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   <subfield code="a">Evolution of Prokaryotic Genes by Shift of Stop Codons</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Anna Vakhrusheva, Marat Kazanov, Andrey Mironov, Georgii Bazykin]</subfield>
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   <subfield code="a">De novo origin of coding sequence remains an obscure issue in molecular evolution. One of the possible paths for addition (subtraction) of DNA segments to (from) a gene is stop codon shift. Single nucleotide substitutions can destroy the existing stop codon, leading to uninterrupted translation up to the next stop codon in the gene's reading frame, or create a premature stop codon via a nonsense mutation. Furthermore, short indels-caused frameshifts near gene's end may lead to premature stop codons or to translation past the existing stop codon. Here, we describe the evolution of the length of coding sequence of prokaryotic genes by change of positions of stop codons. We observed cases of addition of regions of 3′UTR to genes due to mutations at the existing stop codon, and cases of subtraction of C-terminal coding segments due to nonsense mutations upstream of the stop codon. Many of the observed stop codon shifts cannot be attributed to sequencing errors or rare deleterious variants segregating within bacterial populations. The additions of regions of 3′UTR tend to occur in those genes in which they are facilitated by nearby downstream in-frame triplets which may serve as new stop codons. Conversely, subtractions of coding sequence often give rise to in-frame stop codons located nearby. The amino acid composition of the added region is significantly biased, compared to the overall amino acid composition of the genes. Our results show that in prokaryotes, shift of stop codon is an underappreciated contributor to functional evolution of gene length.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2010</subfield>
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   <subfield code="a">Stop codons</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Evolution</subfield>
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   <subfield code="a">Prokaryotes</subfield>
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   <subfield code="a">Frameshifts</subfield>
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   <subfield code="a">Tandem stop codons</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Stop codon read-through</subfield>
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   <subfield code="a">Translation termination</subfield>
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   <subfield code="a">3′UTR</subfield>
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   <subfield code="a">Gene length</subfield>
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   <subfield code="a">Vakhrusheva</subfield>
   <subfield code="D">Anna</subfield>
   <subfield code="u">Department of Bioengineering and Bioinformatics, M.V. Lomonosov Moscow State University, Vorbyevy Gory 1-73, 119992, Moscow, Russia</subfield>
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   <subfield code="a">Kazanov</subfield>
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   <subfield code="u">Institute for Information Transmission Problems, Russian Academy of Sciences, Bolshoi Karenty pereulok 19, 127994, Moscow, Russia</subfield>
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   <subfield code="a">Mironov</subfield>
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   <subfield code="u">Department of Bioengineering and Bioinformatics, M.V. Lomonosov Moscow State University, Vorbyevy Gory 1-73, 119992, Moscow, Russia</subfield>
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   <subfield code="u">Department of Bioengineering and Bioinformatics, M.V. Lomonosov Moscow State University, Vorbyevy Gory 1-73, 119992, Moscow, Russia</subfield>
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   <subfield code="t">Journal of Molecular Evolution</subfield>
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   <subfield code="g">72/2(2011-02-01), 138-146</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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