The DNA present in a single cell of our body gets damaged tens of thousands of times per day and multiplying these to the 37 trillion cells present in our body, we end up with a quintillion DNA errors; every day!
Mutation of the DNA forms the fundamentals of evolution, but at times mutations pose to be harmful. The DNA sequence provides the blue print for the proteins that our cells need to function and thus their damage causes n number of problems, fortunately our cells use various enzyme mediated ways to fix such problems. There are various repair mechanisms working to rectify damaged bases, strand breaks etc.
Sometimes, our DNA fails to maintain the normal Watson & Crick base pairing, this is where DNA Mismatch Repair comes in. It is one of the three types of excision repair. (Others: NER & BER)
Nucleotide Excision Repair: removes a sequence of nucleotides including the damaged ones and replaces by a new sequence of DNA. It removes DNA damage induced by UV light.
Base Excision Repair: directly removes the damaged base and replaces by a correct one
Ex, Uracil Glycosylase, removes uracil mispaired with guanine.
What is Mismatch Repair Mechanism?
MMR is a highly sustained(from bacteria to humans) biological pathway that maintains genetic stability.
Generally DNA polymerases are responsible for synthesizing new DNA strand from template DNA, by 5′ end to 3′ end polymerase activity. Along with this, it also checks whether the purines are paired with their respective pyrimidines or not, this is termed as proofreading activity of DNA polymerase which is accomplished either by 5′ to 3′ or 3′ to 5′ exonuclease activity. If any wrong pairing is detected, it will remove and replace the associated nucleotide and then continue with the replication process.
At times, during such processes few errors remain unattended; this is where MMR knocks off.
It starts right after replication process, it is peculiar to the respective strand and along with repair of mismatched bases it also fixes deletion and insertion mispair errors besides suppressing homologous recombination.(when heteroduplex DNA comprises of extreme mismatched nucleotides)
Commonly polymerase causes disincorporation of one base per 108 bases that are synthesized, whilst MMR reduces this rate to one in every 1011 bases.