Why in the News?

Researchers at Columbia University found that cells can selectively switch off one parent’s copy of a gene. This may explain why some people with harmful mutations remain symptom-free, and it could lead to new diagnostic and therapeutic approaches for genetic disorders.

About the Selective Silencing Mechanism:

• Selective gene silencing refers to the process where cells inactivate one parent’s copy of a gene (either maternal or paternal), resulting in an unequal contribution of the two gene copies to cellular function.
• Previously thought to be rare, recent research reveals that this phenomenon is relatively common and plays a significant role in genetic variability, disease progression, and individual health outcomes.
• Key Features:
  • Inactivation can vary between different cell types (e.g., immune cells and kidney cells).
  • The process is dynamic and may change over time, adding complexity to how genes function in the body.
  • Approximately 1 in 20 active genes in some immune cells exhibit this selective bias.
• Implications for Health:
  • This mechanism helps explain why individuals carrying the same disease-causing mutation can have vastly different symptom severities.
  • It shifts the understanding of genetic diseases, emphasizing the importance of dynamic gene activity patterns alongside static genetic codes.
  • The discovery opens up opportunities for novel diagnostic and therapeutic approaches by focusing on gene expression rather than genetic sequences.

What are its significant applications?

• Selective Gene Manipulation: Therapies could be developed to activate healthy gene copies while suppressing diseased ones, offering a less invasive alternative to traditional genetic editing.
• Improved Understanding of Diseases: Selective gene silencing explains variability in conditions like lupus and cancer, revealing why some individuals remain symptom-free.
• Precision Medicine: By identifying individual patterns of gene expression, personalized treatment options become possible, reducing the need for one-size-fits-all approaches.
• Early Interventions: Recognizing at-risk but asymptomatic individuals allows healthcare providers to implement preventive measures and potentially delay disease onset.
• Protein-Based Therapies: Focusing on selective gene activity aids in detecting and differentiating disease-related proteins from healthy ones, paving the way for targeted, protein-specific drugs.

Get an IAS/IPS ranker as your 1: 1 personal mentor for UPSC 2024

Attend Now