Base-pairing versatility determines wobble sites in tRNA anticodons of vertebrate mitogenomes.

<h4>Background</h4>Vertebrate mitochondrial genomes typically have one transfer RNA (tRNA) for each synonymous codon family. This limited anticodon repertoire implies that each tRNA anticodon needs to wobble (establish a non-Watson-Crick base pairing between two nucleotides in RNA molecu...

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Autores principales: Miguel M Fonseca, Sara Rocha, David Posada
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:0f8aed815bea4e7ea2ce2cb81c2675b02021-11-18T07:19:16ZBase-pairing versatility determines wobble sites in tRNA anticodons of vertebrate mitogenomes.1932-620310.1371/journal.pone.0036605https://doaj.org/article/0f8aed815bea4e7ea2ce2cb81c2675b02012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22590575/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Vertebrate mitochondrial genomes typically have one transfer RNA (tRNA) for each synonymous codon family. This limited anticodon repertoire implies that each tRNA anticodon needs to wobble (establish a non-Watson-Crick base pairing between two nucleotides in RNA molecules) to recognize one or more synonymous codons. Different hypotheses have been proposed to explain the factors that determine the nucleotide composition of wobble sites in vertebrate mitochondrial tRNA anticodons. Until now, the two major postulates--the "codon-anticodon adaptation hypothesis" and the "wobble versatility hypothesis"--have not been formally tested in vertebrate mitochondria because both make the same predictions regarding the composition of anticodon wobble sites. The same is true for the more recent "wobble cost hypothesis".<h4>Principal findings</h4>In this study we have analyzed the occurrence of synonymous codons and tRNA anticodon wobble sites in 1553 complete vertebrate mitochondrial genomes, focusing on three fish species with mtDNA codon usage bias reversal (L-strand is GT-rich). These mitogenomes constitute an excellent opportunity to study the evolution of the wobble nucleotide composition of tRNA anticodons because due to the reversal the predictions for the anticodon wobble sites differ between the existing hypotheses. We observed that none of the wobble sites of tRNA anticodons in these unusual mitochondrial genomes coevolved to match the new overall codon usage bias, suggesting that nucleotides at the wobble sites of tRNA anticodons in vertebrate mitochondrial genomes are determined by wobble versatility.<h4>Conclusions/significance</h4>Our results suggest that, at wobble sites of tRNA anticodons in vertebrate mitogenomes, selection favors the most versatile nucleotide in terms of wobble base-pairing stability and that wobble site composition is not influenced by codon usage. These results are in agreement with the "wobble versatility hypothesis".Miguel M FonsecaSara RochaDavid PosadaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 5, p e36605 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Miguel M Fonseca
Sara Rocha
David Posada
Base-pairing versatility determines wobble sites in tRNA anticodons of vertebrate mitogenomes.
description <h4>Background</h4>Vertebrate mitochondrial genomes typically have one transfer RNA (tRNA) for each synonymous codon family. This limited anticodon repertoire implies that each tRNA anticodon needs to wobble (establish a non-Watson-Crick base pairing between two nucleotides in RNA molecules) to recognize one or more synonymous codons. Different hypotheses have been proposed to explain the factors that determine the nucleotide composition of wobble sites in vertebrate mitochondrial tRNA anticodons. Until now, the two major postulates--the "codon-anticodon adaptation hypothesis" and the "wobble versatility hypothesis"--have not been formally tested in vertebrate mitochondria because both make the same predictions regarding the composition of anticodon wobble sites. The same is true for the more recent "wobble cost hypothesis".<h4>Principal findings</h4>In this study we have analyzed the occurrence of synonymous codons and tRNA anticodon wobble sites in 1553 complete vertebrate mitochondrial genomes, focusing on three fish species with mtDNA codon usage bias reversal (L-strand is GT-rich). These mitogenomes constitute an excellent opportunity to study the evolution of the wobble nucleotide composition of tRNA anticodons because due to the reversal the predictions for the anticodon wobble sites differ between the existing hypotheses. We observed that none of the wobble sites of tRNA anticodons in these unusual mitochondrial genomes coevolved to match the new overall codon usage bias, suggesting that nucleotides at the wobble sites of tRNA anticodons in vertebrate mitochondrial genomes are determined by wobble versatility.<h4>Conclusions/significance</h4>Our results suggest that, at wobble sites of tRNA anticodons in vertebrate mitogenomes, selection favors the most versatile nucleotide in terms of wobble base-pairing stability and that wobble site composition is not influenced by codon usage. These results are in agreement with the "wobble versatility hypothesis".
format article
author Miguel M Fonseca
Sara Rocha
David Posada
author_facet Miguel M Fonseca
Sara Rocha
David Posada
author_sort Miguel M Fonseca
title Base-pairing versatility determines wobble sites in tRNA anticodons of vertebrate mitogenomes.
title_short Base-pairing versatility determines wobble sites in tRNA anticodons of vertebrate mitogenomes.
title_full Base-pairing versatility determines wobble sites in tRNA anticodons of vertebrate mitogenomes.
title_fullStr Base-pairing versatility determines wobble sites in tRNA anticodons of vertebrate mitogenomes.
title_full_unstemmed Base-pairing versatility determines wobble sites in tRNA anticodons of vertebrate mitogenomes.
title_sort base-pairing versatility determines wobble sites in trna anticodons of vertebrate mitogenomes.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/0f8aed815bea4e7ea2ce2cb81c2675b0
work_keys_str_mv AT miguelmfonseca basepairingversatilitydetermineswobblesitesintrnaanticodonsofvertebratemitogenomes
AT sararocha basepairingversatilitydetermineswobblesitesintrnaanticodonsofvertebratemitogenomes
AT davidposada basepairingversatilitydetermineswobblesitesintrnaanticodonsofvertebratemitogenomes
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