Abstract
Transfer RNAs (tRNAs) are widely known for their roles in the decoding of the linear mRNA information into amino acid sequences of proteins. They are also multifunctional platforms in the translation process and have other roles beyond translation, including sensing amino acid abundance, interacting with the general stress response machinery, and modulating cellular adaptation, survival, and death. In this mini-review, we focus on the emerging role of tRNA genes in the organization and modification of the genomic architecture of yeast and the role of tRNA misexpression and decoding infidelity in genome stability, evolution, and adaption. We discuss published work showing how quickly tRNA genes can mutate to meet novel translational demands, how tRNAs speed up genome evolution, and how tRNA genes can be sites of genomic instability. We highlight recent works showing that loss of tRNA decoding fidelity and small alterations in tRNA expression have unexpected and profound impacts on genome stability. By dissecting these recent evidence, we hope to lay the groundwork that prompts future investigations on the mechanistic interplay between tRNAs and genome modification that likely triggers genome evolution.
Introduction
Transfer RNAs (tRNAs) are short non-coding RNAs, approximately 70 to 100 bases long, that play essential roles in translation by linking mRNA codons to their corresponding amino acids, following a set of decoding rules established by the genetic code. They do so by base pairing their anticodon triplets with mRNA codon triplets in the ribosome decoding center and transferring the amino acid attached to its 3′-end in the ribosomal peptidyl transferase center (). This is a critical cellular process that requires tight control of tRNA gene expression, tRNA maturation, tRNA charging, and turnover (). In actively dividing yeast cells, tRNAs represent approximately 15% of total RNA (Warner, 1999), indicating that their genes (tDNAs) are highly transcribed. In general, tDNAs are nucleosome free and are flanked by strongly positioned nucleosomes (Yuan et al., 2005; ). Their transcription is mediated by RNA polymerase III (Pol III) upon recruitment to the promoter by the transcription factors TFIIIC and TFIIIB. TFIIIC binds to the internal A-box and B-box promoter elements and helps recruit the multi-subunit factor TFIIIB to AT-rich sequences upstream of the transcription start site, forming a highly stable TFIIIB–DNA complex that participates in multiple rounds of Pol III recruitment and initiation (Schramm and Hernandez, 2002). In Saccharomyces cerevisiae, the cellular concentration of each tRNA is directly proportional to its gene copy number (). This is particularly important because translation efficiency is described as the degree to which the tRNA pool can accommodate the transcriptome, thus affecting protein production and accuracy (). This interplay is fine-tuned by codon usage, which is under selective pressure and show variation across budding yeast species (). Yet tRNAs have other non-canonical roles in the biological theater beyond their role as adaptors in protein synthesis (reviewed in and Su et al., 2020). For example, tDNAs have roles in chromatin organization and gene regulation and are sites for binding of numerous chromatin proteins, including the architectural structural maintenance of chromosomes (SMC) proteins, nuclear pore proteins, chromatin remodelers, and histone modifiers (; Su et al., 2020).
The 275 tDNAs present in the yeast S. cerevisiae genome are dispersed throughout the linear maps of the 16 chromosomes. Fluorescence in situ hybridization microscopy (FISH) showed that tDNAs cluster at the outer periphery of the nucleolus in a microtubule-dependent manner and or adjacent to centromeres (Thompson et al., 2003). This happens with the assistance of condensing complexes bound at each tDNA gene locus () and requires substantial rearrangements of the genome topology. Whether individual tDNA associations play a role in genome organization is still poorly understood. We review below recent works on how tDNAs and related Pol III promoter elements function as boundary elements that limit chromatin domains (), how they work as barriers to DNA replication fork progression, and how they contribute to the formation of genomic fragile sites (). Beyond their role in the three-dimensional and functional organization of the genome, this review also describes how changes in the tRNA pool can drive genome evolution in fungi.
Roles of tRNA Genes in Chromatin Remodeling and Genome Organization
The three-dimensional organization of the genome can promote long-range genomic rearrangements between interacting loci whose associated chromatin and transcriptional states can be selected through evolution (). In yeast, tRNA genes have been implicated in the spatial organization of the genome by acting as barrier elements and by regulating chromatin structure (; ; Simms et al., 2008; ; ). Evidence that tDNAs can hamper silenced chromatin domains from invading active domains was first obtained in S. cerevisiae (; Simms et al., 2004), where the deletion of a Thr-tRNAAGU gene at the transcriptionally silent HMR mating-type locus resulted in the spread of silencing and consequent repression of the GIT1 gene on chromosome III (). A Gln-tRNAUUG gene has also been shown to block silencing at the S. cerevisiae rDNA locus (RDN1) (). Insulator activity was similarly shown in Schizosaccharomyces pombe, where deletion of a centromeric Ala-tRNA gene led to the spread of pericentromeric heterochromatin and gene silencing (Scott et al., 2006). The precise mechanisms by which tDNAs exert their barrier function remain largely unexplored; however, the assembly of the complete Pol III transcription apparatus does seem to be required for barrier function (; Scott et al., 2006; ). Mutations in internal Thr-tRNA promoter elements, A-box or B-box, at the HMR locus led to deficiencies of TFIIIC and TFIIIB assembly, resulting in the loss of barrier function in S. cerevisiae (). Furthermore, yeast cohesin complex mutants (Δsmc1 and Δsmc3) have impaired tDNA-mediated insulator function ().
A study by mapped cis- and trans-interactions across the entire genome in S. cerevisiae and showed that physical interactions among tDNAs are significantly enriched and that they largely co-localize into clusters associated with the nucleolus or centromeres (). Other studies, using DNA FISH, also showed that some tRNA genes cluster together near centromeres (Thompson et al., 2003). Furthermore, microscopic observations and genome-wide mapping of physical interactions show the co-localization of TFIIIC, cohesins, and other structural proteins at tDNA physical domain borders, suggesting that these insulators are critical players in chromosome folding and organization in the yeast nucleus. Recently, devised a strategy to tackle this topic. They eliminated the internal promoter elements (A-box and B-box) of two tDNAs on the left arm and eight tDNAs on the right arm of chromosome III in S. cerevisiae to generate a “tDNA-less” chromosome where binding of transcription factors TFIIIC and TFIIIB and chromatin proteins was abrogated. This allowed the detailed characterization of chromatin packaging, folding, and nuclear dynamics of chromosome III. Using various approaches, such as MNase-seq, ChIP-seq, RNA-seq, and fluorescence microscopy co-localization analysis, authors showed that (1) tDNA loss affects chromatin structure by disrupting the precise nucleosome positioning outside tDNAs; (2) tDNAs are essential to recruitment of cohesins and condensins; and (3) tDNAs influence centromere clustering, which in turn affects nuclear architecture. Lastly, as in previous studies (; Simms et al., 2004; ), loss of tDNAs alters the long-range interactions of the silenced HML and HMR loci of chromosome III, leading to alterations in gene silencing ().
The discovery of tDNA insulator function in yeast along with the recent advances in uncovering their involvement in the functional and spatial organization of the genome is particularly relevant because they provide a framework for future studies in this field. Furthermore, tDNA insulator functions seem to be conserved from yeast to humans (), and their activities appear to be associated with a significant number of protein complexes whose actions and regulation remain to be determined.
tRNA Genes, R-Loops, and Transposable Elements
tDNAs are often located near naturally occurring genomic fragile sites, and genome-wide studies in S. cerevisiae have detected R-loops at tRNA genes, along with other Pol III transcribed genes (; ; Wahba et al., 2016; Yeung and Smith, 2020). The replication machinery naturally slows down at tDNAs, and DNA helicases must take action to promote the progression of the replication fork (). However, when the direction of DNA replication conflicts with the direction of the tDNA transcription, it leads to replication-fork pausing (; Yeung and Smith, 2020). Head-on replication-fork pausing promotes DNA damage by R-loop formation (Tran et al., 2017). R-loops are stable DNA:RNA hybrid structures with an unpaired DNA strand that naturally blocks replication but can also generate genomic instability (Santos-Pereira and Aguilera, 2015). If left unresolved, R-loops can create replication–transcription conflicts and lead to double-strand breaks which potentially increase DNA recombination (). Tran et al. (2017) showed that tDNAs represent sites of double-strand breaks and of increased recombination events in a series of helicase mutants. Moreover, this phenomenon is also intimately connected with high expression levels of tRNAs and with the fact that tDNAs are usually associated with the pre-initiation complex, i.e., at a ready transcription state, which is a stable multiprotein complex consisting of a constant passage barrier for helicases ().
Comparative genomics of 11 evolutionary-related yeast species showed a prevalence of tRNA genes at DNA breakpoints, which have also been linked to sites of genomic rearrangement (). One of the aspects that could underlie this observation is the preferential integration of transposable elements (TEs) at the proximity of tDNAs (). TEs are mobile self-replicating elements that can integrate themselves in new genomic sites, being a potential source of mutations. There is an underlying assumption that TE insertions are deleterious, and indeed, they are a potential threat to genome integrity. S. cerevisiae has five families of TEs classified as long terminal repeat (LTR) retrotransposons, Ty1 to Ty5. The most abundant and active ones are the Ty1 and Ty2, which, apart from their ORFs, share a high sequence similarity between their LTR sequences (). These long and near-identical sequences scattered in the genome are prone to recombination, particularly ectopic recombination, which allows for an array of rearrangements like deletions, duplications, inversions, and translocations (). It is therefore important that a tight control of retrotransposons’ expression is maintained. Ty1 mobility is regulated by a retrograde mechanism where Ty1 self-encoded elements, like p22, inhibits Ty1’s mobility when an elevated number of copies are present (Saha et al., 2015). This ability in S. cerevisiae was acquired by horizontal transfer from Saccharomyces paradoxus (). Nevertheless, comparative studies have shown that a large percentage of TEs are fixed in the genome (), although there is also evidence for recent Ty insertions at a high rate (), which can be seen as a source of genomic diversity and evolution. Increased retromobility has been observed upon exposure to several stress conditions like UV light () and adenine starvation (Todeschini et al., 2005). Furthermore, in physiological conditions like aging, retromobility has been observed in several species (; ; ). In yeast, reported that during chronological aging, there is an association between Ty1 mobility and the observed genomic instability, particularly in loss of heterozygosity (LOH) events. Important adaptative roles for transposons have also been reported in experimentally evolved yeast. studied the recombination events in evolved strains under glucose limitation and found that almost all detected rearrangements could be traced to ectopic rearrangement between transposons, transposon fragments, or tRNAs. In an experimental evolution study of cells expressing a mutant Ser-tRNA (see below), there were large chromosomal rearrangements mediated by homologous recombination between transposons (). In a large timescale, phylogenetic studies on genome evolution identified tRNAs and transposons at genome breakpoints and rearrangement sites (; ; ). Interestingly, in a comparative evolutionary study between S. cerevisiae and its related species S. paradoxus, S. mikatae, and S. uvarum, all the inversions identified were flanked by tDNAs in an opposite transcriptional orientation (). Thus, it is apparent that tDNAs, or their flaking regions, play an important role in genome innovation and evolution. Although it was not acknowledged in any study (at least to our understanding), it is possible that tDNAs (and their vicinity) represent “silent hotspots” for recombination that, when a particular condition is prolonged, become sites for “rapid” adaptive genomic alterations.
Genomic Changes Associated With tRNA Misexpression
Upon environmental challenges, the organism quickly needs a particular set of defenses to survive. There is a body of evidence on how transcription changes in response to several stresses in yeast (; ). It is, therefore, reasonable to assume that tRNA expression and abundance must also be tuned to follow these changes. Indeed, the tRNA pool dynamically changes to facilitate selective and faster translation of stress-related transcripts (Torrent et al., 2018). The tRNA pool is composed of various tRNA isoacceptor families, each encoded by tDNAs with different copy numbers. tRNA gene families with more copies of the same tDNA decode more frequently used codons, while tRNAs with one gene copy decode rarely used codons, which correlates with the codon usage of protein genes. This establishes the adequate balance between tRNA availability and the usage of its corresponding codon (). Curiously, not all copies of the same tRNA species contribute equally to the tRNA pool, and the loss of a particular copy can have different physiological consequences (). Thus, the multiplicity of copies enables higher expression of tRNAs in high translational demand and enables the tRNA pool to be dynamic enough to allow the dispensability of a particular copy to further expand the tRNA repertoire. This concept was explored by Yona et al. (2013) in a yeast strain with a deletion in the single-copy tDNA tR(CCU)J (), thus eliminating the only cognate tRNA for the AGG codon. Experimental evolution revealed that 200 generations were sufficient for cells to overcome the translational defect. Translational equilibrium was restored by mutating the anticodon of one of the 11 copies of Arg-tRNAUCU from UCU to CCU, without affecting cellular fitness, highlighting how the plasticity of the tRNA pool can overcome translational challenges in changing environments.
Maintaining the proteome’s good health is of extreme importance, but several bacterial and fungal species are able to decrease translation fidelity during stress to functionally diversify the proteome, a phenomenon called adaptive translation (). Although alterations in the identity of a sense codon are a rare phenomenon, several budding yeasts reassigned the CUG codon to serine (Santos and Tuite, 1995) and to alanine (; Riley et al., 2016). The CUG reassignments occurred independently during evolution and involved different tRNA genes that convergently mutated anticodons to CAG (). Candida albicans is the most studied example of adaptive translation, where the identity of the CUG codon was altered to serine but residual leucine identity was still maintained. This results in an ambiguous CUG codon that is translated 97% of the times as serine and 3% as leucine, in standard growth conditions (). This is accomplished by a single Ser-tRNACAG with identity elements for both seryl- and leucyl-tRNA synthetases (Suzuki et al., 1997). However, alteration of the levels of the CUG-decoding tRNA is surprisingly adaptative. engineered a set of C. albicans strains with different combinations of tDNACAG copy number, where one, two, or both copies of the endogenous Ser-tRNACAG genes were deleted and one or two copies of the S. cerevisiae Leu-tRNACAG genes were inserted, thus shifting the ratio of leucine/serine incorporated in the proteome. Strains tolerated increasing Leu incorporation and displayed unexpected phenotypic variability, with highly variable colony and cell morphologies, and increased tolerance to fluconazole and itraconazole. Interestingly, altering the copy number of the CUG decoding tDNAs leads to the rapid accumulation of unique single-nucleotide polymorphisms (SNPs) and LOH events. Strains with higher deregulation of the tRNA pool, and therefore higher levels of Leu incorporation at CUG sites, showed higher number of SNPs, indicating the potential mutagenic effect of tRNA codon misreading. Of note was the fact that strains with the most extreme alterations in the tRNA pool (i.e., with highest level of Leu incorporation) presented a near-complete LOH on chromosome V. A set of genes related with stress response, antifungal drug resistance, filamentous growth, and pathogenesis is located in this chromosome, showing that these alterations are not random and have an adaptative role (). One could hypothesize that the observed genomic alterations triggered by tRNA misexpression are associated with the peculiar features of the C. albicans biology and its highly plastic genome (Selmecki et al., 2010). However, a similar phenotype was also uncovered in S. cerevisiae. experimentally evolved a yeast strain engineered with a mutant Ser-tRNACAG that misincorporates serine at CUG codons. Although this insertion was highly detrimental for fitness, cells were able to adapt to their new condition after 250 generations to their new condition. Genome sequencing showed that tolerance and adaptation to translational stress were achieved by large genomic rearrangements. These repeatedly involved a partial deletion of 127 kb at chromosome V, enriched with genes involved in deubiquitination processes, and a duplication of 540 kb in chromosome IV, enriched with genes involved in glucose uptake. Together, these allowed cells to adapt to imbalances in the tRNA pool that culminate in CUG mistranslation by accelerated protein turnover and a high rate of glucose internalization (). In other words, alterations in the tRNA pool and mRNA decoding accuracy destabilize the proteome in a dynamic way that reciprocates to the genome and produce important adaptive genome instabilities.
Conclusion and Future Perspectives
We highlighted the non-canonical function of tRNAs and tDNAs as drivers of genome evolution (Figure 1) and summarized how tDNA can play a role in the three-dimensional and functional organization of the genome and potentiate genome rearrangements events. Additionally, the discovery that alterations in the yeast tRNA pool generate genome instability associated with phenotypic variation of high adaptation potential adds a new dimension to the study of tRNA-driven genome evolution. Precisely how these mechanisms operate remains to be determined, but future work should elucidate how the tRNA pool provides evolutionary plasticity in environmental changing conditions. It is of high biological importance to understand the complex relationship between the tRNA pool and the genome, since the produced genomic instabilities may be relevant to human diseases, including cancer where extensive tRNA pool alterations and aneuploidies have been observed.
FIGURE 1
Statements
Author contributions
AG and AB: conceptualization, literature study, writing, and editing of the manuscript. MS: editing and revision of the manuscript. All authors listed have made a substantial, direct and intellectual contributions to the work, and approved it for publication.
Funding
This work was supported by FEDER (Fundo Europeu de Desenvolvimento Regional) funds through the COMPETE 2020, Operational Program for Competitiveness and Internationalization (POCI), and by Portuguese national funds via Fundação para a Ciência e a Tecnologia, I.P. (FCT) under the projects PTDC/BIA-MIB/31238/2017 and PTDC/BIA-MIC/31849/2017. The iBiMED research unit was supported by FCT funds under UIDP/04501/2020. AG was supported directly by an FCT grant (SFRH/BD/121358/2016). AB was supported by national funds (OE), through FCT, I.P., in the scope of the framework contract foreseen in numbers 4, 5, and 6 of article 23, of Decree-Law 57/2016 of August 29, changed by Law 57/2017 of July 19.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
tRNA, yeast, chromatin structure, chromosome architecture, genome evolution, genomic instability
Citation
Guimarães AR, Correia I, Sousa I, Oliveira C, Moura G, Bezerra AR and Santos MAS (2021) tRNAs as a Driving Force of Genome Evolution in Yeast. Front. Microbiol. 12:634004. doi: 10.3389/fmicb.2021.634004
Received
26 November 2020
Accepted
01 February 2021
Published
11 March 2021
Volume
12 - 2021
Edited by
Omar Orellana, University of Chile, Chile
Reviewed by
Francisco A. Cubillos, University of Santiago, Chile; Cécile Neuvéglise, Institut National de la Recherche Agronomique, Centre Montpellier, France
Updates
Copyright
© 2021 Guimarães, Correia, Sousa, Oliveira, Moura, Bezerra and Santos.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ana Rita Bezerra, armbezerra@ua.ptManuel A. S. Santos, msantos@ua.pt
This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology
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