Mitotic Cell Cycle & Stem Cells Flashcards

(28 cards)

1
Q

Events of mitotic cell cycle

A

Interphase: G1, S, G2,
Mitosis

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2
Q

What occurs during interphase ?

A

G1: cell synthesis organelles such as mitochondria and ribosomes. Manufacture proteins. Builds up large store of energy.

S: DNA replication. Centrosome duplicated

G2: cell continues to store energy and manufacture organelles and proteins

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3
Q

What is a centrosome ?

A

Nonmembranous organelles found only in animal cell.
Function as the microtubule organising centre (MTOC) to organise th cels microtubule through the cell cycle.

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4
Q

What are centrioles ?

A

Centrioles is where microtubule extend from, forming spindle fibres.
Some spindle fibres attach to the kinetochore of the chromosome forming kinetochore microtubules.

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5
Q

What protein makes up spindle fibres ?

A

Tubulin

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6
Q

Outline prophase

A

Behaviour of chromosomes:
- Chromatin condense into chromsomes (making it visible under light microscope)
- Centrosome moves to opposite ends of the cell developing a pair of centrioles.

Behaviours of nuclear envelope:
- Nucleolus disappears
- nuclear envelope disintegrates

Behaviour of centrioles:
- microtubules extend from centrioles to form spindle fibres
- kinetochore assembles at centromere of chromosome
- some spindle fibres attach to kinetochore

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7
Q

Outline metaphase

A

Behaviour of chromosomes
- chromosomes align on the metaphase plate

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8
Q

Outline anaphase

A

Behaviour of chromsome
- Centrosome of each chromosome divides and two sister chromatids separates
- daughter chromosome formed
- daughter chromosome move to opposite poles of the spindle as kinetochore microtubules shorten

Cell elongates as the non kinetochore microtubules lengthen

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8
Q

Outline telophase

A

Behaviour of chromsomes;
- chromosome uncoil into chromatin

Behaviours of centrioles:
Spindle fibres disintegrate

Behaviour of nuclear ecnelope:
- reforms around chromosome at each pole
- nucleolus reappears

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9
Q
A
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10
Q

Outline cytokinesis in animal cells

A
  • cleavage furrow developed in cell membrane, eventually joining up and separating 2 daughter nuclei
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11
Q

Outline cytokinesis in plant cells

A
  • Series of golgi vesicles line in middle of parent cell and fuse to firm cell plate.
  • Content of golgi vesicles contributes to the cell wall. Membrane of golgi vesicles form cell membrane.
  • cell plate fuse with parent cell separating 2 daughter nuclei
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12
Q

Significance of Mitosis

A

Ensures 2 daughter nuclei formed contained genetically identical sets of chromosomes so that daughter cell is genetically identical to parent cell after cytokinesis.

Maintains genetic stability
- growth, single cell to multicellular organism
- repair
- asexual reproduction

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13
Q

Whatn are the Cell cycle checkpoints

A

G1
G2
M

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14
Q

What is Checked at G1 checkpoint ?

A

Size of cell
Nutrients availability
DNA integrity
Appropriate growth signals

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15
Q

What is checked at G2 checkpoint ?

A

DNA integrity and replication

DNA damage —> stall for repair
DNA damage beyond repair —> p53 triggers cell to undergo apoptosis

16
Q

What is called at M checkpoint ?

A

All chromsomes attached to spindle fibres
Proper tension on paired kinetochores

17
Q

What are the unique features of stem cells ?

A
  1. unspecialised cells
  2. able to differentiate into various cell types under certain conditions to form
    specialised cells
  3. capable of dividing and renewing themselves (self-renewal) for long periods via
    mitotic divisions
18
Q

What is differentiation of stem cells ?

A

Stem cells do not have tissue-specific strictures that allow it to perform superfic functions.

19
Q

What are levels of potency ?

A

Totipotent: diff to any cell type for form a whole organism

Pluripotent: diff into almost any cell type to form any organ

Multipotent: give rise to limited range of cellls and tissues appropriate to their location

Unipotent: give rise to only one type of cell

20
Q

Example of diff potency level

A

Toti: zygotic stem cells

Pluri: embryonic stem cells

Multi: adult stem cells

21
Q

Sugggest how a cell differentiates to firm a specialised cell

A
  1. Receives signal to switch on certain sets of genes ad switch off other sets of gens
  2. Result in different proteins being produced giving rise to different tissue-specific structures
22
Q

Ethical implications of stem cells research

A
  1. Human embryonic stem cellls require destruction of the embryo. Some believe that an embryo has the same moral status as live-born human, which interest ad rights that must be respected. Hence derstruction of the embryo is tantamount to murder
  2. Donors of the coyotes or embryos may not uave consented for theirs to be used for research
  3. Underlying medical completions and risks exist regardless whether donors are fully informed of them
23
Q

What are the major sources of blood stem cells

A

Bone marrow
Umbilical cord

24
Pros and cons of using umbilical cord stem cells for treating diseases in the same individual
Pro: 1. No foreign antigens on cell membrane hence recipients immune system will not reject 2. Can be converted into specialised cells to treats specific diseases Cons: 1. Storage capacity limited and high costs involved 2. Freezer failure cause ells to be damaged or mutated
25
Why do stem cells harvested from burn patients skin need to be treated with chemicals to stimulate proliferation
1. When stem cells are removed from skin, there are no natural growth hormones to stimulate cell division. 2. Addition of chemicals is necessary to stimulate cell division by binding to cell receptors and stimulating cell division
26
Why is it important that scientist ensure high telomerase activities in the iPS cells ?
1. iPS cells need to undergo continuous cell division 2. Telomerase must be present to elongate the telomeres which are shortened after every round of cell division 3. This maintains telomere length to prevent loss of genes through erosion at chromosomal ends
27
Describe role of centromeres:
1. Attach sister chromatids together 2. Site of kinetichore assembly, allowing spidle fibres to attach 3. Alllow separation of homologous chromsomes or sister chromatids