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C G Kozhukhin

Publications and source records attributed to C G Kozhukhin.

2 recordsLinked to original sources

Extendable words in nucleotide sequences.

Previous statistical analyses revealed several peculiarities of nucleotide sequences that preclude their description by existing models and thus allow one to distinguish DNA and RNA sequences from random A,T,G,C-texts. This is a consequence of the unusual distribution of certain words in nucleotide sequences: while the distribution of (most) words is consistent with Markov models of small orders, the distribution of certain words cannot be described by any previous model (anomalies in distribution of homonucleotide/homopurine/homopyrimidine runs, complementary and mirror palindromes, and non-stationary words). In this work we introduce a probabilistic approach that is partly motivated by analogy with linguistics. We also describe another important feature of DNA/RNA sequences: anomalies in distribution of words of poor nucleotide composition. We show that some classes of these words are the major obstacle for the simple Markov description of nucleotide sequences.

Base Sequence

Genome inhomogeneity is determined mainly by WW and SS dinucleotides.

According to the hypothesis of the modular structure of DNA, genomes consist of modules of various nature which may differ in statistical characteristics. Statistical analysis helps in revealing the differences in statistical characteristics and predicting the modular structure. In this connection the question about the contribution of each word of length l (l-tuple) to the inhomogeneity of genetic text arises. The notion of stationary (i.e. relatively evenly distributed over a genome) versus non-stationary l-tuples has been introduced previously. In this paper, the dinucleotide distributions for all long sequences from GenBank were analyzed and it was shown that non-stationary dinucleotides are closely associated with polyW and polyS tracts (W denotes 'weak' nucleotides A or T, while S stands for the 'strong' nucleotides G or C). Thus, genome inhomogeneity is shown to be determined mainly by AA, TT, GG, CC, AT, TA, GC and CG dinucleotides. It has been demonstrated that neither 'codon usage' nor the 'isochore model' can account for this phenomenon.

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