Inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.

Universally conserved positions in ribosomal proteins have significant biases in amino acid usage, likely indicating the expansion of the genetic code at the time leading up to the most recent common ancestor(s) (MRCA). Here, we apply this principle to the evolutionary history of the ribosome before...

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Main Authors: Gregory P Fournier, Justin E Neumann, J Peter Gogarten
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-03-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20208990/?tool=EBI
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spelling doaj-7b7eb2b804c043f481bc091601d164872021-03-03T19:54:48ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-03-0153e943710.1371/journal.pone.0009437Inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.Gregory P FournierJustin E NeumannJ Peter GogartenUniversally conserved positions in ribosomal proteins have significant biases in amino acid usage, likely indicating the expansion of the genetic code at the time leading up to the most recent common ancestor(s) (MRCA). Here, we apply this principle to the evolutionary history of the ribosome before the MRCA. It has been proposed that the experimentally determined order of assembly for ribosomal subunits recapitulates their evolutionary chronology. Given this model, we produce a probabilistic evolutionary ordering of the universally conserved small subunit (SSU) and large subunit (LSU) ribosomal proteins. Optimizing the relative ordering of SSU and LSU evolutionary chronologies with respect to minimizing differences in amino acid usage bias, we find strong compositional evidence for a more ancient origin for early LSU proteins. Furthermore, we find that this ordering produces several trends in specific amino acid usages compatible with models of genetic code evolution.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20208990/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Gregory P Fournier
Justin E Neumann
J Peter Gogarten
spellingShingle Gregory P Fournier
Justin E Neumann
J Peter Gogarten
Inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.
PLoS ONE
author_facet Gregory P Fournier
Justin E Neumann
J Peter Gogarten
author_sort Gregory P Fournier
title Inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.
title_short Inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.
title_full Inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.
title_fullStr Inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.
title_full_unstemmed Inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.
title_sort inferring the ancient history of the translation machinery and genetic code via recapitulation of ribosomal subunit assembly orders.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-03-01
description Universally conserved positions in ribosomal proteins have significant biases in amino acid usage, likely indicating the expansion of the genetic code at the time leading up to the most recent common ancestor(s) (MRCA). Here, we apply this principle to the evolutionary history of the ribosome before the MRCA. It has been proposed that the experimentally determined order of assembly for ribosomal subunits recapitulates their evolutionary chronology. Given this model, we produce a probabilistic evolutionary ordering of the universally conserved small subunit (SSU) and large subunit (LSU) ribosomal proteins. Optimizing the relative ordering of SSU and LSU evolutionary chronologies with respect to minimizing differences in amino acid usage bias, we find strong compositional evidence for a more ancient origin for early LSU proteins. Furthermore, we find that this ordering produces several trends in specific amino acid usages compatible with models of genetic code evolution.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20208990/?tool=EBI
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