D2.1 Flashcards

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1
Q

​List implications of the idea that new cells are only produced from a pre-existing cell. ​

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2
Q

Define cytokinesis.

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3
Q

State the difference between mitosis and cytokinesis.

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4
Q

Compare and contrast cytokinesis in plant and animal cells.

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5
Q

Describe the formation of the cleavage furrow in animal cell cytokinesis.

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6
Q

Describe the formation of the cell wall in plant cell cytokinesis.

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7
Q

State the reason why daughter cells must receive at least one mitochondria during cytokinesis.

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7
Q

State that cytokinesis usually, but not always, results in equal division of the cytoplasm.

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8
Q

State that meiosis is nuclear division that results in reduction of the chromosome number and diversity between genomes.

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8
Q

Outline unequal cytokinesis in yeast budding.

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9
Q

Outline unequal cytokinesis during human oogenesis.

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10
Q

State that mitosis is nuclear division resulting in continuity of the chromosome number and genome.

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11
Q

Outline the cause and consequence of anucleate cells. ​

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12
Q

State that DNA replication occurs before both mitosis and meiosis.

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13
Q

State that DNA replication occurs in S-phase of interphase. ​

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14
Q

Explain how replicated DNA molecules are held together, with reference to chromatid, replicated chromosome, centromere and cohesin.​

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15
Q

Explain how and why chromosomes condense during mitosis and meiosis.

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16
Q

State the role of microtubules and kinetochore motor proteins.

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17
Q

State the names of the four phases of mitosis.

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18
Q

Draw typical eukaryotic cells as they would appear during the interphase and the four phases of mitosis.

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19
Q

Outline four events that occur during prophase.

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20
Q

Outline the process of metaphase, inclusive of the role of microtubules and the kinetochore.

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21
Q

Outline the process of anaphase.

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22
Q

Outline four events that occur during telophase.

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23
Q

Determine the phase of mitosis of a cell viewed in a diagram, micrograph or with a microscope.

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24
Q

Explain what it means for chromosomes to be “homologous.”

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25
Q

Define diploid.

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26
Q

State the human cell diploid number.

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27
Q

Define haploid.

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28
Q

State the human cell haploid number.

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29
Q

List example haploid cells.

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30
Q

Given a diploid number (for example 2n=4), outline the movement and structure of DNA through the stages of meiosis.

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31
Q

Explain why meiosis I is a reductive division.

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32
Q

State that cells are haploid at the end of meiosis I.

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33
Q

Compare meiosis with mitosis.

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34
Q

​Outline the events of prophase, metaphase, anaphase and telophase in meiosis I and meiosis II.

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35
Q

Define nondisjunction.

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36
Q

State the result of nondisjunction during anaphase I and anaphase II.

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37
Q

Describe the cause and symptoms of Down syndrome.​

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38
Q

Explain how meiosis leads to genetic variation in gametes.

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39
Q

Define bivalent.

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40
Q

Describe the process and result of crossing over during prophase I of meiosis.

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41
Q

Draw a diagram to illustrate the formation of new allele combinations as a result of crossing over.

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42
Q

Describe the process and result of random orientation of bivalents during metaphase I of meiosis.

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43
Q

Draw a diagram to illustrate the formation of different chromosome combinations that result from random orientation during meiosis.

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44
Q

List three processes which require cell proliferation.

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44
Q

State that the number of chromosome combinations possible due to random orientation is 2^n.​

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44
Q

Define cell proliferation.

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44
Q

Outline cell proliferation during growth at plant meristems and early-stage animal embryos.

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44
Q

List three processes which require cell proliferation.

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44
Q

Describe skin cell proliferation during cell replacement and tissue repair.​

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44
Q

List the phases of the cell cycle.

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44
Q

Distinguish between interphase, mitosis and cytokinesis.

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44
Q

Outline events of the G1, S, and G2 phases of interphase.

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44
Q

Outline the fate of cells that leave the cell cycle.​

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44
Q

Outline the structures that must be produced by a cell as it grows prior to division.

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44
Q

List example metabolic reactions occurring during cell interphase.​

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44
Q

State the functions of cell cycle checkpoints.

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44
Q

Outline events of the G1, G2 and M checkpoints.

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45
Q

Outline the role of cyclins in controlling the cell cycle.

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45
Q

Interpret a graph of cyclin concentrations throughout the cell cycle.​

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45
Q

Describe how cancer arises, referring to accumulation of mutations over time.

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45
Q

Define and list mutagens.

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45
Q

Explain how mutations to proto- oncogenes and tumor suppressor genes can lead to the development of cancer.​

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45
Q

Compare the rates of cell division and growth and the capacity for metastasis and invasion of neighboring tissues between normal cells and cancerous cells.

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45
Q

Define primary tumor, secondary tumor, benign, malignant, metastasis and cancer.

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45
Q

State the formula for calculation of a mitotic index.

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45
Q

Calculate the mitotic index of a tissue as seen in a micrograph.

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45
Q

Outline the use of mitotic index calculations in diagnosis and treatment of cancer.​

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