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By
Dr. Sonia Goel
SGT University,
Gurugram
 DNA repair is a process by which the cell repairs
mutations that occur in the DNA.
 DNA carries all the necessary information for the
growth and function of the cell, and it is therefore
important that n nay inadvertent change is set right
before it can become detrimental to the cell
 The cell’s DNA repair mechanism continuously scans
the genome to remove or mend such mutations.
 Direct Repair (photoreactivation)
 Excision Repair
a) base excision repair
b) Nucleotide excision repair
 Mismatch repair
 Recombinational repair
 SOS - repair
 Direct repair acts directly on damaged nucleoetides,
converting each one back to its original structure . But only
few types of damaged nucleotides can be repaired directly.
 Example- UV radiations-mediated damages are repaired by
the PHOTOREACTIVATION.
 The UV damages caused in cells are repaired after
exposure of cells in visible light (300-500nm).
 Enzyme ‘DNA photolyase’ (lacks in mutant cell)
activated when exposed to visible light.
 This enzyme absorbs energy, binds to cyclobutane ring
to defective sites of DNA
 Promotes cleavage of bond bw T-T dimer and cause
reverse to original monomeric nucleotides.
Another example of direct repair:
 removal of alkyl group from O⁶-methylguanine.
 More elaborate system in which the damaged
nucleotides is not repaired , but removed from the
DNA.
 In this system, undamaged strand serves as a template
for the reincorporation of correct nucleotide by the
DNA polymerase.
 Types: 1) base excision repair
2) nucleotide excision repair
 Removal of damaged nucleotides base, excision of
short piece of polynucleotide and resynthesis with
DNA polymerase.
ENZYMES INVOLVED:
1. DNA glycocyclase: cleaves N- glycosyl bond to remove
damaged base. (ex.-uracil DNA glycocylcase)
2. AP Endonuclease: cleaves the phosphdieseter bond at
5’ .
3. DNA polymerase: fills the gap
4. DNA ligase: joins the ends.
STEPS:
1. UDG recognizes Uracil.
2. UDG cleaves N- glycosyl
bond
3. UDG flip out Uracil.
4. AP Endonuclease cleaves
phosphodiester bckbone
5. DNA polymerase refills
the gap.
6. DNA ligase seals the nick.
 Versatile process that can remove many forms of DNA
damage by nuclease cleavage on either side of the
damaged bases, removal of the damaged
oligonuclotide, and resynthesis of a patch using the
undamaged strand as the template.
 NER occurs in almost all organisms examined.
 Common feature: modified nucleotides cause a
significant distortion in the DNA helix.
 Disease due to defective NER:
1. Xeroderma Pigmentosum
2. Cockayne syndrome
Uvr system of NER in E. Coli:
 Base pair mismatch occur during DNA replication are fixed by
this repair.
 In E.Coli. ,3 protiens involved : ‘Mut S, Mut L, Mut H’
 Mut S: detects mismatch site & binds to it ; form complex with
Mut L.
 Formed complex recruits Mut H to GATC sequence at
hemimethylated site. This complex intraxct with Mut H by DNA
looping mechanism.
 Mut H: has site specific endonuclease activity that is inactive until
complex encounters a hemimethylated GATC sequence.
 Unmethylated strand is unwound and degraded in 3’ to 5’
direction.
 This segment is replace with new DNA with combined actions of
DNA helicase, SSB, exonuclease, DNA polymerase and ligase.
Mismatch
repair
mechanism
in E.Coli
 The process of filling gap in one strand of dsDNA by
retrieving a homologous single strand from another
dsDNA.
 Occurs after replication (post translation method).
 In E.Coli, when DNA is replicated, dimer prevents the
damaged sites from acting as template. Replication is
forced to bypass it.
 This results in gap in newly synthesised strand, while
other parental strand forms normal complementary
strand.
 Gap opposite the damaged site in one double strand is
filled by taking the homologous ssDNA from normal
duplex.
Recombination
al repair in
E.Coli
 SOS (save our soul) is a global response to DNA
damage in which the cell cycle is arrested and the
DNA repair mutagenesis are induced.
 Sos repair reconstruct the chemical structure of DNA
but the hereditary information is lost.
 Also called inducible repair.
 It involves more than 40 gene which encodes protein
responsible for protection and replication of DNA as
well as repair and mutation.
Mechanism of SOS RESONSE
DNA repair mechanism

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DNA repair mechanism

  • 1. By Dr. Sonia Goel SGT University, Gurugram
  • 2.  DNA repair is a process by which the cell repairs mutations that occur in the DNA.  DNA carries all the necessary information for the growth and function of the cell, and it is therefore important that n nay inadvertent change is set right before it can become detrimental to the cell  The cell’s DNA repair mechanism continuously scans the genome to remove or mend such mutations.
  • 3.  Direct Repair (photoreactivation)  Excision Repair a) base excision repair b) Nucleotide excision repair  Mismatch repair  Recombinational repair  SOS - repair
  • 4.  Direct repair acts directly on damaged nucleoetides, converting each one back to its original structure . But only few types of damaged nucleotides can be repaired directly.  Example- UV radiations-mediated damages are repaired by the PHOTOREACTIVATION.
  • 5.  The UV damages caused in cells are repaired after exposure of cells in visible light (300-500nm).  Enzyme ‘DNA photolyase’ (lacks in mutant cell) activated when exposed to visible light.  This enzyme absorbs energy, binds to cyclobutane ring to defective sites of DNA  Promotes cleavage of bond bw T-T dimer and cause reverse to original monomeric nucleotides.
  • 6.
  • 7. Another example of direct repair:  removal of alkyl group from O⁶-methylguanine.
  • 8.  More elaborate system in which the damaged nucleotides is not repaired , but removed from the DNA.  In this system, undamaged strand serves as a template for the reincorporation of correct nucleotide by the DNA polymerase.  Types: 1) base excision repair 2) nucleotide excision repair
  • 9.  Removal of damaged nucleotides base, excision of short piece of polynucleotide and resynthesis with DNA polymerase. ENZYMES INVOLVED: 1. DNA glycocyclase: cleaves N- glycosyl bond to remove damaged base. (ex.-uracil DNA glycocylcase) 2. AP Endonuclease: cleaves the phosphdieseter bond at 5’ . 3. DNA polymerase: fills the gap 4. DNA ligase: joins the ends.
  • 10. STEPS: 1. UDG recognizes Uracil. 2. UDG cleaves N- glycosyl bond 3. UDG flip out Uracil. 4. AP Endonuclease cleaves phosphodiester bckbone 5. DNA polymerase refills the gap. 6. DNA ligase seals the nick.
  • 11.  Versatile process that can remove many forms of DNA damage by nuclease cleavage on either side of the damaged bases, removal of the damaged oligonuclotide, and resynthesis of a patch using the undamaged strand as the template.  NER occurs in almost all organisms examined.  Common feature: modified nucleotides cause a significant distortion in the DNA helix.  Disease due to defective NER: 1. Xeroderma Pigmentosum 2. Cockayne syndrome
  • 12. Uvr system of NER in E. Coli:
  • 13.  Base pair mismatch occur during DNA replication are fixed by this repair.  In E.Coli. ,3 protiens involved : ‘Mut S, Mut L, Mut H’  Mut S: detects mismatch site & binds to it ; form complex with Mut L.  Formed complex recruits Mut H to GATC sequence at hemimethylated site. This complex intraxct with Mut H by DNA looping mechanism.  Mut H: has site specific endonuclease activity that is inactive until complex encounters a hemimethylated GATC sequence.  Unmethylated strand is unwound and degraded in 3’ to 5’ direction.  This segment is replace with new DNA with combined actions of DNA helicase, SSB, exonuclease, DNA polymerase and ligase.
  • 15.  The process of filling gap in one strand of dsDNA by retrieving a homologous single strand from another dsDNA.  Occurs after replication (post translation method).  In E.Coli, when DNA is replicated, dimer prevents the damaged sites from acting as template. Replication is forced to bypass it.  This results in gap in newly synthesised strand, while other parental strand forms normal complementary strand.  Gap opposite the damaged site in one double strand is filled by taking the homologous ssDNA from normal duplex.
  • 17.  SOS (save our soul) is a global response to DNA damage in which the cell cycle is arrested and the DNA repair mutagenesis are induced.  Sos repair reconstruct the chemical structure of DNA but the hereditary information is lost.  Also called inducible repair.  It involves more than 40 gene which encodes protein responsible for protection and replication of DNA as well as repair and mutation.
  • 18. Mechanism of SOS RESONSE