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BIRSA-101

23 Dec 2025
3 min

In Summary

India launched BIRSA-101, its first indigenous CRISPR-based gene therapy for Sickle Cell Disease, developed by CSIR-IGIB, using advanced gene-editing technology and collaboration with Serum Institute of India.

In Summary

Why in the News?

India launched its 1st indigenous CRISPR-based gene editing therapy called BIRSA-101 for Sickle Cell Disease.

More on News

  • It has been developed by CSIR–Institute of Genomics & Integrative Biology (IGIB).
  • It has been called BIRSA-101 as it has been dedicated to Bhagwan Birsa Munda on his 150th birth anniversary.
  • A technology transfer agreement has been signed between CSIR-IGIB and Serum Institute of India which aims to enable scalable, affordable enFnCas9 CRISPR-based therapies for Sickle Cell Disease and other genetic disorders.

CRISPR Technology and Mechanism

  • CRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats
  • It is a gene-editing technology to selectively modify the DNA of living organisms.

How does it work? 

  • CRISPR leverages a natural defense mechanism of bacteria to cut DNA at a specific location. 
  • When bacteria are attacked by a virus, they record a section of the virus's DNA in their own DNA.
  • Storing part of the virus's genetic code allows the bacteria to "remember" it. 
  • When the same type of virus attacks again, the bacteria use a specific CRISPR-associated protein number 9 (CAS9) to cut the virus's DNA, destroying the virus.
  • In the laboratory, scientists use this same CRISPR/CAS9 system to identify and cut a specific DNA sequence.
  • Main Components:
    • Cas9 Protein: The system uses a Cas protein called Cas9, which acts like molecular scissors to cut DNA.
    • Guide RNA: A guide RNA tells Cas9 where to cut, and the DNA is cut exactly at the spot chosen by this guide.
  • Genome Editing Tools
    • CRISPR-Cas9: It uses a small piece of RNA to guide the Cas9 "cutting" protein to the exact spot in the DNA.
    • Homing Endonucleases (Meganucleases): These are natural enzymes that can find and cut long sections of DNA. 
    • Zinc-Finger Nucleases (ZFNs): They use special protein parts to find the right place in the DNA and then cut it.
    • TALE Nucleases (TALENs): These tools use two parts that come together to cut DNA at a chosen spot.

TnpB-Based Technology

Indian scientists at ICAR–CRRI (Central Rice Research Institute) Cuttack have developed a new genome-editing tool for plants using TnpB proteins which has been granted patent.

  • TnpB Protein: It is a transposon-associated protein that works like a molecular scissor to cut DNA which is much smaller than tools like Cas9 or Cas12a.
    • Transposns/Transposable elements (TEs), also known as "jumping genes," are DNA sequences that move from one location on the genome to another.
  • The compact size of TnpB makes it easier to get into plant cells, including through virus-mediated delivery.

GlowCas9

  • Scientists from Kolkata-based Bose Institute, an autonomous institute under Dept. of Science and Technology (DST), have developed GlowCas9 
  • It is a CRISPR protein that lights up while performing gene editing.
  • It emits light because it is fused with nano-luciferase fragments from deep-sea shrimp, which reassemble and emit light when the Cas9 protein folds correctly.

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