14.2 Cellular Reproduction Flashcards

1
Q

Cdk Inhibitor Arrests Cell Cycle Progression

A
  • p27 alters conformation of Cdk catalytic subunit
  • Inhibits protein kinase activity
  • p27 drapes itself over cdk2 inhibiting the activity
  • age matched but not sized match because p27 has proliferated growth
  • p27 knockout thymus gland huge compared to normal due to increased number of cells
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2
Q

Mitosis

A
  • Process of nuclear division that faithfully partitions duplicated chromosomes
  • Five stages-Prophase, Prometaphase, Metaphase, Anaphase, Telophase
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3
Q

Cytokinesis

A

Division of cell that partitions cytoplasm into two cellular packages

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4
Q

Prophase

A
  • Chromosomal material condenses to form compact chromosomes.
  • Cytoskeleton is disassembled and mitotic spindle is assembled.
  • Golgi complex and ER fragment. Nuclear envelope disperses (partially due to disassembly of lamin protein).
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5
Q

Prometaphase

A
  • chromo start associating with spindle fibres
  • Chromosomal microtubules attach to kinetochores of chromosomes
  • Chromosomes are moved to spindle equator.
  • congressing to plate
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6
Q

Metaphase

A

•Chromosomes are aligned along metaphase plate, attached by chromosomal microtubules to both poles.

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7
Q

Anaphase

A
  • Centromeres split, and chromatids separate.
  • Chromosomes move to opposite spindle poles.
  • Spindle poles move farther apart
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8
Q

Telophase

A
  • Chromosomes cluster at opposite spindle poles.
  • Chromosomes become dispersed.
  • Nuclear envelope assembles around chromosome clusters.
  • Golgi complex and ER reforms.
  • Daughter cells formed by cytokinesis
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9
Q

Condensin and Cohesin

A
  • Condensin-forms loop around DNA loops
  • Cohesin-forms loop around sister chromatids
  • Alternative Model: Cohesin forms molecular bridges between sister chromatids
  • either way it keeps the sis chromo together
  • these is just a way to condense and pack the chimes other than histones
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10
Q

Where along the chromo is it tightly or loosely packed?

A
  • Held tight at centermeere and loose at end.
  • Due to polo-like kinases and aurora b kinase which phophorylate the cohesion, and is inactive along length of chromo but not at centromere. •Phosphatase active counteracts the kinase at centromere.
  • This is where they’re quickly phosphorylated and then quickly dephosphoralated.
  • will only separate at anaphase
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11
Q

Roles Kinetochore Structure

A
  1. Roles
    Site of attachment to mitotic spindle
  2. Location for motor proteins
  3. Component of signaling pathway for cell cycle checkpoint
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12
Q

Kinetochore Structure

A
  • kinetochore has microfillimous called fibrous corona.
    • end associates with kinetocore.
  • Dynene and kineasein moved in particular directions.
  • Dynein – moves toward minus end of microtubule
  • CENP-E (kinesin) – moves toward plus end of mt
  • Depolymerase-specialized kinesin protein responsible for depolymerizing mt during anaphase
  • NDC80 is a multisubunit protein that connects microtubule to kinetochore
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13
Q

Formation of Mitotic Spindle

A
  • Spingle apparatus. Come from either side of the cell.
  • 2 centrosomes make up a centriole MTOC
  • If you look at G1 it’ll only have 1 centrosome. As enters S phase, its synthesis of additional centrosome, as enters into mitosis they migrate to opposite ends. Form spindle apparatus.
  • Phosphorylation of centrosomal protein by Cdk2 initiates duplication
  • these procentrioloes enlongate during G2
  • Centrosomes migrate to opposite poles in mitosis
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14
Q

Abnormal Centrosome Number

A

In this case there’s 3 centrosomes. Chromo don’t know where the metaphase plate is. Abnrnal chromosome segregation can be related to abnormal centrosome segregation, additional duplication.

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15
Q

how to plants assemble a spindle fibre apparatus with the presents of a centrosome?’

A

•centrosomes are unique to animals, none in plants. Different mechanisum, uses 2 headed motor proetins. Jumble of cspindle fibres but there’s these motor proteins present. M.Tubules have plus and minus end. When the proteins grab them they \d then start moving towards the minus end and as they move they pull the m.Tubules togtheretr like a drawstring. Create the equivalent of a centrosome.Plant cells set up the spindle apparatus without the centrosome.

•SUMMARY:
Use 2 headed minus directed motor proteins and associated micro tubules that move towards the minus end and [ ] the minus ends together at the pole of the cell.

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16
Q

Role of Motor Proteins in line up of chromo

A

Deficient for kinesin protein associated with
prometaphase chromosome arms

Motor protein normally provides force
for moving away from poles.

17
Q

Center the Chromo and correct for unbalance in pro metaphase

A
  • Immediately following nuclear envelope breakdown
  • Chromosome become associated with plus end of microtubules
  • Differential polymerization rates regulated by differential pulling force (tension) on chromosomes
  • Chromosome tethered by motors (and Ndc80)
  • Attached to + ends. To get the chromo right dead centre takes balanced. one M.tubule is shorted (rapid loss of tubulin at kinetochore) then the other so the shorter one will grow due to addition of tubulin at the kinetochore. Signalling pathway to promote growth. The model proposed related to the tension from centrosome to the attachment point of the chromo. If you have unequal tension, chromo to far to one side, promote tubular growth. If you have equal tension then balanced polymerization on the m.tubules and depolymerization on the centrosomes.
18
Q

Mitotic Spindle of Animal Cell has 3 types of microtubules

A

Astral microtubules- help position the spindle apparatus, may help determine plane of cytokinesis

Chromosomal microtubules- exert pulling force

Polar microtubules- maintain mechanical integrity of spindle

19
Q

Tubulin Flux at Metaphase

A

Tubulin monomers incorporated at plus ends (kinetochores) (net gain).
Monomers lost at minus ends (centrosome) (net loss).