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A new and updated resource for codon usage tables
BACKGROUND: Due to the degeneracy of the genetic code, most amino acids can be encoded by multiple synonymous codons. Synonymous codons naturally occur with different frequencies in different organisms. The choice of codons may affect protein expression, structure, and function. Recombinant gene tec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581930/ https://www.ncbi.nlm.nih.gov/pubmed/28865429 http://dx.doi.org/10.1186/s12859-017-1793-7 |
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author | Athey, John Alexaki, Aikaterini Osipova, Ekaterina Rostovtsev, Alexandre Santana-Quintero, Luis V. Katneni, Upendra Simonyan, Vahan Kimchi-Sarfaty, Chava |
author_facet | Athey, John Alexaki, Aikaterini Osipova, Ekaterina Rostovtsev, Alexandre Santana-Quintero, Luis V. Katneni, Upendra Simonyan, Vahan Kimchi-Sarfaty, Chava |
author_sort | Athey, John |
collection | PubMed |
description | BACKGROUND: Due to the degeneracy of the genetic code, most amino acids can be encoded by multiple synonymous codons. Synonymous codons naturally occur with different frequencies in different organisms. The choice of codons may affect protein expression, structure, and function. Recombinant gene technologies commonly take advantage of the former effect by implementing a technique termed codon optimization, in which codons are replaced with synonymous ones in order to increase protein expression. This technique relies on the accurate knowledge of codon usage frequencies. Accurately quantifying codon usage bias for different organisms is useful not only for codon optimization, but also for evolutionary and translation studies: phylogenetic relations of organisms, and host-pathogen co-evolution relationships, may be explored through their codon usage similarities. Furthermore, codon usage has been shown to affect protein structure and function through interfering with translation kinetics, and cotranslational protein folding. RESULTS: Despite the obvious need for accurate codon usage tables, currently available resources are either limited in scope, encompassing only organisms from specific domains of life, or greatly outdated. Taking advantage of the exponential growth of GenBank and the creation of NCBI’s RefSeq database, we have developed a new database, the High-performance Integrated Virtual Environment-Codon Usage Tables (HIVE-CUTs), to present and analyse codon usage tables for every organism with publicly available sequencing data. Compared to existing databases, this new database is more comprehensive, addresses concerns that limited the accuracy of earlier databases, and provides several new functionalities, such as the ability to view and compare codon usage between individual organisms and across taxonomical clades, through graphical representation or through commonly used indices. In addition, it is being routinely updated to keep up with the continuous flow of new data in GenBank and RefSeq. CONCLUSION: Given the impact of codon usage bias on recombinant gene technologies, this database will facilitate effective development and review of recombinant drug products and will be instrumental in a wide area of biological research. The database is available at hive.biochemistry.gwu.edu/review/codon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1793-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5581930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55819302017-09-06 A new and updated resource for codon usage tables Athey, John Alexaki, Aikaterini Osipova, Ekaterina Rostovtsev, Alexandre Santana-Quintero, Luis V. Katneni, Upendra Simonyan, Vahan Kimchi-Sarfaty, Chava BMC Bioinformatics Database BACKGROUND: Due to the degeneracy of the genetic code, most amino acids can be encoded by multiple synonymous codons. Synonymous codons naturally occur with different frequencies in different organisms. The choice of codons may affect protein expression, structure, and function. Recombinant gene technologies commonly take advantage of the former effect by implementing a technique termed codon optimization, in which codons are replaced with synonymous ones in order to increase protein expression. This technique relies on the accurate knowledge of codon usage frequencies. Accurately quantifying codon usage bias for different organisms is useful not only for codon optimization, but also for evolutionary and translation studies: phylogenetic relations of organisms, and host-pathogen co-evolution relationships, may be explored through their codon usage similarities. Furthermore, codon usage has been shown to affect protein structure and function through interfering with translation kinetics, and cotranslational protein folding. RESULTS: Despite the obvious need for accurate codon usage tables, currently available resources are either limited in scope, encompassing only organisms from specific domains of life, or greatly outdated. Taking advantage of the exponential growth of GenBank and the creation of NCBI’s RefSeq database, we have developed a new database, the High-performance Integrated Virtual Environment-Codon Usage Tables (HIVE-CUTs), to present and analyse codon usage tables for every organism with publicly available sequencing data. Compared to existing databases, this new database is more comprehensive, addresses concerns that limited the accuracy of earlier databases, and provides several new functionalities, such as the ability to view and compare codon usage between individual organisms and across taxonomical clades, through graphical representation or through commonly used indices. In addition, it is being routinely updated to keep up with the continuous flow of new data in GenBank and RefSeq. CONCLUSION: Given the impact of codon usage bias on recombinant gene technologies, this database will facilitate effective development and review of recombinant drug products and will be instrumental in a wide area of biological research. The database is available at hive.biochemistry.gwu.edu/review/codon. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1793-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-02 /pmc/articles/PMC5581930/ /pubmed/28865429 http://dx.doi.org/10.1186/s12859-017-1793-7 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Database Athey, John Alexaki, Aikaterini Osipova, Ekaterina Rostovtsev, Alexandre Santana-Quintero, Luis V. Katneni, Upendra Simonyan, Vahan Kimchi-Sarfaty, Chava A new and updated resource for codon usage tables |
title | A new and updated resource for codon usage tables |
title_full | A new and updated resource for codon usage tables |
title_fullStr | A new and updated resource for codon usage tables |
title_full_unstemmed | A new and updated resource for codon usage tables |
title_short | A new and updated resource for codon usage tables |
title_sort | new and updated resource for codon usage tables |
topic | Database |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581930/ https://www.ncbi.nlm.nih.gov/pubmed/28865429 http://dx.doi.org/10.1186/s12859-017-1793-7 |
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