Unit 2 Flashcards

1
Q

Prophase

A
  • Nuclear envelope begins to dissolve to see chromosomes
  • spindles appear
  • chromosomes condense
  • centrosomes move to opposite side of the nucleus
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2
Q

Metaphase

A
  • all chromosomes are lined up in middle
  • no nucleus
    -everything is connected
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3
Q

Anaphase

A

-microtubules from opposite poles overlap and push against each other, elongating the cell
-cohesive proteins are cut and sisterhoods are pulled apart

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4
Q

Telaphase

A

-Nucleus starts to reform
-chromosomes start to recoil (histones start to unravel)
-starts to copy DNA and make proteins
- cells actually start to divide

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5
Q

cytokinesis

A

Making the cell into two roughly equal halves

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6
Q

G2

A

chromosomes start condensing
preparing for mitosis

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7
Q

plant cell division- name that phase!!

A
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8
Q

chromatin = _______ + ________

A

DNA + Proteins (histones)

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9
Q

Karyotype

A

the particular array of
chromosomes of an organism

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10
Q

what’s Interphase composed of?

A

G1, S phase, and G2

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11
Q

G1

A

time of cell growth

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12
Q

G2

A

Synthesis of DNA (DNA replication)

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13
Q

S phase

A
  • chromosomes begin to
    condense
  • which means DNA is being copied
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14
Q

Centrioles (microtubule organizing centers)

A

replicate and one centriole
moves to each pole

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15
Q

What happens during the G2 phase to chromosomes?

A

they begin to undergo
condensation, becoming
tightly coiled.

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16
Q

why do we have checkpoints?

A

to make sure everything that should be happening is, so it’s not messed up beofore

17
Q

what’s the most important checkpoint?

A

G1

18
Q

where are most cells?

A

G0 phase

19
Q

what happens to cyclin proteins?

A

is damage is detected, the cyclins downrefulate

20
Q

what’s the last checkpoint?

A

M checkpoint (a.k.a spindle checkpoint)

21
Q

how do you control the cell cycle?

A

Growth factors:
- influence the cell cycle
-trigger intracellular signaling systems

22
Q

example

A

platelet-derived growth factor (PDGF)
- triggers cells to divide during wound
healing

23
Q

what’s density-dependent inhibition?

A

crowded cells stop dividing

24
Q

How do you know if there are cells around you?

A

cell signaling

25
Q

what do most cells exhibit?

A

anchorage dependence = must be attached to a substratum in order to divide

26
Q

what’s different about cancer?

A

Cancer cells exhibit neither density-dependent inhibition nor anchorage dependence

27
Q

what are the Two kinds of genes can disturb the cell cycle when they are mutated?

A
  1. tumor-suppressor genes
  2. proto-oncogenes
28
Q

Tumor-suppressor genes example:

A

P53

29
Q

what’s does P53 do?

A

halts cell division if DNA damage is found and helps damage but if damage is too much then cell undergo apoptosis (death)

30
Q

what’s transformation?

A

Conversion to a cancerous cell

31
Q

Benign tumor

A

If abnormal cells remain only at
the original site

32
Q

Malignant tumors

A

invade surrounding tissues
and undergo (metastasis), may form additional tumors

33
Q

treatment for Benign tumor

A

*Surgery
*Radiation (cancer cells typically can’t repair damage)

34
Q

treatment for Malignant (or suspected malignant)

A

Chemotherapy
*e.g., Taxol stops actively diving cells
*Side effect is hair loss, nausea (these are normal cells that actively divide)

35
Q

what are some Chemotherapy
*e.g., Taxol stops actively diving cells
*Side effect is hair loss, nausea (these are normal
cells that actively divide

A