Development of sense organs Flashcards

1
Q

what are three sensory neuron origins? give examples for each.

A

neural crest - DRG
neural tube - Retina
placodes - olfactory epithelium and some cranial nerves e.g V

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

in c.elegans what do the mechonoreceptors respond to?

A

ranges from gentle body touch to harsh body touch.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what happens to the Q-cell?

A
  • Q-cell divides to produce Q1a and Q1p

- these then divide and one of the daughter cells disappear

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what does Q1p give rise to? what does Q1a give rise to?

A

Q1p gives rise to gentle body touch cell and an interneuron

g1a gives rise to another sensory cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

where is UNC-86 turned on in? what does loss of UNC-86 lead to?

A

UNC-86 turned on only in Q1p
loss of UNC-86 gives loss of touch cell
the cell that should have been Q1p just turns into the mother cell again, this repeats.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

what happens when the MEC-3 protein is lost?

A

the touch cell is transformed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what induces MEC-3 what does this lead to?

A

UNC-86 protein induces MEC-3, these then combine to induce a touch cell specific genes that are involved

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what kind of differentiation does this UNC-86 and MEC-3 form?

A

lineage-dependant differentiation, like an intrinsic blueprint

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

where are drosophila mechonoreceptors derived from?

A

sensory organ precursers

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what gene does SOPs for chordotonal organs express?

A

atonal

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what gene does SOPs for external receptors express?

A

ct

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what happens to numb distribution?

A

it is asymettrically distributed between sp11b and sp11a which are the first division daughter cells.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what does numb do? what is this required for?

A

inhibits the Notch pathway, low NOTCH activity is required for neural fate.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what does one daughter cell that’s going down the neural fate do to the other daughter cell?

A

it inhibits the other daughter cell from going down the neural fate.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what kind of development is the pathway that includes notch and numb?

A

to some extent is can be seen as lineage independant however not completely as there’s ability for plasticity due to cell-cell interactions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what does the drosophilla eye consist of?

A

around 800 ommatidia
8 photoreceptors, R1- R8
and 12 accessory cells

17
Q

what is required for ommadidia formation?
how is this activated?
what does this then activate?

A

Atonal, R8 and Hh are required
atonal is activated in R8 by posterior tip Hh
this activates Notch and delta pathways which produce spaced R8 cells

18
Q

what does subsequent ommatidia development depend on?

A

it depends on cell -cell interactions

19
Q

where is the bridge of sevenless and what does this cause?

A

bridge of sevenless is on R8 and causes R7 to become a photoreceptor and not a cone cell

20
Q

what is development of stereotypy by? whatis this rather than?

A

by competition and rules rather than strict predeterminations

21
Q

in the vertebrate eye:

  • what kind of structure is the retina?
  • what is it derived from?
  • what does is require expression of?
A

it’s a laminar structure
derived from neural and non-neural ectoderm
it requires the expression of Pax-6 (eyeless)

22
Q

how do ventricular progenitors produce types?

A

in sequence

23
Q

are there seperate proginators?

A

no, they can shift their production of one type of neuron to another.

24
Q

what cell types come first in neurogenesis?

A

ganglion cells.

25
Q

what is cell production by the proginator influenced by?

A

the environment?

26
Q

when progenita cells are labelled the 3H-thymadine what can be seen at embryonic 14?
what’s seen postnatally?

A

E14, there’s both rods and RGC however there’s mainly RGCs

postnatally there’s noth Rods and RGCs however there’s more rods

27
Q

if these are mixed together what is seen?

A

have to wait until lecture slide to answer this

28
Q

where does the ear develop from?

A

the otic placode

29
Q

what does the otic placode form into? then?

A

forms into the otic pit and then the otic vesicle (otocyst)

30
Q

where does the VIII ganglion come from?

A

it is placodal, it comes from the otic placode

31
Q

what is hair cell development regulated by?
what cell form with high NOTCH activation?
what cell is formed from low NOTCH activation?
what two things are involved later on in hair cell development?

A

it is regulated by hair-hair interactions
high NOTCH = becomes a supporting cell
low NOTCH = becomes a hair cell
retonoic acid and thyroid hormone are involved later

32
Q

what is altered in human deaf/blindness?

A

Usher Ib myosin VIIa

33
Q

what do Usher Id and If involve?

A

cadherins

34
Q

why are olfactory cells lost regularly? why isn’t this a problem.

A

due to exposure

isn’t a problem because rthere’s progenitor cells in the epithelium ready to make new ones.