Topic 4 (pre-exam) Flashcards

(45 cards)

1
Q

how often does the cell cycle occur, and how long does each stage last?

A

once approximately every 24 hours (circadian rhythms)

interphase - G1: 11 hours; S: 8 hours; G2: 4 hours
mitosis - 1 hour

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2
Q

role of S phase and G2 phase in the cell cycle

A

prepare the cell for division (mitosis)

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3
Q

what is the best way to distinguish living/nonliving matter?

A

cell division; continuity of life based on the reproduction of cells

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4
Q

cell division in unicellular organisms

A

cell division is reproduction; division of one cell replicates the entire organism

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5
Q

purpose of cell division in multicellular organisms

A

needed for:

  • development of a fertilized cell
  • growth
  • repair (i.e. tissue renewal)
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6
Q

what is the result of mitotic vs meiotic cell division?

A

mitotic: daughter cells with identical genetic info (DNA) and 2 sets of chromosomes
meiotic: nonidentical daughter cells (gametes aka sperm and egg cells) with only 1 set of chromosomes

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7
Q

genome

A

all of the DNA in a cell (including in mitochondria and/or chloroplasts)

*can consist of a single DNA molecule (prokaryotes) or a number of DNA molecules eukaryotes)

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8
Q

function and significance of chromosomes

A

DNA is condensed and packaged into chromosomes (with proteins) during prophase

*every eukaryotic species has a characteristic number of chromosomes in each cell nucleus

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9
Q

somatic cells vs gametes

A

somatic cells: non-reproductive; 2 sets of chromosomes

gametes: reproductive; half the chromosomes

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10
Q

chromatin

A

complex of DNA and protein that condenses into chromosomes during cell division; makes up eukaryotic chromosomes

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11
Q

what occurs in preparation for cell divison?

A

DNA is replicated and chromosomes condense

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12
Q

sister chromatids

A

the 2 identical copies of a chromosome after it’s been duplicated that separate during cell division

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13
Q

centromere

A

the narrow waist of a duplicated chromosome, tightly attaches sister chromatids

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14
Q

two phases of eukaryotic cell division

A

mitosis - division of nucleus

cytokinesis - division of cytoplasm

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15
Q

historical breakthrough in observing the cell cycle

A

Walter Flemming developed dyes to observe chromosomes and see their change in form, called the “father of cytogenics”

*various staining techniques today to observe chromosomes

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16
Q

two parts of the cell cycle and their functions:

A

Mitotic (M) phase - mitosis and cytokinesis

Interphase - cell growth and copying of chromosomes in preparation for cell division

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17
Q

phases of mitosis

A

prophase, prometaphase, metaphase, anaphase, telophase

  • cytokinesis underway by late telophase
  • process is still a continuum!!
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18
Q

prophase

A

assembly of mitotic spindle

  • DNA condenses into chromosomes
  • nuclear envelope disappears
  • centrosome (outside of nuclear envelope) replicates in 2; migrates to opposite ends of cell
  • spindle microtubules are assembled and begin to grow out of centrosomes
  • asters extends from each centrosome
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19
Q

centrosomes

A
  • both create and control microtubules

- discovered by Walther Flemming; only in animal cells (unknown where plant microtubules come from)

20
Q

mitotic spindle

A

made of up centrosomes, spindle microtubules, and asters

21
Q

asters

A

radial array of short microtubules extending from each centrosome

22
Q

types of microtubules

A

spindle microtubules

  • kinetochore: attach to kinetochore of chromosomes during prometaphase to pull chromosomes apart during anaphase
  • nonkinetochore: overlap and push against eachother during telophase to elongate cell

other microtubules
- asters: short microtubules that anchor spindle posts to cell membrane

23
Q

prometaphase

A

spindle microtubules attach to kinetochores of chromosomes and begin to move them

24
Q

kinetochores

A

complex of proteins associated with the centromere of chromosomes where spindle fibers attach

25
metaphase
chromosomes lined up at metaphase plate (cell equator) midway between spindle's 2 poles
26
anaphase
sister chromatids separate and move along kinetochore microtubules towards opposite ends of cell - microtubules shorten by depolymerizing at kinetochore ends
27
telophase
nonkinetochore microtubules from opposite poles overlap and push against each other, elongating cell - genetically identical daughter nuclei form at opposite ends of cell
28
how did scientists learn how kinetochores depolymerize?
- scientists used a pig kidney cell in early anaphase - spindle microtubules dyed and part was lasered to remove fluorescence - they monitored change in length on either side of the mark as the chromosomes moved towards the poles - microtubules on kinetochore side shortened, so depolymerization happens at kinetochore end
29
cytokinesis (plants vs animals)
- in animal cells: cleavage furrow forms | - in plant cells: more rigid, so a cell plate forms to divide them
30
binary fission
- method of prokaryote reproduction | - chromosome replicates and 2 daughter chromosomes actively more apart
31
evolution of mitosis
- mitosis evolved form binary fission because prokaryotes existed before eukaryotes - some protists exhibit "in-between" types of cell division
32
what is the molecular control system?
chemical signals in the cytoplasm cause the frequency of cell division to vary with cell type
33
evidence for regulation of cell division coming from the cytoplasm
- mammalian cells at different phases of the cell cycle were fused to form a single cell with 2 nuclei - when cells in S and G1 fused, nucleus of G1 cell immediately entered S phase and DNA synthesized - when cells in M and G1 fused, nucleus of G1 cell began mitosis (spindle formed and chromatin condensed) even though chromosomes had not been duplicated
34
cell cycle control system
directs the sequential events in the cell cycle (like a clock) - both internal and external controls - specific checkpoints control where cell cycle stops until go-ahead signal received
35
important checkpoints in cell cycle control system
most important: G1 checkpoint - cells that get go-ahead will complete other phases and divide; cells that don't get go-ahead signal will exit the cycle and switch into a non-dividing state called G0 phase G2 checkpoint - gives ok for cell division; right before M phase
36
G0 phase
non-dividing state if no go-ahead signal is received at the G1 checkpoint
37
regulatory proteins involved in cell cycle control
cyclins and cyclin-dependent kinases (Cdks) | - actively fluctuate levels during the cell cycle
38
role of MPF
MPF (maturation-promoting-factor) is a cyclin-Cdk complex that gives the cell the go-ahead past the G2 checkpoint, stimulating the mitotic (M) phase - once mitosis completed, cyclins degrade from MPF
39
equation for determining concentrations
C1V1 = C2V2
40
examples of internal cell signaling
when kinetochores not attached to the spindle, a signal is sent to delay anaphase
41
examples of external cell signaling relating to mitosis
growth factors - proteins from some cells stimulate other cells to divide - platelet-derived growth factor (PDGF) - stimulates division of human fibroblast cells density-dependent inhibition - crowded cells stop dividing
42
anchorage dependence
cells must be attached to a substratum in order to divide (most animal cells) *cancer cells often don't have this
43
characteristics of cancer cells
- no density-dependent inhibition nor anchorage dependence - don't respond to cell cycle control mechanisms - may not need growth factors to divide (make their own growth factor, convey growth signal without factor, or have abnormal control system)
44
transformation
process by which normal cells transformed to cancerous cells
45
what do cancer cells do? why are they dangerous?
form tumors - masses of abnormal cells within otherwise normal tissue ***can invade healthy tissue (disrupting functions of organs) and take resources away from the cell