Seminar 6: The cell cycle Flashcards

1
Q

what is & func of histones, what do they produce

A
  • extensively packed DNA
  • their +ve charged r grps bind to -ve phosphate in backbone, forms ionic bonds
    DNA-histone & histone-histone produces nucleosomes
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2
Q

what happens in each stage of interphase?

A

G1: cell growth, ensures enough nutrients for division
S: DNA replication
G2: spindle synthesis begins, prep for mitosis

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3
Q

what happens in prophase?

A
  1. spindle fibres form
  2. chromatin supercoil, becomes more condensed & packed
    (chromosomes are more visible here)
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4
Q

stages of mitosis

A
  1. prophase
  2. prometaphase
  3. metaphase
  4. anaphase
  5. telophase
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5
Q

what happens in prometaphase

A
  1. chromosome attach to spindle
  2. nuclear membrane break down
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6
Q

what happens in metaphase?

A

chromosomes align at centre of cell

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7
Q

what happens in anaphase

A
  1. each identical pair is split at centromere
  2. move to opposite poles of cell
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8
Q

what happens in telophase

A
  1. chromosomes decondense
  2. nuclear membrane reforms
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9
Q

what happens in cytokinesis

A
  1. cells separate
  2. cell wall/membrane forms
    IN PLANTS: vesicles line up b/w cells, fuse to form a plate & secrete their contents, forms CELL PLATE/WALL

IN ANIMALS: cell membrane furrows, contractile ring forms (microfilaments of actin & myosin), forms contraction which pinches cell into 2

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10
Q

how is the cell cycle regulated?

A
  • CDK (always present in cell) will bind w/ cyclin (conc fluctuates, formed when needed) = CDK-cyclin complex
  • binds to proteins & ATP, phosphorylates the protein
  • becuz of added Phosphate, protein shape changes, this either ACTIVATES/DEACTIVATES it to allow PROGRESSION/INHIBITION of cycle
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11
Q

how & when are chromosomes moved to opp poles of cell

A

IN ANAPHASE
1. kinetochores contain motor proteins (kinesin etc): use energy from hydrolysis of ATP to move chromosomes along microtubule
2. kinetochores shorten: brings chromosomes closer to kinetochore
3. causes centromere to move apart, aids in separation

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12
Q

what allows for segregation of sister chromatids

A

movement to opp sides of poles

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13
Q

how is APC inhibited if chromosome isn’t attached properly to spindle

A

occurs at spindle assembly checkpoint (@ end of metaphase)
1. M-phase CDK cyclin will NOT bind to APC & activate it
2. APC cannot bind to separase & activate it
3. Separase can’t remove remaining cohesin (sister chromatids won’t separate)

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14
Q

what makes up the spindle

A

microtubules b/w chromosomes & poles of cell

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15
Q

function of the spindle

A
  • struc that chromosomes attach to
  • keeps 2 poles apart (allows for segragation)
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16
Q

how do microtubules become more stable?

A

connect w/ kinetochores OR w/ other microtubules from other half of cell

17
Q

what grps of microtubules are w/in the spindle

A
  1. POLAR: forms framework, run from 1 end to other
  2. KINETOCHORE MICROTUBULE: form ltr, attach to kinetochore on chromosome, ensures that sister chromatids MOVE TO OPP SIDES
18
Q

why are indv chromatids visible during prophase?

A

because most of cohesin holding them have been removed, only helf by small amount @ centromere (kinetochore)

19
Q

@ what stage do centrosome duplicate & separate

A
  1. S phase = duplicate
  2. start of prophase = separate
20
Q

what is a centrosome

A
  1. organelle near the nucleus (non-membrane bound)
  2. when duplicated, move to opp sides & form the mitotic spindles
21
Q

func of cohesin & condensin

A
  1. cohesin : hold sister chromatids together in G2
  2. condensin : coat DNA molecule & make them more compact
22
Q

how do growth factors work?

A
  1. bind to specific receptors on target cell
  2. activate signal transduction pathways
  3. causes cyclin synthesis
  4. cyclin forms complex w/ CDK
  5. bind to RB & ATP
  6. RB is phosphorylated, changes its 3D shape, inactivating it
  7. RB not func, cell cycle can progress
23
Q

How to regulate CDKs?

A
  1. regulate cyclin prod
  2. if cyclin is absent, CDK = inactive
    Cyclin prod cyclically, @ specific times in cell cycle
24
Q

what does the checkpoint @ each stage check for?

A

G1&G2: Cell damage
S: DNA rep incorrectly & DNA damage
M: chromosomes unattached to spindle

25
Q

how to Cyclin-CDK complexes work?

A
  • allosteric regulation
  • by forming complex, CDK alters shape, exposes its active site, makes it FUNCTIONAL
26
Q

what are growth factors?

A
  • proteins made by cells that can travel to other cells or act on the cells that make them to stimulate cell division
    -They bind to specific receptors on target cells, setting off cell signal transduction inside the cells
  • This can lead to gene expression of cyclins, which will bind to CDK & stimulate cell cycle progression.
27
Q

what are the various levels of packing of genetic info contained in linear DNA

A
  • During interphase, chromosomes are condensed by histone proteins into nucleosomes, these fold over one another to form chromatin fibres.
  • In prophase, the fibres attach as loops to proteins, & these in turn loop extensively to form the chromosome
28
Q

what happens if cohesin wasn’t functional?

A
  • Cohesin proteins joins the chromatids together at their centromere
  • non-functional cohesin protein would prevent chromatids from remaining bound from replication in S phase to metaphase in mitosis
  • Therefore there would be no organisation for kinetochore attachment & thus ineffective segregation of 1 sister chromatid of each replicated chromosome into each daughter cell.