4.3 Flashcards

1
Q
  • All cells derive from other cells.
A
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2
Q
  • Where do all cells come from? Pre-existing cells.
A
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3
Q
  • Cell division is also called the cell cycle.
A
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4
Q
  • What processes does the cell cycle allow for? **Growth
A

repair

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5
Q
  • How many steps are common to all cell division? 4.
A
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6
Q
  • Prokaryotic cells divide by binary fission.
A
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7
Q
  • What regulates binary fission in prokaryotic cells? Environmental signals.
A
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8
Q
  • Eukaryotic cells undergo a more complex cell cycle.
A
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9
Q
  • The eukaryotic cell cycle includes dedicated sections for DNA replication
A

mitosis

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10
Q
  • What is the ori site? Where DNA replication begins in bacteria.
A
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11
Q
  • A mutation in the ori site may prevent replication from initiating properly.
A
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12
Q
  • What might a mutation in the ori site prevent? The formation of two complete copies of the bacterial chromosome.
A
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13
Q
  • What is disrupted if the ori regions cannot move to opposite ends of the bacterial cell? DNA segregation.
A
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14
Q
  • If DNA replication and segregation do not occur correctly in bacteria
A

cytokinesis may be incomplete.

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15
Q
  • What might be the result of incorrect DNA replication and segregation in bacteria? Daughter cells without full genetic material.
A
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16
Q
  • What is the likely outcome of such errors in bacterial cell division? Cell death.
A
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17
Q
  • What are the phases a cell passes through to produce daughter cells by cell division? The cell cycle.
A
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18
Q
  • During which phase is the nucleus visible and do cell functions occur? Interphase.
A
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19
Q
  • The duration of interphase is highly variable.
A
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20
Q
  • How many subphases does interphase have? 3.
A
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21
Q
  • What are the subphases of interphase? **G1
A

S

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22
Q
  • During which phase are chromosomes single (unreplicated)? The G1 phase.
A
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23
Q
  • The duration of the G1 phase is variable
A

from minutes to years.

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24
Q
  • What marks the end of the G1 phase? The G1-to-S transition.
A
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25
Q
  • What commitment is made at the G1-to-S transition? To DNA replication and cell division.
A
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26
Q
  • Some cells enter a resting phase.
A
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27
Q
  • What is the resting phase of the cell cycle called? G0.
A
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28
Q
  • During which phase does DNA replicate? The S phase.
A
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29
Q
  • Where do copied chromosomes remain until mitosis? Together.
A
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30
Q
  • During which phase does the cell prepare for mitosis? The G2 phase.
A
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31
Q
  • What does the cell synthesize in the G2 phase? The structures that move the chromatids.
A
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32
Q
  • What does the M phase include? Mitosis and cytokinesis.
A
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33
Q
  • When does the replication of DNA occur in the cell cycle? During the S phase.
A
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34
Q
  • How are chromosomes described in the G1 phase of the eukaryotic cell cycle? Single (unreplicated).
A
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35
Q
  • What does the cell prepare for in the G1 phase? Division.
A
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36
Q
  • If a nucleus in G2 has 1.6 pg of DNA
A

how much DNA did it have in G1? 0.8 pg.

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37
Q
  • If a cell cannot properly transition from S to G2
A

what might be disrupted? The preparation for mitosis.

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38
Q
  • Cell cycle regulation depends on the action of CDKs.
A
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39
Q
  • What does CDK stand for? Cyclin-dependent kinases.
A
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40
Q
  • What can a protein kinase do? Transfer a phosphate group from ATP to a protein.
A
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41
Q
  • What is the transfer of a phosphate group called? Phosphorylation.
A
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42
Q
  • What does the addition of a phosphate group change in a protein? Shape and function.
A
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43
Q
  • Phosphorylation can switch a protein on or off.
A
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44
Q
  • What type of molecule is a kinase? A protein.
A
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45
Q
  • What can a kinase alter in a protein target? The structure.
A
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46
Q
  • What can kinases do to other proteins? Switch them on and off.
A
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47
Q
  • How does a CDK regulate the cell cycle? By regulating proteins important in the cell cycle.
A
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48
Q
  • What does the name “CDK” imply? That the function of the kinase is dependent on something called cyclin.
A
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49
Q
  • What does cyclin do to the cyclin-CDK complex? Directs it to the target protein.
A
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50
Q
  • How does the kinase change the protein? Through phosphorylation.
A
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51
Q
  • What is the cyclin-CDK complex? Cyclin and Kinase.
A
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52
Q
  • Where do cyclin-CDKs act to regulate cell cycle progress? At cell cycle checkpoints.
A
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53
Q
  • How do cyclin-dependent kinases (CDKs) regulate the cell cycle? **By adding phosphate groups to target proteins
A

altering their activity**.

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54
Q
  • Once interphase is completed
A

what phase does the cell enter? Mitosis.

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55
Q
  • What happens to the replicated DNA during mitosis? It is segregated into two daughter cells.
A
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56
Q
  • What does a eukaryotic chromosome consist of before S phase? **One linear
A

double-stranded DNA molecule bound with many proteins**.

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57
Q
  • What is the complex of DNA and proteins referred to as? Chromatin.
A
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58
Q
  • How many double-stranded DNA molecules does an unreplicated chromosome contain? Only one.
A
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59
Q
  • What is present after replication during S phase? Two double-stranded DNA molecules called sister chromatids.
A
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60
Q
  • What holds sister chromatids together along most of their length? A protein complex called cohesin.
A
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61
Q
  • Where does most of the cohesin remain during mitosis? In a region called the centromere.
A
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62
Q
  • What proteins coat DNA molecules at the end of G2 and the beginning of mitosis to make them more compact? Condensins.
A
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63
Q
  • What proteins largely achieve the packing of DNA? Histones.
A
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64
Q
  • Why are histones positively charged at cellular pH? Because of their high content of the basic amino acids lysine and arginine.
A
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65
Q
  • How does DNA bind to histones? By ionic bonds.
A
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66
Q
  • What do DNA-histone interactions result in? The formation of beadlike units called nucleosomes.
A
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67
Q
  • During interphase
A

what does the chromatin consist of? Single DNA molecules wrapped around vast numbers of nucleosomes.

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68
Q
  • During interphase
A

is DNA accessible to proteins involved in replication and transcription? Yes.

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69
Q
  • What happens to the accessibility of DNA to replication and transcription factors once a mitotic chromosome is formed? It becomes inaccessible.
A
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70
Q
  • What is the genetic outcome of mitosis? Two nuclei that are genetically identical.
A
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71
Q
  • What does mitosis ensure? The accurate segregation of each copy of a eukaryotic cell’s multiple chromosomes into the daughter nuclei.
A
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72
Q
  • What are the five stages of mitosis? **Prophase
A

prometaphase

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73
Q
  • What determines the plane of cell division? The centrosomes.
A
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74
Q
  • What is the dynamic microtubule structure that moves sister chromatids apart during mitosis? The spindle.
A
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75
Q
  • What determines the orientation of the spindle? The centrosome.
A
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76
Q
  • What do centrosomes consist of in many organisms? A pair of centrioles.
A
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77
Q
  • When does the centrosome duplicate? During S phase.
A
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78
Q
  • When do the two centrosomes separate? At the beginning of prophase.
A
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79
Q
  • What do the separating centrosomes identify? The poles toward which chromosomes move during anaphase.
A
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80
Q
  • What do the cells of plants and fungi lack? Centrosomes.
A
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81
Q
  • What do plant and fungal cells have at each end of the cell? Distinct microtubule organizing centers.
A
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82
Q
  • What do the positions of the centrosomes determine in animal cells? The plane where the cell will divide.
A
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83
Q
  • When does the spindle begin to form? During prophase.
84
Q
  • What happens to most of the cohesin during prophase? It is removed.
85
Q
  • What becomes visible during prophase? Individual chromatids.
86
Q
  • Where are sister chromatids still held together during prophase? At the centromere.
87
Q
  • What structures develop in the centromere region late in prophase? Kinetochores.
88
Q
  • What does each of the two centrosomes serve as? **A mitotic center
A

or pole**.

89
Q
  • What forms between the poles and the chromosomes during prophase and prometaphase? Microtubules that make up the spindle.
90
Q
  • What does the spindle serve as? A structure to which the chromosomes attach and a framework keeping the two poles apart.
91
Q
  • What are the two groups of microtubules in the spindle? Polar microtubules and kinetochore microtubules.
92
Q
  • What do polar microtubules do? Form the framework of the spindle and run from one pole to the other.
93
Q
  • What do kinetochore microtubules do? Attach to the kinetochores on the chromosomes.
94
Q
  • What do the two sister chromatids in each replicated chromosome become attached to? Kinetochore microtubules from opposite poles.
95
Q
  • When does the separation of the chromatids occur? At the beginning of anaphase.
96
Q
  • What controls chromatid separation? An M phase cyclin–CDK.
97
Q
  • What does the M phase cyclin-CDK activate? The anaphase-promoting complex (APC).
98
Q
  • What causes separation of sister chromatids? Hydrolysis of the cohesin protein by separase.
99
Q
  • What is the cell cycle checkpoint at the end of metaphase called? The spindle assembly checkpoint.
100
Q
  • What does the spindle assembly checkpoint inhibit if chromosomes are not properly attached? The APC.
101
Q
  • What are chromatids called after separation? Daughter chromosomes.
102
Q
  • What do sister chromatids share? A centromere.
103
Q
  • What do daughter chromosomes have? Their own centromere.
104
Q

Here are 100 fill-in-the-blank questions based on the provided sources

A

presented chronologically:

106
Q
  1. All cells derive from other cells.
107
Q
  1. All cells come from pre-existing cells.
108
Q
  1. Cell division
A

also called the cell cycle

109
Q
  1. The same 4 steps are common to all cell division.
110
Q
  1. Prokaryotic cells divide by binary fission
A

a process regulated by environmental signals.

111
Q
  1. Eukaryotic cells undergo a more complex cell cycle.
112
Q
  1. The eukaryotic cell cycle includes dedicated sections for DNA replication
113
Q
  1. The ori site is where DNA replication begins in bacteria.
114
Q
  1. If the ori site is mutated
A

replication may not initiate properly.

115
Q
  1. A mutation in the ori site may prevent the formation of two complete copies of the bacterial chromosome.
116
Q
  1. Without proper replication
A

the ori regions cannot move to opposite ends of the bacterial cell

117
Q
  1. If DNA replication and segregation do not occur correctly in bacteria
A

cytokinesis may be incomplete.

118
Q
  1. Incorrect DNA replication and segregation in bacteria can result in daughter cells without full genetic material.
119
Q
  1. Such errors in bacterial cell division are likely leading to cell death.
120
Q
  1. The phases a cell passes through to produce daughter cells by cell division is called the cell cycle.
121
Q
  1. During interphase
A

the nucleus is visible and cell functions occur.

122
Q
  1. The duration of interphase is highly variable.
123
Q
  1. Interphase has 3 subphases: G1
124
Q
  1. During the G1 phase
A

chromosomes are single (unreplicated).

125
Q
  1. The duration of the G1 phase is variable
A

from minutes to years.

126
Q
  1. The G1 phase ends at the G1-to-S transition.
127
Q
  1. At the G1-to-S transition
A

commitment is made to DNA replication and cell division.

128
Q
  1. Some cells enter a resting phase called G0.
129
Q
  1. During the S phase
A

DNA replicates.

130
Q
  1. Copied chromosomes remain together until mitosis.
131
Q
  1. During the G2 phase
A

the cell prepares for mitosis.

132
Q
  1. In the G2 phase
A

the cell synthesizes the structures that move the chromatids.

133
Q
  1. The M phase includes mitosis and cytokinesis.
134
Q
  1. The replication of DNA occurs during the S phase of the cell cycle.
135
Q
  1. In the G1 phase of the eukaryotic cell cycle
A

chromosomes are single (unreplicated).

136
Q
  1. In the G1 phase
A

the cell prepares for division.

137
Q
  1. If the nucleus of a cell in G2 has 1.6 pg of DNA
A

it had 0.8 pg of DNA in G1.

138
Q
  1. If a cell is unable to properly transition from S to G2 phase
A

the preparation for mitosis might be disrupted.

139
Q
  1. Cell cycle regulation depends on the action of CDKs.
140
Q
  1. CDK stands for cyclin-dependent kinases.
141
Q
  1. A protein kinase can transfer a phosphate group from ATP to a protein.
142
Q
  1. The transfer of a phosphate group is called phosphorylation.
143
Q
  1. Addition of a phosphate group changes the shape and function of the protein.
144
Q
  1. Phosphorylation can switch a protein on or off.
145
Q
  1. A kinase is a protein.
146
Q
  1. A kinase can alter the structure of a protein target.
147
Q
  1. A kinase can switch other proteins on and off.
148
Q
  1. A CDK regulates the cell cycle by regulating proteins important in the cell cycle.
149
Q
  1. The name “CDK” implies that the function of the kinase is dependent on something called cyclin.
150
Q
  1. Cyclin directs the cyclin-CDK complex to the target protein.
151
Q
  1. The kinase changes the protein through phosphorylation.
152
Q
  1. The whole thing is the cyclin-CDK complex.
153
Q
  1. Cyclin-CDKs act at cell cycle checkpoints to regulate progress through the cell cycle.
154
Q
  1. Cyclin-dependent kinases (CDKs) regulate the cell cycle by adding phosphate groups to target proteins
A

altering their activity.

155
Q
  1. Once the cell cycle is initiated and interphase is completed
A

the cell enters mitosis.

156
Q
  1. During mitosis
A

the replicated DNA is segregated into two daughter cells.

157
Q
  1. A eukaryotic chromosome consists of one or two linear
A

double-stranded DNA molecules bound with many proteins.

158
Q
  1. The complex of DNA and proteins is referred to as chromatin.
159
Q
  1. Before S phase
A

each unreplicated chromosome contains only one double-stranded DNA molecule.

160
Q
  1. After replication during S phase
A

there are two double-stranded DNA molecules called sister chromatids.

161
Q
  1. Sister chromatids are held together along most of their length by a protein complex called cohesin.
162
Q
  1. At mitosis most of the cohesin is removed
A

except in a region called the centromere.

163
Q
  1. At the end of G2 and the beginning of mitosis
A

a second group of proteins called condensins coats the DNA molecules and makes them more compact.

164
Q
  1. The packing of DNA is achieved largely by proteins called histones.
165
Q
  1. Histones are positively charged at cellular pH because of their high content of the basic amino acids lysine and arginine.
166
Q
  1. DNA wraps around histones
A

binding by ionic bonds.

167
Q
  1. DNA-histone interactions result in the formation of beadlike units called nucleosomes.
168
Q
  1. During interphase
A

the chromatin that makes up each chromosome consists of single DNA molecules wrapped around vast numbers of nucleosomes.

169
Q
  1. During interphase
A

the DNA is accessible to proteins involved in replication and transcription.

170
Q
  1. Once a mitotic chromosome is formed
A

its compact nature makes it inaccessible to replication and transcription factors.

171
Q
  1. Mitosis during M phase leads to the production of two nuclei that are genetically identical.
172
Q
  1. Mitosis ensures the accurate segregation of each copy of a eukaryotic cell’s multiple chromosomes into the daughter nuclei.
173
Q
  1. Mitosis is conveniently subdivided into five stages: **prophase
A

prometaphase

174
Q
  1. The centrosomes determine the plane of cell division.
175
Q
  1. The spindle is a dynamic microtubule structure that moves sister chromatids apart during mitosis.
176
Q
  1. The orientation of the spindle is determined by the centrosome.
177
Q
  1. In many organisms the centrosome consists of a pair of centrioles.
178
Q
  1. During S phase
A

the centrosome duplicates.

179
Q
  1. At the beginning of prophase
A

the two centrosomes separate.

180
Q
  1. The separating centrosomes identify the poles toward which chromosomes move during anaphase.
181
Q
  1. The cells of plants and fungi lack centrosomes.
182
Q
  1. Plant and fungal cells have distinct microtubule organizing centers at each end of the cell.
183
Q
  1. The positions of the centrosomes determine the plane where the animal cell will divide.
184
Q
  1. The spindle begins to form during prophase.
185
Q
  1. During prophase
A

most of the cohesin that has held the two products of DNA replication together since S phase is removed.

186
Q
  1. Individual chromatids become visible during prophase.
187
Q
  1. Sister chromatids are still held together by a small amount of cohesin at the centromere.
188
Q
  1. Late in prophase
A

specialized structures called kinetochores develop in the centromere region.

189
Q
  1. Each of the two centrosomes serves as a mitotic center
190
Q
  1. During prophase and prometaphase
A

microtubules form between the poles and the chromosomes to make up the spindle.

191
Q
  1. The spindle serves as a structure to which the chromosomes attach.
192
Q
  1. The spindle also provides a framework keeping the two poles apart.
193
Q
  1. Two groups of microtubules in the spindle are polar microtubules and kinetochore microtubules.
194
Q
  1. Polar microtubules form the framework of the spindle and run from one pole to the other.
195
Q
  1. Kinetochore microtubules attach to the kinetochores on the chromosomes.
196
Q
  1. The two sister chromatids in each replicated chromosome become attached to kinetochore microtubules from opposite poles.
197
Q
  1. Separation of the chromatids occurs at the beginning of anaphase.
198
Q
  1. Chromatid separation is controlled by an M phase cyclin–CDK.
199
Q
  1. The M phase cyclin-CDK activates another protein complex called the anaphase-promoting complex (APC).
200
Q
  1. Separation occurs because one subunit of the cohesin protein is hydrolyzed by separase.
201
Q
  1. A cell cycle checkpoint
A

often called the spindle assembly checkpoint

202
Q
  1. The spindle assembly checkpoint inhibits the APC if one of the chromosomes is not attached properly to the spindle.
203
Q
  1. After separation
A

the chromatids are called daughter chromosomes.

204
Q
  1. Sister chromatids share a centromere.
205
Q
  1. Daughter chromosomes have their own centromere.