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
Telomeres and Telomerase
2:16 minutes
Problem 11b
Textbook Question
Textbook QuestionThere is a problem completing the replication of linear chromosomes at their ends. Describe the problem and identify why telomeres shorten in each replication cycle.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Telomeres
Telomeres are repetitive nucleotide sequences located at the ends of linear chromosomes. They protect the chromosome from deterioration or fusion with neighboring chromosomes. Each time a cell divides, a portion of the telomere is not replicated, leading to gradual shortening over successive replication cycles.
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Telomeres and Telomerase
DNA Replication
DNA replication is the process by which a cell duplicates its DNA before cell division. It involves unwinding the double helix and synthesizing new strands complementary to the original ones. However, due to the nature of DNA polymerase, which cannot fully replicate the ends of linear chromosomes, telomeres become progressively shorter with each replication.
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Hayflick Limit
The Hayflick limit refers to the number of times a normal somatic human cell can divide before cell division stops, which is typically around 40-60 divisions. This limit is largely due to telomere shortening, as critically short telomeres trigger cellular senescence or apoptosis, preventing further replication and contributing to aging and tissue regeneration limitations.
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