Tracts of Adenosine and Cytidine Residues in the Genomes of Prokaryotes and Eukaryotes
- 1 January 1998
- journal article
- research article
- Published by Taylor & Francis in DNA Sequence
- Vol. 8 (6) , 375-383
- https://doi.org/10.3109/10425179809020898
Abstract
Large segments of the S. cerevisiae, C. elegans, D. mela-nogaster, mouse, and human genomes, as well as the genomes of four bacterial species, have been analyzed for the occurrence of tracts of separated, alternating, and mixed adenosine and cytidine residues. Several surprising features have been observed. Although both yeast and nematode DNA are rich in AT base pairs, the genomes of these organisms have widely different biases for long homonucleotide tracts. Yeast has many long tracts of oligoadenosine, while C. elegans has an extraordinary abundance of oligocytidine tracts. Tracts of alternating A-C residues are overrep-resented in most eukaryotic organisms examined. Tracts of mixed adenosine and cytidine residues, however, are especially frequent in the human genome.Keywords
This publication has 16 references indexed in Scilit:
- Whole-Genome Random Sequencing and Assembly of Haemophilus influenzae RdScience, 1995
- H-DNA and Related StructuresAnnual Review of Biophysics, 1994
- Stabilities of double- and triple-strand helical nucleic acidsProgress in Biophysics and Molecular Biology, 1992
- Local Supercoil-Stabilized DNA StructureCritical Reviews in Biochemistry and Molecular Biology, 1991
- Co-polymer tracts in eukaryotic, prokaryotic, and organellar DNADNA Sequence, 1991
- CD studies of double-stranded polydeoxynucleotides composed of repeating units of contiguous homopurine residuesBiopolymers, 1988
- An oligopurine sequence bias occurs in eukaryotic virusesNucleic Acids Research, 1988
- The DNA sequence of the human .beta.-globin region is strongly biased in favor of long strings of contiguous purine or pyrimidine residuesBiochemistry, 1987
- High-salt d(CpGpCpG), a left-handed Z′ DNA double helixNature, 1980
- Molecular structure of a left-handed double helical DNA fragment at atomic resolutionNature, 1979