questions of learning and memory Flashcards

1
Q

how do third order neurones respond selectively to odours

A

sample second order neurones and respond

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2
Q

what are kenyon cells

A
  • in mushroom body
  • each cell only responds to few odours
  • receive input from multiple projection neurons and require multiple simultaneous inputs to fire (thus fire very selectively)
  • sample small regions in PN “coding space”
    recieve dopaminergic transmission and edit behavioural output
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3
Q

how is the dense combinational code turned into a sparse selective code for odour recognition

A

kenyon cells receive input from multiple projection neurons and require multiple simultaneous inputs to fire selectively

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4
Q

what is the GAL4/UAS system

A
  • binary expression system
  • allows us to artificially express arbitrary transgenes in specific cells
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5
Q

what is GAL4

A

yeast transcription factor
- insert into genome and control under enhancer which puts GAL4 into certain cells of body → cellular specificity
- TF binds to DNA sequence = upstream activating sequence → recruits TF to initiate transcription downstream of UAS

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6
Q

what happens if you split the GAL4 system

A

split into 2 separate proteins
1 half = DNA binding domain = binds to uas
1 half = activation domain = recruits tf
only in overlap where both halves of GAL4 expression = zip together and express UAS transgene

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7
Q

what is the mushroom body

A
  • structure in fly brain = olfactory activity
  • forms circuit for associative memory
  • encode dopaminergic neurones = form different compartments of axonal lobe
  • based on punishment = less = approach, more = avoid
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8
Q

how are kenyon cells organised in mushroom body

A
  • cell axons are subdivided into compartments by innervation of mushroom body output neurons (MBONs)
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9
Q

what are MBONS

A

mushroom body output neurons
determines value = good or bad experience
Some MBONs lead to approach/avoidance behaviour when activated optogenetically
activation/deactivation leads to approach and avoidance behaviour

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10
Q

role of DANS

A

dopamine activated neurones
can entrain aversive or appetitive memory

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11
Q

what order are response and conditioned stimulus in for correct conditioning

A

odour -> punishment = avoid
punishment -> odour = relief = approach

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12
Q

how do flies know whether CS or response comes first

A
  1. electrically stim kenyon cells
  2. recording MBON
  3. artificially stim dopa neurone using art receptor + ligand
  4. measure response of MBON to kenyon cell = measures synaptic strength
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13
Q

which type of cells in MB are linked to odour detection

A

kenyon

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14
Q

which type of cells in MB are linked to reward detection

A

DANS

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15
Q

what happens when kenyon cells and DANS are activated at same time

A

activation at same time = synaptic depression

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16
Q

difference between dopr1 and dopr2

A
  • signal through different gpcr pathways
  • 1 = Gs → AC → cAMP
  • 2 = Gq → PLC → IP3 → Ca2+ release
17
Q

how is ER Ca release sensitive to order?

A
  • IP3 receptor = sensitive to Ca
  • Ca = signal for when kenyon cell is active
  • IP3 → Ca = open
  • Ca → IP3 = not open
  • 2 possible binding sites for Ca
  • if no ip3 = only red binding site available = locks receptor into conformation
  • no ca = green is open → channel opens
18
Q

what happens if ca binds to ER channel first

A

ca → locks → no ip3

19
Q

what happens if ip3 binds to ER channel first

A

ip3 → ca binds → open

20
Q

do we have similar odour detection structure as drosophila

A
  • similar structure in cerebellum
    • mossy fibres → more neurones (granule) → purkinje cells
    • synapse between gran and purkinje fibres is modified by climbing fibres
21
Q

what carries error signals

A

climbing fibres modify sinapse between granular and purkinje fibres