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Proliferation: lecture 3

belles11 Inglês 52 flashcards

Proliferation: lecture 3

Flashcards do conjunto (52)

  1. 1What stages can a newborn cell enter into?The newborn cell may drop out of cycle (so called G0 phase) or enter G1
  2. 2Describe the G1 stageIn early G1 the cell
    becomes committed to divide and proteins, organelles and macromolecules are produced. This can take weeks and results in the cell itself becoming bigger in size.
  3. 3Describe the S phase of the cell cycle.The cell commences genome replication in S phase, the only time when DNA
    is synthesised, and a copy of each
    chromosome is produced. This stage takes 8-10 hours and involves the uptake of deoxynucleotides.
  4. 4Describe the G2 phase of the cell cycle.This is a short stage (3-4 hours). It is the second growth stage of the cell and the same processes occur as the G1 phase.
  5. 5How long is the mitotic phase of the cell cycle?minutes- 1 hour
  6. 6Give the order of the stages of cell cycle.G0 <- newborn cell -> G1 -> S -> G2 -> M
  7. 7What are the key decision points in the regulation of the cell cycle?- the entry into S phase - the entry into M phase (known as the G1/S and G2/M checkpoints)
  8. 8What is the overall goal of mitosis?To generate 2 daughter cells and ensure that each inherits one copy (chromatid) of each chromosome
  9. 9Name the phases of mitosis(interphase) prophase, metaphase, anaphase, telophase, cytokinesis
  10. 10Describe what occurs during prophase.-2 pairs of chromosomes condense.
    -cohesin (a protein) forms rings which hold the sister chromatids together
    -The mitotic spindle (mircrotubule structure) forms.
  11. 11What is the name of the transition phase from prophase to metaphase?prometaphase
  12. 12What occurs during prometaphase?-the nuclear envelope breaks down
    -microtubules connect to each centromere via a protein complex called the kinetochore
    -microtubules begin to pull chromosomes towards spindle poles
  13. 13Describe what happens during metaphase.- chromosomes become aligned along cell equator by microtubule tension
  14. 14State the different types of microtubles present in metaphase-astral microtubles -Kinetochore microtubules -interpolar microtubules.
  15. 15What do astral microtubules connect?connect the spindle pole (tubules) to the cell membrane
  16. 16What is the purpose of interpolar microtubules?They connect the 2 spindle poles together.
  17. 17What is the role of the kinetochore microtubules?connect the chromosome to the spindle pole (attach to chromosome at centromere via kinetochore complex.
  18. 18Describe the microtubule movements occuring in prometaphasekinetochore microtubules shorten
    interpolar microtubules lengthen
    pulls chromosome pairs into the midline between spindle poles.
  19. 19what happens in anaphase-cohesin ring holding chromosome pairs together cut by enzyme separase
    -movement of microtubules pulls chromosomes apart.
  20. 20describe the microtubule movements in anaphase-further shortening of kinetochore microtubules
    -lengthening of interpolar tubules
  21. 21Describe the regulation of the cutting of the cohesin ringcatalysed by the enzyme separase
    anaphase promoting complex promotes process
    Securin inhibits process.
  22. 22Briefly describe Tubulin-made of Alpha and Beta subunits
    -can polymerise and depolymerise
  23. 23How are the spindle poles pulled apart during anaphase-astral microtubules shorten
    -helped by 'pushing' from the lengthening interpolar tubules/
  24. 24Describe the process of telophase-chromosomes arrive at cell poles
    -the spindle is broken down
    -nuclear membrane reforms around chromosomes
  25. 25Describe the process of cytokinesis in animal cellsan actin/myosin ring forms around the cell equator, just under the cell membrane. The actin and myosin filaments slide over each other, drawing the ring shut and creating the ‘cleavage furrow’. Cells separated as 'purse string' draws shut
  26. 26Describe the process of cytokinesis in plantsVesicles form across the mitotic spindle, which then fuse to form a cell plate then eventually a new cell wall.
    phragmoplast -> cell plate -> cell wall
  27. 27How is cell shape and movement facilitated in a dividing cell?motor proteins such as kinesin and dyenin move along microtubules and the actin cytoskeleton (ie in cytokinesis)
  28. 28In which direction does dyenin move?+ -> -
  29. 29In which direction does kinesin move?- -> +
  30. 30state the 3 lines of research which gave clues to the regulation of progression through the cell cycle.1)cell fusion experiments
    2)Sea Urchin Embryos
    3)Yeast
  31. 31Describe how cell fusion experiments were used to give clues to the nature of cell cycle control.Fusing a cell in S phase with one in G1 results in G1 nucleus enterinb the S phase early. Fusing a cell from any other phase of the cycle with one in M phase drives the non mitotic nucleus into mitosis.
  32. 32Therefore what can be concluded from the outcome of the cell fusion experiments?That positive factors drive the entry into S and M phases
  33. 33Describe how the sea urchin embryo experiments were conducted.1) isolate cells at same point in cycle (ie embryos dividing in synchrony)
    2) radiolabel proteins and observe intensity differences by running out.
  34. 34What were the results of the sea urchin embryo experiments?revealed that 2 proteins accumulated during interphase and were lost at mitosis. these proteins were named 'cyclins'. cyclin levels fluctuate throughout experiment
  35. 35What type of yeast was used in the yeast experiments?-mutants arrested at specific points in the cell cycle (both in budding yeast -Saccharomyces cerevisiae and fission yeast- Saccharomyces pombe)
  36. 36Describe the process carried out in the yeast experiments."Restoration of Function"
    1) compare normal + mutant CdC mutant phenotypes 2) introduce unknown genes 3)gene which restores cell cycle is involved in G2 stage 4) protein CDK1 identified in correspondence with gene cdc2
  37. 37What does cdk 1 stand for?cyclin dependent kinase 1
  38. 38what is the critical factor for entry into mitosis?a complex of cyclin b and cdk1
  39. 39what is its mode of action?phosphorylates a range of proteins regulating nuclear envelope breakdown, chromosome condensation, and spindle reorganisation, enabling mitosis to proceed.
  40. 40describe the levels of regulation of cdk 1i) requirement for cyclinb which only accumulates prior to mitosis
    ii) cdk1 is inactive unless the tyrosine at position 15 is dephosphorylated
    iii) enzyme controls
  41. 41why does tyrosine 15 phosphorylation inactivate cdk1?tyrosine 15 phosphorylation blocks the ATP binding site of Cdk1, preventing kinase activity.
  42. 42describe how enzymes are able to regulate cdk1 action.2 enzymes identified from genetic studies in yeast.
    Wee1- tyrosine kinase which phosphorylates Cdk1 inactivating it.
    Cdc25- a phosphatase which removes the phosphosphate group activating cdk1.
  43. 43in which stage does cyclinb1 destruction take plate?anaphase
  44. 44in which stage is the mitotic entry stage switch turned 'on'metaphase
  45. 45Draw a diagram showing the progression through the mitotic cycle for the complex and enzymes.Draw a diagram showing the progression through the mitotic cycle for the complex and enzymes.
  46. 46Describe the regulation of entry into S phase.regulated in similar way- but using different unrelated cyclins. (cyclinsA,D+E). and different cyclin dependent kinases. (eg Cdk2 which drives S phase). cyclin degradation and regulation cdk phosphorylation are critical for control.
  47. 47Draw a diagram showing which stages each cdk:cyclin complex regulates.Draw a diagram showing which stages each cdk:cyclin complex regulates.
  48. 48on top of cyclin binding and phosphorylation, what additional regulators are in position?- cdk inhibitors such as the INK4 family and Cip/kip family, which bin to cdks and inhibit their activity.
  49. 49What are Cdk inhibitors (Cdkis) used for in the cell?used to halt the cell cycle in response to external signals or by internal quality control mechanisms (such as those which detect DNA damage). this is a critical defense against mutations that lead to cancer.
  50. 50Describe the process that occurs preventing cells from entering the S phase if DNA damage has been detected.1) ATM and ATR kinases activated 2) both can activate p53 via phosphorylation. (either directly or indirectly) 3) p53 induces expression of genes including p21 (cdk2 inhibitor). 4)prevents cells from entering S phase by blocking cdk2
  51. 51Describe the process that occurs to halt cells which have already entered the S phase, when DNA damage has been detected.1) ATR and ATM activated 2) this activates Chk1 (checkpoint kinase) 3) Chk1 phosphorylates the phosphatase Cdc25 4) Cdc25 unable to dephosphorylate Cdk1 5) cell unable to enter into mitosis.
  52. 52How long is cell cycle arrest maintained for?Cell cycle arrest in G1, S or G2 phase is maintained until DNA is repaired, or if lesions are irreparable, apoptosis results.

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Descrição
how cells cycle
Criado por
belles11 · abr 2016
Atualizado
20 abr 2016
Visualizações
17
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