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MGD Week 1


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B. Lee


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[Front]


How are mitosis and meiosis clinically significant
[Back]


Mitosis - regeneration of tissues - manipulation of stem cells Meiosis - Consequences of faulty meiosis - e.g.) infertility, retardation

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MGD Week 1 - Detalles

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15 preguntas
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How are mitosis and meiosis clinically significant
Mitosis - regeneration of tissues - manipulation of stem cells Meiosis - Consequences of faulty meiosis - e.g.) infertility, retardation
Difference between RNA and DNA
RNA - Single stranded, ribose sugar, uracil DNA- Double stranded, 2-deoxyribose sugar, thymine
Describe the formation of visible chromosomes (under light microscopes) from the double helix structure
In the nucleus - double helix structure of DNA is wrapped around histones to form nucleosomes, which form 'beads on a string DNA' - Nucleosomes tightly packs into solenoid structure, forming 30nm fibres - Fibres are compacted into several hierarchical loops to create highly condensed structure which is visible
Describe what happens in each stages of cell cycle
G1 - Cell content replication - lysosomes, mitochondria etc. doubled - APART from chromosomes S - DNA replication - each of 46 chromosomes are doubled G2 - Cell division preparation - double check of duplicated chromosomes and repair Mitosis - cell division Cytokinesis - division of cytoplasm - parent cell becomes 2 daughter cells with identical genetic information
Describe the stages of mitosis Prophase, prometaphase, metaphase, anaphase, telophase
Prophase - breakdown of nuclear membranes - chromosomes condense Prometaphase - Spindle fibres attach to chromosomes Metaphase - chromosomes align at the middle Anaphase - chromosomes divide and sister chromatids move to opposite poles Telophase - Nuclear membranes form - chromosome decondense - spindle fibre disappears
Give out the purpose of checkpoint 1 and 2 in the cell cycle Also, indicate where they are in the cell cycle
Checkpoint 1 - in between G1 and S - checking process before entering S phase - signifies cells to enter S phase Checkpoint 2 - in between G2 and mitosis - waits for signal to enter mitosis - Checks if everything has been replicated, and if DNA and chromosomes are fully intact
Name the catalyst used in DNA replication and how it catalyzes
DNA polymerase - utilises deoxyribonucleoside triphosphate (dNTP) and joins new nucleotides onto template strand - while the helicase unwind the DNA helicase and primase is removed
What does DNA ligase do
Joins okazaki fragments together on the opposite site of the double helix during elongation - this is because the the helix runs in opposite directions (3' to 5') *note that DNA polymerase acts on a normally running strand (5' to 3') on the oppposite side
Name drugs which may inhibit DNA replication
Cisplatin and BCNU - treat cancer and leukaemia - elongation inhibited Arac and 6-MP - treat acute leukaemia - termination inhibited
How does genetic diversity arise from meiosis
Independent assortment of chromosomes - meiosis I Crossing over
At which stage does crossing over happen? Also describe what happens in that stage in order for crossing over to happen
Prophase I - disintegration of nuclear envelope - formation of tetrad from pair of chromosomes
Difference between meiosis I and meiosis II
Meiosis I - homologous chromosome pair divided Meiosis II - chromatids of each chromosome divided
As gametes are haploid, genetic information must be halved during spermatogenesis and oogenesis. Describe the process of each
Spermatogenesis - spermatogonium->primary spermatocyte-> spermatids-> mature sperm - 48 days Oogenesis - Oogonium, primary oocyte-> polar bodies -> mature ovum - age 12 to 50
How are mitosis and meiosis clinically significant
Mitosis - regeneration of tissues - manipulation of stem cells Meiosis - Consequences of faulty meiosis - e.g.) infertility, retardation
Define genotype and phenotype
Genotype - genetic composition of individual Phenotype - physical appearance of the gene