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Alternative translation start sites are conserved in eukaryotic genomes

Alternative start AUG codons within a single transcript can contribute to diversity of the proteome; however, their functional significance remains controversial. Here, we provide comparative genomics evidence that alternative start codons are under negative selection in vertebrates, insects and yea...

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Detalles Bibliográficos
Autores principales: Bazykin, Georgii A., Kochetov, Alex V.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025576/
https://www.ncbi.nlm.nih.gov/pubmed/20864444
http://dx.doi.org/10.1093/nar/gkq806
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author Bazykin, Georgii A.
Kochetov, Alex V.
author_facet Bazykin, Georgii A.
Kochetov, Alex V.
author_sort Bazykin, Georgii A.
collection PubMed
description Alternative start AUG codons within a single transcript can contribute to diversity of the proteome; however, their functional significance remains controversial. Here, we provide comparative genomics evidence that alternative start codons are under negative selection in vertebrates, insects and yeast. In genes where the annotated start codon (sAUG) resides within the suboptimal nucleotide context, the downstream in-frame AUG codons (dAUG) among the first ∼30 codon sites are significantly more conserved between species than in genes where the sAUG resides within the optimal context. Proteomics data show that this difference is not an annotation artifact and that dAUGs are in fact under selection as alternative start sites. The key optimal, and sometimes suboptimal, context-determining nucleotides of both the sAUG and dAUGs are conserved. Selection for secondary start sites is stronger in genes with the weak primary start site. Genes with multiple conserved start sites are enriched for transcription factors, and tend to have longer 5′UTRs and higher degree of alternative splicing. Together, these results imply that the use of alternative start sites by means of leaky mRNA scanning is a functional mechanism under selection for increased efficiency of translation and/or for translation of different N-terminal protein variants.
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spelling pubmed-30255762011-01-24 Alternative translation start sites are conserved in eukaryotic genomes Bazykin, Georgii A. Kochetov, Alex V. Nucleic Acids Res Genomics Alternative start AUG codons within a single transcript can contribute to diversity of the proteome; however, their functional significance remains controversial. Here, we provide comparative genomics evidence that alternative start codons are under negative selection in vertebrates, insects and yeast. In genes where the annotated start codon (sAUG) resides within the suboptimal nucleotide context, the downstream in-frame AUG codons (dAUG) among the first ∼30 codon sites are significantly more conserved between species than in genes where the sAUG resides within the optimal context. Proteomics data show that this difference is not an annotation artifact and that dAUGs are in fact under selection as alternative start sites. The key optimal, and sometimes suboptimal, context-determining nucleotides of both the sAUG and dAUGs are conserved. Selection for secondary start sites is stronger in genes with the weak primary start site. Genes with multiple conserved start sites are enriched for transcription factors, and tend to have longer 5′UTRs and higher degree of alternative splicing. Together, these results imply that the use of alternative start sites by means of leaky mRNA scanning is a functional mechanism under selection for increased efficiency of translation and/or for translation of different N-terminal protein variants. Oxford University Press 2011-01 2010-09-22 /pmc/articles/PMC3025576/ /pubmed/20864444 http://dx.doi.org/10.1093/nar/gkq806 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Bazykin, Georgii A.
Kochetov, Alex V.
Alternative translation start sites are conserved in eukaryotic genomes
title Alternative translation start sites are conserved in eukaryotic genomes
title_full Alternative translation start sites are conserved in eukaryotic genomes
title_fullStr Alternative translation start sites are conserved in eukaryotic genomes
title_full_unstemmed Alternative translation start sites are conserved in eukaryotic genomes
title_short Alternative translation start sites are conserved in eukaryotic genomes
title_sort alternative translation start sites are conserved in eukaryotic genomes
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025576/
https://www.ncbi.nlm.nih.gov/pubmed/20864444
http://dx.doi.org/10.1093/nar/gkq806
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