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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
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Compositional Features and Codon Usage Pattern of Genes Associated with Parkinson's Disease.
1Department of Zoology, Moinul Hoque Choudhury Memorial Science College, Algapur, Hailakandi-788150, Assam, India. arif.uddin29@gmail.com.
Molecular Neurobiology
|March 15, 2024
Summary
Codon usage bias in Parkinson's disease genes is low, with specific codon patterns observed. Mutation pressure appears to influence this bias in PD-associated genes.
Area of Science:
- Genomics
- Bioinformatics
- Molecular Biology
Background:
- Codon usage bias (CUB) reflects genome organization and gene expression.
- Parkinson's disease (PD) genetics is complex, with limited research on CUB in associated genes.
Purpose of the Study:
- To investigate codon usage patterns and compositional features of PD-associated genes using bioinformatics.
- To identify over-represented and under-represented codons and understand factors influencing CUB in PD.
Main Methods:
- Bioinformatic analysis of protein-coding sequences from PD-associated genes.
- Calculation of improved effective number of codons (Nc) and Nc prime.
- Analysis of GC content, Relative Synonymous Codon Usage (RSCU), Correspondence Analysis (COA), and Neutrality Plot.
Main Results:
- Low CUB indicated by average Nc (42.74) and Nc prime (44.26).
- GC content near 50%, with GC1 highest and GC2 lowest.
- GTG (Val) was the sole universally over-represented codon; other over-represented codons ended in A/T, and under-represented codons ended in G/C.
- Specific codons were absent in certain PD genes (e.g., SNCA1-8).
- COA showed distinct codon usage patterns among PD genes.
- Neutrality plot suggested mutation pressure influences CUB.
Conclusions:
- PD-associated genes exhibit low codon usage bias.
- Specific codon usage patterns and absences are notable in these genes.
- Mutation pressure is a significant factor shaping codon usage bias in Parkinson's disease genetics.
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