Mitosis Phase Flashcards

(42 cards)

1
Q

What is stopped from getting degraded in the spindle assembly checkpoint

A

Cyclin b and securin (allowing anaphase)

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2
Q

Which m cyclin is nuclear and which moves to nucleus from cytoplasm

A

Nuclear is a

Cytoplasmic is b

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3
Q

When does cyclin a get degraded

A

Before prometaphase

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4
Q

When does cyclin b increase / peak and then lower

A

Peak is at prometaphase

Low is met- anaphase

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5
Q

What is the main cdc25 for cdk1 cyclin b activation by removal of wee1/myt1 phos

A

Cdc25b

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6
Q

What kinase is a target of the active cdk1 and cyclin b which causes a positive feedback loop for more activation

A

Polo like kinase

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7
Q

What does plk do in respect to cdk 1 activation

A

Phos of wee and myt inhibiting them

Also phos of cdc25a, and c as well as b which all cause cdk activation

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8
Q

How can cyclin a aswell as main cdc25b be a trigger for mitosis via cdk1 activation

A

When in complex with cdk it allows aurora a activation of plk

Plk then causes a loop via phos of cdc25c

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9
Q

How many centrioles are from centrosomes

A

2

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10
Q

Explain centrosome cycle which duplicates for mitosis

A

In g1 centrosome pulls apart but held by procentrioles

Centrosome is duplicated in s phase

Centrosome disjunction through pulling of procentrioles in s/g2

Full centrosome separation in mitosis and bipolar spindle formation

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11
Q

What is pulling apart of procentrioles called in g2 and what kinase involved

A

Centrosome maturation via plk4

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12
Q

Other than activating cdk1 cyclin b and plk for centrosome maturation, what do plk do

A

Prophase pathway of cohesin ring removal on sister chromatid arms

Cytokinesis in the actin myosin ring

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13
Q

What is aurora a for

A

Spindle integrity

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14
Q

What is aurora b part of

A

Cpc chromosome passenger complex

With incenp, survivin, borealin

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15
Q

Where is aurora b and why

A

Chr arms early eg in mitosis

Moves to centromeres in prometaphase this is so it can aid correct attachment of kinetochores with mt

Via phos of kmn proteins

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16
Q

What spindle attachment is when 1 attaches to each sister

A

Amphitelic

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17
Q

Does amphitelic produce a sac and why

A

No sac is inactive because equal tension

18
Q

What is monotelic

A

When only 1 sister is attached

Produces active sac bc no tension so aurora b present

19
Q

What is syntelic

A

When both mt attach to one sister

Also produces active sac as no tension

20
Q

What is merotelic and why doesn’t this have active sac

A

Both arms attached but 1 has more mt attached

Tension but unequal

21
Q

Which enzyme opposes aurora B action via dephosphorylation

22
Q

When does pp1 get replaced by aurora b

A

Prophase when aurora b on chr arms

23
Q

What inhibits pp1

24
Q

What happens when aurora b moves from arms to centromeres in prometaphase

A

Part of sac

It checks tension. If not there aurora b will cause kinetochore assembly and phos kmn proteins causing proper attachment of k with mt

When this happens anaphase can occur

Aurora b stays in middle of cell and far from kinetochore, allowing kinetochore dissassembly and pp1 increase via i2 degradation from anaphase

25
What is the strong interaction with merotelic and aurora b
Because stay in middle, aurora b can phos of kinetochore subunits and allow proper attachment
26
What does sac block which blocks progression to anaphase
Apc/cdc20
27
What does securin ub do and how does it allow anaphase
Securin degradation activates separase which cleaves cohesin rings around the centromeres = separation
28
Cyclin b causes cdk inactivation and therefore dephos of its substrates , how does this allow anaphase
Spindle elongation and allows chr separation to poles
29
How is cdk 1 inactivation good for telophase and mitotic exit
Nuclear formation and spindle dissassembly
30
What part of sac blocks apc cdc20
Mitotic checkpoint complex mcc
31
What are the key components of mcc
Mad 2 closed, bubr1, bub3
32
What does mad2 closed binding to cdc20 do
Blocks it’s ability to recognise and degrade cyclin b and securin
33
How are cyclins usually recognised by cdc20
N terminal destruction d box Arg and leucine residues
34
What part of apc also recognises substrates
Apc10
35
What occurs for mcc activation
Mps1 phosphorylates KNL1 Allows rzz and other binding like bubr1 and bub3 Rzz recruits mad1 and 2 Mad 2 put into a closed complex which binds cdc20 Attracts others like bubr1 and bub3
36
How does physical separation silence the sac
Aurora B once phos kmn will allow proper kinetochore attachment When tension anaphase occurs Aurora B moves away from kinetochores and stays in middle, allowing pp1 then to dephos and disassemble kinetochores This silences the sac
37
How does p31 comet silence sac by disrupting mcc
Competes with bubr1 for mad2 binding
38
What phosphorylates cdc20 to cause mcc dissassembly and sac turn off
Cdk1
39
What is the cdc20 ub dependant path
Cdc20 can be degraded via p31 comet ub Allows mcc fall off and new cdc20 production without silencing
40
What can dephos knl1 platform protein which blocks mcc assembly
Pp2a phosphatase
41
How is cyclin a degraded even though sac is turned on in prometaphase nuclear degradation
Apc cdc20 can override the sac at this point via long D boxes of cyclin a being recognised
42
What is degraded by cdh1 apc (end of mitosis)
Cdc20 , plk, aurora a and b