2.17 Cell Cycle and Apoptosis Flashcards

1
Q

Confined to a specific part of the body

A

Local Control

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2
Q

Involves multiple organ systems, or the whole body

A

Systemic Control

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3
Q

How do cells reproduce

A

Cell division of existing cells

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4
Q

True or false

DNA replication and cell division must take place in a highly coordinated fashion in eukaryotes

A

True

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5
Q

True or false

Synthesis takes place after mitosis

A

False

M after S

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6
Q

Chromosomes are segregated and packaged into separate nuclei

A

Mitosis

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7
Q

Separation of two nuclei into two genetically identical daughter cells

A

Cytokinesis

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8
Q

Two major processes of M phase

A

Mitosis

Cytokinesis

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9
Q

Nucleolus and nuclear envelope are distinct and the chromosomes are in the form of threadlike chromatin

A

Interphase

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10
Q

Thick, coiled chromosomes, each with two chromatids, are lined up on the metaphase plate

A

Metaphase

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11
Q

Division into two daughter cells is completed

A

Cytokinesis

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12
Q

The chromatids of each chromosome have separated and are moving toward the poles

A

Anaphase

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13
Q

The chromosomes appear condensed, and the nuclear envelope is not apparent

A

Prophase

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14
Q

The chromosomes are at the poles, and are becoming more diffuse. The nuclear envelope is reforming. The cytoplasm may be dividing

A

Telophase

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15
Q

Stages of mitosis

A
Interphase
Prophase
Metaphase
Anaphase
Telophase
Cytokinesis
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16
Q

Bipolar array of microtubules that become attached to the sister chromatids

A

Mitotic spindle

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17
Q

Mitosis depends on the machinery of the ___

A

Mitotic spindle

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18
Q

__ movement towards minus end of microtubules, these minus ends are located towards the centrosome

A

Dynein -mediated

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19
Q

___ movement towards plus end, some microtubule plus ends are attached to the kinetochore

A

Kinesin-mediated

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20
Q

Large protein complex that provides microtubule binding site on the chromosome

A

Kinetochore

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21
Q

Movement of the sister chromatids lining up at metaphase plate and connected to the opposite poles

A

Congression

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22
Q

Holds the sister chromatids together

A

Cohesin

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23
Q

After birth and before the cell gets ready to split

A

G1

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24
Q

Exit for non-proliferating, differentiated cells

Cells remain in a quiescent state

A

G0

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25
Replication
S
26
Getting ready for mitosis
G2
27
Mitosis
M
28
``` Timing Rapidly dividing human cells Mitosis G1 S G2 ```
``` around 24 hours; 0.5 h; 9 h 10 h 4.5 h ```
29
Timing | Rapidly growing yeast cells
around 90 minutes
30
E. coli doubing time
20 m
31
How is the timing maintained?
Dominoes or clocks as model
32
The next phase is dependent on the previous part
Dominoes
33
Schedule is followed
Clock
34
Clock timer that has feedback points for regulation
Control system
35
Checks for cell size, nutrients, growth factors, and DNA damage
G1/S checkpoint | Restriction point
36
Checks if replicated DNA is suitable for cell division - no mutation, appropriate cell size
G2/M checkpoint
37
Check for chromosome attachment to spindle fiber
Metaphase to anaphase checkpoint
38
Heart of the control system
Cyclins and Cyclin-dependent Kinases (CDK)
39
True or false | In control system, cyclins are always present while CDKs are variable
False | The other way around
40
DNA pre-replication complexes are dephosphorylated, and they assemble onto chromosome replication origin
Early G1
41
G1 CDK compelxes are synthesized | These kinases phosphorylate and activate certain transcription factors
Late G1
42
Target of the transcription factors are genes encoding components of the ___ , which is blocked by a specific inhibitors
S-phase CDK complex
43
G1 CDK phosphorylates the inhibitor, targeting it for degradation
Near the start of S-phase
44
Marks the onset of S-phase
Release of S-phase CDK
45
Made during S-phase and G2, but activities are inhibited until DNA synthesis is complete
Mitotic CDK complexes
46
Activation of Mitotic CDK begins at ___
M-phase
47
Targets cohesin regulators for degradation, allowing segragation of sister chromatids
Anaphase promoting complex (APC)
48
Degrades mitotic CDK complexes, resulting in the final mitotic events
APC
49
True or false | Transcription level control is possible after the S phase because DNA is tightly bound as chromosomes
False | Not possible
50
Kinases turn or or off proteins needed after the S phase through ___
Phosphorylation
51
Proteins are controlled via:
Phosphorylation | Degradation
52
Two methods of degradation
Via lysosome | Via ubiquitin-meidated proteasomal degradation
53
only protein that attaches to cohesin because of the presence of enzymes that are specific to both substrates
Ubiquitin
54
True or false | Degradation of the stage-specific proteins ensures one way traffic
True
55
Protein degrading machine
APC
56
APC is regulated by __
Phosphorylation
57
Direct anaphase promoter
APC
58
Protects protein linkages that hold the chromatids, also an inhibitor of separase
Securin
59
When separase is no longer inhibited by securin, it leads to ___
Cohesin degradation
60
G1-CDK
Cyclin D | CDK4, 6
61
G1/S -CDK
Cyclin E | CDK2
62
S - CDK
Cyclin A | CDK2, 1
63
M - CDK
Cyclin B | CDK 1
64
Signal proliferation
Growth factors
65
Cancer drug which is a proteasome inhibitor
Velcade
66
Active ingredient in Velcade
Bortezomib
67
Programmed cell death
Apoptosis
68
Blebbing of the cell
Apoptosis
69
Characterized by extensive tissue damage Cystolic matter spills into the extracellular space through the damaged plasma membrane and this may provoke inflammatory response
Necrosis
70
Apoptosis is triggered by:
Absence of signals from trophic factors Internal conditions in the cell (induced by toxins that enter the cell) External death signals
71
Failure to pass the cell cycle checkpoints leads to __
Cell cycle arrest
72
Gene regulator of the cell cycle | Inhibits the activity of cyclin-CDK complexes upon detection of DNA damage
p53
73
TNF binds to __ (Fas receptor)
Death receptor
74
Binding of TNF to death receptors which activates caspases and leads to appoptosis
External pathway
75
Involved after death signaling
Activation of Caspase 8, 3 | Fomration of apostosome: mitochondrial cytochrome-c, apaf-1 and caspase 9
76
Triggers apoptosis
Plasma membrane (GF withdrawal) Nucleus (irreparable DNA damage) Death receptor signaling ER (unfolded proteins)
77
True or false | Apoptosis is reversible
Depends. | True unless DNA damage is permanent
78
Implications of reversibility when it comes to chemotherapy
Anastasis