Mitosis Worksheet Flashcards

1
Q

How does the cell know that it is ready to enter mitosis?

A

passes G2 checkpoint - DNA is completely replicated and there’s no DNA damage; regulated by MPF

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2
Q

Define interphase and M (mitotic) phase.

A

I: all parts of the cell cycle that aren’t mitosis; subdivided into G1, S, and G2 phases
M: cell division phase where the nucleus and cytoplasm are divided into 2 daughter cells

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3
Q

What are the components of MPF? What is the mechanism that regulates MPF? What are the substrates of MPF?

A

> Cdk1 and Cyclin B
CAK adds P to Thr 161 and Wee1 kinases adds P to Tyr 15 on Cdk1; Thr 161 P for activation, Tyr 15 P for inhibition; when G2 cleared, cdc25 phosphatase dephosphorylates Cdk1 at Tyr 15
condensins, cohesins, MAPs, motor proteins, and lamins

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4
Q

How is the mitotic spindle formed?

A

growth of microtubules out from centrosomes

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5
Q

How do the different types of microtubules form the spindle?

A

> astral - grow from centrosome toward cell periphery; + ends attack to cell cortex through - end directed motor proteins
kinetochore - attach to chromosomes at + ends through kinetochore
chromosomal - attach to ends of chromosomes
polar - from each spindle pole, overlap at + ends at center of cell

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6
Q

What is the role of each type of spindle microtubule in mitosis?

A

> astral - orient the spindle and help to separate spindle poles at anaphase
kinetochore - moves chr. from metaphase plate to spindle pole
chromosomal - positions chr. on metaphase plate
polar - separate spindle poles

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7
Q

What is the mechanism of chromosome alignment on the metaphase plate?

A

> kinetochore microtubules attach to chromosomes at kinetochores –> starts chr. movement (Aurora B involve)
(-) end motor proteins - pull toward centrosomes
(+) end motor proteins (growth of mt’s) - push away from poles
each sister chr. will have a mt attach at a kinetochore –> 1 from each pole
balance of push/pul forces aligns chr. on metaphase plate –> point equidistant from both poles

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8
Q

What is the structure that attaches the chromosomes to the spindle microtubules? Why is it necessary that every chr. have a bipolar attachment to the spindle?

A

kinetochore; to ensure proper segregation at anaphase

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9
Q

What is the spindle checkpoint? Describe its mechanism, including all components.

A

> ensures chr. attached to spindle properly before anaphase
CENP-E attaches to microtubules and BubR1, CENP-E senses tension; if improper attachment, BubR1 adds P to Mad1p–> act. Mad2p –> inhibits APC by preventing Cdc20 binding; when CENP-E sense everything is correct, BubR1 inact. –> Cdc20 binds APC

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10
Q

What are the two parts of anaphase and the processes that take place in each part?

A

A: chr. separate and move to opposite poles due to disassembly of kinetochore microtubules at their + ends; motor proteins also involved
B: polar mt’s elongate and kinesins push poles apart; astral mt’s via dyneins at cell cortex pull poles toward periphery

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11
Q

How is chromosome segregation regulated?

A

motor proteins, kinesins, dyneins, and APC ?

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12
Q

What is the APC, and what are its targets?

A

anaphase promoting complex containing an E3 ubiquitin ligase, targets securin and cyclin B for degradation by the proteasome; securin degraded first; securin inhibits separase (which degrades cohesins); loss of cyclin B inact. Cdk1

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13
Q

How is the nucleus reassembled during telophase?

A

vesicles form around chr., vesicles fuse to form nuc. membrane, nuclear pores reassemble, Lamins A and C imported from cytoplasm to complete nuclear lamina, and chr. decondense

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14
Q

What regulates the formation of the cleavage furrow at cytokinesis?

A

> phosphorylation of myosin
MPF keeps myosin light chain phosphatase in act. state, which keeps myosin in a deP state
MPF declines during anaphse, incr. in Ca2+ act. myosin light chain kinase, P added to myosin

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