Correlations and anticorrelations among nucleotide distributions along the genomes of various organisms
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
- MeSH
- Arabidopsis genetika MeSH
- Drosophila melanogaster genetika MeSH
- druhová specificita MeSH
- Escherichia coli genetika MeSH
- genom bakteriální MeSH
- genom fungální MeSH
- genom rostlinný MeSH
- genom virový MeSH
- genom * MeSH
- Herpesviridae genetika MeSH
- Hominidae genetika MeSH
- lidé MeSH
- myši genetika MeSH
- Retroviridae genetika MeSH
- Saccharomyces cerevisiae genetika MeSH
- sekvenční analýza DNA * MeSH
- statistické modely MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši genetika MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
We have analyzed correlations of nucleotide distributions along more than 50 megabases of the longest sequenced parts of the human, mouse, Drosophila, Arabidopsis, yeast, E.coli and three kinds of viral genomes. The strongest correlations were observed between the distributions of C and G, in particular in the genome of Drosophila. This correlation was much weaker, though still strong, in the human genome and E.coli that exhibited the same level of this correlation. The C/G correlation hardly originates from the isochores because the isochores were not reported to occur in the genomes of Drosophila and E. coil. The genomic distribution curves of adenine and thymine were also positively correlated in all analyzed organisms except for the yeast where they were anticorrelated. Still stronger anticorrelations were, however, observed between the genomic distributions of A and C and between G and T. These genomic distributions anticorrelated almost generally and very strong. These anticorrelations are likely to originate from point mutations resulting from unrepaired GA mispairing as a replication intermediate. The C/A or G/T anticorrelation or compensation is a very strong and general new phenomenon that shapes the genomic nucleotide sequences.
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