Affiliations: [a] Department of Biochemistry and Genetics, Barkatullah University, Bhopal, India
| [b] Pharmaceutical Biotechnology Laboratory, Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia
| [c] Novel Global Community Educational Foundation, Australia & AFNP Med, Austria
| [d] North Caucasus Federal University, Stavropol, Russia | [e] Stavropol State Agrarian University, Stavropol, Russia
Correspondence:
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Correspondence to: Dr. Rekha Khandia, Department of Biochemistry and Genetics, Barkatullah University, Bhopal 462026 MP, India. E-mails: bu.rekha.khandia@gmail.com and rekha.khandia@bubhopal.ac.in.
Abstract: Background:Bim is a Bcl-2 homology 3 (BH3)-only proteins, a group of pro-apoptotic proteins involved in physiological and pathological conditions. Both the overexpression and under-expression of Bim protein are associated with the diseased condition, and various isoforms of Bim protein are present with differential apoptotic potential. Objective:The present study attempted to envisage the association of various molecular signatures with the codon choices of Bim isoforms. Methods:Molecular signatures like composition, codon usage, nucleotide skews, the free energy of mRNA transcript, physical properties of proteins, codon adaptation index, relative synonymous codon usage, and dinucleotide odds ratio were determined and analyzed for their associations with codon choices of Bim gene. Results:Skew analysis of the Bim gene indicated the preference of C nucleotide over G, A, and T and preference of G over T and A nucleotides was observed. An increase in C content at the first and third codon position increased gene expression while it decreased at the second codon position. Compositional constraints on nucleotide C at all three codon positions affected gene expression. The analysis revealed an exceptionally high usage of CpC dinucleotide in all the envisaged 31 isoforms of Bim. We correlated it with the requirement of rapid demethylation machinery to fine-tune the Bimgene expression. Also, mutational pressure played a dominant role in shaping codon usage bias in Bim isoforms. Conclusion:An exceptionally high usage of CpC dinucleotide in all the envisaged 31 isoforms of Bim indicates a high order selectional force to fine tune Bim gene expression.
