Ans: Correct option: Will
remove several nucleotides on one strand.
Explanation: During the DNA
replication some time proofreading fails and the wrong base is
inserted in the growing DNA strand (example adenine with
cytosine) then this is called a mismatch. This
mistake is corrected by the mismatch repair enzymes. Following are
some basic steps of the mismatch repair:
- At first, the MutS
protein recognizes the mismatch site and binds to it.
- MutL protein binds
with the MutS and thus forms the MutS-MutL
complex.
- Now the MutH
protein binds with the DNA strand at GATC
site.
- Due to the looping of the
DNA, the MutS-MutL complex comes close to the MutH
protein.
- After this MutH protein
creates a break in the unmethylated strand by its endonuclease
activity.
- Now several nucleotides flanking
the mismatch are removed.
- DNA polymerase
enzyme fills the gap by adding nucleotides according to the
template.
- The nick is sealed by the enzyme
DNA ligase.
Please see the image below for Steps
1-4.

The explanation for
incorrect options:
- The nucleotides are removed
from only one strand. As template strand is methylated at
the GATC site. But immediately after synthesis, the newly
synthesized strand is not methylated. In this way,
MutH enzyme differentiates the template strand
from the new strand and makes a cut in the only in the new
strand for the removal of nucleotides.
- Several nucleotides (not
only mismatched) near the mismatch site are removed by the
exonuclease enzyme.
- The correct nucleotides are
replaced by the DNA polymerase enzyme.
- Mismatch repair enzymes detect the
mutation and correct it. If the mismatch is not repaired it
may lead to cancer.