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Related Experiment Video

Updated: Aug 23, 2025

Evaluation of LC3-II Release via Extracellular Vesicles in Relation to the Accumulation of Intracellular LC3-positive Vesicles
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Analysis of the Compositional Features and Codon Usage Pattern of Genes Involved in Human Autophagy.

Zarnain Jamil1, Arif Uddin2, Syed Sahajada Mahafujul Alam1

  • 1Applied BioChemistry (ABC) Laboratory, Department of Biological Sciences, Aliah University, Kolkata 700160, India.

Cells
|October 27, 2022
PubMed
Summary

This study analyzes codon usage bias in human autophagy genes, revealing low bias and identifying key evolutionary forces. Understanding these patterns is vital for comprehending autophagy

Keywords:
autophagy-related (ATG) genescodon usage biasminimum free energy (mFE)mutation pressurenatural selection

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Area of Science:

  • Molecular Biology
  • Genomics
  • Evolutionary Biology

Background:

  • Autophagy is crucial in human diseases like cancer and neurodegenerative disorders.
  • Autophagy is regulated by autophagy-related (ATG) genes.
  • Codon usage bias (CUB) analysis offers insights into gene evolution and regulation.

Purpose of the Study:

  • To investigate the nucleotide composition and synonymous codon usage patterns of human autophagy genes.
  • To determine the influence of evolutionary forces on the CUB of these genes.

Main Methods:

  • Retrieved coding sequences (CDS) of human autophagy genes from NCBI.
  • Analyzed nucleotide composition and codon usage patterns using bioinformatics tools.
  • Calculated Effective Number of Codons (ENC) and Relative Synonymous Codon Usage (RSCU).

Main Results:

  • Human autophagy genes exhibit an overall low codon usage bias (mean ENC = 45.05).
  • Genes are marginally rich in GC content, influencing codon usage.
  • Identified 3 over-represented and 10 under-represented codons.

Conclusions:

  • Natural selection and mutational pressure are the primary drivers of CUB in human autophagy genes.
  • Findings contribute to understanding the genome biology and molecular evolution of autophagy.