Regulation of Cell Cycle Flashcards

1
Q

True or False: Rates of cell division will vary depending on cell type

A

True

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2
Q

True or False: There is rapid turn over of cardiac and neurons but a slow turn over of epithelial cells

A

False
There is rapid turn over of epithelial cells but slow turn over of cardiac cells and neurons

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3
Q

G1-S-G2 constitutes ___, one of two major process in the cell cycle

A

Interphase

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4
Q

Mitotic phase consists of: ___ and ___

A

cytokinesis and mitosis

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5
Q

During __ phase of interphase, there is high levels of ___ and synthesis of ____. Further the cell grows and organelles (lysosome and mitochondria) begin to ___ and increase in ___

A

G1; RNA/proteins; duplicate and increase in volume

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6
Q

During S phase, there is transcription and translated mostly for genes related to ____ synthesis and ___

A

DNA; histones

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7
Q

True or False: During S phase, sister chromatids are converted into chromosomes

A

False

During S phase, each chromosome is replicated, forming sister chromatids (attached duplicated chromosomes)

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8
Q

True or False: Heterochromatin (histones) increases towards the end of M phase

A

False
Heterochromatin (histones) increases towards the end of S-phase

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9
Q

During the __ phase of interphase, DNA errors are identified and repaired

A

G2

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10
Q

___ are cylindrical structures that help organize microtubules

A

Centrioles

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11
Q

____ are specific regions of chromosomes that allow for attachment of protein complexes known as kinetochores

A

Centromeres

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12
Q

The centrosome, which is the microtubule organizing center of the cell, is composed of: ___ + ___

A

centrioles; microtubules

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13
Q

____ is made of tubulin and is known to shorten and lengthen rapidly

A

microtubules

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14
Q

True or False: During cell division, the centrosome duplicates

A

True

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15
Q

Attachment of microtubules to ____ will play an important role in separation of sister chromatids during mitosis

A

kinetochores

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16
Q

____ will form a “mitotic spindle” consisting of microtubules during mitosis

A

Centrosomes

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17
Q

Stages of mitosis?

A

1) Prophase
2) Prometaphase
3) Metaphase
4) Anaphase
5) Telophase

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18
Q

During what phase of mitosis does:
-DNA in chromosomes condenses
-kinetochores attach to centromeres
-condensed sister chromatids are formed

A

Prophase

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19
Q

During what phase of mitosis does:
-nuclear membrane break down
-microtubules bind to kinetochores

A

Prometaphase

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20
Q

___ are the names of the microtubules that overlap and become bound to one another during metaphase

A

polar microtubules

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21
Q

During anaphase __ microtubules lengthen, pushing centrosomes to opposite ends of the cell while ___ microtubules shorten, separating sister chromatids

A

polar; kinetochore

22
Q

During ___ phase of mitosis, the kinetochores and mitotic spindles disassemble, nuclear membrane reforms, and chromosomes de-condense. Further: chromosomes are equally separated to opposite poles of the cell

A

Telophase

23
Q

During cytokinesis, a contractile ring—also known as: cleavage furrow—composed of __ and __ proteins forms between cells

A

actin; myosin

24
Q

During ____, the cytoplasm and organelles are separated into two new cells and the membrane of each new cell is sealed off

A

cytokinesis

25
Q

What does the Haylink Limit state?

A

Most human cells can only divide a limited amount of times

26
Q

Cells in ___ phase have exited the cell cycle but remain functional

A

G0

27
Q

True or False: Entry into G0 is always reversible

A

False
Entry into G0 may be permanent or reversible

28
Q

True or False: The Hayflick Limit applies to stem cells

A

False - the Hayflick Limit does NOT apply to stem cells

29
Q

Stem cell converting into a viable and functional neuron, but no longer able to divide, is an example of ___ ____

A

terminal differentiation

30
Q

In response to stress, toxins, lack of nutrients, or damage, a cell can enter G0 where they are viable yet non-dividing. This process, known as ____, involves genetic and metabolic reprogramming.

A

senescence

31
Q

In ____ senescence, cells permanently leaves the cell cycle. In other words, this a non-reversible form of senescence.

A

Replicative senescence

32
Q

An example of___, a reversible state of G0, is memory of t-cells staying in G0 until stimulated to proliferate

A

Quiescence

33
Q

What is a mechanism of replicative senescence?

A

Telomerase shortening

34
Q

True or False: stem cells do not express telomerase but somatic cells do

A

False
Stem cells express telomerase but somatic cells do not. Therefore, the prior cells can replicate infinitely, maintaining telomere length, while the latter eventually undergo senescence due to telomere shortening

35
Q

What domain of the CDK is activated when cyclin binds?

A

kinase domain

36
Q

True or False: Cyclin levels remain constant during the cell cycle while CDK levels rise and fall

A

False
CDK levels remain constant while cyclin levels rise and fall during cell cycle

37
Q

Cyclin D combines with CDK _ and CDK _ to allow for progression through G1

A

CDK4 and CDK6

38
Q

Cyclin _ and _ combine with CDK2 to initiate DNA synthesis in early S-phase

A

E, A

39
Q

Cyclin B combines with CDK1. How does it function?

A

G2/M transition

40
Q

CIP/KIP and INK4 are both what type of inhibitors?

A

cyclin dependent kinase inhibitors (CKI)

41
Q

INK4 inhibitors block cyclin _ binding, stopping the cell cycle at G1

A

D

42
Q

p15, p16, p18, and p19 are all examples of ___

A

INK4 (cyclin dependent kinase inhibitor)

43
Q

CIP/KIP inhibitors block CDK _, inhibiting DNA synthesis

A
44
Q

p21 is an example a ___/___. What makes p21 special?

A

CIP/KIP (cyclin dependent kinase inhibitor)

p21 can inhibit multiple CDK complexes, including cyclin: A, B, D, and E

45
Q

During the ___ checkpoint, the cell checks that kinetochores are bound by microtubules in preparation for cell division

A

spindle/M checkpoint

46
Q

The ___ check point will assess DNA damage and induce DNA repair pathways if needed

A

G2

47
Q

The early G1 check point is ___ while the late G1 check point is ___

A

growth factor dependent; growth factor independent

48
Q

___ factors bind cellular receptors and initiate the cell cycle in early G1. As a result of these factors, there is an increase in ___ _ levels, which activated CDK4/6. Activated CDK4/6 phosphorylates Rb, which changes the structure of Rb, causing it to release E2F

A

Growth ; cyclin D

49
Q

Typically Rb binds and inhibits ___

A

E2F (transcription factor)

50
Q

Activity of E2F up-regulates genes needed for progression of cell cycle, such as ___ _, which moves the cell past the Restriction Point (G1 checkpoint)

A

Cyclin E