etc.
Object name is gkr073i1.jpg). To trace its evolutionary origin we performed a comprehensive phylogenetic analysis which revealed that An external file that holds a picture, illustration, etc.
Object name is gkr073i2.jpg evolved from yeast mitochondrial tRNAHis. To understand this tRNA identity change, we performed mutational and biochemical experiments. We show that Saccharomyces cerevisiae mitochondrial threonyl-tRNA synthetase (MST1) could attach threonine to both An external file that holds a picture, illustration, etc.
Object name is gkr073i3.jpg and the regular An external file that holds a picture, illustration, etc.
Object name is gkr073i4.jpg, but not to the wild-type tRNAHis. A loss of the first nucleotide (G−1) in tRNAHis converts it to a substrate for MST1 with a Km value (0.7 μM) comparable to that of An external file that holds a picture, illustration, etc.
Object name is gkr073i5.jpg (0.3 μM), and addition of G−1 to An external file that holds a picture, illustration, etc.
Object name is gkr073i6.jpg allows efficient histidylation by histidyl-tRNA synthetase. We also show that MST1 from Candida albicans, a yeast in which CUN codons remain assigned to leucine, could not threonylate An external file that holds a picture, illustration, etc.
Object name is gkr073i7.jpg, suggesting that MST1 has coevolved with An external file that holds a picture, illustration, etc.
Object name is gkr073i8.jpg. Our work provides the first clear example of a recent recoding event caused by alloacceptor tRNA gene recruitment.
Transfer RNAs (tRNAs) are adaptor molecules that pair each amino acid with corresponding codons on the mRNA (1). Aminoacyl-tRNA synthetases (aaRSs) attach amino acids to the 3′-terminus of tRNAs (2), and the resulting aminoacyl-tRNAs (aa-tRNAs) are delivered by elongation factors to the ribosome, where codon–anticodon recognition defines the genetic code of life (3). The genetic code was once thought to be universal and frozen (4), but later studies revealed multiple codon reassignment events in nuclear and mitochondrial genomes (5–7). These reassignments include stop-to-sense, sense-to-sense and sense-to-stop codon changes; they have been found in nuclear genomes from all three domains of life. In some bacterial, archaeal and eukaryotic species the UGA codon is reassigned to allow insertion of selenocysteine (Sec), the 21st natural amino acid, in the presence of tRNASec with a UCA anticodon (6,8). In a number of methanogenic archaea a UAG stop codon encodes the 22nd amino acid, pyrrolysine (Pyl), implemented by a tRNAPyl which recognizes UAG (9,10). A major reassignment in mitochondria is recoding UGA to tryptophan (Trp) implemented by a tRNATrp with a mutated anticodon (7). Furthermore, the mitochondria of several yeast species reassigned the AUA codon from isoleucine to methionine (Met) by the abnormal recognition of AUA by tRNAMet (7).
One last codon reassignment in the well-studied organism Saccharomyces cerevisiae is still not understood. In certain budding yeasts (including Saccharomyces, Nakaseomyces and Vanderwaltozyma) the four CUN (N denotes U, C, A or G) codons in the mitochondria are reassigned from leucine (Leu) to threonine (Thr) (11,12). This results from the loss of An external file that holds a picture, illustration, etc.
Object name is gkr073i9.jpg (with a UAG anticodon) that would translate CUN codons, and from the presence of an abnormal An external file that holds a picture, illustration, etc.
Object name is gkr073i10.jpg with an enlarged 8-nt anticodon loop and a UAG anticodon (Figure 1) (11,13). This codon sense change was confirmed by protein sequencing of the S. cerevisiae mitochondrial ATPase (14). Mass spectrometry studies have also validated that at least three CUU and two CUA codons in S. cerevisiae mitochondrial-encoded proteins are recoded as Thr (15). In addition to An external file that holds a picture, illustration, etc.
Object name is gkr073i14.jpg, yeast mitochondria also express a normal An external file that holds a picture, illustration, etc.
Object name is gkr073i15.jpg with a UGU anticodon that reads the ACN threonine codon box (Figure 1). It was shown previously that while mitochondrial extracts from a wild-type (WT) S. cerevisiae strain could attach Thr to both An external file that holds a picture, illustration, etc.
Object name is gkr073i16.jpg and An external file that holds a picture, illustration, etc.
Object name is gkr073i17.jpg, extracts from an MST1 mutant strain could only threonylate An external file that holds a picture, illustration, etc.
Object name is gkr073i18.jpg but not An external file that holds a picture, illustration, etc.
Object name is gkr073i19.jpg (16). Thus it was suggested that MST1 serves as a mitochondrial threonyl-tRNA synthetase (ThrRS) specific for aminoacylation of An external file that holds a picture, illustration, etc.
Object name is gkr073i20.jpg, while a different ThrRS aminoacylates An external file that holds a picture, illustration, etc.
Object name is gkr073i21.jpg in the mitochondria. Three decades after this discovery it is still a mystery how the unusual An external file that holds a picture, illustration, etc.
Object name is gkr073i22.jpg emerged in the mitochondrial genome. Previous hypotheses suggest that An external file that holds a picture, illustration, etc.
Object name is gkr073i23.jpg might have evolved from An external file that holds a picture, illustration, etc.
Object name is gkr073i24.jpg, or alternatively from the missing An external file that holds a picture, illustration, etc.
Object name is gkr073i25.jpg (11,17,18). However, both hypotheses lack convincing experimental evidence. To our surprise, biochemical and phylogenetic analyses demonstrate that An external file that holds a picture, illustration, etc.
Object name is gkr073i26.jpg directly evolved from mitochondrial tRNAHis. Saccharomyces cerevisiae mitochondrial tRNAHis shares high (72%) sequence identity with An external file that holds a picture, illustration, etc.
Object name is gkr073i27.jpg, and a single-nucleotide change converts tRNAHis to a substrate for MST1. Our work thus resolves the long-standing question regarding the origin of An external file that holds a picture, illustration, etc.
Object name is gkr073i28.jpg and its coding response.
Figure 1.
Figure 1.
Nucleotide sequences of S. cerevisiae mitochondrial tRNAs. (A) An external file that holds a picture, illustration, etc.
Object name is gkr073i11.jpg with an 8-nt anticodon loop and a UAG anticodon. (B) An external file that holds a picture, illustration, etc.
Object name is gkr073i12.jpg with a canonical UGU anticodon. (C) tRNAHis with a G−1 (circled, a major anti-determinant for ThrRS). The primary sequences of (more ...)
Cloning, mutagenesis and general methods
Saccharomyces cerevisiae MST1, S. cerevisiae HTS1, Candida albicans MST1 and Schizosaccharomyces pombe MST1 genes were cloned into pET28a expression vector (Novagen) with an N-terminal six-His tag. Expression of recombinant proteins was induced at 37°C for 4 h with 0.5 mM isopropyl β-d-1-thiogalactopyranoside (IPTG) in Escherichia coli strain BL21-codon plus in Luria–Bertani (LB) media. His-tagged proteins were purified according to standard procedures. Mitochondrial tRNA genes were cloned into pUC18 vector (GenScript), and mutations were introduced using QuikChange Site-Directed Mutagenesis Kit (Stratagene).
In vitro assays
In vitro tRNA transcripts were obtained using the T7 RNA polymerase runoff procedure as described (19). Aminoacylation experiments were performed as described (20) in the presence of 100 mM Na-HEPES pH 7.2, 30 mM KCl, 10 mM MgCl2, 2 mM ATP, 25 µM [3H] Thr (100 μCi/ml), 25 µM [3H] His (150 μCi/ml) or 50 µM [3H] Leu (100 μCi/ml), 0.2–9 µM tRNA transcripts and 3–300 nM aaRSs.
Phylogenetic analyses
For phylogenetic analysis of mitochondrial tRNA sequences, tRNAs were predicted in mitochondrial genomes of interest with Erpin/RNAweasel (21,22) and a tRNA profile specific for fungal mitochondria that may be used via our website (http://megasun.bch.umontreal.ca/RNAweasel). Sequence columns representing the sequence positions in the variable loop between the anticodon- and T-loop were removed as the nucleotides in this region are extremely diverse in sequence and length, and phylogenetic analysis was conducted using either a Bayesian [PhyloBayes; (23)] or maximum likelihood approach [RaxML with GTR model; (24)]. For inference of a species tree, an application developed in-house (Mams) was used for automated mitochondrial protein alignment, removal of ambiguous regions in the alignment, and concatenation. Briefly, derived Cob, Cox1-3, Atp6, 9 and Nad1-6 protein sequences are pre-aligned with Muscle (25), alignments are iteratively refined with HMMalign (S. Eddy, http://hmmer.janelia.org) using E-values obtained with respective HMM models as an optimization criterion. Sequence positions that are not aligned with a posterior probability value of 1 are removed from the resulting alignment. This dataset with 22 taxa and 3728 amino acid positions was analyzed using Bayesian inference by PhyloBayes that implements the CAT + GTR model, known to be among the least sensitive to LBA artifacts [(23,26,27), and references therein].
Phylogenetic analysis reveals that An external file that holds a picture, illustration, etc.
Object name is gkr073i29.jpg originated from tRNAHis
The unsolved question of the yeast mitochondrial CUN codon reassignment is the evolutionary origin of An external file that holds a picture, illustration, etc.
Object name is gkr073i30.jpg with an 8-nt anticodon loop and a UAG anticodon. To analyze the An external file that holds a picture, illustration, etc.
Object name is gkr073i31.jpg recruitment, we performed a phylogenetic analysis of all mitochondrial tRNAs of S. cerevisiae and related yeast species using Bayesian inference (Figure 2). Not surprisingly, the 10 organisms with An external file that holds a picture, illustration, etc.
Object name is gkr073i34.jpg are closely related; yet this An external file that holds a picture, illustration, etc.
Object name is gkr073i35.jpg cluster is related to tRNAHis (72% sequence identity between the two respective S. cerevisiae tRNAs; Figure 1). In contrast, An external file that holds a picture, illustration, etc.
Object name is gkr073i36.jpg and An external file that holds a picture, illustration, etc.
Object name is gkr073i37.jpg are definitively distant in the phylogeny (Figures 2, Supplementary Figure S1) and the respective S. cerevisiae tRNAs share only 52% sequence identity. As the phylogenetic signal in tRNA sequences is limited by the small number of informative sequence sites, and not a reliable marker in species phylogenies because of occasional identity shifts [e.g. (28)], we have built a yeast species tree based on mitochondrion-encoded proteins to permit mapping of evolutionary changes to this tree. The result of this phylogenetic analysis (Figure 3) is consistent with a single origin of the 10 yeast species that have a An external file that holds a picture, illustration, etc.
Object name is gkr073i42.jpg homolog with an 8-nt anticodon loop, a clade emerging close to the divergence of Kluyveromyces species and subsequent to Pichia canadensis. Together, these results strongly suggest that An external file that holds a picture, illustration, etc.
Object name is gkr073i43.jpg derived from mitochondrial tRNAHis in an ancestral yeast species.
Figure 2.
Figure 2.
Phylogeny of yeast mitochondrial tRNAs. The phylogenetic analysis with PhyloBayes (default model parameters) contained all tRNA sequences from the species shown in Figure 3. Only the section of the tRNA phylogeny covering the An external file that holds a picture, illustration, etc.
Object name is gkr073i32.jpg and tRNAHis clusters are (more ...)
Figure 3.
Figure 3.
Phylogeny of yeast species based on concatenated mtDNA-encoded protein sequences. The phylogenetic analysis with PhyloBayes and the CAT model is based on 13 mtDNA encoded proteins. All divergence points are supported by posterior probability values of (more ...)
Saccharomyces cerevisiae MST1 threonylates both An external file that holds a picture, illustration, etc.
Object name is gkr073i44.jpg and An external file that holds a picture, illustration, etc.
Object name is gkr073i45.jpg
The mitochondria of all yeast species containing An external file that holds a picture, illustration, etc.
Object name is gkr073i46.jpg have lost the An external file that holds a picture, illustration, etc.
Object name is gkr073i47.jpg gene, leaving An external file that holds a picture, illustration, etc.
Object name is gkr073i48.jpg the only tRNA capable of reading CUN codons. Whereas S. cerevisiae mitochondrial LeuRS (ScmtLeuRS) efficiently attaches Leu to An external file that holds a picture, illustration, etc.
Object name is gkr073i49.jpg (29,30), it could not recognize An external file that holds a picture, illustration, etc.
Object name is gkr073i50.jpg (Figure 4A), confirming that the S. cerevisiae mitochondrial CUN codons are assigned to Thr instead of Leu. It is known that the WT S. cerevisiae strain attaches Thr to An external file that holds a picture, illustration, etc.
Object name is gkr073i56.jpg, and an MST1 deletion strain fails to threonylate An external file that holds a picture, illustration, etc.
Object name is gkr073i57.jpg, resulting in a respiration-deficient phenotype (16). This suggests that MST1 is a putative mitochondrial ThrRS. Compared with bacterial ThrRSs, yeast MST1 enzymes lack an N-terminal editing domain, but share homologous catalytic and tRNA anticodon binding domains. To test aminoacylation of An external file that holds a picture, illustration, etc.
Object name is gkr073i58.jpg directly, the S. cerevisiae MST1 gene was cloned into pET28a for protein overexpression in E. coli. N-terminal His-tagged MST1 was purified to homogeneity and tested in aminoacylation reactions in the presence of [3H] Thr and in vitro transcribed S. cerevisiae tRNAs. Consistent with previous in vivo results (16), ScMST1 was able to charge An external file that holds a picture, illustration, etc.
Object name is gkr073i59.jpg with Thr in vitro (Figure 4B). MST1 could also threonylate An external file that holds a picture, illustration, etc.
Object name is gkr073i60.jpg, which was unexpected as it was previously thought that a second mitochondrial ThrRS was responsible for An external file that holds a picture, illustration, etc.
Object name is gkr073i61.jpg aminoacylation. Steady-state kinetic experiments revealed that ScMST1 recognized An external file that holds a picture, illustration, etc.
Object name is gkr073i62.jpg and An external file that holds a picture, illustration, etc.
Object name is gkr073i63.jpg with high affinity, with Km values of 0.29 and 0.44 µM, respectively (Table 1), suggesting that tRNA modifications (17) are not critical for MST1 recognition. These data, together with previous in vivo results, establishes unequivocally that An external file that holds a picture, illustration, etc.
Object name is gkr073i66.jpg is indeed threonylated by MST1. While we favor that MST1 threonylates An external file that holds a picture, illustration, etc.
Object name is gkr073i67.jpg in vivo, we do not exclude the possibility that a second ThrRS activity is present in yeast mitochondria.
Figure 4.
Figure 4.
Aminoacylation by S. cerevisiae MST1 and HisRS. (A) Leucylation of An external file that holds a picture, illustration, etc.
Object name is gkr073i51.jpg (3 µM) and An external file that holds a picture, illustration, etc.
Object name is gkr073i52.jpg (3 µM) by ScmtLeuRS (0.3 µM). (B) Threonylation of An external file that holds a picture, illustration, etc.
Object name is gkr073i53.jpg (3 µM), An external file that holds a picture, illustration, etc.
Object name is gkr073i54.jpg (3 µM) and tRNAHis variants (3 µM) (more ...)
Table 1.
Table 1.
Threonylation by ScMST1
Loss of G−1 converts S. cerevisiae tRNAHis to a substrate for S. cerevisiae MST1
To provide experimental evidence for the evolution of An external file that holds a picture, illustration, etc.
Object name is gkr073i68.jpg, we examined recognition of tRNAHis variants by MST1. Except in a few α-proteobacteria [(31), and references therein], all known tRNAHis species contain a G at position −1, which is a critical identity element for histidyl-tRNA synthetase (HisRS) [(32,33) and references therein]. Sequence alignments of An external file that holds a picture, illustration, etc.
Object name is gkr073i69.jpg and mitochondrial tRNAHis genes revealed that G−1 addition in tRNAHis comprises one major difference between the two tRNA species (Figure 5). In vitro, ScMST1 failed to charge the WT SctRNAHis transcript with Thr, but deleting G−1 stimulated threonylation of tRNAHis by ScMST1 (Figure 4B). Steady-state kinetic data showed that ΔG−1 tRNAHis gained 4% threonylation activity of the WT An external file that holds a picture, illustration, etc.
Object name is gkr073i72.jpg (Table 1). Compared with An external file that holds a picture, illustration, etc.
Object name is gkr073i73.jpg, ΔG−1 tRNAHis displayed 10-fold lower kcat and 3-fold higher Km values for threonylation by ScMST1. In addition to G−1, other major differences between tRNAHis and An external file that holds a picture, illustration, etc.
Object name is gkr073i74.jpg include an A insertion in An external file that holds a picture, illustration, etc.
Object name is gkr073i75.jpg at position 35, and the discriminator base at position 73 (Figure 5). Changing C73 to A did not improve the threonylation efficiency of ΔG−1 tRNAHis, but inserting A35 in the anticodon loop of ΔG-1 tRNAHis further increased its threonylation activity 5-fold (Table 1). In the presence of G−1, A35 insertion did not allow threonylation of tRNAHis. These results suggest that G−1 is a major anti-determinant in tRNAHis for MST1. In line with this notion, addition of G−1 to An external file that holds a picture, illustration, etc.
Object name is gkr073i76.jpg reduced its threonylation activity 150-fold (Table 1).
Figure 5.
Figure 5.
Sequence alignment of mitochondrial An external file that holds a picture, illustration, etc.
Object name is gkr073i70.jpg and tRNAHis. Three major differences between An external file that holds a picture, illustration, etc.
Object name is gkr073i71.jpg and tRNAHis sequences are indicated by boxes. Cc, Candida castellii; Cg, Candida glabrata; Kt, Kluyveromyces thermotolerans; Nb, Nakaseomyces bacillisporus; Nd, Nakaseomyces (more ...)
G−1 addition allows An external file that holds a picture, illustration, etc.
Object name is gkr073i77.jpg to be histidylated by S. cerevisiae HisRS
ScMST1 efficiently aminoacylates mitochondrial tRNAHis variants lacking G−1. We next investigated the recognition of tRNAHis and An external file that holds a picture, illustration, etc.
Object name is gkr073i78.jpg variants by mitochondrial HisRS. In S. cerevisiae, a single nuclear gene HTS1 containing two open reading frames encodes both the cytoplasmic and mitochondrial forms of HisRS (34). The mitochondrial HisRS (mtHisRS) harbors an extra mitochondria-targeting sequence, yet the predicted mature form of the mitochondrial enzyme is identical to the cytoplasmic HisRS. Previous studies revealed that ScHisRS recognizes both the G−1 and the anticodon of the cytoplasmic tRNAHis (35,36). We overexpressed mature ScmtHisRS in E. coli and purified the enzyme to homogeneity. In vitro aminoacylation reactions showed that ScmtHisRS efficiently charged His to the WT mitochondrial tRNAHis (Figure 4C, Table 2), with a Km value comparable to that of the cytoplasmic tRNAHis (35). Surprisingly, neither deleting G−1 nor inserting A35 in the anticodon loop of mitochondrial tRNAHis significantly affected the aminoacylation activity. However, when both changes were introduced into mitochondrial tRNAHis, the histidylation activity decreased by 80-fold. The discriminator base also appeared to be important for recognition by ScmtHisRS. These results indicate that in the context of S. cerevisiae mitochondrial tRNAHis, G−1 is dispensable for HisRS recognition and the anticodon can alternatively serve as the major identity element. ScmtHisRS was unable to aminoacylate WT An external file that holds a picture, illustration, etc.
Object name is gkr073i80.jpg (Figure 4C). Interestingly, addition of G−1 to An external file that holds a picture, illustration, etc.
Object name is gkr073i81.jpg restored 7% histidylation activity of the WT tRNAHis (Figure 4C, Table 2), further strengthening our argument that the mitochondrial tRNAHis and An external file that holds a picture, illustration, etc.
Object name is gkr073i82.jpg in yeast are closely related during evolution.
Table 2.
Table 2.
Histidylation by ScmtHisRS
MST1 has coevolved with An external file that holds a picture, illustration, etc.
Object name is gkr073i83.jpg to establish CUN codon reassignment in yeast mitochondria
The biochemical and phylogenetic evidence above suggests that An external file that holds a picture, illustration, etc.
Object name is gkr073i84.jpg has evolved from mitochondrial tRNAHis, at a time point close to the divergence of Kluyveromyces species. To understand whether An external file that holds a picture, illustration, etc.
Object name is gkr073i85.jpg could be recognized by MST1 enzymes from other fungal species, we overexpressed and purified MST1s from C. albicans and S. pombe [a non-hemiascomycete ‘fission yeast’ belonging to Taphrinomycotina (37)], and tested them for threonylation of An external file that holds a picture, illustration, etc.
Object name is gkr073i86.jpg. CaMST1 and SpMST1 share 49 and 43% sequence identity with ScMST1, respectively, and both enzymes were able to aminoacylate S. cerevisiae mitochondrial An external file that holds a picture, illustration, etc.
Object name is gkr073i87.jpg (Figure 6A). However, neither CaMST1 nor SpMST1 recognized An external file that holds a picture, illustration, etc.
Object name is gkr073i91.jpg or the tRNAHis variants tested above (Figure 6). These results strongly suggest that MST1 specifically evolved to recognize An external file that holds a picture, illustration, etc.
Object name is gkr073i92.jpg in a group of yeasts comprising S. cerevisiae. Therefore, CUN codon reassignment was completed following the coevolution of MST1 and An external file that holds a picture, illustration, etc.
Object name is gkr073i93.jpg, which established specific protein–tRNA interactions.
Figure 6.
Figure 6.
Threonylation of An external file that holds a picture, illustration, etc.
Object name is gkr073i88.jpg and tRNAHis variants (3 µM) by C. albicans and S. pombe MST1 (0.3 µM). (A) CaMST1 and SpMST1 threonylate An external file that holds a picture, illustration, etc.
Object name is gkr073i89.jpg but not An external file that holds a picture, illustration, etc.
Object name is gkr073i90.jpg. (B and C) CaMST1 and SpMST1 are unable to threonylate tRNAHis variants.
Reassignment of CUN codons from Leu to Thr in yeast mitochondria
CUN codons in the mitochondria of Saccharomyces, Nakaseomyces and Vanderwaltozyma have been previously assigned to Thr (5,11,12). This recoding event is accompanied with the loss of An external file that holds a picture, illustration, etc.
Object name is gkr073i94.jpg and the appearance of An external file that holds a picture, illustration, etc.
Object name is gkr073i95.jpg with an unmodified UAG anticodon (17). Analysis of a mass spectrometry database (PeptideAtlas) confirms that CUU and CUA codons indeed encode Thr in S. cerevisiae mitochondria. CUG and CUC codons are rarely used in yeast mitochondria, and the nature of the amino acid translated by such codons has not been verified experimentally. Given that the unmodified U at the first anticodon position is able to recognize all 4 nt (6,38), and no tRNA bearing GAG or CAG anticodons have been shown to be encoded by or imported into yeast mitochondria (39), it is plausible that CUG and CUC are also decoded by An external file that holds a picture, illustration, etc.
Object name is gkr073i96.jpg as Thr. An external file that holds a picture, illustration, etc.
Object name is gkr073i97.jpg possesses an enlarged anticodon loop with 8 nt (UUUUAGGU), whereas a canonical tRNA anticodon loop consists of 7 nt with the triplet anticodon centered at positions 34–36. In addition to An external file that holds a picture, illustration, etc.
Object name is gkr073i98.jpg, several natural tRNAs have been found to contain eight bases in the anticodon loop, yet such tRNAs decode quadruplet codons instead of triplet codons (40). A question that arises is whether An external file that holds a picture, illustration, etc.
Object name is gkr073i99.jpg can also decode quadruplet codons. In yeast mitochondria, several protein-encoding genes, such as cox1, harbor in-frame CUAA sequences. Decoding of CUAA by a quadruplet anticodon could cause detrimental frameshift translation of these critical mitochondrial proteins. It is thus reasonable to think that An external file that holds a picture, illustration, etc.
Object name is gkr073i100.jpg decodes all four CUN triplet codons but not quadruplet codons.
Evolutionary origin of An external file that holds a picture, illustration, etc.
Object name is gkr073i101.jpg
Our analyses reveal that An external file that holds a picture, illustration, etc.
Object name is gkr073i102.jpg was recruited from mitochondrial tRNAHis. It has been long considered that tRNAs accepting the same amino acid (isoacceptors) evolved by gene duplication from the same common ancestor. However, studies in bacteria demonstrate that several tRNA genes may derive from different amino acid accepting groups (alloacceptors) (41). Naturally-occurring recruitment of alloacceptor tRNA genes was later reported in sponge mitochondria based on phylogenetic studies (28). Our work combines both biochemical and phylogenetic approaches to provide the first clear evidence that alloacceptor tRNA gene recruitment is directly responsible for a recent recoding event, suggesting that such a mechanism might have played an important role in the establishment of the genetic code during evolution.
Phylogenetic analysis suggests that An external file that holds a picture, illustration, etc.
Object name is gkr073i103.jpg likely occurred after the split between Candida and Saccharomyces, subsequent to the divergence of P. canadensis. Interestingly, the C. albicans and C. parapsilosis mitochondrial genomes each contains two copies of the tRNAHis gene but no An external file that holds a picture, illustration, etc.
Object name is gkr073i104.jpg, and the CUN codons in these mitochondria remain assigned to Leu. In Kluvyeromyces lactis, the mitochondrial genome lacks both CUN codons and any tRNA reading such codons (7). Previous studies also suggest that current CUN codons decoded as Thr did not originate from ancestral Leu codons, but instead are derived from codons for other amino acids (18). Although we do not exclude the possibility that the original CUN codons could be ambiguously assigned to both Leu and Thr in certain intermediate yeast species, we favor that the emergence of An external file that holds a picture, illustration, etc.
Object name is gkr073i105.jpg is a late event following the loss of original CUN codons, and such codons have reemerged in present-day yeast mitochondria. We propose that CUN codon reassignment initiated with duplication of the tRNAHis gene, followed by the loss of CUN codons and An external file that holds a picture, illustration, etc.
Object name is gkr073i106.jpg (Figure 7). Next, one copy of the tRNAHis gene evolved to the present-day An external file that holds a picture, illustration, etc.
Object name is gkr073i110.jpg, and MST1 coevolved with An external file that holds a picture, illustration, etc.
Object name is gkr073i111.jpg to form a cognate aaRS/tRNA pair. Finally, the CUN codons reappeared from various other codons and were reassigned to Thr. Our biochemical studies suggest that HisRS could still recognize the intermediate tRNA during the evolution from tRNAHis to An external file that holds a picture, illustration, etc.
Object name is gkr073i112.jpg (Table 2). However, the mitochondrial proteome remained largely unaffected as the CUN codons were not present in the mitochondrial genome during this period.
Figure 7.
Figure 7.
Proposed model for CUN codon reassignment in yeast mitochondria. (1) tRNAHis duplicated in an ancestral yeast species while CUN codons remain assigned to Leu. (2) CUN codons were changed to UUA or UUG decoded by An external file that holds a picture, illustration, etc.
Object name is gkr073i107.jpg, and An external file that holds a picture, illustration, etc.
Object name is gkr073i108.jpg was lost. (3) tRNAHis evolved to (more ...)
Several mechanisms have been proposed to explain the codon reassignment processes, including: (i) codon capture mechanism (42), hypothesizing that a specific tRNA and corresponding codons completely disappear from a genome before a novel tRNA evolves to read such codons; and (ii) ambiguous intermediate mechanism (43), postulating that a tRNA mutant is recognized by more than one aminoacyl-tRNA synthetases, and a codon may be assigned to multiple amino acids in an intermediate state. The latter mechanism is supported by the discovery that in several extant Candida species, the CUG codon is ambiguously decoded by both Leu and Ser due to the presence of a tRNACAG charged by both leucyl- and seryl-tRNA synthetases (12,44). Our work suggests that CUN codons and An external file that holds a picture, illustration, etc.
Object name is gkr073i113.jpg are lost in yeast mitochondria prior to the emergence of An external file that holds a picture, illustration, etc.
Object name is gkr073i114.jpg, which provides a paradigm for the codon capture mechanism and lends support to the evolving genetic code theory.
SUPPLEMENTARY DATA
Supplementary Data are available at NAR Online.
FUNDING
National Institute of General Medical Sciences (grant GM022854 to D.S.); Canadian Research Chair Program (to B.F.L.); Brown-Coxe Post-doctoral Fellowship (to J.L.). Funding for open access charge: National Institute of General Medical Sciences (grant GM022854).
Conflict of interest statement. None declared.
Supplementary Material
Supplementary Data
ACKNOWLEDGEMENTS
We are grateful to Dr Susan Martinis and Jaya Sarkar (University of Illinois at Urbana-Champaign) for the kind gifts of ScmtLeuRS and tRNALeu and Dr Markus Englert for the gift of S. pombe genomic DNA. We thank Dr Lennart Randau (MPI for Terrestrial Microbiology, Marburg, Germany), Patrick O’Donoghue and Ilka Heinemann (Yale University) for insightful discussion and comments.
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