Topic E1 Flashcards

1
Q

What is pattern formation:

A
  • The process in which there is a complex organisation of cell fates in space and time.
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2
Q

What 2 things does pattern formation require?

A
  1. Differential gene expression

2. Signalling between cells (signalling molecules)

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3
Q

What is cell fate?

A
  • The developmental destination of a cell if left undisturbed in the embryo
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4
Q

What are the two main processes in determining cell fate?

A
  1. Cell fate commitment
    a. specification
    b. determination
  2. Differentiation
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5
Q

What is cell fate restriction?

A
  • When the fate of the cell becomes restricted
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6
Q

Describe the two factors within cell fate commitment:

A

a. Specification: the fate of the cell is biased but not irreversible. The cell is capable of differentiating autonomously into its specified form in a dish only- if the cell is transplanted to another part of the embryo it can change fate (as it is exposed to different factors)
b. Determination: the fate of the cell cannot be reversed. The cell will differentiate autonomously according to its determined cell fate both in a dish and if placed in another region of the organism.

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7
Q

What is the process of differentiation?

A
  • The expression of developmental fate in which the cell adopts its final phenotype
  • Differentiated cells express genes to form proteins to allow them to carry out their function and other exit the cell cycle
  • Differentiated is usually a irreversible process (unless forced e.g. iPS cells)
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8
Q

What is cell fate restriction governed by?

A
  1. The cells genome (gene expression)
  2. The cell’s history (the factors it has been exposed to- chromatin marks)
  3. Interaction with its neighbouring cells
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9
Q

What is the difference between epithelial and mesenchymal cells?

A

Epithelial cells: are tightly connected to eachother in sheets/tubes, sit on a basement membrane, cannot move independently, are polarised and display epithelial marker genes e.g. cytokeratin

Mesenchymal cells: are not joined to other cells and are free to move independently around the ECM. They are not poalrised and they express mesenchymal marker genes e.g. Vimettin

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10
Q

What is a fate map?

A
  • A diagram that maps adult tissues or structures to the regions of the embryo that gave rise to that tissue/structure
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11
Q

What are the advantages and disadvantages of invertebrate models?

A

Advantages:

  • Easy to keep
  • Rapid life cycle
  • Fate of most/all cells known

Disadvantages:
- many aspects of development and anatomy are not conserved with humans

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12
Q

What are the advantages and disadvantages of lower vertebrate models? e.g. zebrafish

A

Advantages:

  • Easy to keep
  • Easy to manipulate and access (embryo develops outside maternal body)

Disadvantages:
- Distant from humans- some features not shared

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13
Q

What are the advantages and disadvantages of avian models? e.g. chickens

A

Advantages:

  • A higher vertebrate (closer to humans)
  • Easy to obtain and study (embryo develops in ovo)

Disadvantages:

  • longer life cycle
  • transgenic strategies lag behind those in mice
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14
Q

What are the advantages and disadvantages of mouse models?

A

Advantages:

  • Mouse is a mammal- many of the same organ systems and diseases as humans
  • Advanced transgenics available

Disadvantages:

  • Embryos develop in utero (access is difficult)
  • models can sometimes have different phenotypes as humans to disease
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15
Q

Describe the difference between descriptive studies and manipulative studies:

A

Descriptive studies:
- Observe and study the development of an organism e.g. fate mapping, histology studies etc.

Manipulative studies:
- Altering a system and observing the effects

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16
Q

What is differential gene expression

A
  • Genes being turned on or off in certain cells of the embryo
  • Drives pattern development and differentiation of cells
  • Caused by an interaction between transcription factors and signalling between cells
17
Q

What are transcription factor genes and what is an example?

A
  • Transcription factor genes are genes that code from DNA binding proteins that have transactivation domains that bind to DNA to repress or activate genes
    e. g. homeobox genes
18
Q

What are HOX transcription factor genes?

A
  • Hox genes are clusters of homeobox genes (transcription factors) (4 clusters in mammals; 1 cluster in flies)
  • HOX genes are paralogues and therefore exhibit some functional redundancy
  • Play a key role in patterning of head to tail segmentation of the body
19
Q

What can mutations in HOX genes cause?

A
  • Mutations in HOX genes cause homeotic transformations e.g. one body part takes on features of a more anterior body part e.g. L1 comes to resemble a thoracic vertebrae
20
Q

Role of PAX transcription factors:

A
  • Key role in development of nervous system
21
Q

Role of SOX transcription factors:

A
  • Activated by SRY gene; binds and activates genes important in determining male sex