Cell Biology Flashcards

Introduction to cells, Ultrastructure of cells, Membrane structure, Membrane transport, The origin of cells

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1
Q

State three parts of the cell theory

A
  1. Living organisms are composed of cells
  2. Cells are the smallest units of life
  3. Cells come from pre-existing cells
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2
Q

Outline evidence that supports the cell theory

A
  1. Subcellular components have never been seen to perform the functions of life
  2. Biologists examined tissues from both plants and animals, and saw that every specimen contained at least one or more cell
  3. We have observed cells coming from other cells, but never observed spontaneous generation
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3
Q

Compare the use of the word theory in daily language and scientific language.

A

Daily language: a theory is a guess where there is doubt

Scientific language: a theory is something that has been shown to be true through repeated observations and experiments

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4
Q

Outline the functional characteristics of life

A

Metabolism - organisms carry out chemical reactions such as the synthesis of ATP during cellular respiration

Response - organisms respond and adapt to external stimuli

Growth - organisms increase in size until the cell is too large to function efficiently

Homeostasis - organisms maintain a stable environment within the cell

Reproduction - organisms are able to reproduce (prokaryotes: binary fission, eukaryotes: asexually or sexually)

Nutrition - organisms create or synthesize their own or consumes organic molecules

Excretion - organisms remove waste products

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5
Q

Outline the activities occurring in the volume and at the surface of the cell

A

Volume: many metabolic reactions which require gases and chemical nutrients and produce waste

Surface area: regulates transport of molecules in and out of the cell

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6
Q

Calculate the surface area, volume, and SA:V ratio of a cell

A

SA: length * width

Volume: length * width * height

SA:V ratio: SA / volume

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7
Q

Explain the benefits and limitations of using cubes to model the surface area and volume of a cell

A

Benefits: cubes can be manipulated, visualized, and easily measured

Limitation: most cells are not cubic in shape

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8
Q

Describe the relationship between cell size and the SA:V ratio of the cell

A

As the cell grows bigger, its volume increases and the cell membrane surface expands. However, the volume increases faster than the SA. Therefore, the amount of surface area relative to the volume (SA:V) decreases.

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9
Q

Explain why cells are often limited in size by the SA:V ratio

A

Smaller volume requires fewer metabolic nutrients and waste to be transported through the cell membrane.

Relatively more cell membrane for transporting materials into/out of the cell.

Molecules have shorter distance to diffuse within the cell.

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10
Q

List three adaptations of cells that maximize the SA:V ratio

A

Branching

Microvilli

Folded membranes

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11
Q

Define and provide an example of a multicellular organism

A

An organism that consists of more than one cell. An example is Homo sapien.

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12
Q

Define and provide an example of a unicellular organism

A

An organism that consists of only one cell. An example is paramecium.

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13
Q

Define “emergent property”

A

Properties that arise from the interaction of cellular components.

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14
Q

Provide and example of emergent properties at different hierarchical levels of life

A

1) Cells grouped together to form tissues
2) Organs are then formed from the functional grouping of multiple tissues
3) Organs that interact may form organ systems capable of carrying out specific body functions
4) Organs systems collectively carry out the life functions of the complete organism

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15
Q

Define “tissue”

A

A group or collection of similar cells that work together to perform a specific function within an organism

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16
Q

Outline the benefits of cell specialization in a multicellular organism

A

1) Efficiency in function - specialized cells are more efficient at performing specific tasks compared to generalized cells. For example, red blood cells are specialized for oxygen transport, possessing a unique shape and lacking a nucleus to maximize their capacity for oxygen binding and circulation.
2) Division of labor - cell specialization allows for the division of labor within an organism. This division enables multicellular organisms to perform complex functions more efficiently than single-celled organisms.
3) Formation of tissues and organs - specialized cells organize into tissues with specific functions. In turn, tissues assemble into organs that work together to carry out essential physiological processes.

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17
Q

Define “differentiation”

A

The process during development whereby newly formed cells become more specialized and distinct from one another as they mature

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18
Q

Describe the relationship between cell differentiation and gene expression

A

During differentiation, a cell only uses the genes that it needs to follow its pathway of development. Other genes are unused (turned off)

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19
Q

Define “zygote”

A

The fetus at its earliest stage of development following fertilization, characterized as a diploid cell formed by the fusion of two haploid gametes during fertilization

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20
Q

Define “embryo”

A

A development of the zygote after it has underwent multiple divisions

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21
Q

List 2 key properties of stem cells that have made them on the active areas of research in biology and medicine today

A
  • Unspecialized, which allows scientists to differentiate into any bodily cell (treatment of disease)
  • Divides indefinitely
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22
Q

Explain why stem cells are most prevalent in the early embryonic development of a multicellular organism

A

During early embryonic development, stem cells possess pluripotency, meaning they have the ability to differentiate into many different cell types. They are mostly prominent in the early development of multicellular organisms, as the fetuses require great numbers of tissues to form necessary organs for survival

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23
Q

Contrast the characteristics of embryonic, umbilical cord, and adult somatic stem cells

A

Embryonic:
- Derives from the inner cell mass of the blastocyst
- Pluripotent: potential to differentiate into any cell type in the body

Umbilical cord:
- Derives from the blood or tissue of the umbilical word following childbirth
- Multipotent: more limited potential to differentiate

Adult somatic:
- Derives from various tissues and organs of the adult organism
- Multipotent: even further limited potential to differentiate

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24
Q

Define “totipotent”, “multipotent”, and “pluripotent”

A

Totipotent: can differentiate into any type of cell and can give rise to a complete organism

Pluripotent: can differentiate into all body cells, but cannot give rise to a whole organism

Multipotent: can differentiate into a few closely related types of body cells

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25
Q

Describe features of striated muscle fibers that make them a discrepancy from an atypical cell

A
  • Muscle cells fuse to form fibres that may be very long (>300mm)
  • Multiple nuclei despite being surrounded by a single, continuous plasma membrane
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26
Q

Describe features of aseptate fungal hyphae that make them a discrepancy from an atypical cell

A
  • No dividing cell walls (septa), which results in a shared cytoplasm and multiple nuclei
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27
Q

Describe features of giant algae that make them a discrepancy from an atypical cell

A
  • A single cell can grow to be 100mm
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28
Q

Describe characteristics of Paramecium that enable it to perform functions of life

A
  • Surrounded by small hairs called cilia which allow it to move (responsiveness)
    . Engulf food via a specialized membranous feeding grove called a cytosome (nutrition)
  • Food particles are enclosed within small vacuoles that contain enzymes for digestion (metabolism)
  • Solid wastes are removed via an anal pore, while liquid wastes are pumped out via contractile vacuoles (excretion)
  • Essential gases enter and exit the cell via diffusion (homeostasis)
  • Divide asexually via fission, although horizontal gene transfer car occur via conjunction (reproduction)
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29
Q

Describe characteristics of Scenedesmus that enable it to perform the functions of life

A
  • Gases and other essential materials are exchanged via diffusion (nutrition / excretion)
  • Chlorophyll pigments allow organic molecules to be produced via photosynthesis (metabolism)
  • Daughter cells form as non-motile autospores via the internal asexual division of the parent cell (reproduction)
  • May exist as unicells or form colonies for protection (responsiveness)
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30
Q

Outline why stem cells are used in medical research and treatment

A

Stem cells can differentiate into all cells, meaning that they can be used to treat damaged tissue in medical treatment.

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31
Q

Outline the cause and symptoms of Stargardt’s disease

A

Cause: Gene mutation on gene ABCA4 in fetus

Symptoms: Photoreceptor cells degenerate which leads to a progressive loss of central vision

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32
Q

Explain how stem cells are used in the treatment of Stargardt’s diease

A

Patients are given retinal cells derived from human embryonic stem cells, which are injected into the retina. These cells then divide, providing the patient with healthy retina cells.

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33
Q

Outline the cause of leukemia

A

High levels of abnormal white blood cells which lead to a type of cancer in the blood or bone marrow

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34
Q

Explain how stem cells are used in the treatment of leukemia

A

Hematopoietic stem cells (HSCs) are multipotent stem cells which are harvested from bone marrow, peripheral blood or umbilical cord blood. This may derive from the patient or a suitable donor. Then, the patient undergoes chemotherapy to get rid of the diseased blood cells. Lastly, the HSCs are transplanted back into the bone marrow where they differentiate to form new healthy white blood cells.

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35
Q

Discuss the benefits and drawbacks in using adult stem cells; embryonic stem cells; cord blood stem cells

A

Benefits
- Adult: Effective for certain conditions
- Embryonic: Greatest yield of stem cells
- Umbilical cord: Effective for multiple conditions

Drawbacks
- Adult: Limited in its scope of application
- Embryonic: Destruction of potential living organisms
- Umbilical cord: Availability and access - storing them are costly

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36
Q

Define “magnificaiton”

A

The act of enlarging something

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37
Q

State why the magnification of a drawing or micrograph is not the same as the magnification of the microscope

A

A microscope will always be to scale.

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38
Q

Use a formula to calculate the magnification of a micrograph or drawing

A

M = I / A
I = M * A
A = M / I

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39
Q

Define “trend” and explain why trends are useful in scientific study

A

Can predict how something will be over a period of time.

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40
Q

Outline the major differences between prokaryotic and eukaryotic cells

A

Prokaryotic:
- Cell wall
- Naked DNA
- Flagellum

Eukaryotic:
- No cell wall
- DNA contained within nucleus
-No flagellum

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41
Q

List the functions of the following structures of a prokaryotic cell: cell membrane, nucleoid, plasmid, cytoplasm, ribosome, cell wall, pili, capsule, and flagella

A

Cell membrane:

Nucleoid:

Plasmid:

Cytoplasm:

Ribosome:

Cell wall:

Pili:

Capsule:

Flagella:

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42
Q

Contrast the size of eukaryotic and prokaryotic ribosomes

A

Eukaryotic:

Prokaryotic:

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42
Q

State the meaning and advantages of eukaryotic cells being “compartmentalized”

A

Enzymes and substrates used in a process can be concentrated in a small area.

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43
Q

State structural differences between plant and animal cells

A

Animal cells have only a plasma membrane, whereas plant cells have an additional membrane: the cell wall.

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44
Q

Define “asexual reproduction”

A

An organism’s ability to reproduce by itself.

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45
Q

Outline the steps of binary fission

A

Binary fission is how prokaryotes reproduce asexually. It means splitting in two. The bacterial chromosome is replicated so there are two identical copies. These are moved to opposite sides of the organism, and the wall and plasma membrane are pulled inwards so the cell pinches apart to create two identical cells.

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46
Q

Define “resolution”

A

The ability of the microscope to show two close objects separately in the image.

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47
Q

Compare the functionality of light and electron microscopes

A

Light microscope:
- Resolution: 0.25μm
- Magnification: x 500

Electron microscope:
- Resolution: 0.25nm
- Magnification: x 500,000

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48
Q

State the function of an exocrine gland cell

A

To secrete fluids on the exterior of the body (sweat glands, mammary glands).

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49
Q

Describe the following function of the following structures in an exocrine gland cell: plasma membrane, nucleus, mitochondria, Golgi apparatus, lysosomes, vesicles, and endoplasmic reticulum

A

Plasma membrane:

Nucleus:

Mitochondria:

Golgi apparatus:

Lysosomes:

Vesicles:

Endoplasmic reticulum:

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50
Q

State the function of a palisade mesophyll cell

A
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51
Q

Draw a labeled diagram of a palisade cell from the leaf mesophyll

A
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52
Q

Describe the function of the following structures in a palisade mesophyll cell: cell wall, plasma membrane, chloroplasts, vacuole, nucleus, and mitochondria

A

Cell wall: supports and protects the cell

Plasma membrane: controls entry and exit of substances

Chloroplasts: carries out photosynthesis

Vacuole: transport molecules

Nuclear membrane: protects chromosomes

Mitochondria: synthesizes ATP

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53
Q

Explain why the ultrastructure of prokaryotic cells must be based on electron micrographs

A

They are too small to be seen well enough with a light microscope.

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54
Q

Draw the ultrastructure of E. coli as seen on an electron micrograph

A
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55
Q

Draw and label a diagram the ultrastructure of a generic animal cell

A
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56
Q

Draw and label a diagram of the ultrastructure of a generic plant cell

A
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57
Q

Explain why cells with different functions will have different structures

A

Different structures are specialized for cell functions. Muscle cells will for example have more mitochondria, as these synthesize large amounts of ATP.

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58
Q

Identify ultrastructures visible in a micrograph of a eukaryotic cell

A

Look for rER, mitochondrion, golgi apparatus, nucleus

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59
Q

Given a micrograph of a cell, deduce the function of the cell based on the structure present,

A
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60
Q

With reference to a specific example, explain how an improvement in apparatus allowed for greater understanding of cell structure

A

The structure of membranes:
- First, Davson and Danielli proposed that the membrane of cells are composed of phospholipids and proteins in a sandwich-like structure. This was during the 1930s, and in the 1950s, the first high magnification electron micrographs were produced. This led to the Singer-Nicolson model, which proposed that the membrane was more fluid then the first model proposed.

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61
Q

Draw a simplified diagram of the structure of the phospholipid, including a phosphate-glycerol head and two fatty acid tails

A
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62
Q

Define “hydrophilic” and “hydrophobic”

A

Hydrophilic: water attracting

Hydrophobic: water repelling

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63
Q

Define “amphipathic” and outline the amphipathic properties of phospholipids

A

Having both hydrophobic and hydrophilic properties. A phospholipid has a hydrophilic head and hydrophilic tails.

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64
Q

Explain why phospholipids form bilayers in water, with reference to hydrophilic heads and two hydrophobic hydrocarbon tails

A

Phospholipids form bilayers in water to protect the water-hating tails. The hydrophilic heads are facing outwards, whilst the hydrophobic tails face inwards.

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65
Q

State the primary function of the cell membrane

A
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66
Q

Contrast the structure of integral and peripheral proteins

A

Integral proteins:
- Embedded into the phospholipid bilayer.

Peripheral proteins:
- Attached to an outer surface of the membrane.

67
Q

List at least four functions (with examples) of membrane bound proteins

A
68
Q

Contrast the two types of transport proteins: pumps and channels

A

Pumps: active transport

Channels: facilitated diffusion / passive transport

69
Q

Identify the structure of cholesterol in molecular diagrams

A
70
Q

Describe the structural placement of cholesterol within the cell membrane

A
71
Q

Outline how temperature affects cell membrane fluidity

A
72
Q

Describe the function of cholesterol molecules in the cell membrane

A
73
Q

Draw and label the structure of membranes. Include: phospholipid bilayer, integral proteins spanning the membrane, peripheral proteins on membrane surface, protein channels with a pore, glycoproteins with a carbohydrate side chain, cholesterol between phospholipids in the hydrophobic region

A
74
Q

Describe the observations and conclusions drawn by Davson and Danielli in discovering the structure of cell membranes

A
75
Q

Describe conclusions about cell membrane structure drawn from freeze-etched electron micrograph images of the cell membrane

A
76
Q

Describe conclusions about cell membrane structure drawn from cell fusion experiments

A
77
Q

Compare the Davson-Danielli model of membrane structure with the Singer-Nicolson model

A
78
Q

Explain what models are and their purposes in science

A
79
Q

Explain why models have limitations

A
80
Q

Summarize why scientific models change over time

A
81
Q

Describe why the understanding of cell membrane structure has changed over time

A
82
Q

Describe “simple diffusion”

A
83
Q

Explain two examples of simple diffusion of molecules into and out of cells

A
84
Q

Outline factors that regulate the rate of diffusion

A
85
Q

Describe “facilitated diffusion”

A
86
Q

Describe one example of facilitated diffusion through a protein channel

A
87
Q

Define “osmosis”

A
88
Q

Predict the direction of water movement based upon differences in solute concentration

A
89
Q

Compare active transport and passive transport

A
90
Q

Explain one example of active transport of molecules into and out of cells through protein pumps

A
91
Q

Describe the fluid properties of the cell membrane and vesicles

A
92
Q

Explain vesicle formation via endocytosis

A
93
Q

Outline two examples of materials brought into the cell via endocytosis

A
94
Q

Explain release of materials from cells via exocytosis

A
95
Q

Outline two examples of materials released from a cell via exocytosis

A
96
Q

List two reasons for vesicle movement

A
97
Q

Outline how phospholipids and membrane bound proteins and synthesized and transported to the cell membrane

A
98
Q

Describe how organelles of the endomembrane system function together to produce and secrete proteins (rough ER, smooth ER, Golgi apparatus, vesicles)

A
99
Q

Describe the structure of the sodium-potassium pump

A
100
Q

Describe the role of the sodium-potassium pump in maintaining neuronal resting potential

A
101
Q

Outline the six steps of sodium-potassium pump action

A
102
Q

Describe the structure of the potassium channel

A
103
Q

Describe the mechanism of potassium movement through the potassium channel

A
104
Q

Explain the specificity of the potassium channel

A
105
Q

Describe the action of the “voltage gate” of the potassium channel

A
106
Q

Explain what happens to cells when placed in solutions of the same osmolarity, higher osmolarity, and lower osmolarity

A
107
Q

Outline the use of normal saline in medical procedures

A
108
Q

Define “osmolarity”, “isotonic”, “hypotonic”, and “hypertonic”

A
109
Q

Calculate the percentage change between measurement values

A
110
Q

Determine osmolarity of a sample given changes in mass when placed in solutions of various tonicities

A
111
Q

Define “quantitative” and “qualitative”

A
112
Q

Determine measurement uncertainty of a measurement tool

A
113
Q

Explain the need for repeated measurements in experimental design

A
114
Q

Explain the need to control variables in experimental design

A
115
Q

Discuss implications of all cells formed from preexisting cells

A
116
Q

Outline the four processes needed for the spontaneous origin of cells on Earth

A
117
Q

Outline the experiments of Miller and Urey into the origin of organic compounds

A
118
Q

Define “polymerization”, “monomer”, and “polymer”

A
119
Q

Outline two properties of RNA that would have allowed it to play a role in the origin of life

A
120
Q

State the endosymbiosis theory

A
120
Q

Outline why fatty acids were likely the primary component of the membrane of early cells

A
121
Q

Outline the major events in the origin of eukaryotic cells

A
122
Q

Describe the evidence for the endosymbiotic theory

A
123
Q

Define “spontaneous generation”

A
124
Q

Describe Pasterur’s experiments about spontaneous generation

A
125
Q

Explain why Pasteur’s experiments did not support the idea of spontaneous generation

A
126
Q

Outline historical thinking about spontaneous generation

A
127
Q

Summarize the Redi experiment

A
128
Q

Summarize the Spallanzani experiment

A
129
Q

List reasons why biologists now universally accept that cells only come from preexisting cells

A
130
Q

State the function of mitosis

A
131
Q

List processes which involve mitosis

A
132
Q

State the names of the four phases of mitosis

A

PROPHASE:
- Chromosomes condense
- The two centrosomes move towards opposite poles
- Spindle fibres emerge from the centrosomes
- Nuclear envelope breaks down
- Nucleolus disappears

METAPHASE:
- Centrosomes reach opposite poles
- Spindle fibres continue extending from centrosomes
- Chromosomes line up at equator
- Spindle fibres reach the chromosomes and attach to the centromeres (each sister chromatid is attached to a spindle fibre originating from opposite poles

ANAPHASE:
- Sister chromatids separate at the centromere
- Spindle fibres begin to shorten
- Separated sister chromatids (now called chromosomes) are pulled to opposite poles.
- Cell begins to divide

TELOPHASE:
- Chromosomes arrive at opposite poles and begin to decondense
- Nuclear envelopes begin to reform around chromosomes
- Spindle fibres break down
- New nucleoli form within each nucleus

133
Q

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

A
134
Q

Outline four events that occur during prophase

A
135
Q

Outline the process of metaphase

A
136
Q

Outline the process of anaphase

A
137
Q

Outline four events that occur during telophase

A
138
Q

Describe the structure of a replicated chromosome, include the centromere and sister chromatids

A
139
Q

Explain why chromosomes must condense during mitosis

A
140
Q

Define “cytokineses”

A
141
Q

State the difference between mitosis and cytokinesis

A
142
Q

Contrast cytokinesis in plant and animal cells

A
143
Q

Describe the formation of the cleavage furrow in animal cell cytokineses

A
144
Q

Describe the formation of the middle lamella and cell wall in plant cell cytokinesis

A
145
Q

List examples of metabolic reactions occurring during cell interphase

A
146
Q

Outline events og G1, S, G2, and G0 phases

A
147
Q

Explain the role of cyclin and cyclin-CDK complexes in controlling the cell cycle

A
148
Q

State the role of cyclins D, B, A, and E in the cell cycle

A
149
Q

Define “tumor”, “benign”, “malignant”, “metastasis”, “cancer”, “mutagen”, and “carcinogen”

A

Tumor:

Benign:

Malignant:

Metastasis:

Cancer:

Mutagen:

Carcinogen:

150
Q

Describe why mutagens are not necessarily carcinogens

A
151
Q

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

A
152
Q

Explain the relationship between oncogenes, tumor suppressor genes, and cancer

A
153
Q

Explain the use of correlations to determine the relationship between two variables

A
154
Q

Explain why the existence of a correlation does not necessitate a causal relationship between the two variables

A
155
Q

Calculate a correlation coefficient using Pearson’s R

A
156
Q

Determine if a correlation coefficient value is significant

A
157
Q

Define significant as related to the relationship between two variables

A
158
Q

Use of epidemiological case study information to outline the relationships between smoking and cancer

A
159
Q

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

A
160
Q

State the formula for calculation of a mitotic index

A
161
Q

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

A
162
Q

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

A
163
Q

Outline the discovery of cycling including the role of serendipity

A