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Birsa 101 CRISPR Gene Therapy

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May 26, 2026

Prelims: Current events of national and international importance | Science & Technology

Why in News?

Recently, The Ministry of Tribal Affairs, along with CSIR and CSIR‑IGIB, held a workshop on Birsa‑101, during the Janjatiya Gaurav Utsav 2026.

  • Birsa‑101 – India’s first indigenous CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) based gene therapy for Sickle Cell Disease (SCD).
  • Nomenclature Named after Bhagwan Birsa Munda, marking his 150th birth anniversary.
  • Developed by – CSIR‑IGIB (Council of Scientific and Industrial Research – Institute of Genomics and Integrative Biology), with support from the Ministry of Tribal Affairs.
  • Technological framework – Transferred to Serum Institute of India for manufacturing.
  • Key Features - It works like a precise genetic surgery, capable not only of curing Sickle Cell Disease but also transforming treatment pathways for several hereditary disorders.
  • Uses engineered enFnCas9, a sharper and safer molecular tool than SpCas9 used in Casgevy.

enFnCas9 – (enhanced Francisella novicida Cas9) is a next-generation CRISPR gene-editing platform engineered for ultra-high specificity and efficiency.

SpCas9 (Streptococcus pyogenes Cas9) is the most widely used CRISPR-Cas9 genome editing enzyme.

  • Genome‑wide assays showed up to 1,000‑fold fewer off‑target events compared to conventional CRISPR tools.

Genome-wide assays scan an organism's entire DNA sequence at once. This allows scientists to identify genetic mutations, measure gene activity, and map molecular interactions across the whole genome.

  • Mechanism of Action
    • Direct Root Correction – Birsa 101 corrects the single genetic misprint causing sickle cell disease.
    • Stem Cell Editing – The therapy extracts and edits blood-forming stem cells from the patient's bone marrow to fix the defect.
    • Permanent Cure – Engrafted cells produce healthy blood for patient’s lifetime subject to long‑term clinical follow‑up.
  • Affordability - It is designed to be more affordable than expensive foreign gene therapies like Casgevy and Lyfgenia.
  • National MissionIndia aims to eliminate sickle cell disease by 2047, heavily focusing on tribal welfare across critical belts like Jharkhand, Chhattisgarh, Madhya Pradesh, and Odisha.

Quick Facts

Sickle Cell Disease

  • A hereditary blood disorder caused by a single typo in the genetic code.
  • Red blood cells twist into a crescent or sickle shape, clogging blood vessels.
  • Leads to oxygen starvation of organs, painful crises, and long‑term damage to heart, lungs, and kidneys.

CRISPR

  • It is a revolutionary gene‑editing technology, works like molecular scissors (Cas9 protein) guided by RNA to cut defective DNA.
  • The cell repairs itself using a corrected DNA sequence.
  • Enables scientists to locate and fix errors in DNA with extraordinary precision.

References

  1. India Education Diary | Birsa 101
  2. ORF | Birsa 101
  3. India Today | Birsa 101
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