Chapter 7 : The Cell Cycle and Cell Growth and Differentiation Flashcards

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1
Q

The Cell Cycle Phases

A
- Inter-phase 
G1 - primary growth
S - synthesis = genome replicated 
G2 - secondary growth 
M - mitosis 
- Prophase 
- Metaphase 
- Anaphase 
- Telophase 
C - cytokinesis
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2
Q

Inter-phase

A
  • Lots of activity happening in this phase
  • Cells prepare for mitosis
  • Protein synthesis
  • DNA synthesis
  • Replication of other cellular structures
  • Longest part of cell cycle
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3
Q

The phase of mitosis in eukaryotic cells

A
  • Division of nucleus into 2 nuclei
  • Each nuclei has the same number of chromosomes
  • Occurs in all somatic (body) cells
  • Each new daughter cell has a nucleus complete set of chromosomes
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4
Q

Phases and what occurs in order

A

Prophase :

  • Separates duplicated genetic material carried in -
  • nucleus of a parent cell into 2 identical daughter cells
  • Chromosomes coil up
  • Nuclear envelope disappears
  • Spindle fibres form

Metaphase :

  • Chromosomes line up in middle of the cell
  • Spindle fibres connect to chromosomes

Anaphase :

  • Chromosome copies divide
  • Spindle fibres pull chromosomes to opposite poles

Telophase :

  • Chromosomes uncoil
  • Nuclear envelopes form
  • 2 new nuclei are formed
  • Spindle fibres disappear

Cytokinesis in eukaryotic cells
Cytokinesis :
- Division of the rest of the cell after nucleus divides
- Cytoplasm in animal cells pinch in
- Cell plate forms in plant cells
- After mitosis and cytokinesis the cell returns to interphase

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5
Q

Binary fission / process

A

The division of a cell into 2 without mitosis; the process by which a prokaryotic cell splits to form 2 daughter cells.

Similar to mitosis but occurs in prokaryotic cells as there is only one chromosome and no centromere.

Process includes:

  • DNA replication
  • Chromosome segregation
  • Cytokinesis
  • Produces 2 daughter cells with identical DNA to parent cell

Occurs in eukaryotic cells but only for producing:

  • Mitochondria
  • Chloroplasts
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6
Q

Disruption of cell cycle regulation

Apoptosis :

A
  • Programmed cell death
  • Normal part of an organism’s function
  • Important for development, shaping organs and tissues and removing cells that are old or no longer needed
  • Almost all multicellular organisms have cells that are born to die
  • Failure in Apoptosis can result in many problems, ranging from development defects to cancer
  • Formation of cancer happens when apoptosis is avoided and cells do not die as they should
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7
Q

Example of apoptosis :

A
  • Enables tadpole to lose its tail as it becomes a frog

- Allows human embryo to lose the webbing between its fingers and toes

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8
Q

Cell cycle checkpoints :

A

G0 - resting state

  • Doesn’t divide or preparing for division
  • Occurs outside of cell cycle
  • Damaged cells are located here
G1 checkpoint :
Check for:
- Cell size 
- Nutrients 
- Growth factors 
- DNA damage 

G2 checkpoint
Check for:
- Cell size
- DNA replication

Mitosis checkpoint - spindle assembly checkpoint
Check for:
- Chromosome attachment to spindle

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9
Q

Action of Mutagens in cell cycle

A

Chemical mutagens :

  • Ability to interfere with DNA
  • Interrupts its structure, sequence and replication

Physical mutagens :

  • Ultraviolet light, X rays and nuclear radiation
  • When UV light is absorbed DNA is damaged
  • Mutations in tumor suppressor gene p53 play a critical - role in development of precancerous lesions and have - been implicated in all types of skin cancer

Biological mutagens :

  • Viruses - take over cells
  • Impair cell cycle regulation - results in cancer
  • Cause uncontrolled cell growth
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10
Q

Types of stem cells

A

Stem cells :
Stem cells are undifferentiated cells that have the potential to replicate and to develop into many different kinds of cell

Pluripotent stem cells :
- Capable of giving rise to most but not all tissues of an organism
Example = the inner cell mass

Multipotent stem cells :
Able to give rise to cells that have a specific function
Example = blood stem cells

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11
Q

Adult stem cells

A

Multipotent :
- Form cells of different kinds of tissue
Advantage = patient’s own cells could be used for treatment
- Risks are lower because patient’s immune system won’t reject its own cells
Disadvantage = are pre-specialised
- Blood stem cells only make blood
- Brain stem cells only make brain cells
- Can replace dead or damaged cells
- Bone marrow has multipotent stem cells that give rise - to all cells of the blood

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12
Q

Embryonic stem cells

A
  • Cultured from frozen embryos that are obtained from in-vitro fertilisation clinics (IVF clinics)
  • Ethical issues related to the use of these cells
    Obtaining them requires destruction of an embryo
  • Governments have strict regulations in place for controlling this type of technology
    Advantage = pluripotent
  • Can become any of the cell types of the body
  • More versatile than adult stem cells
    Disadvantage = come from embryo that’s not derived from patient’s own cells
  • Patients immune system may reject them
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13
Q

Sources of stem cells for research and therapy - types

Umbilical cord blood and placental stem cells

A
  • Present in blood in umbilical cord and placenta
  • Once baby is born cells can be extracted from
  • discarded tissue and used for the benefit of children and adults who suffer from bone marrow or blood diseases
  • Stored in case baby requires replacement tissues or organs later in life
  • Obtained after baby is born and there’s no harm to mother or baby
  • Multipotent
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14
Q

Fission

A
  • Single celled eukaryotic or prokaryotic organisms
  • Divide into 2 new organisms
  • Each is an exact copy of parent cell
  • Nucleus is replicated and cytoplasm splits to form 2 new daughter cells
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15
Q

Budding

A
  • New organism is grown on the outside of the parent organism
  • Eventually detaches as its own complete organism
  • Hydra, yeast
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16
Q

Vegetable propagation

A
  • Only in plants
  • Plants grow from cuttings
  • New plant forms through mitosis - genetically identical to parent plant
  • Plant grows - cells undergo differentiation and become specialised
  • Used for agricultural purposes to replicate qualities in plants
17
Q

Spore formation

A
  • 0Spores are hardy self contained capsules - single celled structures
  • Contains exact copy of DNA of the parent
  • Can form an entire new organism in right conditions
  • Spores can survive for hundreds of years and still germinate
  • Prokaryotes, fungi, plants
18
Q

Biological advantages of asexual reproduction

A
  • Does not require a mate
  • Uses less energy
  • Offspring identical to parent
  • Many offspring produced
19
Q

Disadvantages of asexual reproduction in certain situations

A
  • Offspring are genetically identical
  • Parental care of offspring is limited or none
  • Large numbers of offspring may compete for limited resources
  • Lack of genetic diversity
20
Q

Biological cloning - embryo splitting and nuclear transfer

A

Embryo splitting

  • Egg cells (from donor female) are fertilised with male sperm in tissue culture
  • Resulting dividing cells are split and coated to promote division
  • Cells form a blastocyst - implanted into surrogate mother
  • Offspring are twins but born to different mothers
21
Q

Nuclear transfer

A
  • Process made famous in 1996 - Dolly the sheep
  • Nucleus of adult sheep’s mammary cell taken and inserted into ovum - which has nucleus removed
  • Resulting blastocyst transferred to surrogate mother
  • Method has very low success rate for live births
22
Q

Issues of cloning

A

If we’re using adult cells and putting them into eggs to form blastocyst

  • Gamete cells - stem cells in embryo that allows offspring to survive.
  • Not successful as cells are different and the adult cells aren’t stem cells
  • Can’t use adult cells for cloning but you may be able to use adult stem cells instead
  • It is failing because they aren’t using stem cells
23
Q

Application of cloning - agriculture and horticulture

A

Agriculture :

  • Cloning for plants
  • Used to save rare species of plants

Horticulture :
- Common for farm animals for food production

24
Q

SEXUAL REPRODUCTION

A

Combining the ova (egg) and sperm (sex cells/germ cells) of genetically different parents parents, the offspring have a unique mix of genes from the parents.

25
Q

Meiosis

A

Two-phase type of cellular division in which the chromosome number of a cell is halved to the haploid number; meiosis is the basis of gamete formation.
The way the sperm and ova (egg) are formed is through meiosis.

26
Q

MEIOSIS I - Prophase 1

A

Interphase :
Replicating DNA

Prophase I :

  • Chromosomes condense
  • Nucleolus disappears
  • Spindle forms with centrioles (if present) at opposite ends
  • Homologous chromosomes lie side by side - synapsis
  • Pair of homologous chromosomes - maternal and paternal - called bivalent
  • Homologous chromosomes coil around each other immediately
  • Move slightly apart but chromatids remain in contact at certain points - chiasmata
  • At chiasmata chromatids may break and rejoin sometimes rejoining to other chromatids - crossing over
  • Crossing over - results in swapping of parts of DNA along with chromatids
  • Sometimes chromatids rejoin back to same chromatids with no crossing over - have same DNA sequences as before
  • Offspring with different DNA from that in their parents following crossing over - recombinants
  • Crossing over - production of gametes with new parental combinations of DNA and is an important source of genetic variation
27
Q

Meiosis I - Prophase 1

A

Interphase
Replicating DNA

Prophase I :

  • Chromosomes condense
  • Nucleolus disappears
  • Spindle forms with centrioles (if present) at opposite ends
  • Homologous chromosomes lie side by side - synapsis
  • Pair of homologous chromosomes - maternal and paternal - called bivalent
  • Homologous chromosomes coil around each other immediately
  • Move slightly apart but chromatids remain in contact at certain points - chiasmata
  • At chiasmata chromatids may break and rejoin sometimes rejoining to other chromatids - crossing over
  • Crossing over - results in swapping of parts of DNA along with chromatids
  • Sometimes chromatids rejoin back to same chromatids with no crossing over - have same DNA sequences as before
  • Offspring with different DNA from that in their parents following crossing over - recombinants
  • Crossing over - production of gametes with new parental combinations of DNA and is an important source of genetic variation
28
Q

Meiosis I - Metaphase I

A
  • Nuclear envelope breaks down
  • Homologous chromosomes move together to equator of spindle
  • Spindle fibres attach to centromere of each homologous pair
29
Q

Meiosis I - Anaphase I

A

Anaphase I
- Spindle fibres retract towards the poles
Pulling maternal and paternal chromosomes of homologous pairs towards opposite poles of the spindle
- Separation or disjunction of each pair of homologous chromosome occurs independently of other - chromosome pairs

30
Q

Meiosis II - Interphase II

A
  • Brief interphase occurs at the end of meiosis I

- DNA does not duplicate during this interphase

31
Q

Meiosis II - Prophase II

A

Prophase II

New spindle forms at the right angles to the first one

32
Q

Meiosis II - Metaphase II

A

Metaphase II

  • Chromosomes move to equator of spindle
  • Spindle fibres attach to centromere of each chromosome
33
Q

Meiosis II - Anaphase II

A

Anaphase II

  • Spindle fibres retract towards each pole
  • Chromatids separate and move apart from each other
  • Chromatids become the chromosome of daughter cells
34
Q

Meiosis II - Telophase II

A

Telophase II

  • Spindle apparatus disappears
  • Chromosome decondense to thread like form
  • New nuclear envelopes and nucleoli form
35
Q

Meiosis II - Telophase II

A

Telophase II

  • Spindle apparatus disappears
  • Chromosome de-condense to thread like form
  • New nuclear envelopes and nucleoli form
36
Q

Fertilization

A
  • 2 haploid (n) gametes (from each parent) join to form a diploid (2n) zygote
  • All somatic (body) cells are diploid (2n)
    Means they have n pairs of homologous chromosomes - one originally derived from each parent
  • Zygote formed has double the amount of DNA of the gamete
  • Meiosis halves the amount of DNA
  • Fertilisation restores the amount of DNA to required amount for that species
  • Human gametes produced by meiosis contain 23 chromosomes
  • Fertilisation restores number of chromosomes to 46 (23+23=46) = chromosome number in somatic cells
37
Q

Chromosomes and variation

A
  • Number of possible combinations that can occur = 2n (n is the number of haploid chromosomes)
  • Humans have 2^23 possible combinations which is almost 10 million
  • Homologous chromosomes separate and recombine in first division of meiosis, pieces of chromosomes sometimes break and exchange with their homologous pair during crossing over
  • Leads to variations in appearance of offspring
  • Fertilisation provides potential for different combinations of characteristics in offspring because of the chance that particular gametes combine
  • Even though they produce variations in characteristic in sexually reproducing organisms they don’t make new DNA
  • Existing DNA is only reshuffled through different combinations
38
Q

Biological advantages of sexual reproduction

A
  • Gametes with many different combinations of parental chromosomes are possible
  • Offspring are genetically different from parents and from each other
39
Q

Disadvantages of sexual reproduction

A
  • Energy is required to produce organs for sexual reproduction
  • Energy is required to find and attract a male
  • Competition for mates