What would happen to DNA replication in DNA polymerase lost its 3' to 5' exonuclease activity?
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
8. DNA Replication
Overview of DNA Replication
Problem 1d
Textbook Question
In the discussion, we focused on how DNA is replicated and synthesized. We also discussed recombination at the DNA level. Along the way, we encountered many opportunities to consider how this information was acquired. On the basis of these discussions, what answers would you propose to the following fundamental questions?
How do we know that DNA synthesis is discontinuous on one of the two template strands?
Verified step by step guidance1
Recall that DNA replication involves synthesizing new strands complementary to each original template strand, and that the two strands are antiparallel, meaning they run in opposite directions.
Understand that DNA polymerase can only add nucleotides in the 5' to 3' direction, which creates a challenge for replicating the strand oriented 3' to 5'.
Recognize that experimental evidence, such as the discovery of Okazaki fragments, showed that the strand synthesized in the 3' to 5' direction is made in short segments rather than continuously.
Consider the method used in pulse-chase experiments where radioactive nucleotides were incorporated into newly synthesized DNA, revealing short DNA fragments on one strand that were later joined together.
Conclude that these observations demonstrate DNA synthesis is continuous on the leading strand (5' to 3' direction) and discontinuous on the lagging strand (3' to 5' direction), requiring the synthesis of Okazaki fragments that are later ligated.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Semiconservative DNA Replication
DNA replication involves each of the two original strands serving as a template for a new complementary strand, resulting in two DNA molecules each with one old and one new strand. This model explains how genetic information is accurately copied and is foundational to understanding replication mechanisms.
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Semiconservative Replication
Leading and Lagging Strand Synthesis
During DNA replication, one strand (leading) is synthesized continuously in the 5' to 3' direction, while the other strand (lagging) is synthesized discontinuously in short fragments called Okazaki fragments. This occurs because DNA polymerase can only add nucleotides in one direction, necessitating a different mode of synthesis on the antiparallel strand.
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Translesion Synthesis
Okazaki Fragments and Experimental Evidence
Okazaki fragments are short DNA segments formed on the lagging strand during replication. Their discovery through pulse-labeling experiments with radioactive nucleotides provided direct evidence that DNA synthesis is discontinuous on one strand, confirming the bidirectional and asymmetric nature of DNA replication.
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Steps to DNA Replication
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