1-13 Mitosis Flashcards
stages of mitosis
*Interphase: nuclear env intact, no visible chrom
Prophase: chrom consense/visible, bipolar spindle develops
Prometaphase: nuc env dissolves, chrom begin migrate and seen tocontain two chromatids
Metaphase: chrom fully condense and at metaphase plate
Anaphase: centromeres splits, two chromatids pulled opposite poles
Telophase: chrom reach poles and decondense, nucl membrane reforms, cytoplasm starts to divide
*Cytokinesis: cytoplasms division to dive 2 daughter cells
Structural maintenance complex (SMC)
2 complexes that organize chrom during mitosis
chrom cohesion: keeps sister chrom together, unsures sisters apportioned into daughter cells, allows for homology mediated repair, degraded at anaphase to allow for seperation
chrom condensation: compacts chroms, organizes chroms for efficient segregation, uses ATP to pump out chrom loops
Activation of Mitotic Cyclins
- CDK1 binds CyclinB
- CDK1/CyclinB phosphorylated by CDK activating kinase (CAK) and CDK inhibitory kinase (Wee1)
- CDC25 phosphatase removes inactiavting phosphate from CDK1/cyclinB
- active CDK1/cyclinB positive feedbacks to activate Cdc25 for further self activation, cdk1/cyclinB also positive feedbacks by inhibiting CDK inhibitory kinase
Disassembly of nuclear envelope
interphase: nucleus in tact with lamins lining lumen side of membrane
- phosphorylation of nuclear pore proteins and lamins
- degrades membrane and releases chromosomes in prophase/prometaphse
- de-phosphrylation of nuclear pore preotisn and laminns–>telophase starts to reform around daughter chromosomes
- fusion of nuclear envolve vesciles in new daughter cell
kinetochore
distinct layers of core
- centromeric chromatin
- inner kinetochore
- outer kinetochore
- EC/SAC/microtubule binders
interface between chrom and microtubule spindle
microtubule spindle formation
dynamic assembly/disassembly allows growth at + end
if GFP bound the + end stable and grows, if GDP bound catastrophe dynamic instability
allows for anaphase seperation quick snap
motor proteins role in mitosis
regulate spindle formation, microtubule dynamics, chrom alignment
kinesins: + ended motor moves
dyneins: - end motor
3 types of mitosis microtubules
- aster: bind centriole
- kinetochore: bind at centromere and centriole
- interpolar: bind centriole and overlap with motor protein and interpolar from other centriole
Mitotic checkpoint complex
MCC: wait signal that inhibits APC (anaphase promoting complex), APC required for anaphase progression
- prometaphase: “SAC on”, chrom unattached to kinetochore, MCC assembly begins
- metaphase: “SAC off”, MCC assembly inhibits APC until ready
- APC activation: degreade mitottic cyclins, loss of chrom cohesion, separate sister chromatids
APC/C
Anaphse promoting complex
E3 ubiquitin ligase, leads to proteosome mediated degredation, cofactor cdc20 helps specificy targets (cyclinB/cdk1 and securin)
securin
separase
securin: inhibitory protein that bind –>
separase: proteolytic enzyme
APC targets securin for Ub-degredation, separase now free to chew up cohesins and promote metaphse to anaphase transition
Metaphase to anaphase transition events
- MCC no longer made
- APC radibly becomes active
- APC Ubs: mitotic cylin (CyclinB/cdk1), securin, cohesin in cleaved by separase
Anaphase A
Anaphase B
A: shortening of kinetochore microtubules, movement of daughter chrom to poles, forces generated mainly at kinetochores
B: 1. sliding force is generated between interpoalr microtubules from opposites poles to push the poles apart; the interpolar microtubules also elongate 2. a pulling force acts directly on the poles to move them apart
Cytokinesis
signals for location of the contractile ring come from SPINDLE CORTEX interactions and SPINDLE MIDZONE
actinomysin ring pinches off
CyclinB/CDK1 inhibits pinching off
types of errors in chromosome attachment
- amphitelic: goal, all good
- syntelic: both chromatids pulled to one side by two spindles
- monotelic: both chromatids pulled to one side by one spindle
- Merotelic: splits into 3 with one chromatide that was left in middle now making own cell