Mitosis & Meiosis Flashcards

1
Q

What are the 4 stages of the cell cycle & what is the major event in each stage?

A
  1. M
    • mitosis
  2. G1
    • growth
  3. S
    • DNA synthesis
  4. G2
    • “gap” before mitosis
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2
Q

Why is the G1 phase important?

A

cells must increase in volume, othewise each division leads to smaller and smaller cells

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3
Q

What at the 3 major checkpoints & what factors are they trying to assess?

A
  1. Enter mitosis (G2 into M)
    • Is all DNA replicated?
    • Is all DNA damage repaired?
  2. Pull duplicated chromosomes apart (M)
    • Are all chromosomes properly attachd to the mitotic spindle?
  3. Enter S phase (G1 into S)
    • Is the environment favorable?
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4
Q

The shift from one phase into another is dependent on what proteins?

They do this through what mechanism?

A

cyclins

bind to cyclin-dependent kinases (CDK) and activate them, so they can phosphorylate other proteins that perform the functions of that phase

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5
Q

How does the cyclin concentration change throughout the cell cycles?

A

concentration increases steadily until it reaches a maximum, but does not activate until the right time

once transitioned to the next phase, the concentration drops rapidly for that particular cyclin

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6
Q

Describe the process by which cyclins activate CDKs.

A

cyclins bind the appropriate partner CDK, which is phosphorylated at the time of binding – forming an inactive complex

The phosphatase Cdc25 removes the phosphate to activate the complex

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7
Q

CDK activation occurs via what type of feedback loop? How is this helpful?

Descrbribe this process.

A

Positive feedback loop - allows for rapid activation

Cdc25 (phosphatase) must be phosphorylated to be active

It is phosphorylated by a CDK

so, as Cdc25 proteins are phosphorylated, they remove phosphates from moe CDK molecules, which in turn phosphorylates more Cdc25 molecules

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8
Q

What is the name of the molecule responsible for de-phosphorylating the cyclin/CDK complexes?

A

Cdc25

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9
Q

What is the name of the molecule that add the phosphate to the CDK molecules before they bind to cyclin?

A

Wee1

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10
Q

In addition to the phosphorylation directed regulation of cyclin-CDK complexes, how else is the entrance to a new phase controlled?

A

cyclin-dependent kinase inhibitors (CKI)

bind to cyclin-CDK complexes & preven their function – helps to hold cells in a certain stage while concentration of cyclins increases

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11
Q

What are the 3 CKIs?

A

p27

p21

p16

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12
Q

The rapid loss of cyclins at the end of a stage is due to what process?

A

protein degradation initiated by the addition of ubiquitin

this directs them to the proteasome for digestion

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13
Q

What molecule is activated in late S-phase to degrade M and S cyclins? How does it function?

A

Anaphase-Promoting Complex (APC)

adds ubiquiton to M and S phase cyclins, which directs them to a proteosome for degradation

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14
Q

How does the cell block DNA synthesis until it is repaired?

A

Proteins recognize DNA damage and activate a kinase that acts on p53

phosphorylated p53 (active) binds to the promoter for the gene coding p21 & increases transcription

p21 binds to cyclin-CDK complexes as a CKI & blocks S-phase cyclin

Thus, DNA synthesis does not begin until it is repaired & the inhibition is relieved

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15
Q

What are the 2 major proteins involved with condensing DNA strands so they are able to separate within the dividing cell?

A

condensin and cohesin

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16
Q

How are the chromosomes arranged in preparation of division?

A

Loops of DNA are gathered by condensin rings (shortening the length of the chromosome)

The two copies of DNA are attached (1) a the kinetochore and (2) along their length by choesin rings

17
Q

What is the kinetochore?

It is important in what checkpoint?

A

protein complex at the centromere

they attach to the spindle (microtubules)

Spindle microtubules attach to both sides of kinetochore & unless both sides are attached to opposing poles of the cell, mitosis will not proceed

18
Q

What is the name of the short spindle fibers produced once they reach opposite poles?

A

aster

19
Q

How do microtubules adjust their length as they attache to the opposite poles of the cell & the kinetochores?

When do the spindles reach their final length?

A

polymerization makes them longer

depolymerization make them shorter

The spindles reach their final length when the chromosomes align on the metaphase plate

20
Q

What are interpolar microtubules?

A

the spindle fibers grow past the chromosomes & associate with the microtubules from the opposite pole

they will provide the motive force for the chromosomes

motor proteins attach to these & move them relative to each other

21
Q

Describe the steps of removing the cohesin rings.

A
  1. addition of ubiquitin by the APC to a protein called securin
    • securin is in a complex with separase
  2. Degradation of securin allows separase to act on cohesin to degrade it
  3. Releasing the sister chromatids
22
Q

What is happening with centrsomes in each stage of the cell cycle?

A
  • G1: centrosomes with tubules
  • S - G2: replicates
  • M: move apart with short microtubule (aster)
    • some spindles lengthen & attach to centromere
23
Q

What is the region of the chromosome where the spindle attaches?

A

centromere

kinetochore is the protein complex where attachement occurs

24
Q

Why is movement along the spindle during chromosome separation rapid?

A

lots of tension in mitotic spindle during metaphase

25
Q

What are the motor proteins in involved in chromosome separation & what are their individual functions?

A
  • interpolar microtubules push poles apart using kinesin
  • dynein cortex pulls aster microtubles and poles away from center
26
Q

Describe how the chromosomes move toward the periphery of the cell during anaphase.

A
  • Those attached to kinetochores become shorter, bringing the chromosomes closer to the centrosome
  • Interpolar tubules push agains each other using kinesin
  • In the aster, dyenin attaches to the cortex & pulls the aster and spindle close to the cell membrane
27
Q

What are the two divisions that happen in meiosis?

A
  • Reduction Division
    • after replication the centromeres remain intact & one of each homologous pair moves to opposite poles
  • Equational Division
    • no replication has taken place and the centromeres divide to allow the sister chromatids to separate to different cells
28
Q

What stage do the sex chromosomes separate in spermatogenesis?

A

during the reduction division

29
Q

When does recombination occur & how does it begin?

A

It starts to occur when the homologous chromosomes line up in Prophase I

Its begins with a double-stranded break in one chromosome & the invasion of the paired DNA by the broken strand

This induces a new break in the opposite member of the pair & ligation of the different strands

30
Q

What is a Holiday Structure?

A

An X configuration of a homologous pair of chromosomes that occurs durign recombination

All 4 strands are attached and the DNA must be cut and resealed at the junction to separate them into separate chromosomes again

It can up up the X or across the X, then reseal to linear forms

31
Q

How is the role of cohesin different in meiosis as compared to mitosis?

A
  • cohesins bind before replication to bring the homologous pairs together before replication
    • they are _not degrade_d in the reduction division so that each homologue will be a unit sent to a pole intact
    • Spindles tubules sense tension from cohesin rings rather than kinetochore complex when aligning pairs
32
Q

What protein complex is responsible for resolving the Holliday junctions?

A

Synaptonemal Complex at sites of recombination

They surround the homologus pairs & slide along them during anaphase

They are removed by slipping off the ends of the chromosomes

33
Q

What are the stages in which the oocytes spend prolonged periods of time suspended?

A
  • Prophase I: fetus to when follicle begins to grow
  • Metaphase II: from ovulation to fertilization
34
Q

When does meiosis begin in males & how long does it take to develop a mature spermatozoa?

A

any time from puberty onward for a cohort of cells

takes ~ 65 days