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A detailed comparative analysis on the overall codon usage patterns in Hepatitis A virus
Hepatitis A virus (HAV) is a hepatotropic member of the family Picornaviridae. HAV has several unique biological characteristics that distinguish it from other members of this family. Recent and previous studies revealed that codon usage plays a key role in HAV replication and evolution. In this stu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172775/ https://www.ncbi.nlm.nih.gov/pubmed/21296111 http://dx.doi.org/10.1016/j.virusres.2011.01.012 |
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author | D’ Andrea, Lucía Pintó, Rosa M. Bosch, Albert Musto, Héctor Cristina, Juan |
author_facet | D’ Andrea, Lucía Pintó, Rosa M. Bosch, Albert Musto, Héctor Cristina, Juan |
author_sort | D’ Andrea, Lucía |
collection | PubMed |
description | Hepatitis A virus (HAV) is a hepatotropic member of the family Picornaviridae. HAV has several unique biological characteristics that distinguish it from other members of this family. Recent and previous studies revealed that codon usage plays a key role in HAV replication and evolution. In this study, the patterns of synonymous codon usage in HAV have been studied through multivariate statistical methods on 30 complete open reading frames (ORFs) from the available 30 full-length HAV sequences. Effective number of codons (ENC) indicates that the overall extent of codon usage bias in HAV genomes is significant. The relative dinucleotide abundances suggest that codon usage in HAV can also be strongly influenced by underlying biases in dinucleotide frequencies. These factors strongly correlated with the first major axis of correspondence analysis (COA) on relative synonymous codon usage (RSCU). The distribution of the HAV ORFs along the plane defined by the first two major axes in COA showed that different genotypes are located at different places in the plane, suggesting that HAV codon usage is also reflecting an evolutionary process. It has been very recently described that fine-tuning translation kinetics selection also contributes to codon usage bias of HAV. The results of these studies suggest that HAV genomic biases are the result of the co-evolution of genome composition, controlled translation kinetics and probably the ability to escape the antiviral cell responses. |
format | Online Article Text |
id | pubmed-7172775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71727752020-04-22 A detailed comparative analysis on the overall codon usage patterns in Hepatitis A virus D’ Andrea, Lucía Pintó, Rosa M. Bosch, Albert Musto, Héctor Cristina, Juan Virus Res Article Hepatitis A virus (HAV) is a hepatotropic member of the family Picornaviridae. HAV has several unique biological characteristics that distinguish it from other members of this family. Recent and previous studies revealed that codon usage plays a key role in HAV replication and evolution. In this study, the patterns of synonymous codon usage in HAV have been studied through multivariate statistical methods on 30 complete open reading frames (ORFs) from the available 30 full-length HAV sequences. Effective number of codons (ENC) indicates that the overall extent of codon usage bias in HAV genomes is significant. The relative dinucleotide abundances suggest that codon usage in HAV can also be strongly influenced by underlying biases in dinucleotide frequencies. These factors strongly correlated with the first major axis of correspondence analysis (COA) on relative synonymous codon usage (RSCU). The distribution of the HAV ORFs along the plane defined by the first two major axes in COA showed that different genotypes are located at different places in the plane, suggesting that HAV codon usage is also reflecting an evolutionary process. It has been very recently described that fine-tuning translation kinetics selection also contributes to codon usage bias of HAV. The results of these studies suggest that HAV genomic biases are the result of the co-evolution of genome composition, controlled translation kinetics and probably the ability to escape the antiviral cell responses. Elsevier B.V. 2011-04 2011-02-04 /pmc/articles/PMC7172775/ /pubmed/21296111 http://dx.doi.org/10.1016/j.virusres.2011.01.012 Text en Copyright © 2011 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article D’ Andrea, Lucía Pintó, Rosa M. Bosch, Albert Musto, Héctor Cristina, Juan A detailed comparative analysis on the overall codon usage patterns in Hepatitis A virus |
title | A detailed comparative analysis on the overall codon usage patterns in Hepatitis A virus |
title_full | A detailed comparative analysis on the overall codon usage patterns in Hepatitis A virus |
title_fullStr | A detailed comparative analysis on the overall codon usage patterns in Hepatitis A virus |
title_full_unstemmed | A detailed comparative analysis on the overall codon usage patterns in Hepatitis A virus |
title_short | A detailed comparative analysis on the overall codon usage patterns in Hepatitis A virus |
title_sort | detailed comparative analysis on the overall codon usage patterns in hepatitis a virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172775/ https://www.ncbi.nlm.nih.gov/pubmed/21296111 http://dx.doi.org/10.1016/j.virusres.2011.01.012 |
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