author_facet Mrázek, Jan
Karlin, Samuel
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Karlin, Samuel
author Mrázek, Jan
Karlin, Samuel
spellingShingle Mrázek, Jan
Karlin, Samuel
Proceedings of the National Academy of Sciences
Distinctive features of large complex virus genomes and proteomes
Multidisciplinary
author_sort mrázek, jan
spelling Mrázek, Jan Karlin, Samuel 0027-8424 1091-6490 Proceedings of the National Academy of Sciences Multidisciplinary http://dx.doi.org/10.1073/pnas.0700429104 <jats:p> More than a dozen large DNA viruses exceeding 240-kb genome size were recently discovered, including the “giant” <jats:italic>mimivirus</jats:italic> with a 1.2-Mb genome size. The detection of <jats:italic>mimivirus</jats:italic> and other large viruses has stimulated new analysis and discussion concerning the early evolution of life and the complexity and mechanisms of evolutionary transitions. This paper presents analysis in three contexts. ( <jats:italic>i</jats:italic> ) Genome signatures of large viruses tend to deviate from the genome signatures of their hosts, perhaps indicating that the large viruses are lytic in the hosts. ( <jats:italic>ii</jats:italic> ) Proteome composition within these viral genomes contrast with cellular organisms; for example, most eukaryotic genomes, with respect to acidic residue usages, select Glu over Asp, but the opposite generally prevails for the large viral genomes preferring Asp more than Glu. In comparing Phe vs. Tyr usage, the viral genomes select mostly Tyr over Phe, whereas in almost all bacterial and eukaryotic genomes, Phe is used more than Tyr. Interpretations of these contrasts are proffered with respect to protein structure and function. ( <jats:italic>iii</jats:italic> ) Frequent oligonucleotides and peptides are characterized in the large viral genomes. The frequent words may provide structural flexibility to interact with host proteins. </jats:p> Distinctive features of large complex virus genomes and proteomes Proceedings of the National Academy of Sciences
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title Distinctive features of large complex virus genomes and proteomes
title_unstemmed Distinctive features of large complex virus genomes and proteomes
title_full Distinctive features of large complex virus genomes and proteomes
title_fullStr Distinctive features of large complex virus genomes and proteomes
title_full_unstemmed Distinctive features of large complex virus genomes and proteomes
title_short Distinctive features of large complex virus genomes and proteomes
title_sort distinctive features of large complex virus genomes and proteomes
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.0700429104
publishDate 2007
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description <jats:p> More than a dozen large DNA viruses exceeding 240-kb genome size were recently discovered, including the “giant” <jats:italic>mimivirus</jats:italic> with a 1.2-Mb genome size. The detection of <jats:italic>mimivirus</jats:italic> and other large viruses has stimulated new analysis and discussion concerning the early evolution of life and the complexity and mechanisms of evolutionary transitions. This paper presents analysis in three contexts. ( <jats:italic>i</jats:italic> ) Genome signatures of large viruses tend to deviate from the genome signatures of their hosts, perhaps indicating that the large viruses are lytic in the hosts. ( <jats:italic>ii</jats:italic> ) Proteome composition within these viral genomes contrast with cellular organisms; for example, most eukaryotic genomes, with respect to acidic residue usages, select Glu over Asp, but the opposite generally prevails for the large viral genomes preferring Asp more than Glu. In comparing Phe vs. Tyr usage, the viral genomes select mostly Tyr over Phe, whereas in almost all bacterial and eukaryotic genomes, Phe is used more than Tyr. Interpretations of these contrasts are proffered with respect to protein structure and function. ( <jats:italic>iii</jats:italic> ) Frequent oligonucleotides and peptides are characterized in the large viral genomes. The frequent words may provide structural flexibility to interact with host proteins. </jats:p>
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author Mrázek, Jan, Karlin, Samuel
author_facet Mrázek, Jan, Karlin, Samuel, Mrázek, Jan, Karlin, Samuel
author_sort mrázek, jan
container_issue 12
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container_title Proceedings of the National Academy of Sciences
container_volume 104
description <jats:p> More than a dozen large DNA viruses exceeding 240-kb genome size were recently discovered, including the “giant” <jats:italic>mimivirus</jats:italic> with a 1.2-Mb genome size. The detection of <jats:italic>mimivirus</jats:italic> and other large viruses has stimulated new analysis and discussion concerning the early evolution of life and the complexity and mechanisms of evolutionary transitions. This paper presents analysis in three contexts. ( <jats:italic>i</jats:italic> ) Genome signatures of large viruses tend to deviate from the genome signatures of their hosts, perhaps indicating that the large viruses are lytic in the hosts. ( <jats:italic>ii</jats:italic> ) Proteome composition within these viral genomes contrast with cellular organisms; for example, most eukaryotic genomes, with respect to acidic residue usages, select Glu over Asp, but the opposite generally prevails for the large viral genomes preferring Asp more than Glu. In comparing Phe vs. Tyr usage, the viral genomes select mostly Tyr over Phe, whereas in almost all bacterial and eukaryotic genomes, Phe is used more than Tyr. Interpretations of these contrasts are proffered with respect to protein structure and function. ( <jats:italic>iii</jats:italic> ) Frequent oligonucleotides and peptides are characterized in the large viral genomes. The frequent words may provide structural flexibility to interact with host proteins. </jats:p>
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spelling Mrázek, Jan Karlin, Samuel 0027-8424 1091-6490 Proceedings of the National Academy of Sciences Multidisciplinary http://dx.doi.org/10.1073/pnas.0700429104 <jats:p> More than a dozen large DNA viruses exceeding 240-kb genome size were recently discovered, including the “giant” <jats:italic>mimivirus</jats:italic> with a 1.2-Mb genome size. The detection of <jats:italic>mimivirus</jats:italic> and other large viruses has stimulated new analysis and discussion concerning the early evolution of life and the complexity and mechanisms of evolutionary transitions. This paper presents analysis in three contexts. ( <jats:italic>i</jats:italic> ) Genome signatures of large viruses tend to deviate from the genome signatures of their hosts, perhaps indicating that the large viruses are lytic in the hosts. ( <jats:italic>ii</jats:italic> ) Proteome composition within these viral genomes contrast with cellular organisms; for example, most eukaryotic genomes, with respect to acidic residue usages, select Glu over Asp, but the opposite generally prevails for the large viral genomes preferring Asp more than Glu. In comparing Phe vs. Tyr usage, the viral genomes select mostly Tyr over Phe, whereas in almost all bacterial and eukaryotic genomes, Phe is used more than Tyr. Interpretations of these contrasts are proffered with respect to protein structure and function. ( <jats:italic>iii</jats:italic> ) Frequent oligonucleotides and peptides are characterized in the large viral genomes. The frequent words may provide structural flexibility to interact with host proteins. </jats:p> Distinctive features of large complex virus genomes and proteomes Proceedings of the National Academy of Sciences
spellingShingle Mrázek, Jan, Karlin, Samuel, Proceedings of the National Academy of Sciences, Distinctive features of large complex virus genomes and proteomes, Multidisciplinary
title Distinctive features of large complex virus genomes and proteomes
title_full Distinctive features of large complex virus genomes and proteomes
title_fullStr Distinctive features of large complex virus genomes and proteomes
title_full_unstemmed Distinctive features of large complex virus genomes and proteomes
title_short Distinctive features of large complex virus genomes and proteomes
title_sort distinctive features of large complex virus genomes and proteomes
title_unstemmed Distinctive features of large complex virus genomes and proteomes
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.0700429104