ArticleVirus genes2008
Circuit assemblages derived from net dinucleotide values provide a succinct identity for the HIV-1 genome and each of its genes.
Article in Virus genes, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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1 citing paper in PubMed, 1 citations in OpenAlex.
- The biased nucleotide composition of the HIV genome: a constant factor in a highly variable virus.Retrovirology · 2012Review
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1 author at 1 institution in 1 country.
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Abstract
Dinucleotide composition has been recognized as a species-specific characteristic of organisms for more than 20 years. Lang (2000, Bioinformatics, 16, 212-221), found that in Monilinia rRNA a species-specific identity is conserved when dinucleotide counts are compressed into net dinucleotide counts (e.g., 50AC + 20CA = 30nAC) and clusters of net dinucleotides of equal value (e.g., 30nAC + 30nCT + 30nTA = 30ACTA) which were called circuits. This study evaluates circuit assemblages (CAs)--the collection of all net dinucleotide circuits derived from a sequence--in a diverse set of 110 HIV-1 genomes. The circuit composition, which is often based on <or= 15% of the total dinucleotides of a sequence, uniquely characterizes each gene and genome, although the pairwise similarity of the sequences is as low as 70%. Variations in net dinucleotide distributions are associated with structural and functional features of the genome and its proteins. Circuit values of the env signal sequence are different between subtypes that have remained localized and those that have become pandemic. CAs of complete genomes of HIV-1 are similar to other retro-transcribing viruses, and distinct from viroids and single- and double-stranded DNA and RNA viruses. CAs provide a succinct, quantitative, and species-specific description of DNA composition that is consistent with the results of traditional analytic methods at multiple levels of genome organization.
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