7 - Cell Polarity II Flashcards

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1
Q

What hypothesis is the basis of modern day developmental genetics?

A

Cell can generate daughters that are intrinsically different.

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2
Q

What are the 2 main routes in which sister cells can have different fates?

A

1 - The mother cells could divide to generate daughters that have inherited different components.
2 - Daughters could be equal and birth and become different due to exposure to different environmental signals.

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3
Q

What are some important steps in generating polarity and cell fate decisions?

A
  • Establishing the axis of polarity
  • A mitotic spindle positioned along the axis
  • Cell fate determinants distributed differentially to the daughter cells.
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4
Q

What is the role of PAR proteins in cell polarity networks?

A

They form the core.

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5
Q

What is the output of cell polarity networks?

A

One of mutual antagonism with the establishment of opposing and elementary membrane domains.

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6
Q

What happens in the early development of c.elegans?

A

A series of asymmetric cell divisions.

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7
Q

When does polarisation start?

A

When the sperm enters the oocyte.

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8
Q

What does the position of entry of the sperm define?

A

the posterior end of the zygote or the PO cell.

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9
Q

What does the zygote/PO cell do after sperm entry?

A

It divides asymmetrically along the anterior-posterior axis - This produces a large anterior cell (AB) and a smaller posterior cell (P1).

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10
Q

Where did the discovery of PAR genes come from?

A

genetic screening to identify key players in the asymmetric division.

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11
Q

When in symmetry broken in cells?

A

On fertilisation when the sperm delivers the microtubule organising centre (MTOC), which becomes the posterior pole and so defines the axis of polarity.

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12
Q

Why are Par1 and Par2 recruited?

A

To antagonise the anterior Par proteins resulting in the distinct localisations of the par proteins.

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13
Q

What Par proteins are at the anterior cortex?

A

Par3, Par6 and aPkc

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14
Q

What Par proteins are at the posterior cortex?

A

Par1 and Par2

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15
Q

what are neuroblasts?

A

Progenitor cells

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16
Q

Where are neuroblasts found?

A

Within a specific region of an epithelial monolayer called the ventral neuroectoderm.

17
Q

How do the neuroblasts move from their position?

A

They delaminate and undergo repeated rounds of cell division. Which gives rise to a ganglion mother cell (GMC) and a larger atypical daughter cell.

18
Q

What does the ganglion mother cell divide to give rise to?

A

A neuron and a glia cell the apical daughter cell continues to divide.

19
Q

When is polarity established?

A

When the cell is still in the neuroectoderm layer.

20
Q

What happens when the neuroblasts delaminate?

A

Cdc42, Par3 and Par6 are found in a stalk that continues to extend to the epithelium.

21
Q

How does most animal locomotion occur?

A

The cells crawl on the surface of a solid substrate.

22
Q

What are the 3 main activities required for movement?

A

Protrusion, Attachment and Traction.

23
Q

Protrusion is…

A

Pushing out of the plasma membrane in front of the cell.

24
Q

Attachment is…

A

When the actin cytoskeleton in the cell is attached via interacting proteins.

25
Q

Traction is…

A

the bulk of the cell body being drawn forward through a process of contraction.

26
Q

What are filopodia?

A

Micro-spikes which contain a core of actin bundle filaments.

27
Q

What are lamellipodia?

A

Short branch structured actin.

28
Q

What are stress fibres?

A

Bundles of actin filaments involved in the contractility required to move the body of the cell forward.

29
Q

What does cell polarity establishment in cell migration involve?

A

Small Rho GTPases - cCdc42, Rac, Rho.

30
Q

What is chemotaxis?

A

the movement of cells towards or away from a signal such as a diffusible chemical. eg the movement of neutrophil towards the site of bacterial infection.

31
Q

What is the first tissue that emerges during development?

A

Epithelium.

32
Q

Where does the apical side of the epithelium face?

A

The external environs.

33
Q

Where does the basal side of the epithelium face?

A

The basement membrane.

34
Q

what does the polarised cytoskeleton of actin help with?

A

It allows for the apical surface to constrict, which is also important for gastrulation and tubulation.

35
Q

What is epithelial mesenchymal transition (MET)?

A

The rapid loss of epithelial phenotype.

36
Q

What is mesenchymal epithelial transition?

A

the reacquisition of epithelial phenotype.

37
Q

What is epithelial mesenchymal transition important for?

A

Development, it is also important in cancer metastasis