Cell cycle Flashcards
1
Q
Activation of MPF
A
- CDK
- Cyclin
- Phosphorylation of the complex
2
Q
Cyclin dependent kinase inhibitor CKI
A
- interacts with cyclin CDK complex⇒ inhibit kinase activity
- usually in response to environmental signal or damaged DNA ⇒ p53 ⇒ p21 ⇒ inhibition of G1/S CDK cyclin complex
3
Q
Wee kinase
A
- can add an inhibitory phosphate to CDK1 ⇒ inactivation
4
Q
INK CKI
A
- CDK inhibitor
- inhibits cyclin D with CDK4 and CDK6 in G1 phase
5
Q
KIP/CIP CKI
A
- CDK ihibitor
- inhibits cyclin E with CDK2 in G1/S phase
6
Q
G1 phase
A
- Components: Cyclin D + CDK4 + CDK6
- Phsophorylates retinoblstom Rb
- it detaches from E2F ⇒ G1/S transition is possible
7
Q
G1/S phase
A
- Components: Cyclin E + CDK2
- form a complex in late G1
- cyclin E rapidly degraded and released CDK2 forms complex with cyclin A
- this sequence is necessary for the initiation of DNA synthesis in S phase
8
Q
S phase
A
- Components: Cyclin A + CDK2 + CDK1
9
Q
M phase
A
- Components: Cyclin B + CDK1
- transition from G2 ti M
- phsophorylates:
- nuclear lamines
- chromatin condensation
- cytoskeletal rearrangement
- APC activation
10
Q
ATM
A
- protein kinase that is associated with genome
- if DNA contain double-stranded break, the resulting change in the conformation of the chromatin activates ATM
- upon activation ⇒ 1 subunit of activated ATM dimer dissociates + initiates cascade if protein phosphorylation-dephosphorylation events mediated by CHK1 and CHK2 protein kinases
11
Q
CHK1/2
A
phosphorylation of cdc25 (inactivation)
12
Q
Cdc25
A
- Phosphatase
- Removes inhibitory phosphate from CDK
13
Q
p53
A
- gene when activated by CHK ⇒ activates transcription of p21 + other proteins which cause cell apoptosis
14
Q
p21
A
- potent CDK-cyclin inhibitor that can efficiently inhibit the action of all CDKs ⇒ cell cycle stopped to allow time for extensively damaged DNA to be repaired
15
Q
APC
A
- E3 ubiquitin ligase
- marks target cell cycle proteins for degradation in the proteasome
- main function is to trigger the transition from metaphase to anaphase by tagging specific proteins for degradation
- also target mitotic cyclins for degradation ⇒ inactivation of G2/M CDK-cyclin complex ⇒ end of mitosis and cytokinesis
- marks for degradation the anaphase inhibitor, and CDK1 and cyclin B