Positive evolutionary selection on the RIG-I-like receptor genes in mammals.

The mammalian RIG-I-like receptors, RIG-I, MDA5 and LGP2, are a family of DExD/H box RNA helicases responsible for the cytoplasmic detection of viral RNA. These receptors detect a variety of RNA viruses, or DNA viruses that express unusual RNA species, many of which are responsible for a great numbe...

Full description

Bibliographic Details
Main Authors: Ana Lemos de Matos, Grant McFadden, Pedro J Esteves
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3842351?pdf=render
id doaj-5c28c042a31d4ca3931bec6663193acb
record_format Article
spelling doaj-5c28c042a31d4ca3931bec6663193acb2020-11-25T00:47:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01811e8186410.1371/journal.pone.0081864Positive evolutionary selection on the RIG-I-like receptor genes in mammals.Ana Lemos de MatosGrant McFaddenPedro J EstevesThe mammalian RIG-I-like receptors, RIG-I, MDA5 and LGP2, are a family of DExD/H box RNA helicases responsible for the cytoplasmic detection of viral RNA. These receptors detect a variety of RNA viruses, or DNA viruses that express unusual RNA species, many of which are responsible for a great number of severe and lethal diseases. Host innate sentinel proteins involved in pathogen recognition must rapidly evolve in a dynamic arms race with pathogens, and thus are subjected to long-term positive selection pressures to avoid potential infections. Using six codon-based Maximum Likelihood methods, we were able to identify specific codons under positive selection in each of these three genes. The highest number of positively selected codons was detected in MDA5, but a great percentage of these codons were located outside of the currently defined protein domains for MDA5, which likely reflects the imposition of both functional and structural constraints. Additionally, our results support LGP2 as being the least prone to evolutionary change, since the lowest number of codons under selection was observed for this gene. On the other hand, the preponderance of positively selected codons for RIG-I were detected in known protein functional domains, suggesting that pressure has been imposed by the vast number of viruses that are recognized by this RNA helicase. Furthermore, the RIG-I repressor domain, the region responsible for recognizing and binding to its RNA substrates, exhibited the strongest evidence of selective pressures. Branch-site analyses were performed and several species branches on the three receptor gene trees showed evidence of episodic positive selection. In conclusion, by looking for evidence of positive evolutionary selection on mammalian RIG-I-like receptor genes, we propose that a multitude of viruses have crafted the receptors biological function in host defense, specifically for the RIG-I gene, contributing to the innate species-specific resistance/susceptibility to diverse viral pathogens.http://europepmc.org/articles/PMC3842351?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Ana Lemos de Matos
Grant McFadden
Pedro J Esteves
spellingShingle Ana Lemos de Matos
Grant McFadden
Pedro J Esteves
Positive evolutionary selection on the RIG-I-like receptor genes in mammals.
PLoS ONE
author_facet Ana Lemos de Matos
Grant McFadden
Pedro J Esteves
author_sort Ana Lemos de Matos
title Positive evolutionary selection on the RIG-I-like receptor genes in mammals.
title_short Positive evolutionary selection on the RIG-I-like receptor genes in mammals.
title_full Positive evolutionary selection on the RIG-I-like receptor genes in mammals.
title_fullStr Positive evolutionary selection on the RIG-I-like receptor genes in mammals.
title_full_unstemmed Positive evolutionary selection on the RIG-I-like receptor genes in mammals.
title_sort positive evolutionary selection on the rig-i-like receptor genes in mammals.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description The mammalian RIG-I-like receptors, RIG-I, MDA5 and LGP2, are a family of DExD/H box RNA helicases responsible for the cytoplasmic detection of viral RNA. These receptors detect a variety of RNA viruses, or DNA viruses that express unusual RNA species, many of which are responsible for a great number of severe and lethal diseases. Host innate sentinel proteins involved in pathogen recognition must rapidly evolve in a dynamic arms race with pathogens, and thus are subjected to long-term positive selection pressures to avoid potential infections. Using six codon-based Maximum Likelihood methods, we were able to identify specific codons under positive selection in each of these three genes. The highest number of positively selected codons was detected in MDA5, but a great percentage of these codons were located outside of the currently defined protein domains for MDA5, which likely reflects the imposition of both functional and structural constraints. Additionally, our results support LGP2 as being the least prone to evolutionary change, since the lowest number of codons under selection was observed for this gene. On the other hand, the preponderance of positively selected codons for RIG-I were detected in known protein functional domains, suggesting that pressure has been imposed by the vast number of viruses that are recognized by this RNA helicase. Furthermore, the RIG-I repressor domain, the region responsible for recognizing and binding to its RNA substrates, exhibited the strongest evidence of selective pressures. Branch-site analyses were performed and several species branches on the three receptor gene trees showed evidence of episodic positive selection. In conclusion, by looking for evidence of positive evolutionary selection on mammalian RIG-I-like receptor genes, we propose that a multitude of viruses have crafted the receptors biological function in host defense, specifically for the RIG-I gene, contributing to the innate species-specific resistance/susceptibility to diverse viral pathogens.
url http://europepmc.org/articles/PMC3842351?pdf=render
work_keys_str_mv AT analemosdematos positiveevolutionaryselectionontherigilikereceptorgenesinmammals
AT grantmcfadden positiveevolutionaryselectionontherigilikereceptorgenesinmammals
AT pedrojesteves positiveevolutionaryselectionontherigilikereceptorgenesinmammals
_version_ 1725262154141007872