Codon Pattern and Compositional Constraints Determination of Genes Associated with Chronic Periodontitis

Genes (Basel). 2022 Oct 24;13(11):1934. doi: 10.3390/genes13111934.

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.

Keywords: chronic periodontitis; codon usage; genetics relationship of periodontitis; inflammatory disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chronic Periodontitis* / genetics
  • Codon / genetics
  • Codon Usage
  • Genome-Wide Association Study
  • Humans
  • Membrane Proteins / genetics
  • Microtubule-Associated Proteins / genetics
  • Selection, Genetic

Substances

  • Codon
  • WHAMM protein, human
  • Membrane Proteins
  • Microtubule-Associated Proteins

Grants and funding

The research was funded by Researchers Supporting Project (RSP-2021/339), King Saud University, Riyadh, Saudi Arabia and project R-1007/2018, University of Murcia.