Structural and Genetic Determinants of Convergence in the Drosophila tRNA Structure–Function Map
Autor: | David H. Ardell, Julie Baker Phillips |
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Rok vydání: | 2021 |
Předmět: |
0106 biological sciences
Ion-binding pocket Lineage (evolution) Genome Insect 010603 evolutionary biology 01 natural sciences 03 medical and health sciences RNA Transfer Convergent evolution Gene cluster Anticodon Genetics Melanogaster Animals Gene conversion FlyBase : A Database of Drosophila Genes & Genomes Molecular Biology Gene Ecology Evolution Behavior and Systematics 030304 developmental biology Class-informative feature (CIF) 0303 health sciences biology Parallel substitutions biology.organism_classification Structure–function map Drosophila melanogaster Evolutionary biology Transfer RNA Original Article |
Zdroj: | Journal of Molecular Evolution |
ISSN: | 1432-1432 0022-2844 |
Popis: | The evolution of tRNA multigene families remains poorly understood, exhibiting unusual phenomena such as functional conversions of tRNA genes through anticodon shift substitutions. We improved FlyBase tRNA gene annotations from twelve Drosophila species, incorporating previously identified ortholog sets to compare substitution rates across tRNA bodies at single-site and base-pair resolution. All rapidly evolving sites fell within the same metal ion-binding pocket that lies at the interface of the two major stacked helical domains. We applied our tRNA Structure–Function Mapper (tSFM) method independently to each Drosophila species and one outgroup species Musca domestica and found that, although predicted tRNA structure–function maps are generally highly conserved in flies, one tRNA Class-Informative Feature (CIF) within the rapidly evolving ion-binding pocket—Cytosine 17 (C17), ancestrally informative for lysylation identity—independently gained asparaginylation identity and substituted in parallel across tRNAAsn paralogs at least once, possibly multiple times, during evolution of the genus. In D. melanogaster, most tRNALys and tRNAAsn genes are co-arrayed in one large heterologous gene cluster, suggesting that heterologous gene conversion as well as structural similarities of tRNA-binding interfaces in the closely related asparaginyl-tRNA synthetase (AsnRS) and lysyl-tRNA synthetase (LysRS) proteins may have played a role in these changes. A previously identified Asn-to-Lys anticodon shift substitution in D. ananassae may have arisen to compensate for the convergent and parallel gains of C17 in tRNAAsn paralogs in that lineage. Our results underscore the functional and evolutionary relevance of our tRNA structure–function map predictions and illuminate multiple genomic and structural factors contributing to rapid, parallel and compensatory evolution of tRNA multigene families. |
Databáze: | OpenAIRE |
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