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39 Cards in this Set

  • Front
  • Back

Stages of M phase

1. Mitosis


2. Cytokinesis (NOT mitosis)

Dispersed Chromatin vs. Condensed chromatin

Dispersed: easy to transcribe and replicate, hard to separate


Condensed: hard to transcribe and replicate, easy to separate

Cohesin

Protein enzyme to keep sister chromatin together through S and G2 phase and beginning of prophase (In interphase and mitosis)

Protein enzyme to keep sister chromatin together through S and G2 phase and beginning of prophase (In interphase and mitosis)

Method of separating sister chromatin

phosphorylate cohesin (adds - charge), causes homologous chromosomes to lose cohesion except near centromere

Kinetochore

protein complex, one on either side of centromere

Condensin

Protein enzyme to condense DNA, appears at beginning of mitosis (NOT in interphase)

Protein enzyme to condense DNA, appears at beginning of mitosis (NOT in interphase)

Centromere/ Kinetochore placement

Not always at center of mitotic chromosome

Goal of Mitosis (Ploidy)

Equational division, no change in n (always diploid)

Prophase actions

Mitotic spindle begins to form OUTSIDE of nucleus
compact mitotic chromosomes formed with kinetochores on either side of centromere
cytoskeleton, Golgi, ER, and nuclear envelope disassemble

Mitotic spindle begins to form OUTSIDE of nucleus


compact mitotic chromosomes formed with kinetochores on either side of centromere


cytoskeleton, Golgi, ER, and nuclear envelope disassemble

Prophase enzymes

Condensin goes to work, cohesin already present

Prometaphase actions

Cytoplasmic MT from mitotic spindle grab KINETOCHORES (not centromere directly)
Chromosomes oscillate toward center of cell for amphitelic orientation

Cytoplasmic MT from mitotic spindle grab KINETOCHORES (not centromere directly)


Chromosomes oscillate toward center of cell for amphitelic orientation

Amphitelic orientation

sisters face opposite poles

Prometaphase enzymes

cohesin and condensin present

Metaphase actions

Chromosomes align along metaphase plate attached by chromosmal MT
Paired homologous sister chromosomes align along metaphase plate attached by chromosmal MT

Metaphase enzymes

cohesin and condensin present

Anaphase actions

Centromeres split and chromatids separate, move to opposite poles of spindle
Spindle poles move apart

Centromeres split and homologous sister chromatids separate, move to opposite poles of spindle


Spindle poles move apart

Anaphase enzymes

Splitting centromeres show that cohesin disappears


Condensin still present

Telophase actions

Chromosomes cluster and disperse at opposite spindle poles
Nuclear envelope, Golgi, and ER reform

Chromosomes cluster and disperse at opposite spindle poles


Nuclear envelope, Golgi, and ER reform


No mitotic chromosomes at end of telophase


Still considered 1 cell through telophase, but has 2 nuclei

Telophase enzymes

Cohesin gone since Anaphase


Condensin still present but starts to disappear

Mitotic Spindle formation

In prophase outside of nucleus


+ end directed growth

Pericentriolar Material

Acts as microtubule organizational center for cytoplasmic microtubules

Types of Cytoplasmic MT

In prometaphase:


1. Astral MT


2. Chromosomal MT


3. Polar MT

Astral MT

Eminate from centrisome into cytoplasm from the aster (mitotic spindle), anchors centrisome

Eminate from centrisome into cytoplasm from the aster (mitotic spindle), anchors centrisome

Chromosomal MT

Connects from pericentriolar material of centrisome to kinetochore

Polar MT

Extend from centrisome (like chromosomal MT) but attach to other polar MT instead of chromosomes

Cytoplasmic MT growth

Dynamic instability- if not growing, they will shrink


2 Forms of movement Prometaphase

1. Polymerization/depolymerization of tubulin lengthen and shorten MT


2. Cargo and rail action of motor proteins on MT (Kinesin and Dynein)

Polymerization and Depolymerization of tubulin

Way to position chromosomes during prometaphase


Can add or take from tubulin on both + and - end of tubulin (depending on depolymerase)


Non-ATP dependent form of movement, uses dynamic instability to move

Consequence of inhibiting MT growth

Cell division stops (Prometaphase cannot be completed)

Kinesin in Prometaphase

+ end directed growth on MT
Polar MT- sliding kinesin causes poles to move apart (controls distance between poles)

+ end directed growth on MT


Polar MT- sliding kinesin causes poles to move apart (controls distance between poles)

Dynein in Prometaphase

- end directed growth, moves mitotic chromosomes toward - end of chromosomal spindle fibers (toward centromeres)

Colchine and Colcemid

Metaphase Inhibitors- inhibit MT polymerization, stops chromosomes from being pulled apart in Anaphase B so chromosomes "lock" in metaphase state (homologous sister chromatids are still attached at centromere)


Inhibitors are added to cell to create karotypes

When does a spindle checkpoint occur in the cell cycle

In Metaphase before Anaphase


Make sure all chromosomes are lined up before they split in anaphase

What happens when a mitotic chromosome does not reach the metaphase plate when the other 45 do?

Spindle checkpoint: Checkpoint protein binds to the lagging chromosome causing cell cycle arrest, division stops until the chromosome catches up, the protein is removed and the cell cycle continues

Consequences of not having a spindle checkpoint

Genomic instability, increases risk of cancer (but does not directly cause cancer)

Tension and cell arrest

Adding symmetric tension can end cell arrest due to a chromosome being attached only by one spindle fiber (trick cell into continuing division)1

Anaphase A

Chromatids move towards the poles by shortening the chromosomal MT
POLES DON'T MOVE
No ATP needed because chromatids are easy to separate after loss of cohesin, dynamic instability moves MT without ATP

Chromatids move towards the poles by shortening the chromosomal MT


POLES DON'T MOVE


No ATP needed because chromatids are easy to separate after loss of cohesin, dynamic instability moves MT without ATP

Anaphase B

Poles move apart as kinesin drives polar MT apart

Poles move apart as kinesin drives polar MT apart

How would adding a kinesin inhibitor affect anaphase?

Anaphase A would proceed normally but anaphase B would not be able to run properly