author_facet Mrázek, Jan
Karlin, Samuel
Mrázek, Jan
Karlin, Samuel
author Mrázek, Jan
Karlin, Samuel
spellingShingle Mrázek, Jan
Karlin, Samuel
Proceedings of the National Academy of Sciences
Strand compositional asymmetry in bacterial and large viral genomes
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.95.7.3720 <jats:p> Several bacterial genomes exhibit preference for G over C on the DNA leading strand extending from the origin of replication to the ter-region in the genomes of <jats:italic>Escherichia coli</jats:italic> , <jats:italic>Mycoplasma genitalium</jats:italic> , <jats:italic>Bacillus subtilis</jats:italic> , and marginally in <jats:italic>Haemophilus influenzae</jats:italic> , <jats:italic>Mycoplasma pneumoniae</jats:italic> , and <jats:italic>Helicobacter pylori</jats:italic> . Strand compositional asymmetry is not observed in the cyanobacterium <jats:italic>Synechocystis</jats:italic> sp. genome nor in the archaeal genomes of <jats:italic>Methanococcus jannaschii</jats:italic> , <jats:italic>Methanobacterium thermoautotrophicum</jats:italic> , and <jats:italic>Archaeoglobus fulgidus</jats:italic> . A strong strand compositional asymmetry is observed in β-type but not α- or γ-type human herpesviruses featuring G &gt; C downstream of oriL and C &gt; G upstream of oriL. Dinucleotide relative abundances (i.e., dinucleotide representations normalized by the component nucleotide frequencies) are consonant with respect to the leading and lagging strands. Strand compositional asymmetry may reflect on differences in replication synthesis of the leading versus lagging strand, on differences between template and coding strand associated with transcription-coupled repair mechanisms, on differences in gene density between the two strands, on differences in residue and codon biases in relation to gene function, expression level, or operon organization, or on differences in single or context-dependent base mutational rates. The absence of strand asymmetry in the archaeal genomes may reflect the presence of multiple origins of replication. </jats:p> Strand compositional asymmetry in bacterial and large viral genomes Proceedings of the National Academy of Sciences
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title Strand compositional asymmetry in bacterial and large viral genomes
title_unstemmed Strand compositional asymmetry in bacterial and large viral genomes
title_full Strand compositional asymmetry in bacterial and large viral genomes
title_fullStr Strand compositional asymmetry in bacterial and large viral genomes
title_full_unstemmed Strand compositional asymmetry in bacterial and large viral genomes
title_short Strand compositional asymmetry in bacterial and large viral genomes
title_sort strand compositional asymmetry in bacterial and large viral genomes
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.95.7.3720
publishDate 1998
physical 3720-3725
description <jats:p> Several bacterial genomes exhibit preference for G over C on the DNA leading strand extending from the origin of replication to the ter-region in the genomes of <jats:italic>Escherichia coli</jats:italic> , <jats:italic>Mycoplasma genitalium</jats:italic> , <jats:italic>Bacillus subtilis</jats:italic> , and marginally in <jats:italic>Haemophilus influenzae</jats:italic> , <jats:italic>Mycoplasma pneumoniae</jats:italic> , and <jats:italic>Helicobacter pylori</jats:italic> . Strand compositional asymmetry is not observed in the cyanobacterium <jats:italic>Synechocystis</jats:italic> sp. genome nor in the archaeal genomes of <jats:italic>Methanococcus jannaschii</jats:italic> , <jats:italic>Methanobacterium thermoautotrophicum</jats:italic> , and <jats:italic>Archaeoglobus fulgidus</jats:italic> . A strong strand compositional asymmetry is observed in β-type but not α- or γ-type human herpesviruses featuring G &gt; C downstream of oriL and C &gt; G upstream of oriL. Dinucleotide relative abundances (i.e., dinucleotide representations normalized by the component nucleotide frequencies) are consonant with respect to the leading and lagging strands. Strand compositional asymmetry may reflect on differences in replication synthesis of the leading versus lagging strand, on differences between template and coding strand associated with transcription-coupled repair mechanisms, on differences in gene density between the two strands, on differences in residue and codon biases in relation to gene function, expression level, or operon organization, or on differences in single or context-dependent base mutational rates. The absence of strand asymmetry in the archaeal genomes may reflect the presence of multiple origins of replication. </jats:p>
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author Mrázek, Jan, Karlin, Samuel
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author_sort mrázek, jan
container_issue 7
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container_title Proceedings of the National Academy of Sciences
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description <jats:p> Several bacterial genomes exhibit preference for G over C on the DNA leading strand extending from the origin of replication to the ter-region in the genomes of <jats:italic>Escherichia coli</jats:italic> , <jats:italic>Mycoplasma genitalium</jats:italic> , <jats:italic>Bacillus subtilis</jats:italic> , and marginally in <jats:italic>Haemophilus influenzae</jats:italic> , <jats:italic>Mycoplasma pneumoniae</jats:italic> , and <jats:italic>Helicobacter pylori</jats:italic> . Strand compositional asymmetry is not observed in the cyanobacterium <jats:italic>Synechocystis</jats:italic> sp. genome nor in the archaeal genomes of <jats:italic>Methanococcus jannaschii</jats:italic> , <jats:italic>Methanobacterium thermoautotrophicum</jats:italic> , and <jats:italic>Archaeoglobus fulgidus</jats:italic> . A strong strand compositional asymmetry is observed in β-type but not α- or γ-type human herpesviruses featuring G &gt; C downstream of oriL and C &gt; G upstream of oriL. Dinucleotide relative abundances (i.e., dinucleotide representations normalized by the component nucleotide frequencies) are consonant with respect to the leading and lagging strands. Strand compositional asymmetry may reflect on differences in replication synthesis of the leading versus lagging strand, on differences between template and coding strand associated with transcription-coupled repair mechanisms, on differences in gene density between the two strands, on differences in residue and codon biases in relation to gene function, expression level, or operon organization, or on differences in single or context-dependent base mutational rates. The absence of strand asymmetry in the archaeal genomes may reflect the presence of multiple origins of replication. </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.95.7.3720 <jats:p> Several bacterial genomes exhibit preference for G over C on the DNA leading strand extending from the origin of replication to the ter-region in the genomes of <jats:italic>Escherichia coli</jats:italic> , <jats:italic>Mycoplasma genitalium</jats:italic> , <jats:italic>Bacillus subtilis</jats:italic> , and marginally in <jats:italic>Haemophilus influenzae</jats:italic> , <jats:italic>Mycoplasma pneumoniae</jats:italic> , and <jats:italic>Helicobacter pylori</jats:italic> . Strand compositional asymmetry is not observed in the cyanobacterium <jats:italic>Synechocystis</jats:italic> sp. genome nor in the archaeal genomes of <jats:italic>Methanococcus jannaschii</jats:italic> , <jats:italic>Methanobacterium thermoautotrophicum</jats:italic> , and <jats:italic>Archaeoglobus fulgidus</jats:italic> . A strong strand compositional asymmetry is observed in β-type but not α- or γ-type human herpesviruses featuring G &gt; C downstream of oriL and C &gt; G upstream of oriL. Dinucleotide relative abundances (i.e., dinucleotide representations normalized by the component nucleotide frequencies) are consonant with respect to the leading and lagging strands. Strand compositional asymmetry may reflect on differences in replication synthesis of the leading versus lagging strand, on differences between template and coding strand associated with transcription-coupled repair mechanisms, on differences in gene density between the two strands, on differences in residue and codon biases in relation to gene function, expression level, or operon organization, or on differences in single or context-dependent base mutational rates. The absence of strand asymmetry in the archaeal genomes may reflect the presence of multiple origins of replication. </jats:p> Strand compositional asymmetry in bacterial and large viral genomes Proceedings of the National Academy of Sciences
spellingShingle Mrázek, Jan, Karlin, Samuel, Proceedings of the National Academy of Sciences, Strand compositional asymmetry in bacterial and large viral genomes, Multidisciplinary
title Strand compositional asymmetry in bacterial and large viral genomes
title_full Strand compositional asymmetry in bacterial and large viral genomes
title_fullStr Strand compositional asymmetry in bacterial and large viral genomes
title_full_unstemmed Strand compositional asymmetry in bacterial and large viral genomes
title_short Strand compositional asymmetry in bacterial and large viral genomes
title_sort strand compositional asymmetry in bacterial and large viral genomes
title_unstemmed Strand compositional asymmetry in bacterial and large viral genomes
topic Multidisciplinary
url http://dx.doi.org/10.1073/pnas.95.7.3720