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Flashcards

Cell Division

Lareyna Mcmenemy MD2002 Inglês 41 flashcards

Flashcards do conjunto (41)

  1. 1G0 phaseQuiescent (inactive) cells
  2. 2G1 phaseGap phase
    Decides if conditions are correct for cell division
  3. 3S phaseSynthesis / replication of DNA
  4. 4G2 phaseCheck genetic info has been accurately replicated & is ready to move to mitosis
  5. 52 decisions of M phaseMitosis - nuclear division
    Cytokinesis - cytoplasmic divison
  6. 6What is CDK?Cyclin Dependent Kinases (enzyme)
    Family of proteins that control the cell cycle
  7. 7How does CDK work?Works as a heterodimer ∴ enzymatic activity is related to the conc. of cyclin subunit
  8. 8How is CDK activated?Inactive CDK-cyclin complex forms
    Phosphorylated at 2 sites by an inhibitory kinase & an activating kinase BUT remains inactive
    Activating phosphatase removes the inhibitory phosphate leaving an active CDK-cyclin complex
  9. 9Activity pattern of mitotic cyclinLow activity in the early stages
    High activity in the entry to mitosis
  10. 10Cyclin expression patternCyclin D - coupled with CDK4/6 in G1 phase
    Cyclin E - coupled with CDK2
    Cyclin A - which substitutes its kinase partner for CDC2 on entry to G2 phase
    Cyclin B - CDC2 complex
  11. 11What is the R-point?Most important regulatory stage in the cell cycle
  12. 12Accumulation & destruction of Cyclin BAt end of mitosis it undergoes ubiquitination - creating a polymer ∴ signalling to the cell to destroy the protein
    The cyclin part is then destroyed & the CDK is inactivated
  13. 133-step process of Ubiquitination1. Ubiquitin binds E1 (ubiquitin-activating enzyme)
    2. Ubiquitin is transferred to E2 (conjugation enzyme)
    3. E2 complexes with E3 (ubiquitin protein ligase).E3 recognises which proteins need to be ubiquintated & catalyses the catalyse of the ubiquitination
  14. 14Structure of a proteasomeComplex of many proteins
    Core particle in middle forming a channel, with a regulatory particle on top & bottom
  15. 15What do proteasomes do?Destruction happens here
    Proteins in the regulatory particle recognises the ubiquitin & start to cleave it off ∴ it can be res-used & unfold the protein so it can move in an energy dependent manner ∴ can move through the core particle in which it will be chopped into amino acids to be lost out the bottom
  16. 16CDK inhibitorsInhibitors transcription can be induced if conditions are incorrect for cell division
    They structurally interfere with & inactivate CDK
  17. 17How is S phase gene expression repressed?Retinoblastoma proteins in unphosphorylated ∴ its active & bound to a transcription factor
  18. 18What happenes when the cell is ready to divide / move into S phase?CDK inhibitor is inactivated contributing to the activation of CDK which phosphorylated the retinoblastoma protein making it inactive ∴ the transcription factor E2F becomes active & synthesis of S phase genes can occur
  19. 19What is Cdc6?One of a group of proteins which form a pre-replicative complex
  20. 20Function of the pre-replicative complexBind an ORC (Origin Recognition Site) - when in this form DNA polymerase can't bind ∴ DNA replication can't start
  21. 21What happens when the cell moves into S phase?CDK phosphorylates it cdc6 ∴ it falls off the pre-replicative complex & a proper replication fork can be assembled at the origin of replication & DNA synthesis can begin
  22. 22How is recombination of phosphorylated cdc6 avoided?Degradation by ubiquitin specific pathway
  23. 23What are the 2 main mech. of response to DNA damage?p53 - involved in directing transcription of CDK inhibitors
    Activation of checkpoint specific protein CHK2 which inhibits cdc25 (phosphatase responsible for final step in CDK activation
  24. 24Stages of MitosisProphase
    ↓
    Pro-metaphase
    ↓
    Metaphase
    ↓
    Anaphase
    ↓
    Telophase
    ↓
    Cytokinesis
  25. 25ProphaseMitotic spindle begin to form & organise
    Nucleolus disappears but membrane is intact
  26. 26PrometaphaseChromosomes finish condensing
    Nuclear envelope breaks down
  27. 27MetaphaseChromosome align & attach to central spindle
  28. 28Important checkpoint in metaphaseSpindle checkpoint
    - chromosomes must attach to the spindle in such a way that they are under slight tension & each chromatid is attached to a microtubule from the opposite end of the spindle
  29. 29AnaphaseChromosomes separate out to opposite ends of the spindle
  30. 30CytokinesisCytoplasm is split into 2 daughter cells
    - done via a contractile ring of actin & myosin at the central point
  31. 31How is DNA condensed?Specific proteins form 'handcuffs' around DNA & help them become more condensed
  32. 32When is max. DNA condensation reached?Metaphase
  33. 33How is the spindle formed?The centrosome comprises 2 centrioles which are replicated in the cell cycle & start to organise the microtubules even before mitosis is fully underway
  34. 34How does nuclear envolope break down occur?One of CDKs targets in mitosis is the nuclear lamins - proteins found in nuclear envelope
    CDK phosphorylates them ∴ breakdown of the envelope occurs
  35. 35How do chromosomes attach to the spindle?Through constricted regions present at the centromere & require a specific protein called kinetochore
  36. 36What holds sister chromatids together?Cohesion complex
  37. 37Example of a defect in cohesionRoberts Syndrome
    chromosomes are not held together ∴ are more spread out that desirable
  38. 38Function of separaseTo break cohesins into amino acids so chromosomes can move apart
  39. 39Function of anaphase promting complexThe activity of APC is regulated to prevent separase activating at the wrong time in the cell cycle
  40. 40How is separase activated?Separase is normally held inactively as a dimmer by securin and inhibitory protein, BUT at the right time in the cell cycle the APC is an E3 ubiquitin ligase & targets securin for degradation
  41. 41What can result from a defect in the spindle checkpoint?Aneuploid cells
    - cells with the wrong number of chromosomes ∴ long-term abnormalities & prolonged uncontrolled proliferation

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MD2002 FlashCards sobre Cell Division, criado por Lareyna Mcmenemy em 26-04-2018.
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