Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp

Detalhes bibliográficos
Autor(a) principal: Massey, Steven E.
Data de Publicação: 2003
Outros Autores: Moura, Gabriela, Beltrão, Pedro, Almeida, Ricardo, Garey, James R., Tuite, Mick F, Santos, Manuel A. S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/27694
Resumo: Using the (near) complete genome sequences of the yeasts Candida albicans, Saccharomyces cerevisiae, and Schizosaccharomyces pombe, we address the evolution of a unique genetic code change, which involves decoding of the standard leucine-CTG codon as serine in Candida spp. By using two complementary comparative genomics approaches, we have been able to shed new light on both the origin of the novel Candida spp. Ser-tRNA(CAG), which has mediated CTG reassignment, and on the evolution of the CTG codon in the genomes of C. albicans, S. cerevisiae, and S. pombe. Sequence analyses of newly identified tRNAs from the C. albicans genome demonstrate that the Ser-tRNA(CAG) is derived from a serine and not a leucine tRNA in the ancestor yeast species and that this codon reassignment occurred approximately 170 million years ago, but the origin of the Ser-tRNA(CAG) is more ancient, implying that the ancestral Leu-tRNA that decoded the CTG codon was lost after the appearance of the Ser-tRNA(CAG). Ambiguous CTG decoding by the Ser-tRNA(CAG) combined with biased AT pressure forced the evolution of CTG into TTR codons and have been major forces driving evolution of the CTN codon family in C. albicans. Remarkably, most of the CTG codons present in extant C. albicans genes are encoded by serine and not leucine codons in homologous S. cerevisiae and S. pombe genes, indicating that a significant number of serine TCN and AGY codons evolved into CTG codons either directly by simultaneous double mutations or indirectly through an intermediary codon. In either case, CTG reassignment had a major impact on the evolution of the coding component of the Candida spp. genome.
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spelling Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida sppUsing the (near) complete genome sequences of the yeasts Candida albicans, Saccharomyces cerevisiae, and Schizosaccharomyces pombe, we address the evolution of a unique genetic code change, which involves decoding of the standard leucine-CTG codon as serine in Candida spp. By using two complementary comparative genomics approaches, we have been able to shed new light on both the origin of the novel Candida spp. Ser-tRNA(CAG), which has mediated CTG reassignment, and on the evolution of the CTG codon in the genomes of C. albicans, S. cerevisiae, and S. pombe. Sequence analyses of newly identified tRNAs from the C. albicans genome demonstrate that the Ser-tRNA(CAG) is derived from a serine and not a leucine tRNA in the ancestor yeast species and that this codon reassignment occurred approximately 170 million years ago, but the origin of the Ser-tRNA(CAG) is more ancient, implying that the ancestral Leu-tRNA that decoded the CTG codon was lost after the appearance of the Ser-tRNA(CAG). Ambiguous CTG decoding by the Ser-tRNA(CAG) combined with biased AT pressure forced the evolution of CTG into TTR codons and have been major forces driving evolution of the CTN codon family in C. albicans. Remarkably, most of the CTG codons present in extant C. albicans genes are encoded by serine and not leucine codons in homologous S. cerevisiae and S. pombe genes, indicating that a significant number of serine TCN and AGY codons evolved into CTG codons either directly by simultaneous double mutations or indirectly through an intermediary codon. In either case, CTG reassignment had a major impact on the evolution of the coding component of the Candida spp. genome.Cold Spring Harbor Laboratory Press2020-02-27T11:57:29Z2003-04-01T00:00:00Z2003-04info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/27694eng1088-905110.1101/gr.811003Massey, Steven E.Moura, GabrielaBeltrão, PedroAlmeida, RicardoGarey, James R.Tuite, Mick FSantos, Manuel A. S.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T11:53:37Zoai:ria.ua.pt:10773/27694Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:00:23.566488Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp
title Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp
spellingShingle Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp
Massey, Steven E.
title_short Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp
title_full Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp
title_fullStr Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp
title_full_unstemmed Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp
title_sort Comparative evolutionary genomics unveils the molecular mechanism of reassignment of the CTG codon in Candida spp
author Massey, Steven E.
author_facet Massey, Steven E.
Moura, Gabriela
Beltrão, Pedro
Almeida, Ricardo
Garey, James R.
Tuite, Mick F
Santos, Manuel A. S.
author_role author
author2 Moura, Gabriela
Beltrão, Pedro
Almeida, Ricardo
Garey, James R.
Tuite, Mick F
Santos, Manuel A. S.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Massey, Steven E.
Moura, Gabriela
Beltrão, Pedro
Almeida, Ricardo
Garey, James R.
Tuite, Mick F
Santos, Manuel A. S.
description Using the (near) complete genome sequences of the yeasts Candida albicans, Saccharomyces cerevisiae, and Schizosaccharomyces pombe, we address the evolution of a unique genetic code change, which involves decoding of the standard leucine-CTG codon as serine in Candida spp. By using two complementary comparative genomics approaches, we have been able to shed new light on both the origin of the novel Candida spp. Ser-tRNA(CAG), which has mediated CTG reassignment, and on the evolution of the CTG codon in the genomes of C. albicans, S. cerevisiae, and S. pombe. Sequence analyses of newly identified tRNAs from the C. albicans genome demonstrate that the Ser-tRNA(CAG) is derived from a serine and not a leucine tRNA in the ancestor yeast species and that this codon reassignment occurred approximately 170 million years ago, but the origin of the Ser-tRNA(CAG) is more ancient, implying that the ancestral Leu-tRNA that decoded the CTG codon was lost after the appearance of the Ser-tRNA(CAG). Ambiguous CTG decoding by the Ser-tRNA(CAG) combined with biased AT pressure forced the evolution of CTG into TTR codons and have been major forces driving evolution of the CTN codon family in C. albicans. Remarkably, most of the CTG codons present in extant C. albicans genes are encoded by serine and not leucine codons in homologous S. cerevisiae and S. pombe genes, indicating that a significant number of serine TCN and AGY codons evolved into CTG codons either directly by simultaneous double mutations or indirectly through an intermediary codon. In either case, CTG reassignment had a major impact on the evolution of the coding component of the Candida spp. genome.
publishDate 2003
dc.date.none.fl_str_mv 2003-04-01T00:00:00Z
2003-04
2020-02-27T11:57:29Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/27694
url http://hdl.handle.net/10773/27694
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10.1101/gr.811003
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dc.publisher.none.fl_str_mv Cold Spring Harbor Laboratory Press
publisher.none.fl_str_mv Cold Spring Harbor Laboratory Press
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