Respuesta :
Answer:
Lost 5′ – 3′ polymerase activity = no DNA synthesis to fill gaps caused by removing RNA primers
Lost 5′–3′ exonuclease activity = no RNA primer removal during DNA replication
Lost 3′–5′exonuclease activity = decreased polymerase fidelity
Explanation:
DNA polymerase I wouldn't have the ability to synthesize new DNA strands if the 5' -> 3' polymerase activity was lost. Loss of the 5' --> 3' exonuclease activity would cause the RNA primers used to initiate replication to not be removed by DNA polymerase I. 3'–5' exonuclease activity participates in DNA repair, meaning that the loss of 3'–5' exonuclease activity would cause decreased polymerase fidelity.
Lost 5′–3′ polymerase activity leads to 'no DNA synthesis to fill gaps caused by removing RNA primers'. Moreover, lost 5′–3′ exonuclease activity leads to 'no RNA primer removal during DNA replication'; whereas lost 3′–5′ exonuclease activity leads to a decreased polymerase fidelity.
In prokaryotic organisms, DNA polymerase I is an enzyme required during DNA replication.
The lost 5′–3′ polymerase activity (option a) leads to 'no DNA synthesis to fill gaps caused by removing RNA primers' (Option 5).
This enzyme (DNA polymerase I) catalyzes the addition of nucleotides to the 3' end of the DNA strand.
Exonuclease activity refers to the removal of nucleotides at the ends of a polynucleotide chain (DNA strand).
The lost 5′–3′ exonuclease activity (option b) leads to 'no RNA primer removal during DNA replication' (Option 1).
This enzyme also connects the Okazaki fragments in the lagging DNA strand by deleting RNA primers and then replacing ribonucleotides with deoxyribonucleotides.
Finally, the lost 3′–5′ exonuclease activity (option c) leads to a decreased polymerase fidelity (Option 2).
The term 'polymerase fidelity' of a DNA polymerase refers to the accuracy in the process of DNA replication from a given template.
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