(Molecular Biology) Why does deamination of 5-methylcytosine lead to hot spots for spontaneous mutations?
Repairing systems that act on G-T mismatches have a bias on replace T with a C ..but this is not good as removal of U from G-U mismatches.Due to the above reason deamination of 5 methyl cytosine only leads to mutation rather than deamination of cytosine or correction.Possibility of mutation are always in CPG islands due to the random occurance of deaminated 5- methyl cytosine.Failure lies in our repairing systems actually.The greater probability of mutation are being avoiding by our DNA itself by replacing Uracil with Thymine.But the second most powerful mutation spot are these deaminated 5-methyl cytosine area.But onething is that because of the mutation only variation possible in population that ensures it's survival in world.At the same time this causes unnecessary human genetic disease in germline.
(Molecular Biology) Why does deamination of 5-methylcytosine lead to hot spots for spontaneous mutations?
(Molecular Biology) What is the "second genetic code" and how does it relate to tRNA and synthetases? How many different synthetases are there in total in most organisms and why is their specificity important?
Why would the answer be a and b? I just chose a. What is it
about b that also makes it correct?
9. In the human genome, CpG dinucleotides are often methylated. When exposed to deaminating agents, 5-methylcytosine becomes thymine. Which of the following mutations are can be explained by deamination of methylated CpG? a. 5'-TATCGAGA-3' to 5' -TATTGAGA-3' b. 5' -TATCGAGA-3' to 5'-TATCAAGA-3' c. 5' -TATGCAGA-3' to 5'-TATGTAGA-3' d. all of the above e. a and b only
Why do loss of function mutations in p53 often lead to mutations in other genes? See Section 19.6 (Page) O p53 normally functions as a tumor suppressor to stop the cell cycle after DNA damage occurs. O p53 normally functions as a tumor suppressor that encourages cell growth by triggering specific phases of the cell cycle O p53 normally functions as a proto-oncogene to stop the cell cycle after DNA damage occurs. O p53 normally functions as a proto-oncogene that...
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