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TOPIC : DNA Damage- Pyrimidine Dimer and
DNA Repair- Photoreactivation
NAME – Vivek kumar
COURSE –Microbiology
Bangalore University
• Pyrimidine dimers are molecular lesions formed from thymine or
cytosine bases in DNA via photochemical reactions.
• Ultraviolet light induces the formation of covalent linkages by
reactions localized on the C=C double bonds.
• Two common UV products are cyclobutane pyrimidine dimers (CPDs,
including thymine dimers) and 6,4 photoproducts.
• These lesions alter the structure of DNA and consequently inhibit
polymerases and arrest replication.
Types of dimers
• Cyclobutane – A cyclobutane pyrimidine dimer (CPD) contains a four
membered ring arising from the coupling of the C=C double bonds of
pyrimidines. Such dimers interfere with base pairing during DNA
replication, leading to mutations.
• 6,4-photoproducts – 6,4-photoproducts or 6,4 pyrimidine-
pyrimidones, results from the formation of a bond between C6 of one
pyrimidine base and C4 of the another pyrimidine base. Spore
photoproduct lyase provides another enzymatic pathway for repair of
thymine photodimers.
DNA Repair - Photoreactivation
• Photoreactivation repair mechanism can be used to repair a specific
DNA damage, called as Pyrimidine dimers.
• Those DNA who have their thymines as 3H- labelled are ultraviolated-
irradiated damaged.
• By this rule a repairable DNA is identified.
Initiation
• Photolyase enzyme binds to the DNA and creates
enzyme-DNA complex.
Repairing
• Absorption of visible light and activation of the
enzyme and then the thymine dimer is monomerized.
Release
• After repairing release of enzyme.
Reference
• Molecular Biology by David Freifelder , Narosa Publishing House, Page
no.277-284
• David S. Goodsell (2001). “The Molecular Perspective: Ultraviolet
Light and Pyrimidine Dimers” PMID 11423677
THANK
YOU

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Dna damage and repair (Photoreactivation)

  • 1. TOPIC : DNA Damage- Pyrimidine Dimer and DNA Repair- Photoreactivation NAME – Vivek kumar COURSE –Microbiology Bangalore University
  • 2. • Pyrimidine dimers are molecular lesions formed from thymine or cytosine bases in DNA via photochemical reactions. • Ultraviolet light induces the formation of covalent linkages by reactions localized on the C=C double bonds. • Two common UV products are cyclobutane pyrimidine dimers (CPDs, including thymine dimers) and 6,4 photoproducts. • These lesions alter the structure of DNA and consequently inhibit polymerases and arrest replication.
  • 3.
  • 4. Types of dimers • Cyclobutane – A cyclobutane pyrimidine dimer (CPD) contains a four membered ring arising from the coupling of the C=C double bonds of pyrimidines. Such dimers interfere with base pairing during DNA replication, leading to mutations. • 6,4-photoproducts – 6,4-photoproducts or 6,4 pyrimidine- pyrimidones, results from the formation of a bond between C6 of one pyrimidine base and C4 of the another pyrimidine base. Spore photoproduct lyase provides another enzymatic pathway for repair of thymine photodimers.
  • 5.
  • 6. DNA Repair - Photoreactivation • Photoreactivation repair mechanism can be used to repair a specific DNA damage, called as Pyrimidine dimers. • Those DNA who have their thymines as 3H- labelled are ultraviolated- irradiated damaged. • By this rule a repairable DNA is identified.
  • 7. Initiation • Photolyase enzyme binds to the DNA and creates enzyme-DNA complex. Repairing • Absorption of visible light and activation of the enzyme and then the thymine dimer is monomerized. Release • After repairing release of enzyme.
  • 8.
  • 9. Reference • Molecular Biology by David Freifelder , Narosa Publishing House, Page no.277-284 • David S. Goodsell (2001). “The Molecular Perspective: Ultraviolet Light and Pyrimidine Dimers” PMID 11423677