Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/22247
Title: Codon Pattern and Compositional Constraints Determination of Genes Associated with Chronic Periodontitis
Authors: Rzhepakovsky, I. V.
Ржепаковский, И. В.
Keywords: Inflammatory disease;Genetics relationship of periodontitis;Chronic periodontitis;Codon usage
Issue Date: 2022
Citation: Khandia, R., Pandey, M., Rzhepakovsky, I.V., Khan, A.A., Legaz, I. Codon Pattern and Compositional Constraints Determination of Genes Associated with Chronic Periodontitis // Genes. - 2022. - 13 (11), статья № 1934. - DOI:10.3390/genes13111934
Series/Report no.: Genes
Abstract: Genome-wide association studies showed the relationship of NIN, ABHD12B, WHAMM, AP3B2, and SIGLEC5 with chronic periodontitis. The study’s objective was to investigate different molecular patterns and evolutionary forces acting on the mentioned genes. The investigation of molecular patterns encompasses the study of compositional parameters, expression profile, physical properties of genes, codon preferences, degree of codon bias, determination of the most influential codons, and assessment of actions of evolutionary forces, such as mutations and natural selection. The overall compositional analysis revealed the dominance of A and G nucleotides compared to T and C. A relatively low codon usage bias is observed. The CTG codon is the most overused codon, followed by TCC. The genes, AP3B2 and SIGLEC5, preferred GC-ending codons, while NIN, ABHD12B, and WHAMM preferred AT-ending codons. The presence of directional mutational force and natural selection was found to operate codon usage in genes envisaged, and selective forces were dominant over mutational forces. Apart from mutation and selection forces, compositional constraints also played imperative roles. The study enriched our knowledge of specific molecular patterns associated with the set of genes significantly associated with chronic periodontitis. Further studies are warranted to identify more genetic signatures associated with the disease
URI: http://hdl.handle.net/20.500.12258/22247
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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